After 44 years of pain, one win stands between Ash Barty and immortality: Aus Open final LIVE – Fox Sports

After 44 years of pain, only Slam final debutant Danielle Collins stands between Ash Barty and immortality in tonights Australian Open womens singles final.

The French Open and Wimbledon champion is trying to become the first Australian to win the Australian Open since Chris ONeil in 1978.

Follow Ash Barty vs Danielle Collins in the Australian Open final below from 7:30pm EST!

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PREVIEW, via AFP

Multi-talented Ashleigh Barty has been a professional cricketer, won a golf tournament and collected two tennis Grand Slam titles, with a third beckoning at the Australian Open on Saturday night.

Few athletes can boost such a varied sporting resume, but the down-to-earth Australian has taken it in her stride.

Widely seen as one of the nicest players on tour, the 25-year-old began playing tennis as a child in Brisbane.

But it was a trip to the Australian Open for a training camp when she was 11 or 12 that proved to be the spark that drove her to where she is today.

To see how professional it was and to see everyone going about their business was really eye-opening. My first taste of it was in the juniors and I loved it, she said this week.

I think being able to get a taste of that kind of lit the flame. You wonder what you can achieve. You wonder what you can do.

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The Australian went on to win the junior Wimbledon title as a 15-year-old in 2011.

But the expectations that came with success took their toll and she made a shock decision three years later to ditch tennis for cricket, signing for Brisbane Heat in the inaugural Womens Big Bash League.

In short, I think I needed just to find myself, Barty said when reflecting on that time of her life.

I felt like I got twisted and maybe a little bit lost along the way in the first part of my career.

While cricket gave her a different perspective about sport, the lure of tennis was never far away and driven by an ambition to taste success again at Wimbledon she returned after a season away.

The break worked wonders and she went from strength-to-strength. Barty broke through for her maiden Grand Slam triumph at the French Open in 2019, became Australias first womens world number one since Evonne Goolagong-Cawley and finally won a cherished Wimbledon crown last year.

So dominant has she been that she ended 2021 as the top-ranked player for a third consecutive year, joining Steffi Graf, Martina Navratilova, Serena Williams and Chris Evert as the only women to achieve the feat.

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Barty should have returned to Paris to defend her Roland Garros title in 2020, but she pulled out over coronavirus fears and picked up her golf clubs instead.

And on a course designed by Greg Norman near Brisbane, she won the Brookwater Golf Club womens title with a commanding 7 and 5 triumph in the matchplay final.

Is there anything you cant do?, asked one social media user at the time.

Barty finetuned her golf game playing rounds with fellow Grand Slam winner Pat Rafter and her long-time boyfriend Garry Kissick, who has been by her side since 2016 and often posts supportive messages on social media.

They got engaged in November, sparking a frenzy of congratulations from fellow tennis stars.

Barty attributes much of her success to her close-knit team, which includes not just Kissick but her family and long time coach Craig Tyzzer, routinely referring to we rather than I when she speaks of her tennis exploits.

Everyone is equally important. Were all equal, she said of her team. I mean, the experiences weve been able to share together have been remarkable, for my whole team. My family, starts with my family, my sisters.

Obviously my professional team who contribute so much time and energy into my career and help me try and live out my dreams.

I genuinely cannot thank them enough for the time and effort they put in to someone else.

AUSTRALIAN OPEN 2022 - Day 13 - Order of Play and Results

Rod Laver Arena

Day session from 12pm

Junior Girls Singles Final: [1] Petra Marcinko (CRO) vs [8] Sofia Costoulas (BEL)

Junior Boys Singles Final: [1] Bruno Kuzuhara (USA) vs [4] Jakub Mensik (CZE)

Night session from 7:30pm

Womens Singles Final: [1] Ash Barty (AUS) vs [27] Danielle Collins (USA)

Mens Doubles Final: Thanasi Kokkinakis (AUS)/Nick Kyrgios (AUS) vs Matt Ebden (AUS)/Max Purcell (AUS)

Follow all the latest from the Australian Open below!

If you cant see the blog, tap here.

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After 44 years of pain, one win stands between Ash Barty and immortality: Aus Open final LIVE - Fox Sports

Violin decomposes as it is eaten by a mushroom in a one-year timelapse – Classic FM

28 January 2022, 12:43

A one-year timelapse of a decomposing violin accompanies German composer, Sven Helbigs, latest work.

The Reishi mushroom is a reddish brown varnished kidney-shaped cap fungus. Nicknamed the mushroom of immortality in English, the mushroom has long been thought to be a talisman of luck, healing, and wellness in Chinese culture.

This fungus is usually found growing on hardwood trees in particular, oaks in warm climates, such as Asia, the South Pacific, Southern Europe and the Southeastern United States.

But one type of wood you probably wouldnt expect to find the fungus on, is the wood of a violin.

In the music video for composer Sven Helbigs latest track,Metamorphosis (meaning a great change in appearance or character), a violin is seen slowly being eaten by aReishi mushroom over the course of a year.

Recorded via timelapse, the result is the eerie decomposition of an instrument like weve never seen before (watch above).

Read more: Funky fungi? Meet the musicians making melodies out of mushrooms

In the music video teaser trailer, Helbig asks the audience, Can you drink a violin?.

For those stumped by his questioning, Reishi mushroom is often made into a tea. According to the tea company Twinings website, Reishi has long been used to manage allergies, autoimmune diseases, sleep patterns, and asthma, due to its immune system-boosting qualities.

The mushroom growing on the Metamorphosis violin is eventually harvested after a year of growth and made into tea. The last imagery we see in the music video is that of a cup of tea being poured.

Seeing the violin used as a type of soil in this scenario perhaps creates more questions than it answers for the viewer. Does the instrument have more value as a part of todays classical music world, or as food for this mushroom of immortality?

Read more: Worlds first vegan violin replaces animal hide glue with wild berries

Helbig is a double ECHO Classical Music Award winner and the co-founder of the Dresdner Sinfoniker, one of the leading symphony orchestras specialising in contemporary music. Other musicians involved in the video include the Mondna Quartet, hornistsAnne Grethen, Jrg Brckner and Robinson Wappler, andtuba player Tom Gtze.

Helbig performs with the London Contemporary Orchestra on 27 April at the Purcell Room, Southbank Centre in London.

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Violin decomposes as it is eaten by a mushroom in a one-year timelapse - Classic FM

Rockies First Baseman Todd Helton Not Elected To Hall Of Fame – CBS Denver

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Rockies First Baseman Todd Helton Not Elected To Hall Of Fame - CBS Denver

Silencing a faulty gene may uncover clues to rare forms of ALS – National Institutes of Health

News Release

Monday, January 24, 2022

NIH-funded preclinical study identifies potential therapeutic approach to treat ALS.

Using an experimental drug, researchers were able to suppress a mutated amyotrophic lateral sclerosis (ALS) gene. Studies in mice demonstrate that the therapy could show promise in treating rare, aggressive forms of ALS caused by mutations in the fused in sarcoma (FUS) gene. The study, published in Nature Medicine, was funded in part by the National Institute for Neurological Disorders and Stroke (NINDS), part of the National Institutes of Health.

