All posts by medical

Biochemistry Analyzers Market: A Latest Research Report to Share Biochemistry Analyzers Industry Insights and Dynamics By 2026 – Market Strategies

The research report on the global Biochemistry Analyzers marketprovides a comprehensive outlook of the equipment and technological devices employed in the manufacturing of the Biochemistry Analyzers market products. From industry chain analysis to cost structure analysis, the report examines various factors of the industry, including production and end-use segments of the Biochemistry Analyzers market. The current trends in the pharmaceutical industry have been highlighted in the report to evaluate their influence on the overall output of the Biochemistry Analyzers market. The Biochemistry Analyzers Market analyzed in this study is speculated to grow at a CAGR of XX% during the forecast period (2019-2026).

Fill in your details to get your hands on an Exclusive Sample of this Report @ https://www.marketexpertz.com/sample-enquiry-form/71860

Competitive Landscape:

The Biochemistry Analyzers market is moderately competitive and includes numerous key players. When looking at market share, few industry players predominantly constitute the worldwide market. With the growing awareness among patients and high prevalence of diseases like cancer, new companies are also expected to find their way into the market in the near future.

Some of the major players engaged in the market are :

Roche Diagnostics GmbH, Siemens AG, Beckman Coulter Inc., Abbott Diagnostics Inc., Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Hologic, Inc., Randox Laboratories Ltd., Awareness Technology, Inc., Transasia Biomedicals Ltd, Nova Biomedical Corp.

Results of the latest scientific undertakings for the development of new Biochemistry Analyzers products have also been considered. Factors that can potentially influence the leading industry players to implement synthetic sourcing of market products have also been studied in this investigative report. The inferences drawn in this study are valuable for any company operating in the industry. Every organization contributing to the global production of the Biochemistry Analyzers market products has been profiled in this report, in order to study the insights on cost-effective manufacturing methods, competitive landscape, and new avenues for applications.

Biochemistry Analyzers Market Segmentation:

Type of Biochemistry Analyzers Market:

Semi-automated Biochemistry Analyzer, Fully Automated Biochemistry Analyzer

Application of Biochemistry Analyzers Market:

Clinical Diagnostics, Bioreactor Byproduct Detection, Drug Development Applications, Others

Grab Your Report at an Impressive Discount! Please Click Here @ https://www.marketexpertz.com/discount-enquiry-form/71860

The varying scenarios across the global market have been examined in this study, providing an overview of how the Biochemistry Analyzers products have established their place in this rapidly-evolving sector. Industry participants will be able to formulate their strategies and tactics by assessing the speculated market size for the forecast mentioned in the report. Favorable regional markets for the Biochemistry Analyzers have been described, which are expected to impact the global expansion strategies of the leading organizations. Additionally, key manufacturers have been profiled comprehensively in this research report.

In market segmentation by geographical regions, the report has analyzed the following regions-

North America

Europe

China

Japan

Middle East & Africa

India

South America

Others

With the existing market standards evaluated, this research report also explains the latest strategic initiatives and patterns of the market players in an unbiased way. The report can be construed as a presumptive business record that can aid the readers functioning in the global market devise their plans effectively, to reach the desired position in the market in the forecast period.

Read the Comprehensive Report with a meticulous TOC and panoramic coverage of the [emailprotected] https://www.marketexpertz.com/industry-overview/biochemistry-analyzers-market

Report Methodology:

The data contained in this report has been derived through both primary and secondary research methodologies.

Primary research methodology includes interaction with service providers, suppliers, and industry professionals. Secondary research methodology entails a thorough examination of relevant literature like company annual reports, financial reports, and exclusive databases.

This report provides:

Request customized copy of Biochemistry Analyzers report

We are grateful to you for reading our report. If you wish to find more details of the report or want a customization, contact us. You can get a detailed information of the entire research here. If you have any special requirements, please let us know and we will offer you the report as you want.

Need to customized? Ask Our Expert @ https://www.marketexpertz.com/customization-form/71860

Continued here:
Biochemistry Analyzers Market: A Latest Research Report to Share Biochemistry Analyzers Industry Insights and Dynamics By 2026 - Market Strategies

Researcher who uncovered the sex life of marsupials awarded Academy’s most prestigious medal – Australian Academy of Science

December 09, 2019

A scientist whose research has transformed our understanding of Australias iconic mammals has been recognised by the Australian Academy of Science. Professor Marilyn Renfree AO FAA has been awarded the Academys highest honour in the biological sciencesthe Macfarlane Burnet Medal and Lecture.

