All About Chemistry: ASU’s Offense is Clicking and Ready for the Shortened Season – College Times

By Kendall Rooker

For ASUs new offensive coordinator, Zak Hill, starting the seven-game season on November 7 is a relief.

It is good to be back out at practice and have a future goal, he says. You can feel the energy. Its exciting knowing well get to play. It was frustrating seeing other teams play. Now, for us, we got to stay focused on day to day. It is a daily process.

The offense is clicking in its first few weeks of practice, thanks to the Sun Devils getting in a few spring practices before the COVID-19 pandemic hit.

Hill and Prentice Gill, the assistant recruiting coordinator and wide receiver coach, agree the spring sessions helped young players get a preview of the offense.

The spring practices helped a lot. It helps Jayden, Gill says about quarterback Jayden Daniels.

We need elite QB play as organizing moving pieces around, when 5 (Daniels number) is used to it. When our guys get lost out there, Jayden can move pieces around and help them. If we didnt have it, it would be hard to function right now.

The receiving core for the Sun Devils has improved; it added the freshman pieces it would like to use this season to add depth. Not only are they adding depth, one of the captains is graduate student Frank Darby, who is returning this season. Hes helping incoming freshmen play at the collegiate level.

Frank leads by example, Gill says.

He is an older guy who cares about the positive direction of the team. He is constantly watching other guys and trying to correct different things. It holds him to a high standard. He is getting better himself, and I keep pushing him to not only being a captain but to be our No. 1 guy.

Incoming freshmen include wide receivers Johnny Wilson and LV Bunkley-Shelton.

Johnny and LV are people we need for depth and the playmaking ability; theyre what we needed to push this group. Theyre dynamic in their own ways, Gill says.

The Sun Devils plan to use Wilson in the slot position. At 6-foot-7, 220 pounds, Wilson will create great matchups, Gill says.

When Daniels returned to practice in early October, he worked on offense and his relationships with Hill and head coach Herm Edwards. Daniels showed off changes he made during the quarantine.

It helped me when COVID did hit to go back home and put on some more weight and come back out here to get bigger, put on some more weight and get more muscle mass to take more hits, he says.

Daniels relationship with Edwards is 100% real, Hill says. Hes witnessed them walking to practice and chatting in the coachs office.

As for Hill, Daniels and his new offensive coordinator have chemistry.

It is exciting going to someone (like Hill) to talk to him about what he wants to do, Daniels says. I feel like now I know the offense, know the details of everything I want to do and I built a relationship with coach Hill.

Daniels is confident in knowing the offense and in his receiving corps led by Darby and the supporting cast around him.

We knew, coming into the season, Frank was taking the leadership role, and we got a good supporting class around him that are receivers who are hungry and playing to win, Daniels says.

Although Daniels is happy to be preparing for the season, it was rough for him to adapt to playing in November and starting camp in October. It is a different offseason from usual; usually camp would start in August.

It has been difficult. By now were in season, he says.

I would rather be in camp right now and getting ready to play than not playing this whole fall and watching people on TV play. It has been hard, the transition to wanting to play and keeping the focus and angles we have.

The Sun Devils are set to start their 2020 season at USC at 10 a.m. Saturday, November 7.

They will play six other games for their full season, and the Pac-12 championship will be December 18.

The games will be played without fans until January, when the Pac-12 revisits it. CT

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All About Chemistry: ASU's Offense is Clicking and Ready for the Shortened Season - College Times

Health Matters: Neurology and the Keto Diet – NBC2 News

Its high in fat, moderate in protein, and low in carbohydratesthe ketogenic diet is known for helping patients lose weight. But sleep medicine Dr. Jose Colon says, if done correctly, the diet can improve more than just your weight. Being on a ketogenic diet or being in a state of ketosis, has been shown to help with epilepsy and many other disorders as well, Dr. Jose Colon, a sleep medicine physician with Lee Health.

Doctors use the ketogenic diet to help treat patients with seizures. The ketogenic diet is very effective in epilepsy but its also been shown to be helpful in many other medical disorders, from weight loss to diabetes, type two diabetes, insulin resistance, it can help with PCOS, and it helps brain function from pediatric to geriatric, from autism to Alzheimers, he said.

The keto diet can also benefit patients who suffer from sleep disorders. Ive had several patients also have successful treatment of narcolepsy as well with the ketogenic diet. One of the things with narcolepsy is that your brain is in a sleepy state and high carbohydrate states turn off your alerting neurons so it can help with that disorder as well, said Dr. Colon.

Doctors can help patients successfully adapt and maintain a ketogenic diet. A lifestyle change that can benefit their overall health.

View More Health Matters video segments at LeeHealth.org/Healthmatters/

Lee Health in Fort Myers, FL is the largest network of health care facilities in Southwest Florida and is highly respected for its expertise, innovation and quality of care. For more than 100 years, weve been providing our community with personalized preventative health services and primary care to highly specialized care services and robotic assisted surgeries. Lee Health Caring People. Inspiring Care.

Visit LeeHealth.org

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Global Interventional Neurology Device Market Seeking Growth from Emerging Markets, Growth Revenue, Study Drivers, Restraints and Forecast 2024 -…

Global Interventional Neurology Device market presents an in-depth scenario which is segmented according to Interventional Neurology Device manufacturers, product type, applications, and regions. This segmentation will provide deep-dive analysis of the Interventional Neurology Device industry for identifying the growth opportunities, Interventional Neurology Device development trends and factors limiting the growth of the market. This report offers forecast market information based on past and present Interventional Neurology Device industry situations and growth aspects.

Initially, the report presents the Interventional Neurology Device market overview covering product description, market analysis, market dynamics, Interventional Neurology Device opportunities and market share. Secondly, global Interventional Neurology Device report conducts a qualitative analysis to present the key manufacturers profile, Interventional Neurology Device market share, market size, sales volume, gross margin analysis.

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All the key regions covered in Interventional Neurology Device report are North America, Europe, Asia-Pacific, South America, Middle East and Africa. The Interventional Neurology Device market share and market outlook of each region from 2019-2026 are presented in this report. A deep study of Interventional Neurology Device market dynamics will help the market aspirants in identifying the business opportunities which will lead to accumulation of revenue. This segment can effectively determine the Interventional Neurology Device risk and key market driving forces.

The Interventional Neurology Device report is segmented to provide a clear and precise view of the global Interventional Neurology Device market statistics and market estimates. Interventional Neurology Device report Data represented in the form of graphs, charts, and figures will show the Interventional Neurology Device growth rate, volume, target consumer analysis. This report presents the crucial data to all Interventional Neurology Device industry aspirants which will facilitate useful business decisions.

Interventional Neurology Device Market Breakdown By Manufacturers (2019-2026):

Merit Medical Systems, IncW.L. Gore & AssociatesJohnson and JohnsonPenumbra, Inc.MedtronicMedikit Co., Ltd.StrykerTerumo CorporationMicroport Scientific Corporation

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Global Interventional Neurology Device Market Details Based on Product Category:

Carotid artery angioplasty & stentingEmbolization & coilingNeurothrombectomy Devices

Global Interventional Neurology Device Market Details Based On Key Product Applications:

Treatment of Cerebral AneurysmsTreatment of Cerebral VasospasmVertebroplasty

Region-Wise Interventional Neurology Device Market Analysis Can Be Represented As Follows:

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Part 1: This part enlists the global Interventional Neurology Device market overview, covering the basic market introduction, market analysis by type, applications, regions. The major Interventional Neurology Device producing regions include North America, Europe, Asia-Pacific, Middle-East, and Africa. Interventional Neurology Device industry states and outlook(2019-2026) is presented in this part. In addition, Interventional Neurology Device market dynamics stating the opportunities, market risk, key driving forces are studied.

Part 2: This part covers Interventional Neurology Device manufacturers profile based on their business overview, product type, and application. Also, the sales volume, Interventional Neurology Device product price, gross margin analysis, and Interventional Neurology Device market share of each player is profiled in this report.

Part 3 and Part 4: This part presents the Interventional Neurology Device competition based on sales, revenue, and market share of each manufacturer. Part 4 covers the Interventional Neurology Device market scenario based on regions. Region-wise Interventional Neurology Device sales and growth (2029-2026) is studied in this report.

Part 5 and Part 6: These two sections cover the North America and Europes Interventional Neurology Device industry by countries. Under this the Interventional Neurology Device revenue, market share of the countries like USA, Canada, and Mexico is provided. Under Europe Interventional Neurology Device report includes, the countries like Germany, UK, France, Russia, Italy, Russia and their sales and growth is covered.

Part 7, Part 8 and Part 9: These 3 sections covers Interventional Neurology Device sales revenue and growth for the regions like Asia-Pacific, South America, Middle East & Africa. Under these regions Interventional Neurology Device report covered, the countries like China, Japan, Korea, India, Brazil, Columbia, Argentina, Egypt, Saudi Arabia, Nigeria and South Africa. The sales and growth in these regions are presented in this Interventional Neurology Device industry report.

Part 10 and Part 11: This part depicts the Interventional Neurology Device market share, revenue, sales by product type and application. The Interventional Neurology Device sales growth seen during 2015-2019 is covered in this report.

Part 12 and Part 13: This part provides forecast information related to Interventional Neurology Device market(2029-2026) for each region. The sales channels including direct and indirect Interventional Neurology Device marketing, traders, distributors, and future trends are presented in this report.

Part 14 and Part 15: These parts present Interventional Neurology Device market key research findings and conclusion, research methodology, and data sources are covered.

Thus, Global Interventional Neurology Device report is a complete blend covering all the vital market aspects.

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Global Interventional Neurology Device Market Seeking Growth from Emerging Markets, Growth Revenue, Study Drivers, Restraints and Forecast 2024 -...

