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Monthly Archives: July 2017
Decoding human genome: Scientists creating yeast DNA from scratch – Zee News
Posted: July 25, 2017 at 11:46 am
New Delhi: Scientists say they are building yeast DNA from scratch, paving the way towards creating new organisms in the lab, amid huge scientific hurdles and public scrutiny.
The initiative being discussed at the New York City meeting in May - Genome Project-write (GP-write) - has been surrounded by worries over creating unnatural beings in the labs.
For the notable project, the group of researchers aim to synthesise from scratch all 23 chromosomes of the human genome and insert them into cells in the lab.
While scientists are yet to come to a conclusion on a specific road map for moving forward of the project, creating a human genome from scratch is a tremendous scientific and engineering challenge, which they believe will hinge on developing new methods for synthesizing and delivering DNA.
The GP-write consortium members believe that turning to human genome synthesis will also enable new cell therapies and other medical advances.
The overall project is still under development, and scientists are also unclear where funding will come from.
The synthetic genomes and chromosomes already constructed by scientists are by no means simple, but to synthesize the human genome, scientists will have to address a whole other level of complexity.
Our genome is composed of more than 3 billion bases across 23 paired chromosomes. And to synthesize the human genome could mean scientists will have to address a whole other level of complexity.
The GP-Write project is being managed by the Center of Excellence for Engineering Biology, a new non-profit organisation.
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Decoding human genome: Scientists creating yeast DNA from scratch - Zee News
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This app analyzes your genome to help you lose weight – New York Post
Posted: at 11:46 am
Could your sweat (or saliva) be a clue to a successful weight loss regime?
The weight-loss app Lose It! and Silicon Valley DNA analytics start-up Helix on Monday released embodyDNA, a service that analyzes 16 different traits as they relate to weight loss, nutrition, fitness and sensitivities to certain foods. It measures everything from body mass index and the metabolism of nutrients to muscle mass and gluten tolerance to give people insights into their genetic makeup, says Kevin McCoy, senior vice president of business development at the Boston-based Lose It.
It costs $190 for a new customer or $110 if you are previous Helix customer. 23AndMe provides ancestry information, but there several other companies provide DNA analysis and nutrition programs to help with weight loss, including DNAFit, Fitness Genes and Nutrigenomix. They can cost as much as $289, depending on the plan. (Privacy policies vary for each service, but Lose It users must opt into their data being aggregated anonymously for future research.)
There are over 100 locations across the genome that play roles in various obesity traits, according to this 2015 study of more than 500,000 genetic samples published in the journal Nature by researchers at the University of Michigan. The large number of genes makes it less likely that one solution to beat obesity will work for everyone and opens the door to possible ways we could use genetic clues to help defeat obesity, senior study author Elizabeth Speliotes said.
But other more recent studies put less emphasis on the link between obesity and DNA. While genotype plays a role in obesity, another 2016 study in the British Medical Journal found that individuals carrying a gene that might give them a propensity for obesity respond equally well to a change in diet, physical activity and/or drug-based weight loss treatments. A genetic predisposition to obesity can be at least partly counteracted through such interventions, it concluded.
Some fitness experts are also sanguine about the usefulness of these DNA analytic services for dieting. Anne Machalinski, a writer for Self magazine and marathon runner, tried Fitness Genes service and was told she had an increased obesity risk and had muscles that recovered quickly from exercise. These recommendations are essentially common sense of the eat less and move more variety, she wrote for Self, plus a push for resistance, strength and high intensity interval training.
Still, as this 2016 study in the British Medical Journal concluded, DNA analysis can motivate people to lose weight. It can be a life or death decision: Weight gain in early and middle adulthood will increase health risks later in life, researchers at the Harvard T.H. Chan School of Public Health said last week. People who gained 5 to 22 pounds before aged 55 increased their risk of premature death, chronic diseases and decreased the likelihood of achieving healthy aging, it found.