The study models how promising gene-targeting therapies can move expeditiously from pre-clinical development to clinical testing, said Amelie Gubitz, Ph.D., program director at NINDS. There is a desperate need for innovative approaches to treating ALS.

ALS, also known as Lou Gehrigs disease, is a fatal neurological disorder that causes the degeneration of motor neurons in the brain and spinal cord. People with ALS rapidly lose muscle strength and eventually their ability to move, swallow, and breathe. Most cases of ALS are sporadic, but at least 10% of cases are familial, or due to mutations in various genes. Mutations in the gene FUS cause severe forms of ALS, referred to as FUS-ALS, including a rare type that begins in adolescence or young adulthood.

In the study, Neil Shneider, M.D., Ph.D., the Claire Tow Associate Professor of Motor Neuron Disorders and Director of the Eleanor and Lou Gehrig ALS Center at Columbia University, New York City, and his team delayed the onset of motor neuron degeneration in mice by using an antisense oligonucleotide drug designed to silence FUS by blocking cells from making specific proteins. Following encouraging results, they administered the drug to a patient with ALS.

Compared to normal mice, mice with a mutated FUS gene had higher levels of insoluble FUS and other ALS-related proteins in their brains and spinal cords. Mice with higher doses of mutant FUS in motor neurons experienced rapid neurodegeneration that began early in life, much like FUS-ALS patients.

The study establishes a mouse model that is highly disease-relevant, said Dr. Shneider. In mice, we found that FUS toxicity was due to a gain of function and was dose-dependent, suggesting that we could treat FUS-ALS by silencing the FUS gene.

In 2019 Dr. Shneider met an individual with ALS in search of therapies that may help her disease. Inspired by her story, Dr. Shneider teamed up with a pharmaceutical company to develop a personalized therapy designed to target the FUS mutation.

In mice, injecting a single dose of the drug into the ventricles, fluid-filled spaces surrounding the brain, delayed the onset of inflammation and motor neuron degeneration by six months. The drug also knocked down levels of FUS by 50% to 80% in the brain and spinal cord. Following drug administration, insoluble forms of other ALS-associated proteins were also cleared.

Under a compassionate use protocol reviewed by the U.S. Food and Drug Administration, Dr. Shneider administered the drug to the patient it had been designed for. The patient received repeated infusions of the drug into her spinal canal for 10 months. During the treatment, the patients rate of motor function deterioration slowed. The patient tolerated the treatment well and there were no medically adverse effects.

The study is an example of a precision medicine, bench-to-bedside effort, said Dr. Shneider. We began with the mouse model to establish a rationale for the drug, conducted efficacy studies in the mouse, moved the drug into a human, and collected valuable data that was ultimately used to support a larger Phase 3 clinical trial.

Treatment began more than six months after clinical onset, by which time the disease had already significantly advanced. As is typical with juvenile-onset FUS-ALS, the disease progressed rapidly, and the patient died from complications of the disease.

By studying the patients brain and spinal cord tissue, researchers found that the drug silenced FUS throughout the nervous system and reversed the toxic nature of FUS and other disease-related proteins. Compared to tissue from untreated FUS-ALS patients and healthy controls, FUS protein aggregatesa pathological hallmark of this form of ALSwere sparse, suggesting that they may have been cleared by the drug. Tissue samples were provided by the New York Brain Bank of Columbia University.

The protein made from the FUS gene has been shown to be important for various cellular processes. Prior studies in mice suggest that FUS mutations result in the production of an abnormal protein that forms clumps, or aggregates, leading to motor neuron damage. By targeting the faulty gene in a way that suppresses toxic FUS activity, gene silencing products like the antisense oligonucleotide drug could potentially reduce or prevent disease progression.

The results were used to support a clinical trial testing the drug in patients with FUS-ALS (NCT04768972).

This study was supported by grants from the NIH (NS106236), Nancy Perlman, Tom Klingenstein, and the Judith and Jean Pape Adams Charitable Foundation.

NINDSis the nations leading funder of research on the brain and nervous system.The mission of NINDS is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.

About the National Institutes of Health (NIH):NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov.

NIHTurning Discovery Into Health

Korobeynikov, V.A., et al. Antisense oligonucleotide silencing of FUS expression as a therapeutic approach in amyotrophic lateral sclerosis. Nature Medicine, January 24, 2022. DOI: 10.1038/s41591-021-01615-z

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Silencing a faulty gene may uncover clues to rare forms of ALS - National Institutes of Health

Omicron BA.2: Should we be worried? – Medical News Today

A new version of the Omicron variant of SARS-CoV-2, known as BA.2, has emerged. Although experts are unsure about its effects, they know that it is spreading quickly and has 20 mutations in the area that most COVID-19 vaccines target.

Scientists first identified the BA.2 subvariant of Omicron in India and South Africa in late December 2021. Since then, it has spread to several countries, including the United States, the United Kingdom, and Israel.

The subvariant virus has also spread rapidly in Denmark, increasing from 20% of all COVID-19 cases in the country in week 52 of 2021 to 45% in the second week of 2022.

Despite its rapid spread in the country, initial analyses show no difference in hospitalizations between the BA.2 subvariant and the original form of Omicron, also known as BA.1.

Studies, however, are still ongoing to understand the infectiousness of BA.2, alongside how effective vaccines are against it.

While BA.2 is not currently a variant of concern, public health officials in the U.K. have taken enough interest in its spread to designate it as a variant under investigation.

To understand more about the emerging subvariant, Medical News Today spoke with six experts in public health, immunology, and infectious diseases.

Omicron has three main [subvariants] BA.1, BA.2, and BA.3 according to the World Health Organization (WHO), Dr. Donald C. Vinh, associate professor in the Department of Medicine at McGill University, Canada, told MNT.

Up until now, the overwhelmingly large majority of all Omicron cases has been BA.1. However, in some places, the BA.2 has emerged and has spread faster than BA.1, he went on to note.

This sister variant, which is still Omicron, is interesting because it seems to be displacing Omicron in certain parts of the world, Dr. Amesh A. Adalja, senior scholar at Johns Hopkins Center for Health Security, told MNT. There is speculation that it may be more transmissible than its sibling.

How the fast spread of the BA.2 subvariant may affect public health is still under investigation.

The Omicron SARS-CoV-2 variant has been interesting to scientists because of its comparatively (i) higher number of mutations, which [] allow it to partially evade peoples immune response; (ii) higher transmissibility and pathogenicity, i.e., its greater ability to infect and cause disease; and (iii) lower virulence, i.e., its lower ability to cause severe disease, Dr. Richard Reithinger, Ph.D., vice president of global health at RTI International, explained.

The big question for newly identified variants and subvariants such as omicron BA.2 is how these above three characteristics vary from the original SARS-CoV-2 virus [variant] or the Omicron variant and why.

Dr. Richard Reithinger, Ph.D.

If some countries are now reporting a surge in the proportion of BA.2 subvariant infections, is it because the additional mutations make it more transmissible or allow it to evade the immune response more easily than the other Omicron subvariants? Will BA.2 result in the same clinical pathology as the Omicron parent variant (B.1.1.529) and subvariants (BA.1 and BA.3)? Also, how do current therapeutic options and vaccines fare against BA.2?