For half a century the committed reproductive and developmental biologist and conservationist from the University of Melbourne has been using the tammar wallaby, a small macropodid marsupial native to South and Western Australia, to study their reproduction and development.

Professor Renfree has developed contraceptive strategies for kangaroos and koalas and established marsupials as unique biomedical models for understanding human reproduction.

She is now a world authority on marsupial reproduction and development and has pioneered research on some of Australias most iconic creatures including kangaroos, koalas and now echidnas.

And with passion for her work as strong as ever, she has no plans of slowing down. Professor Renfree has just embarked on the worlds first study of the development of the embryo and newly hatched pouch young from the echidna.

Professor Renfree said hardly anything was known about marsupials when she started out.

Im passionately Australian and I really wanted to work on something Australian but when I started honours I said to my prospective supervisors: I wanted to do biochemistry and fieldwork. And they laughed at me. Well, Im still really doing biochemistry and fieldwork.

Her first paper published from her PhD in 1972 was aNaturepublication.

In her distinguished career Professor Renfree has made numerous research breakthroughs. In research with colleagues Professor Renfree conducted the first genome sequencing of an Australian marsupial, the tammar wallaby, providing new information on their evolution.

She also showed that certain genes directly control sexual development during pregnancy and even after birth in marsupials, providing a new understanding of the relative influence of genes versus hormones in sexual differentiation in all mammals. With colleagues she also discovered a new hormone pathway that explains some human disorders of sexual development.

Professor Renfree said Australia is sitting on a biological goldmine because it is home to a unique assembly of mammalsthe marsupials and monotremes.

The impact of Australias recent bushfires on Australian mammals has highlighted Australia and the worlds fascination with these special animals. We really need to put more effort, time and money into conserving and doing research on them, Professor Renfree said.

Australia has the distinction of having the worst record of mammal extinctions of any developed country and thats not a record you want to be proud of.

Professor Renfree said the Academy award is a huge honour.

Im receiving it on behalf of all of my students, PhD students and postdocs and collaborators. Without them I could have only done a fraction of what I've done, Professor Renfree said.

She was nominated for the medal by Professor James Angus FAA from the University of Melbourne.

Professor Renfree is a pioneer and forward thinker who has an ability to excite and inspire scientists from around the world by providing new insights through the study of the unique evolutionary innovations in the reproductive systems of marsupials and monotremes, Professor Angus said.

The basic science and the clinical impact of her work for humans are as important as the direct benefits of her work for Australias marsupials. Her research has undoubtedly opened the eyes of the academic world and beyond to the value of these iconic Australian mammals both for their intrinsic interest and as unique biomedical models.

Professor Renfree will receive the medal and give a lecture at the Academys Science at the Shine Dome event in May 2020. The Macfarlane Burnet Medal and Lecture honours the contributions to science by Sir MacFarlane BurnetOMKBMDFAAFRSNobel Laureate.

See the original post here:
Researcher who uncovered the sex life of marsupials awarded Academy's most prestigious medal - Australian Academy of Science

Biochemistry Analyzers Market to Receive Overwhelming Hike in Revenues by 2026 – Montana Ledger

GlobalBiochemistry Analyzers Market: Overview

The report details an exhaustive account of the global biochemistry analyzers market along with numerous associated factors. Some of these factors that are included in the report are drivers, restraints, competitive analysis, latest trends and opportunities, geographical outlook, and many other aspects. The study covered in the report spans a forecast period from 2018 to 2028. From an overall perspective, the report is expected to exist as a valuable insight to businesses which are already operating in the global biochemistry analyzers market, as well for those who intend to newly establish themselves in this environment.

GlobalBiochemistry Analyzers Market: Market Potential and Restraints

Widespread advancements in the medical field have primarily been responsible for driving the global biochemistry analyzers market. Moreover, with rising geriatric population, the numbers of health issues are gradually increasing, thereby increasing demand for relevant treatments that involve biochemical analyzers. In addition, these analyzers possess a high rate of identification of a specific pathogen, consequently providing high clarity and accuracy.