On the plus side, theres also plenty of other common sense data to help people stay fit and healthy. Americans log nearly 6 percent more calories on Saturdays than any other day of the week, and an extra 3 percent calories than normal on Fridays, according to separate analysis of millions of calorie counters from Lose It! Breakfast and dinners on weekends when people are either with friends or kicking back are also a time for a spike in calories over other mornings (by between 6.5 percent and 7 percent).
And Americans who are keeping tabs on their weight might also do well to watch the clock. Snacks that are better for you such as nuts, vegetable slices or fruits peak at around noon, followed by a slightly smaller rise in savory and sweet snacks at that, according to market research company The NPD Group, but sweet snacks such as candy, chocolate and ice-cream peak in the evening just after 8 p.m. A third of snack and/or appetizers are consumed during lunch or dinner.
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This app analyzes your genome to help you lose weight - New York Post
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Tomorrow Night, Regent College, Adam and the Genome – Patheos (blog)
Posted: at 11:46 am
Since 1982 the Gallup Poll [a repost of RJSs post because tomorrow night Dennis and I will be giving a public lecture at Regent College(Vancouver) on our project] has been asking Americans about their views on evolution and human origins. This week they released the results of their most recent survey conducted in early May of this year (here). The question posed (with the order of options randomized):
Which of the following statements comes closest to your views on the origin and development of human beings:
The answers have changed modestly over the last 35 years, with the most significant change an increase in the percentage of those who are comfortable with no guidance at all. This has increased from 9 to 19% over the years, with a concomitant decrease in those who see God involved in the process in one way or another. The plot to the right summarizes the data reported by Gallup. Ive added error bars at the +/- 4% level reported for the current poll as this helps to clarify the reliability of the results.
The latest poll is noteworthy in that it marks the first time that creation in their present form within the last 10000 years was not the clear favorite and the first time this response dropped below 40%. Whether this is a blip (similar to the dip in 2010) or represents a trend remains to be seen. It is encouraging, however, that the drop in the young creation view is countered by an increase in those comfortable with God guiding development over millions of years rather than an increase in the no guidance position.
The Gallup report analyzes these results according to religious views, church attendance, and education level. There are no real surprises here those who attend church regularly are far more likely to agree choose the young creation view (65% of weekly attenders). The results also correlate strongly with education. The difference between the respondents with and without a college degree is striking. Postgraduate education has a smaller influence.
Is a change afoot? An enormous number of book have been published over the last decade wrestling with the questions of evolution and Christian faith. Ive reviewed or commented on several dozen books on this blog, with more on the way (I am not sure of the exact number Ive read and reviewed I stopped counting and returned to writing this post when I passed 36 on the shelves in my study). I am currently working through Adam and the Genome, Evolution and the Fall, Science and Christianity, and The Emergence of Personhood, three of which focus on the questions raised by human evolution.
Most of the books that have been, and are being, published work through the theological and biblical questions raised by evolution. This is significant. As a church we are digging into the important questions. These book are being published (often by relatively conservative Christian publishers) and are being read. At the recent BioLogos conference, one author noted that publishers who shied away from his work a decade ago as too controversial are approaching him about the possibility of publishing his next book.
Although resistance remains, I have found far more willingness to listen and understand than was common a decade ago. Dennis Venema recently made a similar observation on a post at BioLogos: A Decade of Evolutionary Creation: Milestones and Signposts.
Evolutionary creation is a viable option for understanding and making sense of Gods world.
Do you think there is an increased openness to evolutionary creation?
If so, what is driving this change?
If you wish to contact me directly you may do so at rjs4mail [at] att.net.
If interested you can subscribe to a full text feed of my posts at Musings on Science and Theology.
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Tomorrow Night, Regent College, Adam and the Genome - Patheos (blog)
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What’s next in consumer genetics? Helix’s ‘app store for your genome’ – Genetic Literacy Project
Posted: at 11:46 am
A Silicon Valley startup called Helix is betting on the notion that not only do people want to learn more about their DNA, but theyll also pay to keep interacting withit.
the company, which was founded in 2015 with $100 million from genomics giant Illumina, is launching its much-anticipated online hub where people can digitally explore their genetic code by downloading different applications on their computers or mobile devices. Think of it as an app store for your genome
From the consumer side, people will have to get their genes sequenced only once, then they can choose from different apps in categories like ancestry, fitness, health, and nutrition and pay as they go
One company, Exploragen, says it can tell you about your sleep patternslike whether youre a morning person or a night owl Another company, Dot One, willexamine the tiny portion of your genes that makes you different from everyone else and print that unique code onto a customized fabric scarf
A third company, Insitome, has an app that will determine what percentage of your DNA you inherited from Neanderthals and how those traits are relevant to your health.