Global Impact of Covid-19 on Interventional Neurology Device Market to Record Significant Revenue Growth During the Forecast Period 20202025 |…

Interventional-Neurology-Device-Market

Global Interventional Neurology DeviceMarket report forecast 2020-2025 investigate the market size, manufactures, types, applications and key regions like North America, Europe, Asia Pacific, Central & South America and Middle East & Africa, focuses on the consumption of Interventional Neurology Device market in these regions. This report also covers the global Interventional Neurology Device market share, competition landscape, status share, growth rate, future trends, market drivers, opportunities and challenges, sales channels and distributors.

Global Interventional Neurology Device Market are mentioned in the competition landscape, company overview, financials, recent developments and long-term investments. Various parameters have been studied while estimating the market size. The revenue generated by the leading industry participants in the sales of the Interventional Neurology Device markethas been calculated through primary and secondary research.

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Top Key players profiled in the Interventional Neurology Device market report include:Medtronic, Johnson and Johnson, Terumo Corporation, Penumbra, Inc., Merit Medical Systems, Inc, W.L. Gore & Associates, Microport Scientific Corporation, Medikit Co., Ltd., Stryker and More

Market by Type Embolization & coiling Neurothrombectomy DevicesMarket by Application Treatment of Cerebral Aneurysms Treatment of Cerebral Vasospasm Vertebroplasty

global Interventional Neurology Device market report also highlights key insights on the factors that drive the growth of the market as well as key challenges that are required to Interventional Neurology Device market growth in the projection period. Here provide the perspectives for the impact of COVID-19 from the long and short term. Interventional Neurology Device market contain the influence of the crisis on the industry chain, especially for marketing channels. Update the industry economic revitalization plan of the country-wise government.

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Years Considered to Estimate the Market Size:History Year: 2015-2019Base Year: 2019Estimated Year: 2020Forecast Year: 2020-2025

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Key point summary of the Global Interventional Neurology Device Market report:

Detailed TOC of Interventional Neurology Device Market Report 2020-2025:1 COVID-19 Impact on Interventional Neurology Device Market Overview1.1 Product Definition and Market Characteristics1.2 Global Interventional Neurology Device Market Size1.3 Interventional Neurology Device market Segmentation1.4 Global Macroeconomic Analysis1.5 SWOT Analysis2 COVID-19 Impact on Interventional Neurology Device Market Dynamics2.1 Interventional Neurology Device Market Drivers2.2 Interventional Neurology Device Market Constraints and Challenges2.3 Emerging Market Trends2.4 Impact of COVID-192.4.1 Short-term Impact2.4.2 Long-term Impact3 Associated Industry Assessment3.1 Supply Chain Analysis3.2 Industry Active Participants3.2.1 Suppliers of Raw Materials3.2.2 Key Distributors/Retailers3.3 Alternative Analysis3.4 The Impact of Covid-19 From the Perspective of Industry Chain4 Interventional Neurology Device Market Competitive Landscape4.1 Industry Leading Players4.2 Industry News4.2.1 Key Product Launch News4.2.2 M&A and Expansion Plans5 Analysis of Leading Companies5.1 Company A5.1. Company Profile5.1.2 Business Overview5.1.3 Interventional Neurology Device market Sales, Revenue, Average Selling Price and Gross Margin (2015-2020)5.1.4 Interventional Neurology Device market Products Introduction5.2 Company B5.2.1 Company Profile5.2.2 Business Overview5.2.3 Interventional Neurology Device market Sales, Revenue, Average Selling Price and Gross Margin (2015-2020)5.2.4 Interventional Neurology Device market Products Introduction6 Interventional Neurology Device Market Analysis and Forecast, By Product Types6.1 Global Interventional Neurology Device Market Sales, Revenue and Market Share by Types (2015-2020)6.2 Global Interventional Neurology Device Market Forecast by Types (2020-2025)6.3 Global Interventional Neurology Device Market Sales, Price and Growth Rate by Types (2015-2020)6.4 Global Interventional Neurology Device Market Revenue and Sales Forecast, by Types (2020-2025)7 Interventional Neurology Device Market Analysis and Forecast, By Applications7.1 Global Interventional Neurology Device Market Sales, Revenue and Market Share by Applications (2015-2020)7.2 Global Interventional Neurology Device Market Forecast by Applications (2020-2025)7.3 Global Interventional Neurology Device Market Revenue, Sales and Growth Rate by Applications (2015-2020)7.4 Global Interventional Neurology Device Market Revenue and Sales Forecast, by Applications (2020-2025)Continued

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Corlieve Therapeutics SAS Closes Seed Financing to Develop Therapies for Severe Neurological Conditions – Yahoo Finance

PARIS, Nov. 2, 2020 /PRNewswire/ -- Corlieve Therapeutics today announced the closing of its seed financing led by Kurma Partners and IDinvest Partners, together with Pureos Bioventures. Corlieve is focused on developing novel therapeutics for severe neurological disorders.

Corlieve's lead program employs a novel AAV gene therapy approach for the treatment of refractory temporal lobe epilepsy (TLE), the most commonly diagnosed focal epilepsy in humans. The program is based on pioneering science from INSERM, CNRS, Aix Marseille University and the University of Bordeaux, and is being developed in collaboration with REGENXBIO Inc. (Maryland, US), a leading gene therapy company. In addition, Corlieve has licensed REGENXBIO's NAV AAV9 technology for the TLE program. Corlieve is led by Chief Executive Officer Richard Porter, Ph.D., who brings to the Company over 25 years of neuroscience leadership experience in the pharmaceutical and biotech industries, including most recently as Chief Operating Officer of Therachon Holding AG until its acquisition by Pfizer in July 2019.

"I am excited to build Corlieve on a strong scientific foundation and with valuable support from our partners and investors," said Dr. Porter. "Our novel approach allows us to bring potentially game-changing treatments to patients with neurological diseases."

Corlieve's board will consist of Vanessa Malier, Managing Partner at Kurma, Anja Harmeier, Partner at Pureos Bioventures and Olivier Danos, Ph.D., Chief Scientific Officer of REGENXBIO.

"The formation of Corlieve with REGENXBIO is another validation of our approach to build companies on the basis of leading French science combined with a strong technology partner. We at Kurma are thrilled to support this emerging science to tackle TLE," said Ms. Malier.

"Our mission at REGENXBIO is to develop and enable the use of our proprietary NAV Technology Platform to advance new gene therapies for diseases with significant unmet needs," said Dr. Danos. "We are pleased to collaborate with Corlieve in this application of our NAV AAV9 technology to potentially treat patients suffering from TLE, for which better treatment modalities are needed."

Story continues

About Corlieve TherapeuticsCorlieve Therapeutics is a biotechnology company focused on bringing novel therapeutic options to patients with severe neurological disorders. The lead project is targeting aberrantly expressed kainate receptors in the hippocampus of patients with TLE using a gene therapy approach.

About KurmaKurma Partners is a key European player in the financing of Innovation in Healthcare and Biotechnology, from pre-seed to growth capital, notably through Kurma Biofund I through III and Kurma Diagnostics, as well as via strategic partnerships with prestigious European research and medical institutions.

About IDinvestIdinvest Partners is a leading European mid-market private equity firm. With 8bn under management, the firm has developed several areas of expertise including innovative start-up venture capital transactions; mid-market private debt, i.e. single-tranche, senior and subordinated debt; primary and secondary investment and private equity advisory services.

About Pureos BioventuresPureos Bioventures is a newly formed venture capital fund, advised by Bellevue Asset Management. Pureos invests exclusively in private innovative drug development companies, with a special emphasis on the next generation of biological drugs and drug modalities. The fund's portfolio companies are built on scientific excellence to develop therapies across a broad indication spectrum including oncology, immunology, ophthalmology, rare diseases and neuroscience. Pureos has built a team with deep investment, operating and clinical expertise, that strives to impact patients' lives by advancing innovative treatments for devastating diseases.

About REGENXBIOREGENXBIO is a leading clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy. REGENXBIO's NAV Technology Platform, a proprietary adeno-associated virus (AAV) gene delivery platform, consists of exclusive rights to more than 100 novel AAV vectors, including AAV7, AAV8, AAV9 and AAVrh10. REGENXBIO and its third-party NAV Technology Platform Licensees are applying the NAV Technology Platform in the development of a broad pipeline of candidates in multiple therapeutic areas.

Contact: Amy Conrad, 858-366-3243, amy@juniper-point.com

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Corlieve Therapeutics SAS Closes Seed Financing to Develop Therapies for Severe Neurological Conditions - Yahoo Finance

Global Neurology Software Market Expected to Reach highest CAGR: Epic, Athenahealth, Nextgen, healthfusion, Allscripts etc. – The Think Curiouser

This versatile composition of research derivatives pertaining to diverse concurrent developments in the global Neurology Software market is poised to induce forward-looking perspectives favoring unfaltering growth stance.

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Vendor Profiling: Global Market_Keywor Market, 2019-25:

DROT Analysis Driver Assessment: This section of the report also clearly identifies the major growth enablement triggers and drivers that push the growth trajectory.

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Understanding Competition Spectrum: Global Neurology Software Market

In addition to the above, this dedicated research report representing the current and historical developments in the global Neurology Software market have been prioritized exponentially in report contents to ensure seamless growth oriented business discretion amongst frontline players

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North America (U.S., Canada, Mexico) Europe (U.K., France, Germany, Spain, Italy, Central & Eastern Europe, CIS) Asia Pacific (China, Japan, South Korea, ASEAN, India, Rest of Asia Pacific) Latin America (Brazil, Rest of L.A.) Middle East and Africa (Turkey, GCC, Rest of Middle East)

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The report offers a clear and accessible estimation of the global Neurology Software market that are presented as value based and volume based estimations. The report is mindfully structured to present all market relevant information which are designed and presented in the form of graphs, charts and tables to allow market players quickly decipher the peculiarities to invoke mindful business decisions

Global Neurology Software Market: Understanding Scope In-depth research and thorough evaluation of the various contributing factors reveal that the global Neurology Software market is estimated to perform decently in forthcoming years, reaching a total valuation of xx million USD in 2019, and is further poised to register xx million USD in 2025, growing at a healthy CAGR of xx%. This elaborate research report also houses extensive information of various market specific segments, elaborating further on segment categorization comprising type, application as well as end-user sections which successively influence lucrative business discretion.