According to Dr. Reithinger, these are some of the questions that public health experts must take into consideration while keeping this subvariant under observation.

While researchers are still gathering data on how BA.2 may affect the population at large, laboratory studies have already verified many of its molecular properties.

BA.2 is missing the spike 69-70 mutations, so it does not cause S gene target failure, making it harder to identify on PCR tests, Dr. Anna Ssentongo, assistant professor of public health at the Penn State College of Medicine, told MNT.

Because of this, BA.2 was nicknamed the stealth variant, she explained.

Dr. Ssentongo added that BA.2 has more than 20 mutations in its spike protein, which is a target of many COVID-19 vaccines because the virus uses it to enter healthy cells. Although this difference may make BA.2 more resistant to vaccines, further research is necessary to confirm any effects.

Similar to its parental lineage (Omicron), it is expected to be highly transmissible and result in less severe disease than the Delta or Beta variants, especially if one is fully vaccinated and even better boosted, added Dr. Reithinger. However, ultimately, this would have to be confirmed by ongoing laboratory and clinical studies, which are expected to provide results in the next couple of weeks.

Dr. Vinh agreed that before drawing any conclusions on how the subvariant may affect public health, further research is necessary:

It is important to mention that there are very limited data on clinical differences between BA.2 and BA.1. Specifically, we have no firm data to know if BA.2 is more contagious, results in more severe disease, or can evade immunity better than BA.1. Nonetheless, early data from Denmark and the U.K. suggest that BA.2 may be more contagious than BA.1.

When MNT asked whether we should be concerned about BA.2, Dr. Pavitra Roychoudhury, research associate at the Vaccine and Infectious Disease Division at the University of Washington, explained: It remains to be seen how BA.2 will compete against currently circulating viruses [], and also whether it causes more severe disease. [] We will continue to monitor frequencies of BA.2 through the use of genomic surveillance.

Dr. Adalja agreed that much remains to be seen: We know that this has been a variant that has been present since the early days of Omicron and that it has some similar and some distinct mutations. It is unclear, as of now, whether it is more transmissible. [It] likely has the same characteristics when it comes to vaccine efficacy and severity.

It is too early to know what role [BA.2] may play. Its likely that it will just be part of the Omicron wave and they extend it over time and eventually become the dominant version of Omicron. More study is needed.

Dr. Amesh Adalja

However, Dr. Barton F. Haynes, director of the human vaccine institute in the Department of Medicine at the Duke University School of Medicine, said that due to its molecular changes, there might be cause for concern regarding BA.2.

We are worried that because it is so different than Omicron BA.1, it may escape current vaccines and Omicron BA.1-neutralizing antibodies, he noted. To this point, we are working to study the Omicron BA-2 virus to see whether current vaccine-induced neutralizing antibodies neutralize it.

Whether BA.2, or any other Omicron subvariant or other SARS-CoV-2 variant, there is irrefutable evidence that existing vaccines are quite effective in protecting people against infection and highly effective in protecting people from developing severe disease or worst case scenario dying upon SARS-CoV-2 infection, explained Dr. Reithinger.

Additionally, even if vaccinated, people should consider adhering to nonpharmaceutical interventions, such as face masks, physical distancing, and handwashing, particularly when in crowded and/or high transmission environments, he advised.

For live updates on the latest developments regarding COVID-19, click here.

Excerpt from:
Omicron BA.2: Should we be worried? - Medical News Today

Gene therapy of prostate cancer using liposomes containing perforin expression vector driven by the promoter of prostate-specific antigen gene -…

This article was originally published here

Sci Rep. 2022 Jan 27;12(1):1442. doi: 10.1038/s41598-021-03324-6.

ABSTRACT

Perforin secreted from cytotoxic lymphocytes plays a critical role in cancer immunosurveillance. The aim of this study was to investigate the therapeutic potential of liposomes containing perforin expression vector driven by the promotor of prostate-specific antigen (PSA). The anti-tumor effect of perforin was analyzed using prostate cancer (PC) PC-3 cells in which perforin expression was controlled by Tet-on system (PC-3PRF cells). Liposomes encapsulating PSA promoter-driven perforin expression vector (pLipo) were constructed for its specific expression in PC. The anti-tumor effect of pLipo was evaluated in vitro using docetaxel-resistant PC 22Rv1 PC cell line, 22Rv1DR, and PC-3 cells in the presence of human peripheral blood mono nuclear cells (PBMCs) and also in vivo using male nude mice bearing 22Rv1DR cell-derived tumor xenograft. Induction of perforin significantly inhibited growth of PC-3PRF cells. Treatment with pLipo induced perforin expression in 22Rv1DR cells expressing PSA but not in PC-3 cells lacking it. Treatment with pLipo at a low concentration was prone to inhibit growth of both cell lines and significantly inhibited growth of 22Rv1DR cells when co-incubated with PBMCs. The combined use of pLipo at a high concentration with PBMCs showed nearly complete inhibition of 22Rv1DR cell growth. Intravenous administration of pLipo via tail vein increased the level of perforin in tumor and serum and significantly decreased the tumor volume. Our results suggest that liposome-mediated PC-specific expression of perforin could be a novel therapy for advanced PC.

PMID:35087064 | DOI:10.1038/s41598-021-03324-6

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Gene therapy of prostate cancer using liposomes containing perforin expression vector driven by the promoter of prostate-specific antigen gene -...

Wellness Wednesday: neurologist concerned about Multiple Sclerosis trend hes seen throughout the pandemic – WSYR

SYRACUSE, N.Y. (WSYR-TV) Central New York has the highest population of patients with Multiple Sclerosis (MS) in the nation. Doctors have been speculating why for years, and it may be getting worse.

A neurologist at St. Josephs Health is concerned about the trend hes seen throughout the pandemic.

Dr. Fahed Saada recently treated a 24-year-old man. His brain and spine were riddled with lesions. Hes in the early stages of MS and joins a growing list of Saadas patients, adding to a trend no neurologist wants to see.

Ive never seen so many acute Multiple Sclerosis cases over the years compared to this past year and I dont know why.

Saada says other viruses can increase our risk, but it will be years before we learn COVID-19s contributions, if any. In the meantime, more people are getting sick.

Early treatment can give patients some improvement, but over time, MS progresses.

The disease disrupts the brains ability to send messages to the rest of the body. Theres no cure, and eventually, it causes permanent damage to the nerves.

These lesions, if theyre not treated appropriately and quickly, they become what we call black holes in the brain.

Its hard to stop an uptick in cases when doctors dont know whats causing it.

However, neurologists do know that places north of the equator are at a higher risk because patients with MS have low vitamin D levels.

Doctors also know we here in Central New York dont get a lot of sunlight in the winter.

For now, though, Saada says its a medical mystery doctors desperately want to solve.

Saada says a vitamin D supplement may help boost your prevention, but you should always talk to your doctor before making any changes to your medication and supplements.

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Wellness Wednesday: neurologist concerned about Multiple Sclerosis trend hes seen throughout the pandemic - WSYR

8 Things Neurologists Do When They Have A Headache – HuffPost

Whether stress-induced or genetic, headaches are a common condition that can affect anyone. This includes neurologists AKA the specialists who treat headache disorders.