The GLP aggregated and excerpted this blog/article to reflect the diversity of news, opinion, and analysis. Read full, original post:A DNA App Store Is Here, but Proceed with Caution
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What's next in consumer genetics? Helix's 'app store for your genome' - Genetic Literacy Project
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Large malaria genome study highlights surprising number of potential drug targets – The Pharmaceutical Journal
Posted: at 11:46 am
Source: Sinclair Stammers / Science Photo Library
In the first large-scale study of malaria gene function, researchers at the Wellcome Trust Sanger Institute analysed more than half of the genes in the genome of one species of malaria parasite,Plasmodium berghei
The genomes of malaria parasites contain many genes of unknown function. However, knowing the genes and pathways that contribute to parasite growth is critical to guiding the discovery of new drug targets.
In the first large-scale study of malaria gene function, researchers at the Wellcome Trust Sanger Institute analysed more than half of the genes in the genome of one species of malaria parasite, Plasmodium berghei. To do this, they measured the growth rates in mice of 2,578 P. berghei knockout mutants, each of which were tagged with a unique barcode.
It was found that during a single blood stage of its life cycle, the P. berghei parasite requires around two-thirds of the genes looked at to develop normally.
Publishing their results in Cell[1] (13 July), the researchers say that this shows there are many more potential targets for new antimalarial drug development than previously thought.
Citation: Clinical Pharmacist, CP July 2017 online, online | DOI: 10.1211/CP.2017.20203236
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Jeff Broin receives George Washington Carver Award – Wallace’s Farmer
Posted: at 11:46 am
Jeff Broin, CEO of POET, the worlds leading producer of biofuels, received the George Washington Carver Award at a July 24 ceremony at the BIO World Congress in Montreal. The Carver Award recognizes significant contributions by individuals in the field of industrial biotechnology and its application in biological engineering, environmental science, biorefining and biobased products.
I am very humbled by this award. George Washington Carver was an historic leader in finding new potential in agricultural products to meet the worlds needs, Broin said. Thats what we strive to do each day at POET, whether its producing biofuel from starch and cellulose or finding new or better ways to produce co-products such as distillers grain, corn oil, fiber, liquefied CO2 and more. I believe agriculture is the key to solving many of our worlds challenges.
Related: POET DSM Opens First Commercial Cellulosic Ethanol Plant in the U.S.
Creating new markets for ag products
Carver was a true visionary," Broin said. "At POET, we follow that vision, developing additional products and bioprocesses to replace petroleum-based products. We believe the agricultural potential of the world is virtually untapped. The world is beginning to learn that we need to return to the sun, the soil and the seed.
Jeff Broin is one of the great innovators and entrepreneurs in the industrial biotechnology sector, said Brent Erickson, executive vice president of BIOs Industrial & Environmental Section. He ranks among the most influential leaders in agriculture as well. Biofuels have created new markets for agricultural products and rejuvenated rural America. Jeff Broin has positioned POET at the forefront of developing cellulosic ethanol and improving the economics of biofuel production.
As POET CEO, Broin grew the company from a 1-million-gallon-per-year facility in 1987 into the world's largest biofuels producer, with 1.8 billion gallons of annual fuel production and 10 billion pounds of high-protein animal feed, among other products.
Success in developing new technology
Broin says POET has always placed a high priority on research, from the laboratories at its headquarters in Sioux Falls, South Dakota, to its pilot plant/research facility in Scotland, South Dakota, to its commercial-scale demonstration cellulosic biofuel plant in Emmetsburg, Iowa, as part of POET-DSM Advanced Biofuels. This focus has led to industry-leading technology such as BPX (POETs proprietary no-cook production process), total water recovery technology, unique corn oil and distillers grains products, cellulosic biofuel development and more.