The report also entails a dedicated section and chapter to offer market relevant highlights denoting consumption and production activities. The report also entails sectional representation of thorough barrier evaluation and threat probabilities. The report clearly highlights the details of vendor activities and promotional investments, crucial to ensure high return on investments.

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Minaris Regenerative Medicine to Significantly Expand Manufacturing Capacity for Cell and Gene Therapies in Germany and Japan – b3c newswire

MUNICH, Germany and YOKOHAMA, Japan , November 02, 2020 / B3C newswire / -- Minaris Regenerative Medicine (Minaris), a leading global contract development and manufacturing organization for cell and gene therapies, wholly owned by Showa Denko Materials Co., Ltd., announced today a total investment of 64.5 million USD to significantly expand its facilities in Europe and Asia.

European facility expansion:

A new state of the art facility will be built in the proximity of the existing site in Ottobrunn near Munich, Germany with a total investment of 40.7 million USD. The new facility will operate according to GMP standards (FDA and EMA) and be dedicated to clinical and commercial manufacturing as well as development services for cell and gene therapies. The multi-storey building with a total of 6,650 sqm will initially more than double Minaris existing capacity in Europe by providing additional clean rooms, quality control laboratories, warehousing, cryo-storage and office space. It will have a modular design with the possibilities to go from single room to ball room design and to flexibly change between grade B and grade C configuration. The new facility is expected to be operational early 2023 and will allow for additional expansion of clean rooms according to client demand and specifications, thus more than tripling the current clean room capacity.

We are very pleased to expand our capacity to support the growing demand of clients who continue to care for an increasing number of patients in the future, said Dusan Kosijer, Managing Director of Minaris Regenerative Medicine GmbH.

Asian site expansion:

A new facility will also be established adjacent to the existing facility in Yokohama, Japan allowing for an additional 4,000 sqm which will double the capacity for commercial manufacturing of regenerative medicine. The new facility is scheduled to start operations in October 2022. The investment of 23.8 million USD is part of a strategy to establish a center for cancer immunotherapy and somatic stem cells.

The European and Asian expansions complement the opening of the new commercial facility in Allendale, New Jersey, USA announced in January this year. Our investment in the facility expansions of all our three regional sites confirms our commitment to contract development and manufacturing for the cell and gene therapy industry, commented Kazuchika Furuishi, PhD, Corporate Officer and General Manager, Regenerative Medicine Business Sector of Showa Denko Materials Co., Ltd. Our global offering to our clients with sites in USA, Germany and Japan enables us to advance our clients life-saving therapeutics to patients in need around the world.

About Minaris Regenerative MedicineMinaris Regenerative Medicine is a global contract development and manufacturing organization (CDMO) for cell and gene therapies. We offer our clients high value clinical and commercial manufacturing services, development solutions, and technologies. We are pioneers in the field with more than 20 years experience providing outstanding quality and reliability. Our facilities in the US, Europe, and Asia allow us to supply patients worldwide with life-changing therapies. Minaris Regenerative Medicine is wholly owned by Showa Denko Materials Co., Ltd.

For more information, please visit http://www.rm.minaris.com

Conversion rate: 1 Euro = 1.14 UDS, 105 Yen = 1 USD

Contact

Minaris Regenerative Medicine GmbHLuc St-Onge, Ph.D.Global Head of Sales and MarketingThis email address is being protected from spambots. You need JavaScript enabled to view it.+49 (0)89 700 9608-0

Keywords: Investments; Regenerative Medicine; Genetic Therapy; Induced Pluripotent Stem Cells; Mesenchymal Stem Cells; Allogeneic Cells; Hematopoietic Stem Cells; Dendritic Cells; Adult Stem Cells; Lymphocytes; Europe; Asia; Japan; Industry

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Minaris Regenerative Medicine to Significantly Expand Manufacturing Capacity for Cell and Gene Therapies in Germany and Japan - b3c newswire

Avantor Discusses Cell & Gene Therapy Production Trends Through the Lens of COVID-19 – PRNewswire

Avantor executives joined other industry leaders at virtual Cell & Gene Therapy Bioprocessing & Commercialization Conference

Panels discussed critical topics including process efficiency and scaling solutions

RADNOR, Pa., Nov. 2, 2020 /PRNewswire/ --Executives from Avantor Inc. (NYSE: AVTR), a leading global provider of mission-critical products and services to customers in the life sciences, advanced technologies and applied materials industries, recently provided expert insight at the Cell & Gene Therapy Bioprocessing & Commercialization Virtual Conference. Cell and gene therapy (C>) are two of the most revolutionary applications driving the biopharmaceutical industry.

In separate panel discussions with other global industry leaders, Dr. Ger Brophy, EVP, Biopharma Production at Avantor and Claudia Berrn, SVP, Business Development and Commercial Operations at Avantor, each addressed novel considerations and challenges facing the biopharmaceutical industry, including the impact of COVID-19. They highlighted innovation to help drive the creation and commercialization of life-changing, personalized C> treatments.

In a panel on the evolution of C> and the path toward scalability and manufacturability of these treatments, Dr. Brophy gave his perspective on this growing need for the bioprocessing industry.

"Genuine progress is being made in the long-standing battle to effectively treat and control disease, and cell & gene therapies will only continue to unlock new frontiers in medicine," said Dr. Brophy. "We're beginning to see more clearly the issues that need to be addressed, and know that if products are to scale and become more accessible to patients worldwide, there needs to be efficiency in operations. There is an absolute requirement for automation, both to reduce variability and to generate process efficiencies. At Avantor, we are ready to make the essential materials and technologies available to companies leading the charge and treating patients. Innovation and agility are central to how we're partnering with the industry to resolve these issues."

On a separate panel, Ms. Berrn highlighted how the industry is navigating the challenges and impact of the global pandemic, from the fragmentation of supply chains to clinical trial disruption.

"In this critical moment for the industry and the world, it is more important than ever for leaders in the cell & gene therapy community to come together to strategize and share ideas," said Ms. Berrn. "Avantor is actively working with the world's leading pharmaceutical and biotechnology companies to accelerate the production of novel treatments. Collectively, our goal is to mitigate any challenges in the process of taking a groundbreaking treatment from its initial scientific discovery to delivery in treating patients."

Avantor provides products for biopharma production workflows, including cell and gene therapy offering. Search 'Avantor biopharma' in your browser.

About AvantorAvantor, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers. Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries.We set science in motion to create a better world. For information, visit avantorsciences.com and find us on LinkedIn, Twitter and Facebook.

Robert DonohoeSenior Director, Corporate CommunicationsAvantorM: 484-688-4730[emailprotected]

Source: Avantor and Financial News

SOURCE Avantor and Financial News

http://avantorsciences.com

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Avantor Discusses Cell & Gene Therapy Production Trends Through the Lens of COVID-19 - PRNewswire

Sloan Kettering Institute, Bluebird Bio in court trial over gene therapy deal – Crain’s Chicago Business

Then, Girondi claimed, Sloan Kettering mothballed his work to favor Bluebird, whose chief executivehad a prior business relationship with the cancer center's boss.

Girondis rage has been fueled by Bluebirds trajectory since then: its thalassemia treatment was approved last year by the European Union and at $1.8 million per patient will be among the most expensive.

In my neighborhood, theyd have gotten ball batted for similar behavior, said Girondi, a self-described former street tough from the South Side of Chicago whosbeen using such talk to describe his adversaries for years.

Now, Girondi is finally getting his day in court. Having survived years of legal challenges, which have portrayed his case as absurd and Girondi himself as erratic and ill-tempered, his trial began on Thursday.Errant is seeking hundreds of millions of dollars in damages, according to court filings.

The trial promises a rare glimpse into the not uncommonly messy marriage of medical researchers and for-profit companies, and it will showcase a slew of revealingdocuments and emails that have emerged in the court file, including one that Girondis lawyers described in court as the smoking gun.

Written in June 2010 by Nick Leschly, then interim president of Genetix Pharmaceuticals, which was renamed Bluebird Bio a few months later, the emailsaid:Pat Girondineed to shut him down.

The recipient of the email, another Genetix executive, responded by saying they need to be nice, suck up, etc. to Girondi, so they can review valuable data from a Sloan Kettering scientist with whom Errant was collaborating.

Both Sloan Kettering and Bluebird deny Errants allegations.

Sloan Kettering is vigorously defending itself in court, said Jorge Lopez, executive vice president and general counsel for Memorial Sloan Kettering Cancer Center, in a statement. We also disagree with EGTs characterizations of the case and of the Courts rulings. He declined further comment.

In court filings, Sloan Kettering has argued that Girondis company, called EGT for short,wasnt tricked but rather was short of money and repeatedly failed to meet obligations outlined in its deal.

The evidence shows that EGTs case is the fantasy of a defunct company and its founder that refuse to accept responsibility for their own failure, an attorney for Sloan Kettering Institute wrotein a July 8, 2019 filing.

Bluebirds attorney, Jeffrey Eilender, said the court record has disproved Errantsclaim of a conspiracy between Sloan Kettering Institute, referred to as SKI in court filings, and Bluebird, as well as an allegation that Bluebird gleaned secrets from Girondis company.

None of the evidence relied upon by EGT shows a material issue as to the ultimate fact: none suggests in any way that there was an agreement between Bluebird and SKI to defraud EGT, Bluebirds lawyers wrotein a July 8, 2019 court filing. In fact, EGT does not even explain how or why the facts it cites are relevant here (they are not); it just throws everything at the wall to see if it sticks.