Headache is any pain affecting the head, upper face or upper neck. Headaches are called primary when they arise from biological changes within the brain itself, Robert Kaniecki, the director of the UPMC Headache Center in Pittsburgh, told HuffPost. These include migraine headaches, tension-type headaches, and cluster headaches.

Migraine-induced headaches cause additional symptoms such as nausea, sensitivity to light and noise, fatigue, visual disturbances and more. People may also experience secondary headaches if there is another underlying illness or cause for the headache, Kaniecki said.

Worldwide, headache disorders are considered one of the most common yet under-treated disorders of the nervous system. Additionally, a 2018 study found that one in six people in the U.S. reported having a migraine or severe headache over a three-month period.

HuffPost spoke to neurologists about the things they personally do when experiencing a headache, and why these go-to strategies work.

Find a calming space.

Creating a quiet and relaxing environment is often the first step some neurologists take to alleviate headache pain.

If I have a headache, I rest or lie down for as long as I can, and it doesnt depend on the time of day, said Faye Begeti, a neurology doctor and neuroscientist in the U.K. With migraines in particular, people usually find that they have to lie down in a quiet, dark room.

Distract your mind.

With busy schedules and responsibilities, taking a quick siesta isnt always feasible. Rami Burstein, a professor of anesthesia and neuroscience at Harvard Medical School, explained that he tends to utilize relaxing distractions when he cant power nap in the workplace.

As contrary as it may sound, walking can be helpful and reading, Burstein said.

Figure out your triggers.

Understanding your headache triggers can serve as both a preventative and in-the-moment approach to address pain.

Most of my migraine attacks are visually triggered or are triggered when I am ambivalent or worried about a decision or situation. The latter is a bit harder to control, but its fascinating to recognize, said Jan Lewis Brandes, the director and founder of the Nashville Neuroscience Group. Red wine can be a trigger for me, so I am careful about not having more than a few ounces.

Additionally, a common headache trigger is sleep disturbances. Theres a misconception that headaches are primarily caused by sleep deprivation, but Begeti explained that sticking to a consistent sleep schedule may be more important than the amount of sleep you get every night.

This is something that I didnt know when I was at university, so I would reliably have a headache every single Saturday after staying up late the day before, and sleeping in on the weekend, Begeti said.

Westend61 via Getty Images

Get hydrated ASAP.

Many neurologists pay closer attention to what they drink when experiencing headache pain. As simple as it sounds, water is your best friend when you have a headache or migraine.

Kristina Lopez, an assistant professor at the West Virginia University Rockefeller Neuroscience Institute and headache specialist, said that her headaches are typically a signifier that she needs to up her hydration. While Lopez explained that researchers arent quite sure why drinking water eases headache pain (there are a number of theories), its a cheap and safe preventative and as-needed treatment strategy.

I finally took my own advice and started getting a consistent eight hours of sleep and drinking more water, Lopez said. Its wild how much better I feel.

Try drinking a little coffee, too.

Though it may seem counterintuitive, caffeine can actually be a remedy for headaches. Brandes said that drinking a cup of coffee is the first step she takes when combatting a migraine attack, followed by drinking a glass of water and taking medication.

Caffeine causes blood vessels to narrow and restricts blood flow around the brain, which can relieve pain. However, moderation is key: Consuming caffeine on the regular may have the opposite effect, leading to withdrawal headaches if you suddenly stop drinking your morning espresso or green tea.

Eat smaller meals throughout the day.

Interestingly, another personal tip from Kanieki is to break snacks and meals into five to six portions throughout the day.

This is because low blood sugar may exacerbate headache pain, along with migraine symptoms. Try swapping up your meal times or breaking down bigger meals into smaller parts that you eat intermittently and see if it helps.

Take pain relievers when necessary.

Depending on the severity of her headache, Begeti will take over-the-counter pain medication such as non-steroidal anti-inflammatory drugs (aka NSAIDs) or acetaminophen. However, be sure to keep track of the amount of pain relievers you take: Begeti noted that she limits her monthly intake of over-the-counter pain medication to under 10 days a month to avoid medication-overuse headaches.

If you are experiencing more severe pain or symptoms, it may be worth a trip to the neurologist to see if you could benefit from prescription medication.

I get migraine attacks and will take a triptan an as-needed migraine pain medication and a nausea medication when I feel an episode coming on, Lopez said.

Remember that some factors are outside of your control.

While some things can help you prevent headache pain, its important to note that not every headache can be linked to lifestyle or environmental factors.

Sometimes there are no notable triggers to headaches, Begeti said. A big part of why people get headaches is due to genetics, and I see headaches that run in families.

Headache pain can range from mild to debilitating. Trying neurologist-approved strategies until you find what specifically works for you may help to alleviate your pain in the long run. Establishing a unique, at-home routine is vital to treating these conditions effectively.

Its important to listen to your body. I find that a headache may resolve if I do that and it certainly prevents it from getting worse, Begeti said.

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8 Things Neurologists Do When They Have A Headache - HuffPost

Diagnosis and management of functional neurological disorder – The BMJ

Our search found 37 bedside clinical tests or groups of tests for motor FND (functional weakness and functional movement disorder) that had some formal validation (table 2). Sample size varied between 8 and 107 patients with FND. Most investigations of positive signs were conducted in a single study or a small number of studies (maximum five for the Hoover sign), allowing for the calculation of pooled specificity and sensitivity by merging data from different studies. Five studies reported on the inter-rater reliability of positive signs.

Overall, the specificities of validated signs are high, ranging from 64% to 100%; however, the sensitivities are lower, ranging from 9% to 100%. Inter-rater reliability of these signs is overall good to excellent (defined as values: <0.2 poor/0.21-0.4 fair/0.41-0.6 moderate/0.61-0.8 good/>0.8 excellent).

General signs common to all FND presentations are: variability of the symptom, which can be observed during history taking and examination, and effortful or grimacing expression while following the examiners instructions during examination. If suspecting a functional movement disorder, test oculomotor function to show abnormal eye movements and in particular convergence spasm,100 even if the patient did not endorse this as a concern during history taking.

When assessing gait, look for typical positive signs such as monoplegic leg dragging, excessive visible effort (huffing and puffing sign),50 falling toward support (chair nearby, table, wall), excessive slowness, hesitation or caution, non-economic posture (for example knee flexed), and knee buckling (sudden loss of tone at each step).101 Asking a patient with severe gait disorder to propel a chair while sitting on it will show improvement in FND.51

When assessing hemifacial spasm, look for typical signs such as long contraction of more than three seconds, lip pulling (tonic deviation of the lip, often the lower one) sometimes with platysma contraction, and lack of other Babinski sign for hemifacial spasm (other Babinski sign=eyebrow elevation on the side of the spasm).102 Positive signs for functional orofacial movements in comparison with tardive dyskinesia are: lack of chewing movements, lack of self-biting, lingual movements without mouth movements, and abnormal speech.45 A large case series (61 patients) that focused on facial functional movement103 reported involvement of the lip as the most frequent (60.7%, with the lip pulling feature).