Request Brochure of Biochemistry Analyzers Market Report

https://www.transparencymarketresearch.com/sample/sample.php?flag=B&rep_id=50526

These characteristics make the use of the biochemical analyzers more suitable than other alternatives, thereby boosting growth in the global biochemical analyzers market. Technological advancements are expected to increase even more in the near future, consequently projected to further stoke expansion in the global biochemical analyzer market. Increasing use of the analyzers in drug monitoring, drug abuse detection, and drug provision, owing to rise in the number of health conditions too is notably contributing towards growth witnessed by the global biochemistry analyzers market.

However, this market is hindered owing to several factors. A prominent obstacle present in its growth involves lack of expertise and shortage of necessary manpower required to provide the treatments that involves use of biochemistry analyzers in remote and underdeveloped regions. Owing to this, the market remains restrained geographically. Moreover, high costs of manufacturing the analyzer compounds might cause difficulties for small-scale healthcare centers to afford the required equipment.

In addition, there are several complexities involved with carrying out medical processes that make use of the analyzers. Due to this, people might prefer traditional and cheaper alternatives, which is notably hampering progress in the global biochemistry analyzers market. Nonetheless, key players are soon expected to introduce cost-effective analyzer production procedures, thus blanketing most restraints affecting the global biochemistry analyzers market.

Request for a Discount on Biochemistry Analyzers Market Report

https://www.transparencymarketresearch.com/sample/sample.php?flag=D&rep_id=50526

GlobalBiochemistry Analyzers Market: Geographical Outlook

This market is mainly spread across North America, Europe, Asia Pacific, the Middle East and Africa, and Latin America. Of these, a strong medical infrastructure in North America has made this region hold a leading stance with maximum market share. Many organizations are growing in the global biochemistry analyzers market in North America owing to the availability of necessary funds, mainly to conduct research and develop new and efficient treatments. However, apart from North America, Asia Pacific too showcases a splendid growth present in the global biochemistry analyzers market. This is majorly due to the introduction and utilization of various treatment procedures wherein biochemistry analyzers play a huge role. In addition, several companies are pouring extensive investments in developed economies located in Asia Pacific, which is anticipated to strengthen the market in this region.

GlobalBiochemistry Analyzers Market: Competitive Landscape

This market depicts the presence of a substantially competitive vendor landscape, with the presence of a handful of players exerting their respective dominance. Regulation of treatment costs, achieving geographical expansion, and bringing forth medical treatment efficiency are key strategies implemented by most players operating in the global biochemistry analyzers market. Abbott Diagnostics Inc., Hologic, Inc., Transasia Biomedicals Ltd., Beckman Coulter Inc., Roche Diagnostics GmbH, Siemens AG, Randox Laboratories Ltd., Awareness Technology, Inc., Shenzhen Mindray Bio-Medical Electronics Co., Ltd., and Nova Biomedical Corp., are chief players operating in this sector.

About Us

Transparency Market Research is a next-generation market intelligence provider, offering fact-based solutions to business leaders, consultants, and strategy professionals.

Our reports are single-point solutions for businesses to grow, evolve, and mature. Our real-time data collection methods along with ability to track more than one million high growth niche products are aligned with your aims. The detailed and proprietary statistical models used by our analysts offer insights for making right decision in the shortest span of time. For organizations that require specific but comprehensive information we offer customized solutions through adhoc reports. These requests are delivered with the perfect combination of right sense of fact-oriented problem solving methodologies and leveraging existing data repositories.

TMR believes that unison of solutions for clients-specific problems with right methodology of research is the key to help enterprises reach right decision.

ContactTransparency Market ResearchState Tower,90 State Street,Suite 700,Albany NY 12207United StatesTel:+1-518-618-1030USA Canada Toll Free:866-552-3453Email:[emailprotected]Website:http://www.transparencymarketresearch.com

Read the original:
Biochemistry Analyzers Market to Receive Overwhelming Hike in Revenues by 2026 - Montana Ledger

Introducing the Autophagy and Proteostasis Collection – PLoS Blogs

The importance of proteostasis is becoming increasingly apparent as disrupted proteostasis and dysregulation of proteostasis-associated networks has been linked with aging and many age-associated diseases such as Alzheimers, Parkinsons and Huntingtons disorders. In recognition of the importance of this subject, PLOS ONE, alongside PLOS Biology, launched a Call for Papers on the topic of Autophagy and Proteostasis earlier this year. We welcomed a range of submissions that provided insight into the molecular and cellular machinery, and mechanisms that regulate autophagy and the crosstalk of this process with other protein quality control pathways to ensure proteostasis. These studies also underline the importance of all these cellular pathways in pathophysiological conditions and aging. The Guest Editors are Sharon Tooze (Francis Crick Institute, United Kingdom), Fulvio Reggiori (University Medical Centre Groningen, The Netherlands) and Thorsten Hoppe (Institute for Genetics and CECAD Center for Aging Research, University of Cologne, Germany).