As for Leschlys email saying that Girondi needed to be shut down, Eilender said it referred to Girondi,not the company. Why? Because with all due respect to Mr. Girondi, hes a nudnik, Eilender told the court at January 2019 hearing, explaining Girondi had becomea nuisance.

Leschly wasnt available for an interview, but he has previously expressed his opinions about Girondi and his firm.

Errant is toothless and the guy behind it is completely insane, truly, Leschly wrote in a 2012 email to an investment analyst.

Thalassemia is an inherited blood disorder in which the body doesnt produce enough hemoglobin, the substance in red blood cells that carriesoxygen. Moderate and severe, or beta,cases require frequent blood transfusions and can result in early death.

In 1992, Rocco Girondi was diagnosed with a more severe form of the blood disorder. He was two years old. The next year, Girondi retired from what he describes as a lucrative trading career to devote himself to finding a cure.

Girondi, 62, isnt your typical biotech entrepreneur. A high school dropout, he was listed as one of America's most eligible bachelors in Playgirl magazine in 1988 and appeared on the Oprah Winfrey Show in an episode on male chauvinists. (A copy of the show wasnt readily available; Girondi said he had defended both a mans and a woman's right to work, but believed one should stay home if they have children).A 1987 article about him in Chicago Magazine is entitled Fonzie Gets Rich. He left Chicago decades ago for Italy, where he occasionally performs in concert, playing blues and rock andthe occasional Italian ballad. But hestill speaks in the blunt, sometimes salty, manner of the Chicago neighborhood where he grew up.

He had some money at a time when few others showed interest in gene therapy. By 2000, Girondi began providing financial support to researchers at Sloan Kettering, including Dr. Michel Sadelain, who had brought thalassemia under control in mice, according to Errants complaint. Those researchers had developed a method to replace defective genes in thalassemia patients with a healthy copy. The plan used a modified virus known as a vector to deliver the genetic material into the cells.

At that time, gene therapy was relatively new and scarred by missteps, including a patient who had died after undergoing treatment. In 2005, Sloan Kettering granted a license to develop Sadelains potential gene therapy treatment to the only interested party, Errant Gene Therapeutics, according to the complaint.

Progress was slow and hampered by delays, according to Girondi and his lawyers. But by 2010, Errant had manufactured enough of the medicine to start clinical trials, his lawyers say in court papers.

Girondi said the relationship between his company and Sloan Kettering changedsoon after Craig Thompsons hiring as president and chief executive officer of Memorial Sloan Kettering Medical Centerwas announced in August 2010. By that fall, he said it was clear his company was on the outs.

It ended very strangely, Girondi said. I think thats the best way to say it.

Sadelain didnt respond to messages seeking comment.

Thompson, 67, had previously worked at the University of Pennsylvania, where he had been director of the Abramson Cancer Center. He also co-founded a company called Agios Pharmaceuticals in 2007with the goal of unlocking a new field of discovery in cellular metabolism.

Agiosreceived an infusion of $33 million from several venture capital firms in 2008 including Third Rock Ventures, where Leschly the future Bluebird CEO -- was a partner. Leschly also served as Agioss interim chief business officer,according to a 2010 Bluebird press release. A few months later, when Thompson began his job at Sloan Kettering, he was listed as being on Agioss scientific advisory board.

In September, 2010, Sloan Kettering asked Errant for physical possession of the vector to complete a study which it said was necessary to move forward with clinical trials, according to Errants lawyers. Errant delivered the vector and never got it back, the lawyers said.

Sloan Kettering said in court documents that by 2010, Errant had defaulted on its obligations, and that following arbitration and a new deal the following year, all rights granted to Errant in the 2005 deal reverted to Sloan Kettering.

Thompson started his job at Sloan Kettering in November, 2010. That same month,Sloan Ketteringmet with Bluebird and gave them a technical demonstration on Errants vector, sharing confidential information that served as a preludeto a more formal agreement the next year, according to Errants lawyers.

In November 2010, Bluebirds board of directors in 2010 weighedthe pros and cons of collaborating withSloan Kettering, according to Errants court filings. Among the positives? Eliminates the most threatening competitor, according to thepresentation, which is part of the court record.

Andrew Maslow, a former Sloan Kettering executive, said in an interview thathe made the decision to pursue a collaboration with Bluebird, not Thompson. One reason was the improving landscape for gene therapy, and another was Bluebirds capabilities, he said.

These guys are the real thing. They are totally capable, he said. They were just the opposite of Pat.

While Errant squabbled with Sloan Kettering, Bluebird continued to move toward commercialization of its treatment.

Bluebirds treatment for transfusion-dependent thalassemia patients, Zynteglo, was approved by the European Union last year, and the company plans to apply for U.S. approval in 2021. But thats just the beginning. The gene therapy is also intended foruseas a treatment for sickle cell disease(SCD). It could ultimately generate $1 billion a year in annual sales, according to Bloomberg Intelligence.

These therapies have the potential to transform the lives of patients with thalassemia and SCD,said Marc Engelsgjerd, a biotech analyst at Bloomberg Intelligence, who called the treatments groundbeaking.

Leschly, for one, has already benefited. He has pocketed roughly $78 million from stock sales since the company went public in 2013, according to data compiled by Bloomberg. Girondi and Sadelain have been left to contemplate what might have been.

We could have gotten an incredible product and a Nobel Prize, Sadelain said, in a May 2015 phone call that Girondi recorded, also part of the court file. And right now, we have nothing.

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Sloan Kettering Institute, Bluebird Bio in court trial over gene therapy deal - Crain's Chicago Business

Cell Therapy Manufacturing Market is estimated to reach close to USD 10 Billion by 2030, claims Roots Analysis – PRnews Leader

The approval of KYMRIAH, YESCARTA, Alofisel and Zyntelgo has increased the interest of pharma stakeholders in cell therapies; further, owing to the technical challenges in this field, outsourcing manufacturing operations has become a necessity

Roots Analysis has announced the addition of Cell Therapy Manufacturing Market (3rd Edition), 2019 2030 report to its list of offerings.

Owing to various reasons, the demand for cell therapies is anticipated to increase over the coming years. Therefore, both therapy developers and contract service providers may need to strengthen their capabilities and expand available capacity. In this context, automation is expected to be a key enabler within the cell therapy manufacturing and contract services industry.

To order this 500+ page report, which features 160+ figures and 250+ tables, please visit this link

Key Market Insights

More than 160 organizations claim to be engaged in cell therapy manufacturingThe market landscape is dominated by industry players, representing more than 60% of the total number of stakeholders. Amongst these, over 55 are large or mid-sized firms (having more than 50 employees).

100+ players focused on T-cell and stem cell therapiesMost of these players are focused on manufacturing T-cell therapies, including CART, TCR or TILs. It is worth highlighting that more than 35 organizations claim to have necessary capabilities for the manufacturing of both types of therapies.

Presently, 70+ companies have commercial scale capacityAs majority of the cell therapy products are in clinical trials, the demand is high at this scale. However, it is worth noting that several players (~50%) have already developed commercial scale capacity for cell therapies.

Europe is currently considered a current hub for cell therapy productionMore than 220 manufacturing facilities have been established by various players, worldwide; of these, 35% are in Europe, followed by those based in North America. Other emerging regions include Australia, China, Japan, Singapore, South Korea and Israel.

50+ facility expansions reported between 2015-2019More than 85% of the expansions are related to setting up of new facilities across different regions. Maximum expansion activity was observed in the US and in certain countries within the Asia Pacific regions.

20+ companies offer automated solutions to cell therapy developersPlayers that claim to offer consultancy services related to automation include (in alphabetical order) Berkeley Lights, Cesca Therapeutics, Ferrologix, FluDesign Sonics, GE Healthcare and Terumo BCT. Further, we identified players, namely (in alphabetical order) Fraunhofer Institute for Manufacturing Engineering and Automation IPA, Invetech, KMC Systems, Mayo Clinic Center for Regenerative Medicine and RoosterBio, that offer consultancy solutions related to automation.

Partnership activity has grown at an annualized rate of 16%, between 2014 and 2018More than 200 agreements have been inked in the last 5 years; majority of these were focused on the supply of cell-based therapy products for clinical trials. Other popular types of collaboration models include manufacturing process development agreements (16%), services agreements (12%) and acquisitions (10%).

By 2030, developed geographies will capture over 60% of the market shareAsia Pacific is anticipated to capture the major share (~36%) of the market by 2030. It is also important to highlight that financial resources, technical expertise and established infrastructure is likely to drive cell therapy manufacturing market in Europe, which is estimated to grow at a CAGR of ~26%.

To request a sample copy / brochure of this report, please visit this link

Key Questions Answered

The USD 10+ billion (by 2030) financial opportunity within the cell therapy manufacturing market has been analyzed across the following segments:

The report features inputs from eminent industry stakeholders, according to whom the manufacturing of cell therapies is largely being outsourced due to exorbitant costs associated with the setting-up of in-house expertise. The report includes detailed transcripts of discussions held with the following experts:

The research covers profiles of key players (industry and non-industry) that offer manufacturing services for cell-based therapies, featuring a company overview, information on manufacturing facilities, and recent collaborations.

For additional details, please visithttps://www.rootsanalysis.com/reports/view_document/cell-therapy-manufacturing/285.html or email [emailprotected]

You may also be interested in the following titles:

Contact:Gaurav Chaudhary+1 (415) 800 3415+44 (122) 391 1091[emailprotected]

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Cell Therapy Manufacturing Market is estimated to reach close to USD 10 Billion by 2030, claims Roots Analysis - PRnews Leader

Tetra Therapeutics Announces Positive Topline Results from Phase 2 Study of BPN14770 in Patients with Fragile X Syndrome – BioSpace

Nov. 2, 2020 13:00 UTC

Study shows significant cognitive improvement in domains related to language and caregivers reported improved language and daily functioning

Lead drug candidate continues to be safe and well-tolerated

GRAND RAPIDS, Mich.--(BUSINESS WIRE)-- Tetra Therapeutics, a wholly owned subsidiary of Shionogi & Co. Ltd., today announced positive topline results from its Phase 2 exploratory study in adult patients with Fragile X Syndrome (FXS). The study evaluated its lead candidate, BPN14770, a first-in-class phosphodiesterase4D (PDE4D) allosteric inhibitor. In this single-center, randomized, placebo-controlled, two-way crossover study, BPN14770 demonstrated excellent safety as well as benefits on cognitive function and behavior in 30 patients with FXS.