The George Washington Carver Award is also sponsored by the Iowa Biotechnology Association. Joe Hrdlicka, executive director of the Iowa Biotechnology Association, said, Jeff Broin has created an environment at POET where new ideas thrive throughout the value chain of new economic opportunities for American agricultural producers and rural communities. His business model truly reflects the ideas and passion spawned by George Washington Carver a century ago.
Past Carver Award Recipients:
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Mutation explains why some men live to 100 – ISRAEL21c
Posted: at 11:46 am
Just as smaller animals of a given species generally live longer than their larger cousins, one might expect that taller humans are genetically programmed to sacrifice longevity for height.
But its not that simple.
A major multinational study of 841 men and women from across four populations found lower levels of insulin-like growth factor 1 (IGF-1) in men living to age 100 and yet most of them were taller than men in the younger control group.
The apparent explanation for this head-scratcher is that some long-lived men and only men have a genetic mutation that makes their growth hormone receptors more sensitive to the effects of the hormone. The cells absorb less growth hormone, yet protein expression is increased by several times.
This mutation seems to be responsible for their ability to live about 10 years longer than the control group of 70-year-old men without the mutation, even though they have a lower amount of growth hormone and are about 3 centimeters (1.18 inches) taller.
The lead author of the study is Prof. Gil Atzmon of Albert Einstein College of Medicine in New York and head of the Laboratory of Genetics and Epigenetics of Aging and Longevity at the University of Haifa. Since 2001, Atzmon has been studying the human genome and its impact on aging and longevity.
Longevity genes
The researchers working with Atzmon looked at four elderly populations: 567 Ashkenazi Jews in the Longevity Genes Project at Einstein, 152 from a study of Amish centenarians, and the rest from an American cardiovascular health study and a French longevity study.
In 2008, the Longevity Genes Project found a genetic mutation in the IGF-1 receptor of some women, though its not the same as the one affecting mens lifespan.
We knew in the past that genetic pathways associated with growth hormone were also associated with longevity and now we have found a specific mutation whose presence or absence is directly related to it, said Atzmon.
This study makes it an established fact that there is a relationship between the function of the growth hormone and longevity. Our current goal is to fully understand the mechanism of the mutation we found to express it, so that we can allow longevity while maintaining quality of life, he added.
The 16 researchers involved the study, published June 16 in Science Advances, are associated with institutions in Israel and France as well as the US states of New York, Maryland, California, Vermont, Massachusetts and Washington.
Clue to longer life
While more research is needed to understand why the receptor mutation affects longevity and why it happens only in men, the study suggests that making a slight change in this specific piece of DNA could possibly make people live longer.
Although the presence of the mutation almost certainly ensured longevity, Atzmon stressed that many other factors affect longevity and that many men without the mutation also live to 100 and older.
Atzmon is one of the principal researchers in the Longevity Genes Project at Einstein along with Israeli endocrinology specialist Dr. Nir Barzilai.
Their groundbreaking 10-year study of healthy Ashkenazi Jews between the ages of 95 and 112 and their children attempted to understand why humans dont all age at the same rate, and why only one in 10,000 individuals lives to 100.
The centenarians were found to have genetic protective factors (longevity genes) that overcame factors such as diet and lifestyle.
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Mutation explains why some men live to 100 - ISRAEL21c
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The Internet of Living Things – Scientific American (blog)
Posted: at 11:46 am
10 A.M.It is hot and sultry in the slums of the Campina Barreto neighborhood on the north side of Recife, in Brazil, and a public health worker named Glaucia has just taken a blood sample from a young, pregnant patient. Glaucia feeds it into a portable sequencer the size of a USB stick, plugs the sequencer into her computer and waits for the results. The device identifies genetic markers of the Zika virus, but flags the fact that this is a mutated strain that could be resistant to existing vaccines. She reports the information to her colleague, Franco, at the nearest hospital and to public health authorities. They need to know that this could signal the start of an outbreak.