We are happy to launch this Collection today, which includes five studies published in PLOS ONE that highlight the relevance of autophagy and other pathways such as the ubiquitin proteasome-system in maintaining protein homeostasis. In human cells, Ferreira et al. showed that when the STUB1/CHIP ubiquitin ligase is inactivated, cells increase secretion of extracellular vesicles (EVs) enriched in ubiquitylated or stabilized proteins, suggesting that cells use these EVs to dispose of proteotoxic material. Studying another E3 ubiquitin ligase, Si and colleagues investigate the mechanism for Pink1- and Parkin-mediated mitophagy in indirect flight muscles in Drosophila melanogaster, and showed that Pink1/Parkin are crucial for muscle function in aged muscles in an Atg1-dependent manner. Autophagy also plays crucial roles in the fungus Aspergillus niger and Kaur and Punekar revealed that acidogenic growth appears to mimic a nutrient deficient condition, and acidogenic growth and metabolism are compromised in atg1 and atg8 strains of A. niger.

In addition, two papers in the Collection showcase research investigating proteostasis dysfunction in disease states, and potential ways to modulate autophagy for therapeutic uses. Aviazidis et al. study proteostasis network dysfunction caused by unbalanced karyotypes using human Downs syndrome fibroblasts, showing that decreased abundance of SNARE family members STX17 and VAMP8 maybe responsible for reducing autophagic flux by impairing autophagosome-lysosome fusion. Bhaskar et al. identify lipoarabinomannan (LAM), a crucial lipid component of the Mycobacterium indicius pranii cell-wall, as an inducer of autophagy that leads to the enhancement of co-localization between Mycobacteriaum tuberculosis and phago-lysosomes, and increased clearance of this bacterium in macrophages.

Papers will continue to be added to the Collection as they are published. Stay tuned for new articles and additional insights on this important topic.

Fulvio Reggiori

Fulvio Reggiori is a Professor and Section Head of Molecular Cell Biology at the Department of Biomedical Sciences of Cells and Systems of the University Medical Centre Groningen, The Netherlands. Fulvio obtained in his PhD in Biochemistry from the University of Fribourg, Switzerland, in the laboratory of Professor Andreas Conzelmann. Subsequently, he moved to the MRC Laboratory in Molecular Biology in Cambridge to join the laboratory of Dr. Hugh Pelham, UK in 1998. In 2001, Fulvio moved to the University of Michigan in Ann Arbor, USA to the laboratory of Professor Daniel Klionsky, where he started working on different aspects of the molecular mechanisms of autophagy in yeast. In 2005 he was appointed as an Assistant Professor at the Department of Cell Biology of the University Medical Center Utrecht, The Netherlands before becoming an Associate Professor in 2011. Fulvio moved his lab in 2015, to the Department of Department of Biomedical Sciences of Cells and Systems of the University Medical Center Groningen where he became Professor. His research continues to investigate the molecular mechanisms of autophagy using Saccharomyces cerevisiae as a model organism as well as understanding the interaction between autophagy and pathogens, in particular viruses.

Sharon Tooze

Sharon Tooze is a Senior Group Leader at the Francis Crick Institute, London, UK. She has a long-standing interest in understanding organelle biogenesis using molecular cell biology approaches. Sharon received her PhD and undertook a postdoctoral research position in Wieland Huttners lab at the European Molecular Biology Laboratory (EMBL). She established a lab at Imperial Cancer Research Fund, UK which later became known as the Cancer Research UK London Research Institute. In 2015 she moved her lab to the Francis Crick Institute where her research continues to focus on autophagy. Her current interests are focused on expanding our knowledge of the core autophagy proteins in mammalian cells at the molecular level, in particular the autophagy proteins which initiate the formation of the autophagosome.

Thorsten Hoppe

Thorsten Hoppe is a Professor at the Institute for Genetics and the Center for Aging Research (CECAD) at the University of Cologne, Germany. He received his PhD from the University of Heidelberg working in the lab of Stefan Jentsch at the Center for Molecular Biology in Heidelberg (ZMBH) and the Max Planck Institute of Biochemistry in Martinsried. He undertook is postdoctoral work in the Department of Molecular Neurogenetics in the group of Ralf Baumeister at the LM-University of Munich before setting up his own group in 2003 at the Centre for Molecular Neurobiologie at the University of Hamburg (ZMNH). In 2008 he moved his lab to the Institute for Genetics and was Acting Director from 2011 to 2013. His research focuses on understanding the role proteostasis plays in aging and age-associated diseases.