BPN14770 is a novel therapeutic agent that selectively inhibits phosphodiesterase4D (PDE4D). In preclinical studies, BPN14770 promoted the maturation of connections between neurons, which is impaired in patients with FXS, the most common genetic form of Autism.

We are very excited about the results of this study, said Mark Gurney PhD, Founder and Chief Executive Officer of Tetra. In addition to being safe and well tolerated, treatment with BPN14770 led to significant cognitive improvement, specifically in the language domains, and we also saw a clinically meaningful benefit in overall daily functioning. These findings validate our approach to treating this disease through a mechanism that addresses a core deficit in the disorder. On behalf of the entire Tetra team, I want to sincerely thank the patients, families and investigators who participated in this study as well as the FRAXA Research Foundation, for their assistance in this study.

The Phase 2 clinical trial was a randomized, placebo-controlled, two-way crossover study. Each period was 12 weeks in duration with no washout between periods. The study enrolled 30 adult male subjects age 18-41 years with FXS due to >200 CGG repeats in the FMR1 gene. Subjects received daily oral doses of 25 mg twice a day of BPN14770 or placebo. Parents/caregivers and physician raters were blinded to treatment. Study enrollment occurred between July 9, 2018 and July 31, 2020. All subjects completed both treatment periods, although carryover effects limited the primary statistical analysis to Period 1. The following results, therefore, describe the outcomes for patients who received BPN14770 during Period 1, compared to those who received placebo.

Cognitive assessments using the NIH-Toolbox revealed significant benefit in Oral Reading Recognition (LSMean Difference +2.80, p=0.0157), Picture Vocabulary (+5.79, p=0.0342), and Cognition Crystallized Composite Score (+5.29, p=0.0018). Parent/Caregiver ratings using 100 point Visual Analog Scales revealed benefit that was judged to be clinically significant in Language (LSMean Difference +14.04, p=0.0051) and Daily Functioning (+14.53, p=0.0017). The benefit of BPN14770 was maintained up to 12 weeks after the crossover from drug to placebo. BPN14770 was very well tolerated in the Phase 2 trial with few adverse events.

These results offer hope for Fragile X Syndrome patients and their parents said Dr. Elizabeth Berry-Kravis, pediatric neurologist, Rush University Medical Center, and principal investigator. The preponderance of clinical outcome measures were in favor of the drug. These included performance-based as well as parent and physician-rated scales which suggests a meaningful impact on the global FXS disease process. I find it exciting that we have a drug that potentially addresses a core deficit in FXS, a decrease in cAMP, that has been documented in patients as well as in the fly and mouse models of the disorder.

About the Phase 2 Trial

The Phase 2 clinical trial was a randomized, placebo-controlled, two-way crossover study in 30 adult male patients with FXS, ages 18-45, to assess the safety and efficacy of BPN14770. The study was conducted at Rush University Medical Center, Chicago, Illinois by principal investigator Elizabeth M. Berry-Kravis, M.D., Ph.D. with financial support from the FRAXA Research Foundation. Additional information is available through clinicaltrials.gov (Identifier: NCT03569631).

About BPN14770

BPN14770 is a novel therapeutic agent that selectively inhibits phosphodiesterase-4D (PDE4D) to increase the levels of cAMP, a key signaling molecule, in brain. In preclinical models, BPN14770 promotes the maturation of connections between neurons, which is impaired in patients with Fragile X Syndrome, an indication for which BPN14770 has received Orphan Drug Designation from the U.S. Food and Drug Administration (FDA). This unique mechanism of action has the potential to improve cognitive and memory function in devastating CNS disorders, including FXS, Alzheimer's disease and other dementias, learning/developmental disabilities and schizophrenia. BPN14770 currently is approved for investigational use only by the FDA.

About Tetra Therapeutics

Tetra Therapeutics, a wholly owned subsidiary of Shionogi & Co., Ltd., is a clinical stage biotechnology company developing a portfolio of therapeutic products that will bring clarity of thought to people suffering from Fragile X syndrome, Alzheimers disease, traumatic brain injury, and other brain disorders. Tetra uses structure-guided drug design to discover mechanistically novel, allosteric inhibitors of the phosphodiesterase 4 (PDE4) enzymes, a family of enzymes that play key roles in memory formation, learning, neuroinflammation, and traumatic brain injury. Tetra Therapeutics is headquartered in Grand Rapids, Michigan. For more information, please visit the companys website at http://www.tetratherapeutics.com.

About Shionogi

Shionogi & Co., Ltd. is a major Japanese research-driven pharmaceutical company dedicated to bringing benefits to patients based on its corporate philosophy of supplying the best possible medicine to protect the health and wellbeing of the patients we serve. The company currently markets products in several therapeutic areas including anti-infectives, pain, cardiovascular diseases, and gastroenterology. The Shionogi pipeline is focused on infectious disease, pain, CNS, and oncology. For more information on Shionogi & Co., Ltd., visit https://www.shionogi.com/global/en/.

Forward Looking Statement

This announcement contains forward-looking statements. These statements are based on expectations in light of the information currently available, assumptions that are subject to risks and uncertainties which could cause actual results to differ materially from these statements. Risks and uncertainties include general domestic and international economic conditions such as general industry and market conditions, and changes of interest rate and currency exchange rate. These risks and uncertainties particularly apply with respect to product-related forward-looking statements. Product risks and uncertainties include, but are not limited to, completion and discontinuation of clinical trials; obtaining regulatory approvals; claims and concerns about product safety and efficacy; technological advances; adverse outcome of important litigation; domestic and foreign healthcare reforms and changes of laws and regulations. Also, for existing products, there are manufacturing and marketing risks, which include, but are not limited to, inability to build production capacity to meet demand, unavailability of raw materials and entry of competitive products. The company disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise.

View source version on businesswire.com: https://www.businesswire.com/news/home/20201102005309/en/

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Tetra Therapeutics Announces Positive Topline Results from Phase 2 Study of BPN14770 in Patients with Fragile X Syndrome - BioSpace

Human Reproductive System – Male and Female Reproductive …

Overview

Reproduction can be defined as the biological process of producing a new individual or an offspring identical to the parents. This process ensuresthe increase in the number of individuals of a species when conditions are favourable. It is one of the fundamental characteristics of living things and an essential life process.

There are two types of reproduction asexual and sexual.

Sexual Reproduction This process of reproduction is very complex that involves the formation and transfer of gametes, followed by fertilization, the formation of the zygote, andembryogenesis.

Asexual Reproduction This process of reproduction involves only one parent and the new offspring produced is genetically similar to the parent.

Also read:Asexual Reproduction

All human beings undergo a sexual mode of reproduction. In this process, two parents are involved in producing a new individual. Offspring are produced by the fusion of gametes (sex cells) from each parent. Hence, the newly formed individual will be different from parents, both genetically and physically. Human reproduction is an example of sexual reproduction.

In human beings, both males and females have different reproductive systems; hence, they are known to exhibit sexual dimorphism. Males have testes- also calledtesticles, while the females have a pair of ovaries.

Also read:Sexual Reproduction

The reproduction in human beings involves the fusion of male and female gametes produced in their reproductive system. The male reproductive system is different from the female reproductive system, both in structure and in function.

Male Reproductive System

The male gametes, i.e., sperms are produced within the male reproductive system. Sperms are small unicellular structures with a head, middle piece, and a tail.

The male reproductive system consists of :

Explore more:Male Reproductive System

Female Reproductive System

The female reproductive system is active before, during and after fertilization as well. It consists of the following parts:

Female reproductive system has two functions

During puberty, eggs in the ovaries start to mature. One of the ovaries releases the matured ovum in every 28 to 30 days and is called ovulation.

The process of fusion of sperm with egg (ovum) to produce zygote is called fertilization. Fertilization is a crucial stage of reproduction in human beings. The fertilized egg is called the zygote. Zygote starts to divide into many cells and develops into an embryo.

Embryo moves into the uterus and gets attached to its walls. This process is referred to as implantation, and the implanted embryo eventually develops into a fetus.

Learn more about reproduction in human beings, its types, process, significance and other related topics atBYJUS Biology

Reproduction is a fundamental biological process of producing young ones or offspring, which are identical to their parents.

Fertilization is the fusion of male and haploid female gametes (egg and sperm) resulting in the formation of a diploid zygote.

Cell Differentiation is the process through which a young and immature cell develops into a specialized and matured cell.

The process of reproduction in humans usually begins with copulation, followed by the Pre-fertilization, Fertilization, and Post-fertilization. During this fundamental process, both male and female reproductive organs play an important role.

In Biology, the trimester system mainly refers to three months. A complete pregnancy period lasts for 38-40 weeks or 9 months from the first day of your last menstrual period to the birth of the baby. This period is divided into three stages, which are collectively called trimesters.

Parturition is the process of delivering the baby after the completion of pregnancy or a fully grown developed fetus and placenta from the uterus to the vagina to the outside world. This process occurs in three stages, which includes:

Humans reproduce their young ones sexually by the interaction between the male and female reproductive organs.

Sexual Reproduction is carried out by a set of events and are divided into three stages: Pre-fertilization, Fertilization, and Post-fertilization

Reproduction is a fundamental biological process carried out by different living organisms to produce their young ones or offspring. In human, reproduction plays a significant role in the continuity of species from one generation to another generation. Without reproduction, there would no life existing on the planet earth.