This scenario is imaginary, but researchers around the world now use pocket-size genomic sequencers to rapidly detect resistant pathogenic strains in hospitals, explore microbial diversity in Antarctic ice valleys, and diagnose infectious agents in food supply and aboard spaceships (the device works in microgravity). In 2015, for example, Johanna Rhodes from Imperial College London relied on portable sequencers to identify the genetic makeup of Candida auris, a multidrug-resistant fungal pathogen that had caused an outbreak in a London hospital. The same year, a research team from Birmingham University flew to Guinea and used the same technology to detect strains of Ebola in human blood. In a few months, they had sequenced 142 Ebola genomes on the spot, producing results less than 24 hours after receiving an Ebola-positive sample.
But what if sequencer-equipped researchers were able to transmit what theyre learning directly to others? Imagine students in universities becoming the first sequencing line of defense by detecting bacteria resistant to antibiotics and educating their neighbors about them. Imagine the same neighbors equipped with portable sequencers to identify microorganisms in soils capable of fighting resistant pathogens. These new bio-citizens would be socially responsible actors who use biology as the main language to understand themselves and the world around them, playing an increasing role in protecting global health and ecosystems.
This is the utopian version of what visionaries call the second genomic revolution, where sequencing our genomes and those of other species becomes a pervasive data market in which DNA is the primary currency. Yet we must remain lucid about who will primarily contribute and who will reap the rewards of streaming our DNA to the cloud. The way forward is to make sure that this trove of data does not benefit only those who already reign over our digital infrastructures but build counter powers, global commons where citizens can learn to turn their own data into innovations.
The new lab-in-your-hand technology is the product of Oxford Nanopore Technologies, a British company, whose ambition is to democratize genomic sequencing. Its sequencer, called MinION is as small as a USB-stick and easy to use for any apprentice scientist who knows how to prepare samples of blood, bodily fluids or water to be fed into the device. Such preparation is easily done by amateur biologists in DIY bio labs. Researchers and clinicians across the world have now adopted these portable sequencers, some to detect foodborne outbreaks in hospital, others to analyze the DNA of new species in the jungle. As early skepticism fades away, industry giants (Illumina and Roche) and newcomers (Genapsys) alike are showing interest in following Oxford Nanopores head start in portable sequencing.
If the ambition is to promote more distributed use of genomic sequencing, users also need a ready-made platform for interpreting genetic data. Oxford Nanopore has designed an intelligent cloud lab, Metrichor, to be used for genomics data storage in conjunction with smartphone apps that interpret the meaning of DNA sequences.
The convergence of automation technologies, intelligent algorithms and cloud computing is progressively making genomics available to less skilled actors. While this does not necessarily ensure democratization, it does enable us to imagine it. And so, what if it actually happens?
The world around us would be equipped with increasingly sophisticated bio-sensing capacity: the ability to identify the genetic composition of our bodily fluids, species surrounding us and microorganisms on our skins and in our backyards. Portable genomic sequencers in our pockets and cell phones would become part of our networks of sensorswhat we already call the Internet of things (IoT).
The attributes of a new bio-citizen then look like this: scientists, patients, congressmen, employeeseveryonewill be monitoring the DNA of their own bodies on shared cloud labs. Portable genomic sequencers, the size of a USB stick and connected to our smartphones, would also be integrated to our most strategic technical systems, including agro-food facilities, airports, battlefields and hospitals. These DNA-reading sensors would identify the nature, transmission paths and mutations of deadly viruses, engineered bacteria and even forgotten lethal pathogens that could one day be freed by the melting permafrost. In their home, individuals would have access to liquid biopsies blood tests that could track their most vital biomarkers and identify at an early stage the pieces of DNA shredded by a cancer tumor or a viral agent. If millions of citizens were streaming these data to the cloud, they would build the most powerful data set for preventive and precision medicine the world has ever known. The genetic identity of any living thing, then, acquires a new life on the Internet. We enter the age of the Internet of living things (IoLT).
The amount of genomics data to be stored, curated and protected in the digital bio-space will keep growing, requiring powerful and expensive computing platforms. It will create a complex architecture with new needs related to the governance of such an increasingly data-driven society.