Go here to see the original:
Introducing the Autophagy and Proteostasis Collection - PLoS Blogs

Koeppe Recognized for Service as ABI Institutional Director at University of Arkansas – University of Arkansas Newswire

Chieko Hara, University Relations

From left, Dan Sui, vice chancellor for research and innovation; Roger Koeppe, Distinguished Professor of chemistry and biochemistry; and Robert "Bobby" McGehee, executive director of Arkansas Biosciences Institute and dean at UAMS Graduate School

Science and engineering researchers at the University of Arkansas use research awards from the Arkansas Biosciences Institute to improve the health of Arkansans and prevent smoking-related illnesses.

Seed funding from the institute, a statewide consortium consisting of five research institutions, often enables researchers to produce preliminary results that help them and the university compete for large grants from federal agencies, such as the National Science Foundation and the National Institutes of Health.

As the U of A's institutional director and ABI representative for 11 years, Roger Koeppe, Distinguished Professor in the Department of Chemistry and Biochemistry, helped many colleagues secure funding from the institute. Koeppe was recognized for his service Thursday during a faculty town hall meeting to discuss future funding priorities and strategies of the Arkansas Biosciences Institute. The meeting was hosted by Dan Sui, vice chancellor for research and innovation.

"ABI funds have made a huge difference on this campus, certainly in terms of biosciences research, but also as leverage to attract and recruit top investigators," Sui said. "Obviously, Roger has been responsible so much its success on this campus, and we want to recognize his enormous contribution."

Earlier this semester, Chancellor Joe Steinmetz appointed Sui to serve as the new ABI institutional director.

The Arkansas Biosciences Institute was established as a result of Arkansas' share of the 1998 nationwide tobacco settlement. Health care leaders in the state sought a productive way to disperse the state's share of the settlement. TheArkansas Biosciences Institutewas created as a conduit for research that could help reduce or prevent smoking-related illnesses.

Arkansas voters endorsed the proposed Tobacco Settlement Proceeds Act of 2000, and the Arkansas Legislature enacted the provisions of that proposal as Acts 1569 through 1580 of 2001. Part of that legislation established the institute as a consortium of five research institutions: the University of Arkansas, the University of Arkansas System Division of Agriculture, the University of Arkansas for Medical Sciences, Arkansas State University and Arkansas Children's Hospital. Since ABI's beginning, scientists at these institutions have focused on biomedical and agricultural research with medical implications.

Robert "Bobby" McGehee, executive director of the Arkansas Biosciences Instituteand dean at University of Arkansas for Medical Sciences Graduate School, also recognized Koeppe during Thursday's meeting. He and Koeppe served together for more than a decade.

McGehee said Arkansas is one of only two states that uses all of its tobacco settlement money for heath inititatives and healthcare research. Sui said the university will continue to use ABI funds to make new strategetic investments in biosciences research.

Link:
Koeppe Recognized for Service as ABI Institutional Director at University of Arkansas - University of Arkansas Newswire

Does the ‘genetics revolution’ unsettle you? Here is a guide, and reasons to be hopeful – Genetic Literacy Project

Its that time of year again an avalanche of ads urging us to drool into tubes so companies can spit back verdicts on our pasts, presents, and futures. Judging from my emails, those unceasing ads have inspired many questions about genetics in general.

Among the emails that pinged in recently:

So I started a list of my e-mails, with apologies to Hillary, and extracted three recurring themes: transgender identity, when a human life begins, and by far the largest group: interpreting DNA test results, either consumer or clinical.

What do you think about a new studythat found 20 genetic markers of transgender identity? asked a reporter from The Times of London In March 2018. Id suggested just such a study a year earlier, which hed found here.

Impressed with the study, I agreed to comment. But the reporter forgot to distinguish me from the researcher, and so throughout Europe, I was suddenly an expert on transgender genes. And that inspired some telling emails.

The first, from a trans woman born in 1948, shared her 70-page story:

As far back as I can remember I thought nothing of going into my mothers closet, pulling down her nightgowns, and putting them on. They were soft, they smelled of her, and they felt so perfect. This was me. Everything feminine fascinated me. Anything male repelled me. I wanted to emerge myself in the female world. But no matter what I did, I just couldnt look like Mommy.