Both sexual and asexual are two different modes of reproduction. Sexual mode reproduction takes place in all multicellular organisms including humans, animals, and higher plants. Asexual mode reproduction occurs only in lower invertebrates and other simpler living species such as amoeba, bacteria, and hydra.

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Human Reproductive System - Male and Female Reproductive ...

Brain waves with the same beat as "Call Me Maybe" induce dissociative states – Massive Science

Dieting is notoriously difficult. Thanks in part to evolution, we love foods that are high in calories. Not only that, but once we have experienced the kind of high-calorie foods that surround us in the modern world, more nutritionally-balanced foods become much less attractive. But why?

To understand how the brain makes dieting so difficult, and high-calorie foods so tempting, the authors of a recent study turned to mice, where they could record and manipulate the activity of specific neurons involved in energy balance and reward. They asked how exposing mice to high-calorie foods affected their consumption of, and neural responses to, regular foods.

When researchers gave the mice access to both high-fat (HFD) and standard (SD) diets, mice completely stopped eating the SD almost immediately, and preferred the HFD. They then removed the HFD, and saw that mice still ate very little SD, and so lost substantial weight. This devaluation of regular food was so strong that even fasting mice presented with an SD ate very little they would only eat a lot if the HFD was available. Just experiencing the HFD for 24 hours was enough time to make the SD less tasty.

Suzanne Beaky

To see how HFD exposure affects the brains response to food, the scientists recorded the activity of AgRP neurons, a population of neurons that is active during hunger and controls energy balance, and midbrain dopamine neurons, which release dopamine as a signal of reward. Exposure to the HFD greatly reduced the response of both groups of neurons to the SD: afterward, these neurons would only respond strongly to the HFD. Regular food became less rewarding, and less satiating, than high-calorie food.

Under normal conditions, AgRP neurons would only respond to food when a mouse is hungry. But after HFD withdrawal (mimicking dieting), the AgRP neurons became so sensitive to HFD that they would respond even if the mouse was not hungry. This could explain why when we diet, high-calorie foods are so hard to resist these foods become rewarding even when we arent hungry.

This study suggests that exposure to a HFD alters the brains response to food so that only high-calorie foods are rewarding and satiating, while more nutritionally-balanced foods become less valuable. And, abstaining from high-fat foods might just make our brains' hunger centers responsive to these foods even when were not hungry, making it difficult to resist the urge to binge. Research on the circuits that regulate food intake will potentially lead to therapies that allow us to manipulate these biological urges and control the obesity epidemic.

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Brain waves with the same beat as "Call Me Maybe" induce dissociative states - Massive Science

New case study shows that COVID-19-positive people don’t transfer the virus through donated eggs – Massive Science

Dieting is notoriously difficult. Thanks in part to evolution, we love foods that are high in calories. Not only that, but once we have experienced the kind of high-calorie foods that surround us in the modern world, more nutritionally-balanced foods become much less attractive. But why?

To understand how the brain makes dieting so difficult, and high-calorie foods so tempting, the authors of a recent study turned to mice, where they could record and manipulate the activity of specific neurons involved in energy balance and reward. They asked how exposing mice to high-calorie foods affected their consumption of, and neural responses to, regular foods.

When researchers gave the mice access to both high-fat (HFD) and standard (SD) diets, mice completely stopped eating the SD almost immediately, and preferred the HFD. They then removed the HFD, and saw that mice still ate very little SD, and so lost substantial weight. This devaluation of regular food was so strong that even fasting mice presented with an SD ate very little they would only eat a lot if the HFD was available. Just experiencing the HFD for 24 hours was enough time to make the SD less tasty.

Suzanne Beaky

To see how HFD exposure affects the brains response to food, the scientists recorded the activity of AgRP neurons, a population of neurons that is active during hunger and controls energy balance, and midbrain dopamine neurons, which release dopamine as a signal of reward. Exposure to the HFD greatly reduced the response of both groups of neurons to the SD: afterward, these neurons would only respond strongly to the HFD. Regular food became less rewarding, and less satiating, than high-calorie food.

Under normal conditions, AgRP neurons would only respond to food when a mouse is hungry. But after HFD withdrawal (mimicking dieting), the AgRP neurons became so sensitive to HFD that they would respond even if the mouse was not hungry. This could explain why when we diet, high-calorie foods are so hard to resist these foods become rewarding even when we arent hungry.

This study suggests that exposure to a HFD alters the brains response to food so that only high-calorie foods are rewarding and satiating, while more nutritionally-balanced foods become less valuable. And, abstaining from high-fat foods might just make our brains' hunger centers responsive to these foods even when were not hungry, making it difficult to resist the urge to binge. Research on the circuits that regulate food intake will potentially lead to therapies that allow us to manipulate these biological urges and control the obesity epidemic.

Read the rest here:
New case study shows that COVID-19-positive people don't transfer the virus through donated eggs - Massive Science

Fertility treatment and COVID-19: lessons from, and for, lockdown – BioNews

2 November 2020

This year has seen a variety of measures and restrictions the most stringent and fiercely debated being 'lockdowns' introduced around the world in order to address the COVID-19 pandemic. This week, England is due to enter a lockdown which is expected to last for at least a month. What will this mean for fertility patients?

Authorities in England hope to avoid mandatory closure of clinics, of the sort that was imposed during the UK's previous lockdown. The country's fertility regulator the Human Fertilisation and Embryology Authority (HFEA) has said that there are currently 'no plans to implement a national closure of fertility clinics', but has noted that 'we expect all clinics to demonstrate how their service can be safely maintained and how they can minimise any possible further impact on the wider NHS'.

There are important lessons to be learned from the UK's previous lockdown, as well as from the experiences of other countries, when it comes to supporting fertility patients through these challenging times. That is why this coming Thursday (5 November) the day that England's new lockdown measures are expected to begin the Progress Educational Trust (PET) will be holding a free-to-attend online event, from 5pm-6.30pm (GMT), entitled 'Lessons from Lockdown: How to Improve Support for Fertility Patients'.

At this event, we will begin by looking back at early April 2020, when UK fertility clinics closed their doors. This disrupted and delayed the treatment of thousands of patients. An atmosphere of uncertainty prevailed, with little clarity as to when treatments could resume, how waiting lists and funding arrangements would be affected, or how patients would be prioritised once clinics reopened.

This situation added to the stress and anxiety experienced by many patients. Infertility can be associated with a sense of lack of control, even at the best of times, and for some patients this feeling was intensified during and after lockdown.

Things improved in May, when the HFEA issued guidance allowing clinics to begin reopening if they could meet certain criteria (see BioNews 1045). Even then, however, the situation was inconsistent across the UK. Some patients were able to resume treatment almost immediately, while others grew increasingly frustrated because they were unable to access information, make plans or receive adequate support.

Thursday's event which we are producing in partnership with University College London's EGA Institute for Women's Health, with sponsorship from CooperSurgical will explore questions including:

What have been the greatest concerns and anxieties of fertility patients during the recent period?

What support do fertility patients need in such circumstances? And what support have they actually received?

What lessons should be taken on board by fertility clinics, policymakers and others, as we enter another lockdown?

How can fertility patients best be supported in relation to COVID-19? Or in the event of a different disease pandemic? Or in any such period of widespread disruption and uncertainty?

To help us answer these questions, we will be hearing from academics who have led research into fertility patients' experiences of the pandemic (Professor Jacky Boivin and Dr Zeynep Gurtin), from a patient and advocate whose own fertility treatment has been disrupted (Seetal Savla), and from a fertility counsellor who has been supporting patients during this difficult period (Carmel Dennehy).

All are welcome to attend Thursday's event. Find out more here, and register for your free place here.

After this week, we will continue to explore these issues at PET's annual conference, which for the first time we will be holding entirely online. The conference is entitled 'Fertility, Genomics and COVID-19', and is taking place from 9.15am-5.30pm (GMT) on Wednesday 9 December.

The conference will open with a session entitled 'The Impact of COVID-19 on the Fertility Sector', where speakers will include the chair of the HFEA (Sally Cheshire), the chair of the British Fertility Society (Dr Jane Stewart) and a leading figure in medical ethics (Professor Julian Savulescu).

The conference will close with a session entitled 'Resuming Treatment: What Can European Countries Learn from One Another?', featuring an international lineup of speakers (Dr Anna Veiga, Dr Luca Gianaroli, Dr Edgar Mocanu and Dr Nathalie Vermeulen) from the COVID-19 Working Group of the European Society of Human Reproduction and Embryology.

The conference's other sessions are detailed in the full timetable, and many other speakers are listed in the full lineup. Register to attend here, and note that the Institute of Medical Ethics has provided funding for 20 medical students to attend the conference free of charge to apply for one of these places, please email.

As with all of PET's public events, Thursday's 'Lessons from Lockdown' event and next month's 'Fertility, Genomics and COVID-19' conference will devote substantial time to letting you put questions and comments to the speakers. At our online events, you have the additional option of making contributions either identifiably or anonymously.

2020 continues to be a turbulent year, but PET is more determined than ever to provide you with a wide variety of information, opinion and opportunities for discussion. See details of all our upcoming events here, and if you are able to do so, please support our efforts by becoming a registered Friend of PET.

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Fertility treatment and COVID-19: lessons from, and for, lockdown - BioNews

Urine test reveals quality of your diet — and whether it’s the best fit for your body – Jill Lopez

Scientists have completed large-scale tests on a new type of five-minute urine test that measures the health of a person's diet, and produces an individual's unique urine 'fingerprint'.

Scientists at Imperial College London in collaboration with colleagues at Northwestern University, University of Illinois, and Murdoch University, analysed levels of 46 different so-called metabolites in the urine of 1,848 people in the U.S.