When assessing movements of the trunk, look for the typical positive sign of asymmetry in strength of the sterno-cleido-mastoid muscle.53 A functional Romberg sign is described as large movements of imbalance with sudden steps and no falls and improvement with cognitive distraction or numbers drawn on the back.48

When assessing episodes of cataplexy (brief, symmetrical loss of muscle tone with retained consciousness precipitated by strong emotions) look for positive signs54 such as lack of sudden facial expression change, facial jerks or grimaces, postural dyscontrol (head drop, trunk fall), in addition to preserved tendon reflexes (which typically disappear during cataplexy associated with narcolepsy).

When assessing upper arm weakness, look for discordance or inconsistency in strength (at different instances during the examination), as well as a give-way/collapsing pattern, drift without pronation, and/or co-contractions of agonist and antagonist muscles preventing movement of the tested joint. As a cautionary note, give-way/collapsing pattern of weakness is common in patients with pain limited weakness (and pain limited weakness should not be mistaken for functional limb weakness).104 In cases of complete hand plegia, involuntary abduction of the fifth finger can be seen when the patient is asked to do a forced abduction against the examiners resistance on the healthy hand.58 The flex-ext sign, which is the equivalent of the Hoover sign,105 can be elicited as follows: the involuntary flexion of the arm at the elbow that occurs when the patient focuses on extending the healthy elbow against the examiners resistance is better than the voluntary flexion.59

When assessing lower limb weakness, also look for discordance/inconsistence, give-way/collapsing weakness, co-contractions, and the Hoover sign.61 The classical way to describe a positive Hoover sign is when the involuntary hip extension (when the patient focuses on flexing the healthy leg against the examiners resistance) is stronger than the voluntary hip extension. A similar pattern can be found during leg abduction60: when the patient is asked to do a forced abduction with both legs against the examiners resistance, the weak leg will have a stronger involuntary abduction than when the voluntary abduction is tested. In patients with severe unilateral leg weakness, positioning passively the leg in flexion with the soles on the bed (spinal injury test)62 shows a discordance in strength as the weak leg will not fall on the side, as expected in complete weakness.

When assessing tremor, typical signs are distractibility, entrainment, and increase in amplitude with weight load on the wrists. In addition, look for variability in amplitude, frequency, and direction of tremor.63 A whack a mole sign can be seen106: when the limb affected by tremor is immobilized by the examiner, the tremor appears in another body segment (head, trunk, other arm, or legs).

No validated clinical signs are available for assessing dystonia, but a pattern of adult sudden onset fixed dystonia (typically clenched fist sparing thumb and index finger107) or equinovarus foot is suggestive of functional dystonia.108 Associated prominent pain and other FND signs can help support the diagnosis.109

When assessing tics, no validated signs are available but clinical clues can help identify functional tics110111: lack of premonitory urge and inability to suppress the movement, female preponderance, additional FND symptoms, lack of response to anti-tic medication, and absence of family history. In functional tics, the cranial region is less affected, the type of tic is often blocking (ie, interferes with voluntary action) and pali, echo, and copro phenomenon are less common.

Overall, the evidence for rule-in motor signs shows very high specificity, which advocates for their routine use in clinical practice. A range of educational pictorial and video libraries illustrate many of these signs.2101102112113 Too much emphasis on a single sign, however, can lead to false positives. In a cohort of 190 patients diagnosed with a neurological disorder, 37 (20%) had at least one positive functional neurological sign.91 Interestingly, regression analysis showed that this 20% of the cohort had typical risk factors known in patients with FND, suggesting that the presence of positive signs in this subgroup could either be false positives or indicate the presence of an FND comorbidity. Keep in mind the possibility that the patient has both FND and another neurological disorder: recent reports describe functional neurological signs in a subset of patients with Parkinsons disease114115 or multiple sclerosis.116 Overall, data from a systematic review and a prospective study underscore that rates of misdiagnosis in FND since 1970 (once confirmed) are low, and between 1% and 4%.117118

Recently, efforts have been made to integrate additional clinical features in the process of diagnosis, such as, for example, abrupt onset, fluctuations of the motor symptom, comorbid pain, and fatigue.119 The presence of these features should raise the index of suspicion and prompt a more systematic search of signs positive for FND.

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Diagnosis and management of functional neurological disorder - The BMJ

Characteristics of peer-based interventions for individuals with neurological conditions: a scoping review – DocWire News

This article was originally published here

Disabil Rehabil. 2022 Jan 27:1-32. doi: 10.1080/09638288.2022.2028911. Online ahead of print.

ABSTRACT

PURPOSE: Peer-based interventions are increasingly popular and cost-effective therapeutic opportunities to support others experiencing similar life circumstances. However, little is known about the similarities and differences among peer-based interventions and their outcomes for people with neurological conditions. This scoping review aims to describe and compare the characteristics of existing peer-based interventions for adults with common neurological conditions.

MATERIALS AND METHODS: We searched MEDLINE, CINAHL, PsychInfo, and Embase for research on peer-based interventions for individuals with brain injury, Parkinsons, multiple sclerosis, spinal cord injury, and stroke up to June 2019. The search was updated in March 2021. Fifty-three of 2472 articles found were included.

RESULTS: Characteristics of peer-based intervention for this population vary significantly. They include individual and group-based formats delivered in-person, by telephone, or online. Content varied from structured education to tailored approaches. Participant outcomes included improved health, confidence, and self-management skills; however, these varied based on the intervention model.

CONCLUSION: Various peer-based interventions exist, each with its own definition of what it means to be a peer. Research using rigorous methodology is needed to determine the most effective interventions. Clear definitions of each program component are needed to better understand the outcomes and mechanism of action within each intervention.IMPLICATIONS FOR REHABILITATIONRehabilitation services can draw on various peer support interventions to add experiential knowledge and support based on shared experience to enhance outcomes.Fulfilling the role of peer mentor may be beneficial and could be encouraged as part of the rehabilitation process for people with SCI, TBI, Stroke, PD, or MS.In planning peer-based interventions for TBI, Stroke, SCI, PD, and MS populations, it is important to clearly define intervention components and evaluate outcomes to measure the impact of the intervention.

PMID:35085058 | DOI:10.1080/09638288.2022.2028911

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Characteristics of peer-based interventions for individuals with neurological conditions: a scoping review - DocWire News

Neurologists React to CMS’ Proposed NCD Decision on Anti-Amyloid Monoclonal Antibodies for Alzheimer’s Disease in the Latest from Spherix Global…

EXTON, Pa., Jan. 27, 2022 /PRNewswire/ -- On January 11th, the Centers for Medicare and Medicaid Services (CMS)' proposed Medicare reimbursement of FDA-approved anti-amyloid monoclonal antibodies (mAbs) be limited to clinical trials under Coverage with Evidence Development (CED). Days later, Spherix surveyed 75 U.S. neurologists and Alzheimer's disease specialists (including five follow-up interviews) to evaluate their awareness of and opinions on this unprecedented event.

The resulting insights are part of a two-wave Special Topix: Impact of CMS Reimbursement Decision on Alzheimer's Disease Therapies service. The second wave will be fielded immediately following the publication of the final determination.