Without access to the cloud, as provided by Google and Amazon, many biomedical projectsfrom J. Craig Venters Human Longevity to genome-wide analyses focused on autism and Alzheimerscould hardly have taken shape. Google and Amazon offer a deal too tempting to refuse: the most sophisticated cybersecurity strategies as well as analytical speed and power. These services seldom come free; universities, companiesin the future, hospitals, doctors and citizenswill likely keep paying for each genome to be stored, analyzed or transferred to a different repository.
Another hard truth is that most analyses of genomic data are comparative, meaning what can be learned about a new and potentially important genomic sequence is based on some existing point of reference. Yet, genomic sequences of interest risk being held by private databasesthink 23andMethat gain a competitive advantage by selling access to their genetic gold.
As a consequence of the growing number of players that may be involved in the process of generating, collecting and processing the data, determining the legal ownership of such data may prove increasingly complex. Like our personal information gathered by the IoT, our genetic secrets might end up trapped by 10,000-word-long consumer agreements.
The powerful and lucrative alliance between genetics and a data-driven society has already made tech giants in Silicon Valley and Seattle the new masters of our digital identities. If we consider the current privatization of consumers data and the erosion of digital privacy, it is not difficult to imagine, in the future, large corporations using their vast computing and machine-learning platforms to commodify continuous streams of genetic data about humans and ecosystems. Global conflicts over ownership would have to be balanced by open-source efforts to ensure that research, data and technological tools primarily serve the public good. The Global Alliance for Genomics and Health is an example, a thriving effort to share genomes across disciplinary and geographical boundaries.
For the Internet of living things to realize its promises, U.S. policymakers and regulators, in collaboration with technologists, should have an ambitious conversation about global data commons. How open and resilient should our big data architectures be, in particular those used for monitoring vital public health and environmental factors?
Experts will also need to consider the challenge and cost of ensuring accuracy when dealing with biological and microbial samples. One can imagine an IoLT node monitoring for Ebola virus and sending a positive signal, which, if not substantiated, could cause panic. The potential of monitoring for biological threats is enormous, but methods to validate data and address personal and collective liability issues are needed.
What is more troubling as we slowly enter the age of ubiquitous genomics sequencing is that we face an increasing socio-economic disparity between the technological elitesSilicon Valley or the new Shenzhen tech Eldoradoand the majority of citizens, the ones who provide data. While I have no hope that this gap will soon be closed, the next decade will first tell us if the new bio-citizen is just in our imagination.
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The Internet of Living Things - Scientific American (blog)
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Stanford announces new Center for Definitive and Curative Medicine – Stanford Medical Center Report
Posted: at 11:45 am
It is a privilege to lead the center and to leverage my previous experience to build Stanfords preeminence in stem cell and gene therapies, said Roncarolo, who is also chief of pediatric stem cell transplantation and regenerative medicine, co-director of the Bass Center for Childhood Cancer and Blood Diseases and co-director of the Stanford Institute for Stem Cell Biology and Regenerative Medicine. Stanford Medicines unique environment brings together scientific discovery, translational medicine and clinical treatment. We will accelerate Stanfords fundamental discoveries toward novel stem cell and gene therapies to transform the field and to bring cures to hundreds of diseases affecting millions of children worldwide.
The center consists of several innovative pieces designed to allow the rapid development of early scientific discoveries into the clinic that in the past have languished. This includes an interdisciplinary team of basic and clinical scientists to shepherd nascent therapies developed at Stanford. The team will be headed by associate directors Matthew Porteus, PhD, associate professor of pediatrics, and Anthony Oro, MD, the Eugene and Gloria Bauer Professor and professor of dermatology.
To help with clinical development, the center boasts a dedicated stem cell clinical trial office with Sandeep Soni, MD, clinical associate professor of pediatrics, as medical director. In addition, the center has dedicated clinical trial hospital beds in the Bass Center for Childhood Cancer and Blood Diseases located on the top floor of the soon-to-open LucilePackardChildrensHospital. From work performed by scientists over the past decade, the center already has a backlog of nearly two dozen early stage therapies whose development the center will accelerate.