Metabolites are considered to be an objective indicator of diet quality - and are produced as different foods are digested by the body, say the research team, who published their findings in the journalNature Food.

The work was funded by the U.S. National Institutes of Health and Health Data Research UK.

Dr Joram Posma, author of the research from Imperial's Department of Metabolism, Digestion and Reproduction said: "Diet is a key contributor to human health and disease, though it is notoriously difficult to measure accurately because it relies on an individual's ability to recall what and how much they ate. For instance, asking people to track their diets through apps or diaries can often lead to inaccurate reports about what they really eat. This research reveals this technology can help provide in-depth information on the quality of a person's diet, and whether it is the right type of diet for their individual biological make-up."

The findings revealed an association between 46 metabolites in urine, and types of foods or nutrients in the diet. For instance, certain metabolites correlated with alcohol intake, while others were linked to intake of citrus fruit, fructose (fruit sugar), glucose and vitamin C. The team also found metabolites in urine associated with dietary intake of red meats, other meats such as chicken, and nutrients such as calcium. Certain metabolites were also linked with health conditions - for instance compounds found in urine such as formate and sodium (an indicator of salt intake) are linked with obesity and high blood pressure.

Professor Paul Elliott, study co-author and Chair in Epidemiology and Public Health Medicine at Imperial said: "Through careful measurement of people's diets and collection of their urine excreted over two 24-hour periods we were able to establish links between dietary inputs and urinary output of metabolites that may help improve understanding of how our diets affect health. Healthful diets have a different pattern of metabolites in the urine than those associated with worse health outcomes."

In a second study also published inNature Foodby the same Imperial team, in collaboration with Newcastle University, Aberystwyth University, and Murdoch University and funded by the National Institute for Health Research, the Medical Research Council and Health Data Research UK, the team used this technology to develop a five-minute test to reveal that the mix of metabolites in urine varies from person to person.

The team says the technology, which produces an individual's urine 'fingerprint', could enable people to receive healthy eating advice tailored to their individual biological make-up. This is known as "precision nutrition", and could provide health professionals with more specific information on the quality of a person's diet.

Dr Isabel Garcia-Perez, author of the research also from Imperial's Department of Metabolism, Digestion and Reproduction explained: "Our technology can provide crucial insights into how foods are processed by individuals in different ways - and can help health professionals such as dieticians provide dietary advice tailored to individual patients."

Dr Garcia-Perez added that the team now plan to use the diet analysis technology on people at risk of cardiovascular disease.

The researchers say this urine 'fingerprint' can be used to develop an individual's personal score - called the Dietary Metabotype Score, or DMS.

In their experiments, the team asked 19 people to follow four different diets - ranging from very healthy (following 100 per cent of World Health Organisation recommendations for a balanced diet), to unhealthy (following 25 per cent WHO diet recommendations).

The team found that people who strictly followed the same diet had varied DMS scores.

The team's work also revealed that the higher a person's DMS score, the healthier their diet. A higher DMS score was also found to be associated with lower blood sugar, and a higher amount of energy excreted from the body in urine.

The team found the difference between high energy urine (i.e. high DMS score) and low energy urine (low DMS score) was equivalent to someone with a high DMS score losing an extra 4 calories a day, or 1,500 calories a year. The team calculate this could translate to a difference of 215g of body fat per year.

The next step is to investigate how a person's urine metabolite fingerprint may link to a person's risk of conditions such as obesity, diabetes and high blood pressure. Professor Gary Frost, co-author of the research and Chair in Nutrition and Dietetics at Imperial said: "These findings bring a new and more in-depth understanding to how our bodies process and use food at the molecular level. The research brings into question whether we should re-write food tables to incorporate these new metabolites that have biological effects in the body."

Professor John Mathers, co-author of research and Director of the Human Nutrition Research Centre at Newcastle University said: "We show here how different people metabolise the same foods in highly individual ways. This has implications for understanding the development of nutrition-related diseases and for more personalised dietary advice to improve public health."

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Urine test reveals quality of your diet -- and whether it's the best fit for your body - Jill Lopez

Meet the tsetse fly, the supermom of the insect world – Advanced Science News

Tsetse flies, which miraculously birth young bigger than the mother, show us what science is about.

Image credit: Lee Haines et al. 2020

Across most of the animal kingdom, offspring are born smaller than their parents. Astonishingly, several families of insects, including tsetse flies, break this simple rule, and mothers produce offspring their own size or even larger.

An international team from the Liverpool School of Tropical Medicine and the universities of Bristol, Greenwich, Stellenbosch and California Riverside, have published an essay in BioEssays that describes this extreme reproductive strategy in tsetse flies, how it might have evolved, and what it means for controlling this disease-transmitting insect.

It is difficult to fathom a female giving birth to a single offspring that weighs more than she does.Since we are familiar with human babies, which weigh approximately 6% of the mothers pre-pregnancy weight, this feat is unthinkable. Even a blue whale calf, the largest baby in the world, weighing an impressive 2700 kg at birth, is only 1.5% of the mothers weight.

Now, imagine giving birth to a massive baby every ten days for the rest of your life!Unlike most insects, which are egg-layers, female tsetse flies give birth to only one baby at a time. This results in a slow life history in which the females must be continually pregnant and long-lived to produce sufficient offspring to sustain the species. This type of tremendous maternal investment makes one wonder how natural selection could favor this highly implausible trait.

For tsetse flies, producing enormous offspring is possible thanks to two main factors. First, tsetse have a diet consisting exclusively of protein-rich blood, and they can consume over twice their body weight in blood every few days. This allows the female to produce vast quantities of a highly nutritious, milk-like substance to feed a rapidly growing larva. Second, tsetse do not possess the physiological constraints of mammals, such as the pelvic girdle, which prevent birthing of large babies.

Understanding this strange reproductive strategy can help scientists reduce fly populations and control the diseases tsetse flies transmit. Since tsetse larvae remain protected within their mothers uterus and the pupae are hidden in the soil, controlling tsetse populations is restricted to targeting only adult flies. This contrasts strongly with controlling egg-laying insects, like mosquitoes, where all stages of insect development are susceptible to insect control campaigns. For tsetse, the slow breeding cycle means that you only need to kill a few percent of the adult female flies per day to eradicate a population.

Currently, insecticide applied to cattle and artificial host-like baits, such as tiny targets are used successfully to control tsetse populations in disease-endemic areas, such as Uganda and the Democratic Republic of the Congo.These small, easily deployable and low-cost insecticide-impregnated targets kill both male and female adult tsetse upon contact. Other tsetse control strategies, like releasing sterile males or manipulating the fly microbiome, can be more challenging to implement as large numbers of tsetse must first be reared prior to treatment (irradiation or genetic modification of symbiotic bacteria) followed by field release.

Tsetse populations must, undeniably, be controlled to prevent disease transmission.However, they should also be recognized as biologically fascinating creatures in their own right as they contribute to biodiversity and species richness in tsetse-endemic regions. In areas where human and animal health are not threatened, the preservation of these flies will give us insight into the evolution of pregnancy and motherhood.

Using tsetse flies as a model organism to study pregnancy, we can investigate how environmental changes and stress affect the mothers ability to produce high quality offspring. In an analogous situation, if a human mother is malnourished, her baby may not be born strong enough to fight off infectious diseases.

Tsetse flies are a captivating species to study for many reasons beyond their unique reproduction. In the words of Professor Glyn Vale, OBE, who has dedicated his life to the control and eradication of tsetse fly populations in many countries across the African continent:

I went to Zimbabwe (then Rhodesia) as a young man wanting to walk with lions and elephants, but I got ambushed by a tsetse fly who reckoned it could give me more fun and a better chance to be useful. It taught me that its distinctive feeding habits have seemingly inevitable chains of consequences that interweave and reach far going through matters such as the amazing reproductive system of the flies, their geographical limits, and their impact on human and animal health.

All of these biological issues ensured that eventually the trail led into lively debates over the appropriateness of widely differing technologies and strategies for control. Thus, the tsetse that I first met 55 years ago has kept its promise to give me, in its own way, exactly what I was really after: a varied, adventurous, and challenging walk on the wild side.

Check out the video Burrowing for knowledge for more background about the project, led by Dr. Sinead English at the University of Bristol and funded by the BBSRC and Royal Society

Reference: Lee R. Haines, et al. Big Baby, Little Mother: Tsetse Flies Are Exceptions to the Juvenile Small Size Principle. BioEssays (2020). DOI: 10.1002/bies.202000049

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Meet the tsetse fly, the supermom of the insect world - Advanced Science News

The Science of What Uncertainty Can Mean for Your Mind, Body – ScienceBlog.com

This process, by which certain pieces of information are selectively transmitted between different parts of the brain, often involves synchronization between the brain rhythms in these regions. The prefrontal cortex plays an essential role in this process, and can determine which information to pay attention to and which to ignore. It makes decisions based on signals from other parts of the brain, like the hippocampus, where anxiety neurons reside.

Sohals lab measured the synchronization between brain rhythms in the hippocampus and prefrontal cortex during times when mice had to make decisions. Brain regions must collaborate to make these decisions explore that open field? Stay hidden?

Without synchronization, the brain would have a harder time deciding whats important, what to focus on. Sohals lab sees these kinds of problems with appropriately filtering information as important parts of schizophrenia, autism, and anxiety disorders.

But, Sohal reiterates that anxiety is essential. We have to have anxiety. Otherwise we would do things that are overly dangerous. Anxiety is a basic part of our existence, he says. But pathological situations arise when for whatever reason the brain doesnt seem to be able to tune anxiety properly, and so its avoid, avoid, avoid.

Aoife ODonovan said that in most cases the human brain is quite good at managing anxiety.

We can think in the abstract about multiple scenarios and outcomes and prepare ourselves for them before they even happen, she says. The problem is that imagining and predicting and preparing for bad outcomes can take a toll on us psychologically and biologically.