Another transgender woman wrote:

I would love to have that degree of certainty that a genetic study would show. Parents would be able to perhaps work with their children instead of ignoring it either intentionally or out of ignorance.

A recent email from 58-year-old Edith brought up nature v nurture:

Two of my nine nieces and nephews are transitioning. My family has an overall fluid concept of gender identity, which we discussed with each other before either child made it known they were trans. I find myself wondering if this is true in other families.

Me too.

I repost 17 timepoints whenever womens reproductive rights are threatened, or I read or hear a comment that indicates ignorance of biology. The idea of the list came to me when considering that an embryos genome turns on at day 5, but it cant possibly exist at that point outside of a womans body.

One woman asked about fetal rights. Her ex had given her an herbal abortion tea without her knowledge when she was pregnant. Her baby so far is healthy, but she wants a court to recognize the tea-poisoning as child abuse. At what point in utero does a fetus have rights? It seems to vary state to state, she wrote.

Celia Collias, a statistics major at the University of North Carolina, offered a compelling perspective: distinguishing two types of viability. Natural ability to be physiologically independent for a human fetus is around 24 weeks. Technologically assisted viability for a human fetus is 21 weeks.

If we dont use natural viability as the cut off for reproductive rights, Ms. Collias argues, then those rights will erode as technology sets back the age of assisted viability:

Technologically assisted viability is not free. If we allow that to be the benchmark, its going to cost society a lot to care for all those fetuses where would that money come from?

Good question.

Is he really my brother? asked the woman who sent me scanned columns of genetic markers. I circled 16 of 38 that they share and sent it back: Yes.

I dont have mutations in BRCA1 or 2, so Im ok, right? I do have a mutation in ATM (or p53 or CHEK2 or PTEN or RAD51 or a few dozenothers). Inherited mutations for cancer risk go beyond the most common ones in the BRCA pair, and altogether they account for only 5 percent of cases. Yes, shes at high risk.

BRCA brings up the limited variant problem. Consumer DNA tests, for cancer or single-gene diseases, are likely to check for only the most common variants, such as a handful of mutations in the CFTR gene behind cystic fibrosis, which has more than 1,700. These health reports may provide a false sense of reassurance and should not be used for making any health decisions without confirmation testing, said Edward Esplin, MD, of Invitae, a clinical testing company, at the American Society of Human Genetics conference in October, catalyzing a flood of headlines.

I had a prenatal screen for 125 genes and one is a variant of uncertain significance. What the heck is a VUS? Do I have a mutation or not?

A VUS is a gene variant that isnt common, but hasnt shown up in someone with a disease and reported in the medical literature. Yet. I explain here.

My ethnicity estimate changed overnight. Huh? When an ancestry company adds a new group to its database of reference populations, the sections of those pie charts can shift, or a new one appear.

Im 20 weeks pregnant. The fetus has a microduplication of chromosome 18. Is that a problem? The healthy dad-to-be also had the tiny extra bit of DNA. So, no.

I just found out that I have an extra Y chromosome. Ive had severe acne since my early teens, and today Im 62 and weigh 295 pounds. Im a biker, football player, and served time for selling pot. Did my extra chromosome get me arrested?

Probably not. Being in the wrong place at the wrong time, before decriminalization, was more likely at fault.

Because most of my email brings up medical matters, heres a short guide to getting help in making sense of DNA test results related to health. (For interpreting ancestry findings, the International Society of Genetic Genealogy is an excellent resource.)

Its important to distinguish consumer DNA tests, which anyone can take by purchasing a kit and spitting or swizzling a cheekbrush, from clinical DNA tests, which a health care provider orders and the FDAs Clinical Laboratory Improvement Amendments (CLIA) regulate.

Like mushrooms materializing after a warm rain, articles, websites, books and companies are springing up to help consumers navigate test-taking and interpretation.

Finding an expert specifically trained at the graduate level in genetics a genetic counselor, PhD geneticist, or MD with genetics/genomics training is challenging because their priorities are in clinical testing, not the entertainment/education space that the consumer companies so ceaselessly promote. Other scientists may be helpful molecular biologists, biochemists but genetics as a discipline transcends DNA, including developmental, transmission, and population and evolutionary genetics too. Ancestry testing in particular melds these levels of genetics.