Key takeaways from the first wave of research include:

Indeed, according to an interviewed neurologist, "To pre-judge before the data is submitted on the other three products is unfair. I don't think that that's reasonable because one of them may show a significant clinical improvement."

One neurologist noted, "If Lilly had very strong data on clinical benefit [with donanemab], not just clearing of amyloid, and on the side effect profile, I hope that CMS would change its decision for that particular drug."

Positive cognitive and functional data with acceptable safety from at least one of the ongoing Phase III programs with anti-amyloid mAbs would positively impact neurologists' currently low willingness to participate in such trials.

As mentioned by one interviewed neurologist, "The FDA is very concerning. As you probably are aware, the advisory committee, which were all neurologists and memory disorder neurologists, almost unanimously recommended against it [Aduhelm's approval] and then the FDA went around and said yes, so you lose a lot of confidence right now. My confidence in CMS is much better, much improved. I think they did the right thing. I think this is necessary. Too expensive and too potentially harmful to just willy-nilly start using these medications. We need to know definitively that these are really beneficial."

While CMS' draft NCD decision is specific to anti-amyloid mAbs, the Special Topix report also captures insights on the potential impact that the proposal could have on emerging therapies for Alzheimer's disease with alternative mechanisms of action (i.e., non-amyloid-targeted).

About Special Topix

Special Topix: Impact of CMS Reimbursement Decision on Alzheimer's Disease Therapies (US)includes two waves of research, collecting feedback from U.S. neurologists and Alzheimer's disease specialists about their awareness of and opinions on CMS' draft and final National Coverage Determination (NCD) decision on FDA-approved mAbs targeting amyloid for the treatment of Alzheimer's disease. The waves of research will field immediately following the releases of the draft and final NCD decisions.

Therapies covered include:

Learn more about our services here.

About Spherix Global Insights

Spherix Global Insights is a hyper-focused market intelligence firm that leverages our own independent data and expertise to provide strategic guidance, so biopharma stakeholders make decisions with confidence. We specialize in select immunology, nephrology, and neurology markets.

All company, brand or product names in this document are trademarks of their respective holders.

For more information, contact:

Virginia Schobel, Neurology Franchise Head

info@spherixglobalinsights.com

http://www.spherixglobalinsights.com

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Longer Decompression Time and Early Transport Time After Spinal Cord Injury Are Linked to Higher Impairment… – Physician’s Weekly

For a retrospective cohort study, researchers wanted to determine if there was a link between early decompressive surgery and the influence of transport time on traumatic spinal cord injury (tSCI) patients neurological outcomes. tSCI was a life-changing incident leaves a person permanently unable or unable to function. There was a lot of debate over when the best time is for surgical decompression in tSCI patients. The goal of the research was to compare the neurological results of tSCI patients who had early vs. late surgical decompression and the effect of transit time on neurological outcomes. A total of 84 patients with tSCI who required surgical decompression were studied. Time to decompression classification cutoffs was determined using regression analysis. The following subgroups of patients were identified: As a percentage of total or admitting hospital time to decompression, 0 to 12 or greater than 12 hours. It was discovered how the American Spinal Injury Association Impairment (AIS) Grade changed from admission to discharge. In addition, the influence of transport duration on AIS grade conversion was evaluated, with patients being divided into 2 groups: those who travelled for less than 6 hours and those who travelled for more than 6 hours. Confounding factors such as age, injury severity, and AIS grade had no significant differences (P>0.05) among the time to decompression subgroups. Patients who got decompression within 0 to 12 hours had considerably (P<0.0001) better average ASIA grade improvements (0.76). Patient transport periods of fewer than 6 hours were linked to a significantly larger conversion of AIS grade to less impaired states (P=0.004). According to the findings, decompression within 12 hours and short transport periods (<6 hours) are linked to significant improvements in neurological outcomes.

Link:journals.lww.com/spinejournal/Abstract/2022/01010/Early_Decompression_and_Short_Transport_Time_After.10.aspx

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Longer Decompression Time and Early Transport Time After Spinal Cord Injury Are Linked to Higher Impairment... - Physician's Weekly

Clarkson Ph.D. Candidate Wins Travel Award to Attend the American Society for Biochemistry and Molecular Biology Conference – Clarkson University News

Madhuri Jayathirtha

Madhuri Jayathirtha of Bangalore, India will travel to Philadelphia, PA, on April 2-5th to attend and present her work at the ASBMB conference. The ASBMB 2022 Graduate Student Award will support her travel.

Jayathirtha is a Ph.D. candidate at Clarkson University who works in the Biochemistry and Proteomics Group under the supervision of Dr. Costel C. Darie, an Associate Professor in the Department of Chemistry & Biomolecular Science.

Jayathirtha will present her project entitled "Mass Spectrometry based Proteomics to Investigate and characterize the Human Jumping Translocation Breakpoint (hJTB) Protein using cancer cell lines. This study is used to investigate the function of human JTB. JTB protein is required for normal cell division. If you have too much of this protein, you get cancer, mostly prostate and breast cancer. Investigating the function of this protein will help in testing it as a potential serum biomarker for the identification of breast cancer.

I am very happy about the travel award, said Jayathirtha. This will be my first time at this ASBMB conference. Since my research completely focuses on cell biology and biochemistry, I am excited to present my work and discuss my project with the other members of the society, ended Jayathirtha.

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Clarkson Ph.D. Candidate Wins Travel Award to Attend the American Society for Biochemistry and Molecular Biology Conference - Clarkson University News

Zero Gravity Solutions, Inc.’s Announces the Publication of an Important Research Paper in the International Journal of Biochemistry Research and…

BOCA RATON, Fla.--(BUSINESS WIRE)--Zero Gravity Solutions, Inc. (ZGSI or the Company) (Pink Sheets: ZGSI), an agricultural biotechnology company, announced that the International Journal of Biochemistry Research and Review has published a peer reviewed research paper outlining the mechanism by which the Companys technology activates plants innate disease defenses. In this illustrative case study, the Company identified new plant biomarkers expressed when a plant is under fungal attack and demonstrated how our technology successfully triggers plants natural fungal defenses, a response known as priming. The findings validate the technologys mode of action and pave the way for the Company to broaden its product suite with proprietary priming elicitors that enable plants to sustainably increase yield and protect against disease.

Identifying the molecular mechanism of BAM priming and the specific biomarkers it causes to express is a scientific breakthrough for the Company. Our research validates our theory that a plant's natural defenses are triggered by the Company's priming technology, stated Dr. Ravi Pottathil, Zero Gravity Solutions Chief Science Officer. We believe the next generation of sustainable agricultural solutions will come from priming applications. We intend to introduce novel elicitor formulations as part of our priming technology platform in the near future based upon the biomarkers we have identified.

The Company expects that use of priming technologies will be the next category of agricultural product innovation to achieve green and sustainable agriculture practices. The Companys technology platform, which has been validated through numerous third-party trials both domestically and internationally, is at the forefront of an expected increasing use of priming agents as potent tools to mitigate plant disease.

"The findings of our recent research, combined with the ongoing commercial success of our BAM-FX product, reinforces our position that our priming technology is a leading edge innovation that will continue to contribute strongly to the tools that a grower has available to naturally boost the biological potential of their crops," said Timothy Peach, CEO/CFO of Zero Gravity Solutions, Inc.