The problem is that imagining and predicting and preparing for bad outcomes can take a toll on us psychologically and biologically.

AOIFE ODONOVAN,PHD, ASSOCIATE PROFESSOR OF PSYCHIATRY

ODonovans lab works with people with PTSD, who show exaggerated reactions to perceived threats. In these cases, our cognitive strength can be turned against us. Our bodies react to hypothetical threats as if they are right in front of us cue stress hormones and sweaty palms.

And that may be more commonplace now.

Because so many people worldwide are living in a state of anxiety at least partly due to the effects of the pandemic, social unrest, and climate change we might see more people showing these kinds of biased responses to new or preexisting potential threats, she says.

When a state of uncertainty drags on for months, our protective cognitive mechanisms can do more harm than good.

In the short-term, these responses prepare us for positive action and protect us against the potential for injury and infection that came with stressors in our evolutionary past. In the long-term, prolonged activation of the biological stress response can have toxic effects on the brain and the rest of the body, increasing risk for both psychiatric disorders and chronic physical diseases.

Theres no telling the future and, so far, no way to turn off our anxiety neurons, so how can we better cope with uncertainty? ODonovan suggests limiting exposure to the news and instead prioritizing behaviors that allow our anxious bodies to return to baseline. That means meditating, exercising, sleeping well, and nurturing social connections.

At the community level, this long-term uncertainty strains the relationships we need to maintain.

Social connection is key to making people feel safe, but our social relationships are also under strain due to social distancing and other factors. As much as possible, we need to use technology to maintain our social ties and take care of one another during these times, she said.

We may not be able to shed our current, collective uncertainty, but we can share the burden. Community, ODonovan says, has never been more important.

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The Science of What Uncertainty Can Mean for Your Mind, Body - ScienceBlog.com

Viewpoint: Rightwing packing on Supreme Court means ERA more crucial than ever to protect Women’s Rights – Blog – The Island Now

It is so curious how right-wing, Trumpers see mask-wearing mandate for public health as tyranny but cant wait to force women to bear babies, even if her own life is at stake, even if a 15-year old girl was raped by a relative.

But Amy Coney Barrett wants to go further than banning abortion even non-surgically using medication and denying a womans right to make her own health, reproduction, and family decisions.

She has indicated her inclination to ban contraceptives, fertility procedures like IVF, and Im betting would oppose any medical research that involved stem cells from fetal material (the breakthrough drug cocktail that Trump took for COVID-19 came from fetal material).

And what is next?

Women being prosecuted if they miscarry? Women being forced to isolate, prevented from traveling across state lines when pregnant, as some states have already tried to legislate? Thats what is at the heart of personhood essentially giving a fetus more rights than its mother (and who should decide what that fetus wants? Well the government!)

The U.S. Constitution guarantees religious freedom but specifically bars the establishment of religion what is known as separation of church and state.

That means that Barrett is free to follow her own conscience and religious beliefs for her own life if she opposes abortion, but it does not give her, or the government, the right to impose her religious beliefs on someone else. If government mandated mask-wearing is tyranny, what is denying a womans right to control her own body, her own destiny, to have the same ability for self-determination and fulfillment as a man?

It makes the woman a slave of the state, chattel, a broodmare, but not a full, equal citizen, not a full human being, as Supreme Court Justice Ruth Bader Ginsburg argued so many years ago.

State actions, like New York State codifying the principles of Roe v. Wade into state law, will not be enough to protect a womans dignity, equality, or liberty if the activist regressive justices on the Supreme Court create a new principle of personhood the notion that a fetus has all the rights of a living sentient being even if it is only a cluster of cells.

What, you cant hear the fetus say whether it wants to live in pain with a prognosis of a very early death? Well, The government will decide on behalf of the fetus.

Wow, makes those mask-wearing mandates make the Nanny State look ridiculous; this is (still) the Daddy State.

Roe v Wade should not have been decided based on the premise of privacy and property, but on the 14th amendments guarantee of Equal Protection. Justice Ruth Bader Ginsburgs (R.I.P.) argument for gender equality stemmed from the same argument for racial equality.

Since RBG first used this argument in 1973, things have improved for women, it is true, but as this latest stolen lifetime appointment to the Supreme Court shows, it is fragile. Barrett said that Roe is not settled law, because it has always been controversial, thus broadcasting her intent to vote to overturn it at her earliest opportunity.

But consider this: a government that can ban abortion can also mandate abortion (think China).

But its not just Equal Protection between women and men. Striking down Roe altogether or giving states the ability to impose extraordinary barriers that effectively overturn a womans right to choose means that women in some states, and women in certain economic and social strata will have more rights than others by their sheer ability to travel to obtain an abortion. It is the same as why the Supreme Court realized that Marriage Equality needed to be federal and not left up to individual states.

Someone tweeted back at me during the Senate confirmation hearing for Amy Coney Barrett, who insists she is an originalist and only interprets law based on the original intent of the Founding Fathers (as if that can be divined) that abortion is not in the Constitution.

Well, the framework for the entire nation contains only 4,500 words and none of them are freedom, God or women (but it does contain the words Post Offices and Post Roads).

Indeed, the newly formed states were so wary of a new tyranny that a Bill of Rights had to be added (originally 12), and even that was forged in compromise and had to be amended and added to multiple times. Originalism is the biggest judicial fraud ever concocted.

Trumps Supreme Court-packing with ultra-conservative, undemocratic justices who conveniently divine what the founding Fathers were thinking according to their own political sensibilities and expediencies and who is occupying the Oval Office, means that the Equal Rights Amendment is more important than ever.

When Democrats take back the Senate, the House and the White House, they need to pass a law extending the validity of the state votes on the ERA, since Virginia just became the 38th state, and the last one needed to ratify, and then adopt it into the Constitution.

But this is all the more reason a Blue wave must sweep Joe Biden into the White House with overwhelming margins and the Democrats in control of the Senate, so that through law-making, versus judicial fiat, we restore health care, environmental protection, voting rights, womens rights, civil rights and equal protection under the law. And yes, if necessary, expand the court to restore balance and justice.

Women, who came out by the millions the day after Trumps inauguration, again took the streets of Washington and other cities in the final days before Election Day. Its not hyperbole to say everything is on the line, one said.

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Viewpoint: Rightwing packing on Supreme Court means ERA more crucial than ever to protect Women's Rights - Blog - The Island Now

Software helping break the silence about sex in Rwanda – The New Times

Talking about sex is almosttaboo in Rwanda. The age of sexual debut is dropping below 15 and adolescents report high levels of coercion in their first sexual experiences.

The majority of new HIV infections are in young girls and teen pregnancy rates are rising.

Studies show that these trends are driven primarily by absence of candid conversations about sexual and reproductive health and relationships with adolescents.

Leveraging on the current digital boom in the country, a local group is using a chatbot to break that silence.

A chatbot simply is software that allows humans and computers to talk to each other as if it is two humans chatting.

The technology was developed by a local NGO known as the Rwanda Womens Network (RWN) and a Canadian market research firm, Rival Technologies in partnership with Proteknn Foundation for Innovation and Learning, also a Canadian Foundation.

Via Facebook Messenger, young adolescents from remote areas are using a chatbot dubbed IrindeBot to learn about sexual and reproductive health and rights (SRHR) and relationships.

Users can also initiate a conversation via Menya Wirinde (learn so you can protect yourself) Facebook page or replying to the page posts.

For the past six months, the technology was tested and proved promising for scaling up.

The bot is targeting at-risk youth and their parents or caregivers for frank conversations about sex and relationships, developers say.

Developers opted for Facebook because of popularity especially in the youth, including in rural communities. According to StatCounter, a database of global internet statistics, Facebook owns 56 per cent of social media market share in Rwanda.

Today, over 5,000 users have talked to the bot of whom about 1,200 have gone through the full two hours of content and quizzes.

How it works

The chatbot works in Kinyarwanda or English, text or audio, depending on user preference. First users search for IrindeBot on Facebook. Click on Send Message and type anything like Hi, the chatbot replies instantly with an option to choose a language.

From there, you trade brief introductions (you must be 13 years old or older) before diving into a more serious, honest and private chat.

Using a combination of simple text, audio, mini dramas and image selection, IrindeBot is also accessible to users with low literacy. Unlike most media platforms such as radio, the chatbot allows for a two-way interaction with fun, according to Gisle Umutoniwase, the coordinator IrindeBot project.

The technology has some downsides, however. IrindeBot is not powered by artificial intelligence, so you can only select buttons and enter a limited amount of text (only when asked). But it allows a user to upload comments and questions and receive a response from a trained, human associate.

Also, you cant go back and change your responses and weak connectivity can block the conversation.

Overcoming pertinent issues

Topics about sexuality in many Rwandan households are frowned upon, says Mary Balikungeri, founder and director of RWN.

We are trying to find innovative ways to engage young people on the issues of SRHRs in a fun way to learn and share and not feel judged at all, Balikungeri said.

IrindeBot is providing straight-up answers to the most sensitive questions about sex, gender-based violence, love and reproduction. Balikungeri observed that it is helping parents realise the importance of dialoging about sex and not as taboo but as part of peoples health.

The initiative sheds light on how digital technology may be useful to tackle emerging issues.

Traditional social norms, lack of access to accurate information and poverty are some of the reasons behind growing numbers of teen mothers, premature marriages and high HIV infections among young people.

These issues led us to think about how to shape accurate information that is tailored and friendly to adolescents, said Andrew Ndahiro, a gender activist and deputy director at RWN.

Backers of the technology plan to scale it up to more target groups such as the privileged class of young people on Instagram. They are also expanding to other countries including Kenya, Brazil and India.

In order to cater for those who dont have access to mobile phones, RWN had young people in communities and provided them with shareable smartphones.

editor@newtimesrwanda.com

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Software helping break the silence about sex in Rwanda - The New Times