Assuming a sit-down with an expert to intrepret consumer DNA data isnt happening easily, here are some places to turn.

A longstanding helpful website is Genetics Home Reference, from the NIH.

A newer resource is this report from ConsumersAdvocate.org. Their researchers recently sent DNA anonymously to 9 leading consumer DNA testing companies, interpreted the data, and then wrote a detailed, clear analysis that compares the services, privacy/security measures, online resources, and cost of tests.

Consumer DNA testing is a fast-growing industry with over 26 million users worldwide. That number is expected to grow to 100 million by 2021, Sam Klau, Community Outreach at the organization, told me.

An excellent new book is DNA Nation: How the Internet of Genes is Changing Your Life, by PhD molecular biologist Sergio Pistoi. And my human genetics textbook will be out in a new edition in September. Ive added a chapter called The Genetics of Identity, inspired by having my past rewritten recently thanks to ancestry testing.

The testing company websites, like that of 23andme, provide clear and well-written info on interpreting test results. But without any prior knowledge of genetics, misinterpretation and misplaced angst can arise.

Does the average person know the difference in significance between revealing a pattern of genome-wide single-base variations (SNPs) associated with elevated risk of a trait or illness, and detecting a well-studied mutation in a single gene?

The raw data dump from consumer DNA testing can be overwhelming, and to paraphrase Elizabeth Warren: Theres a company for that. A consumer can pay to avoid bushwhacking through dense SNP forests.

Strategene, for example, is a genetic reporting tool that uses 23andMe data to identify SNPs in a few dozen well-studied, health-related genes, and not every SNP under the sun. The $45 is a sound investment; it would take hours to sort through Google Scholar to DIY. But the client needs to know about the limited variant issue of checking only for common SNPs.

(I was briefly fooled into confusing the company with 1980s biotech giant Stratagene, but its off by one letter and one capitalization. The only person named on the company website is a naturopath referred to many times as Dr., which wouldnt necessarily denote a genetics expert.)

Im curious to see how soon the medical profession catches up. Right now, genetic counselors in the US number only about 5,000. But professional organizations are stepping in. The American College of Medical Genetics and Genomics, for example, offers online continuing medical education, ACMG Genetics 101 for Healthcare Providers.

But doctors Ive encountered recently still go deer-in-the-headlights when I ask a genetics question, just to be obnoxious. And so a company like ActXmakes sense in helping medical professionals keep pace with the growing tide of patients coming in waving consumer DNA test results. The company helps physicians and patients apply 23andMe raw data to select drugs, order clinical tests to help diagnose specific conditions, and to confirm carrier status for single-gene diseases.

When I started my career as a Drosophila geneticist, mutating flies to grow legs out of their heads, I never imagined at-home DNA testing. When I started my career as a science writer and textbook author, I still couldnt have predicted at-home DNA testing. Now that its here, Im thrilled that DNA science has become so much more tangible and practical. Yet we must use the information in our strings of A, C, T, and G wisely.

Ricki Lewis is the GLPs senior contributing writer focusing on gene therapy and gene editing. She has a PhD in genetics and is a genetic counselor, science writer and author of The Forever Fix: Gene Therapy and the Boy Who Saved It, the only popular book about gene therapy. BIO. Follow her at her website or Twitter @rickilewis

Read the original:
Does the 'genetics revolution' unsettle you? Here is a guide, and reasons to be hopeful - Genetic Literacy Project

New Data from Ambry Genetics Showed Concurrent RNA and DNA Testing Identified More Patients with Hereditary Breast Cancer than DNA Testing Alone -…

ALISO VIEJO, Calif., Dec. 10, 2019 /PRNewswire/ --Researchers atAmbry Genetics(Ambry), a leading clinical genetic testing lab, will announce new data showing that conducting RNA and DNA tests for hereditary cancer risk at the same time identifies more patients with mutations that increase cancer risk than DNA testing alone. To be presented at the San Antonio Breast Cancer Symposium (SABCS) this week, the data come from a study of 746 patients with breast cancer that received +RNAinsight, paired RNA and DNA genetic testing for hereditary cancer risk.

Standard DNA testing for hereditary cancer risk excludes large portions of DNA, thereby missing some mutations. In addition, DNA testing can produce inconclusive results and fail to determine that an error in our DNA increases cancer risk. These limitations impact patients and their families because doctors may not have the information needed to recommend appropriate preventive, early detection, or therapeutic steps. Additionally, relatives may not be referred for genetic testing and obtain the care they would otherwise have gotten if they had learned they had mutations.