The referenced published research paper is available at: https://journalijbcrr.com/index.php/IJBCRR

About Zero Gravity Solutions, Inc.

Zero Gravity Solutions, Inc. is an agricultural biotechnology public company with technology derived from and designed for Space with significant applications here on Earth. These technologies are focused on providing valuable solutions to challenges facing world agriculture. The commercialization activities are being executed through ZGSIs two operating subsidiaries, BAM Agricultural Solutions, Inc. and Specialty Agricultural Solutions, Inc.

This press release may contain certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Investors are cautioned that such forward-looking statements involve risks and uncertainties, including without limitation, acceptance of the Companys products, increased levels of competition for the Company, new products and technological changes, the Companys dependence on third-party suppliers, and other risks detailed from time to time in the Companys periodic reports filed with the Securities and Exchange Commission. Except as required by applicable law or regulation, Zero Gravity Solutions undertakes no obligation to update these forward-looking statements to reflect events or circumstances that occur after the date on which such statements were made.

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Zero Gravity Solutions, Inc.'s Announces the Publication of an Important Research Paper in the International Journal of Biochemistry Research and...

Public Discourse and General Alumni Association Host Science and Democracy Speaker Series | Newsroom – UNC Health and UNC School of Medicine

The UNC Program for Public Discourse and General Alumni Association host Science and Democracy, an online Abbey Speaker Series event featuring a discussion about the interplay of science and politics this February.

The UNC Program for Public Discourse and General Alumni Association will hostScience and Democracy, an online Abbey Speaker Series event featuring a discussion about the interplay of science and politics. Contributors includeScience editor-in-chief and former UNC-Chapel Hill chancellor Holden Thorp 86 and Luana Maroja, associate professor of biology and chair of the Biochemistry and Molecular Biology Program at Williams College.

The event will take place February 8th at 5:30 p.m., and the discussion will be moderated by Chris Clemens, Jaroslav Folda Distinguished Professor of Physics and Astronomy at the University of North Carolina at Chapel Hill.

The event takes place over Zoom and is free and open to the public.Registration is available here.

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Public Discourse and General Alumni Association Host Science and Democracy Speaker Series | Newsroom - UNC Health and UNC School of Medicine

University of Arizona Awarded the 2022 Beckman Scholars Program – University of Arizona News

Undergraduate researchers of today are the scientists of tomorrow. Supporting students to be independent, critical thinkers is essential, and giving them access to research opportunities helps to strengthen their own futures as well as the future of scientific research. As part of this effort, the Beckman Scholars Program provides the opportunity for exceptional undergraduate students in the chemical and biological sciences to grow as scientists through independent research and mentoring.

A prestigious award, the Beckman Scholars Program is only awarded to a handful of institutions that meet the criteria. These institutions must demonstrate a commitment to undergraduate research, have successfully competed at the national level for scientific research funding, and have dedicated faculty who have demonstrated an outstanding ability to mentor undergraduate students. As such, it is a great honor that one of this years 2022 Beckman Scholars Program grants has been awarded to the University of Arizona following a competitive process administered by the Arnold and Mabel Beckman Foundation. Pictured right are UArizona's last four Beckman Scholars: Catherine Weibel, Amanda Warner, Randall Eck, and Jamie Takashima.

The 2022 UArizona Beckman Scholars Program is being led by Dr. Daniela Zarnescu, a Molecular and Cellular Biology faculty member and experienced Beckman Mentor. Faculty mentors are drawn from three UArizona departments within the College of Science: Chemistry and Biochemistry, Ecology and Evolutionary Biology, and Molecular and Cellular Biology. The Program will be housed under the Undergraduate Biology Research Program (UBRP) and administered by Ms. Marisa Lester, UBRP Assistant Program Director. UBRP is an ongoing UArizona research initiative that has been on campus since 1988 and is designed to teach students science by involving them in research. UBPR will provide additional support for the selected Beckman Scholars by integrating them into a peer network of fellow undergraduate researchers as well as having the scholars participate in and co-lead workshops.

The 2022 award supports six undergraduate students, two a year for three years. Beckman Scholars will be selected through a careful process that includes an original research proposal that demonstrates the students creativity, analytical skills, and familiarity with the scientific process. Selected scholars will work with a faculty mentor on an independent research project. These mentors, who are also members of UBRP, were recruited based on their scientific expertise, experience working with undergraduates, and demonstrated mentoring commitment. The new scholars will also be supported by previous Beckman Scholars.

As part of the program, Beckman Scholars are encouraged to author a peer-reviewed publication of their research. This will help the students to develop their scientific writing skills as well as to better understand the peer-review process. Scholars will also develop leadership and professional skills by inviting and arranging for an eminent scholar to speak each year at a Beckman Lecture. These speakers will be supported by committed funds from Dr. Betsy Cantwell, the UArizona Senior Vice President for Research. Additionally, the scholars will communicate their research with the public through appearing on the weekly KXCI Community Radio program Thesis Thursday.

An important aspect of the recruitment and selection of scholars and mentors is a commitment to diversity, equity, and inclusion. Ethnic and racial minorities, people with disabilities, and first-generation students are often underrepresented in scientific research programs. As such, the 2022 Beckman Scholars Program will actively recruit and select students from the diverse student body of the University of Arizona. Additionally, Beckman mentors of the program represent a diverse group of faculty across the three participating departments.

Beckman Scholars are leaders amongst their peers and significant contributors to their respective areas of research. Beckman alumni have continued onward to professional and graduate programs at some of the world's more prestigious institutions. Receiving this award showcases the excellence in undergraduate research at the University of Arizona. For more information about the program at UArizona and the application process, please visit:https://ubrp.arizona.edu/programs/beckman-scholars-program.

By:Christine Acosta

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University of Arizona Awarded the 2022 Beckman Scholars Program - University of Arizona News

Qualitative Analysis of Heparin Sodium Market 2022-2028 Strategical Assessment of Shenzhen Hepalink, Bioibrica, Nanjing King-friend, Pfizer, Dongcheng…

The Research report provides an in-depth analysis of the impact of COVID-19 on numerous segments within the Heparin Sodium market-supported product types, applications, and key players like (Shenzhen Hepalink, Bioibrica, Nanjing King-friend, Pfizer, Dongcheng Biochemicals, Changshan Biochemical, and more) across various countries around the world. Further, the Heparin Sodium market report additionally provides insights into market developments, trends, provide and demand changes across numerous regions across the globe. The market is predicted to witness continuing growth throughout the forecast from 2022 to 2028. It commits various factors affecting industry like market environment, various policies of the government, past data and market trends, technological advancements, upcoming innovations, market risk factors, market restraints, and challenges within the industry. Then it analyzed the worlds main region market conditions, including the demand and supply chain analysis and industry rate of growth etc. At the top, the report introduced a new project SWOT analysis, investment feasibility analysis, and investment return analysis.