The center will provide novel therapies that can prevent irreversible damage in children, and allow them to live normal, healthy lives, said Mary Leonard, MD, professor and chair of pediatrics and physician-in-chief at Stanford Childrens Health. The stem cell and gene therapy efforts within the center are aligned with the strategic vision of the Department of Pediatrics and Stanfords precision health vision, where we go beyond simply providing treatment for children to instead cure them definitively for their entire lives.
One of the unique features of the center is its close association with the recently opened $35 million Stanford Laboratory for Cell and Gene Medicine, a 23,000-square-foot manufacturing facility located on California Avenue in Palo Alto. One of the first of its kind in the world, the laboratory has the ability to produce newly developed cell and gene therapy therapies according to the Good Manufacturing Practice standards as required for patient treatment.
Headed by executive director David DiGiusto, PhD, the lab can produce diverse cellular products for patient use, such as genetically corrected bone marrow cells for sickle cell anemia, genetically-engineered skin grafts for children with the genetic disease epidermolysis bullosa or genetically-engineered lymphocytes to fight rejection and leukemia.
We are fortunate that Stanford researchers have created such a strong portfolio of innovative candidate therapeutics to develop, said DiGusto. The capabilities of the laboratory will bridge the gap between research and clinical investigation so that the curative potential of these exciting cell and gene therapies can be realized.
For more information about the center, or for information about trials associated with the center, please see https://med.stanford.edu/ptrm/faculty.html, or contact Jennifer Howard at jmhoward@stanford.edu.
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Stanford announces new Center for Definitive and Curative Medicine - Stanford Medical Center Report
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Regenerative medicine startup Rodeo Therapeutics raises $5.9M for drugs to regenerate tissue – GeekWire
Posted: at 11:45 am
Dr. Sanford Markowitz, founder of Rodeo Therapeutics. (Case Western Reserve University Photo)
If you could write a medical wish-list of futuristic technologies, regenerating tissue would be pretty high up there. It could do things like treat a variety of inflammatory conditions and even help cancer patients regrow healthy cells.
A new Seattle-based biotech startup, Rodeo Therapeutics, is hoping its technology can make tissue regeneration a reality, and it has just raised a $5.9 million Series A round from Seattle-based biotech fund Accelerator Corporationto make it happen.
The general idea is simple: Rodeo is hoping to use small-molecule therapies a category most drugs fall into that stimulate the bodys natural regeneration process, like when a skinned knee heals.
Its first focus is to develop a treatmentfor inflammatory bowel disease and one that can help cancer patients cells grow quickly following stem cell transplants. But those goals are just the beginning.
The ability to stimulate the bodys natural processes for tissue regeneration and repair has broad therapeutic potential in disease settings such as ulcerative colitis and in hemopoietic recovery following bone marrow transplantation. Rodeo Therapeutics is focused on developing small-molecule therapies that stimulate these processes and enable new approaches to address serious medical conditions that today have a substantial unmet medical need, said Rodeo Therapeutics founder and cancer researcher Dr.Sanford Markowitz.
The company is currently working on drugs that inhibit an enzyme called 15-PGDH, which has been shown to speed up regenerative processes.
The startup was founded by Markowitz and Dr. Stanton Gerson, researchers at Case Western University, along with Dr.Joseph Ready, a researcher at the University of Texas Southwestern Medical Center.
Its technology is based on their work. Markowitz is an expert in gastrointestinal cancers, where inflammation can cause serious problems; Dr. Gerson specializes in stem cell and genetic research along with gene therapies and cancer drug development; and Dr. Ready works in regenerative medicine and cancer, specifically synthetic and medicinal chemistry.
The startups corporate office is currently in Accelerator Corporations facilities in Seattle, with its founders in Dallas and Cleveland. Rodeos early operations will be overseen by Accelerator, and the funds CEO Thong Le is currently servingas Rodeos CEO.
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Regenerative medicine startup Rodeo Therapeutics raises $5.9M for drugs to regenerate tissue - GeekWire
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