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Further, the report presents profiles of competitors in the Heparin Sodium market include:

The report provides an accurate analysis of the changing competitive dynamics. It provides a forward-looking perspective on the various factors that drive or restrict market growth. It provides a five-year forecast evaluated based on Heparin Sodium market growth projections. Helps in understanding the key product segments and their future, to gain a complete view of the market, and make informed business decisions by performing an in-depth analysis of the market segments.

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Men’s and Women’s Cross Country Earn All-Academic Honors – Southern Virginia – Southern Virginia University News

NEW ORLEANS The Men's and Women's Scholar-Athlete of the Year and All-Academic Athletes for the 2021 NCAA Division III Cross Country season were announced on Thursday by the U.S. Track & Field and Cross Country Coaches Association (USTFCCCA).

Both the men's and women's cross country teams earned USTFCCCA All-Academic Team honors, with the men's team recording a cumulative team GPA of 3.2, while the women's team recorded an impressive 3.59 cumulative GPA.

For the women's team, three Knights were awarded All-Academic Athletes, consisting of Bayleigh Redd, Sasha Willie, and Ashley Brewer, majoring in Biochemistry.Quin Meyer, majoring in Business Management, and Kaelen Ruder, majoring in Physical Therapy, represented the men's team.

The group played key roles for their teams in their 2021campaigns, finishing in the top 25 percent at the 2021 NCAA Division III South Region Cross Country Championships. Their performances, along with their academic achievements, qualified themselves for USTFCCCA All-Academic Awards.

Follow @knightxctf on Instagram and Twitter for more updates and details on the team.

Full USTFCCCA Release

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Men's and Women's Cross Country Earn All-Academic Honors - Southern Virginia - Southern Virginia University News

Biochemical Oxygen Demand Analyzer Market Competitive Analysis With Growth Forecast Till 2027 – UkrAgroConsult

The Latest released Global Biochemical Oxygen Demand Analyzer Market Report 2021-2027 provides 100+ data Tables, Pie Chat, Graphs & Figures spread through Pages and easy to understand detailed analysis.

The Global Biochemical Oxygen Demand Analyzer Market Report provides an in-depth assessment of the given sectors current position and central factors.The study considers the present scenario of the Biochemical Oxygen Demand Analyzer market and its market dynamics for the period 2021-2027. It covers a detailed overview of several market growth enablers, restraints, and trends. The report offers both the demand and supply aspects of the market. It profiles and examines leading companies and other prominent ones operating in the market.

Top Key Players in the Global Biochemical Oxygen Demand Analyzer Market: HachLovibondXylemSkalarMANTECH-IncMettler ToledoThermo Fisher ScientificVELP ScientificaAQUALYTICLAR Process AnalysersKORBI

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This report elaborates the market size, market characteristics, and market growth of the Biochemical Oxygen Demand Analyzer industry, and breaks down according to the type, application, and consumption area of Biochemical Oxygen Demand Analyzer. The report also conducted a PESTEL analysis of the industry to study the main influencing factors and entry barriers of the industry.

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Portable BOD AnalyzerOnline BOD AnalyzerOthers

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Municipal Wastewater Treatment PlantsIndustrial Production FacilitiesLaboratoriesOthers

Regional Analysis:

North America (United States, Canada and Mexico)Europe (Germany, France, UK, Russia and Italy)Asia-Pacific (China, Japan, Korea, India, Southeast Asia and Australia)South America (Brazil, Argentina, Colombia)Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa)

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Who are the Leading key players and what are their Key Business plans in the Global Biochemical Oxygen Demand Analyzer market? What are the key concerns of the five forces analysis of the Global Biochemical Oxygen Demand Analyzer market? What are different prospects and threats faced by the dealers in the Global Biochemical Oxygen Demand Analyzer market? What are the strengths and weaknesses of the key vendors?

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Ground-Breaking Study Reveals Dynamics of DNA Replication ‘Licensing’ | Newsroom – UNC Health and UNC School of Medicine

This research, led by Jean Cook, PhD, and Liu Mei, PhD, at the UNC School of Medicine, may help explain why certain parts of the genome become highly mutable in some cancers.

CHAPEL HILL, NC A new study from scientists at the UNC School of Medicine has illuminated an important process that occurs during cell division and is a likely source of DNA damage under some circumstances, including cancer.

The scientists, who reported their findings in Nucleic Acids Research, devised a sophisticated experimental platform for studying the process called origin licensing. Cells use this process to regulate, or license the replication of their genomes during cell division.

The researchers revealed for the first time the dynamics of this process. They showed in particular how these dynamics differ and bring different risks of DNA damage during replication in the two basic states of genomic DNA, the euchromatin state which is relatively loose and open for gene activity, and the heterochromatin state which is wound more tightly to silence gene activity.

Our findings may help explain, for example, why certain portions of the genome are relatively susceptible to DNA damage during replication in some cancer cells, said study senior author Jean Cook, PhD, professor of biochemistry and biophysics at the UNC School of Medicine and member of the UNC Lineberger Comprehensive Cancer Center.

Origin licensing occurs in the initial, preparatory phase of cell replication, known as the G1 phase. It involves sets of special enzymes that attach to the DNA in chromosomes at various locations where DNA-copying is to originate. The enzymes essentially license the copying of DNA so that cells dont copy their genomes more than once.

Cook and other scientists have described in prior studies the basic process of origin licensing, and have identified proteins that make it happen. But this study, for the first time, revealed in detail how the process unfolds over time in cells as they prepare for cell division. Study first author Liu Mei, PhD, a postdoctoral fellow in the Cook laboratory, combined still and time-lapse microscopic imaging techniques to accomplish this feat.

What Liu did was incredibly painstaking and meticulous, a technical tour de force, Cook said.

As an initial demonstration of her experimental platform, Mei compared the origin licensing process, with its loading of licensing enzymes, in the two main states of the genome euchromatin and heterochromatin. She found an important difference.

Essentially heterochromatin more compacted DNA loads these licensing enzymes relatively late compared to what we observe in the more open euchromatin, Mei said.

This finding hinted, at least, that in dividing cells with an abnormally shortened G1 phase, the more compacted DNA in the cell genome might never be fully licensed for replication, potentially resulting in large mutations during replication and even cell death. Confirming this possibility, the researchers found that when they artificially shortened the G1 phase in test cells, there was significantly more under-replication and DNA damage in heterochromatin regions of the cells genomes, compared to the euchromatin regions.

Cells can have a shortened G1 phase for different reasons, including due to cancer. Thus the study suggests that the genomic instability or tendency to develop more mutations of some cancer types, as well as the genomic locations of that instability, might be explained in part by faulty origin licensing.

The study also establishes the researchers experimental platform as a tool for further studies of origin licensing dynamics and genomic instability, studies that might someday yield new strategies against cancers, for example.

The consequences of differential origin licensing dynamics in distinct chromatin environments was co-authored by Liu Mei, Katarzyna Kedziora, Eun-Ah Song, Jeremy Purvis, and Jean Cook, all at UNC Chapel Hill.

Funding was provided by the National Institutes of Health (R01GM102413, R01GM083024, R35GM141833, R01-GM138834).

Media contact: Mark Derewicz, 919-923-0959.

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Ground-Breaking Study Reveals Dynamics of DNA Replication 'Licensing' | Newsroom - UNC Health and UNC School of Medicine