Adding RNA to DNA testing overcomes these limitations for a substantial number of patients as it provides considerably more evidence than DNA testing alone about whether our DNA has mutations.

The data showed that adding RNA genetic testing to DNA testing increased the diagnostic yield the number of people found to have a mutation that increases cancer risk across 16 hereditary breast and/or ovarian cancer genes. As a result of +RNAinsight, five breast cancer patients were identified to have mutations in clinically-actionable genes that would have otherwise been missed completely or the patient would have received inconclusive results if they had received DNA testing only. These findings included three women with mutations in BRCA1/2, one woman with a mutation in ATM, and one woman with a mutation in PMS2. Additionally, paired RNA and DNA genetic testing decreased the number of inconclusive results, giving patients more definitive answers about whether their breast cancers were hereditary. Additional results will be presented on an expanded breast cancer cohort at the meeting on Saturday, December 14th.

"These data further prove that paired RNA and DNA genetic testing for hereditary cancer should be the industry standard," said Holly LaDuca, MS, CGC, senior manager of Ambry's clinical affairs research. "Our research has consistently shown that +RNAinsight provides clinicians with more accurate results, better informing patient care."

Researchers from Ambry will also present at SABCS new data from a pre-and post-test clinician survey that assessed how genetic testing for hereditary cancer impacted medical management, such as screening recommendations. The survey found that positive genetic testing results frequently lead to changes in management recommendations in both high risk (e.g. BRCA1) and moderate risk (e.g. ATM) genes. Changes to mammogram, breast MRI, and/or preventive surgery options were reported in 77.3% of positive individuals. Moreover, medical management changes largely adhered to published guidelines, indicating that cliniciansare applying recommendations appropriately based on test results.

"With this survey data, clinicians are showing us that they truly do use genetic testing results to implement personalized recommendations, which can be life-saving for a patient," said Carrie Horton, MS, CGC, senior researcher in Ambry's clinical affairs team. "These data provide further evidence that genetic testing is essential to comprehensive cancer care. Continued study in this area will aid clinicians, laboratories, health plans, and ultimately patients."

Below are summaries of each of the four studies that Ambry will present at SABCS 2019.

Friday, December 13, 5:00- 7:00 PM CST

P5-07-06,Black M, et. al., Performance of Polygenic Risk Score Combined with Clinical Assessment for Breast Cancer Risk

Saturday, December 14, 7:00 9:00 AM CST

P6-08-35,Horton C, et. al., Impact of Multigene Panel Testing on Medical Management: Preliminary Results of a Pre- and Post- Test Clinician Survey

P6-08-08,LaDuca H, et. al., Concurrent DNA and RNA Genetic Testing Identifies More Patients with Hereditary Breast Cancer than DNA Testing Alone

P6-08-04,Yadav S, et. al., Germline Mutations in Cancer Predisposition Genes in Patients with Invasive Lobular Carcinoma of the Breast

ABOUT AMBRY GENETICS

Ambry Genetics, as part of Konica Minolta Precision Medicine, excels at translating scientific research into clinically actionable test results based upon a deep understanding of the human genome and the biology behind genetic disease. Our unparalleled track record of discoveries over 20 years, and growing database that continues to expand in collaboration with academic, corporate and pharmaceutical partners, means we are first to market with innovative products and comprehensive analysis that enable clinicians to confidently inform patient health decisions. We care about what happens to real people, their families, and the people they love, and remain dedicated to providing them and their clinicians with deeper knowledge and fresh insights, so together they can make informed, potentially life-altering healthcare decisions. For more information, please visitambrygen.com.

For more information on risk factors for hereditary cancer, please visit cancer.gov's fact sheet on hereditary cancer and genetic testing.

ABOUT +RNAINSIGHT

+RNAinsight, paired with Ambry Genetics' hereditary cancer DNA tests, uses next-generation sequencing to concurrently analyze a patient's DNA and RNA, another layer of genetic information. +RNAinsight identifies more patients who have mutations that increase their cancer risks than through standard DNA-only testing by overcoming limitations of DNA testing. +RNAinsight enables more accurate identification of patients with increased genetic risks for cancer, finds actionable results that may otherwise be missed, and decreases the frequency of inconclusive results. +RNAinsight is now available through doctors and genetic counselors around the country. For more information on +RNAinsight, please go toambrygen.com/RNAinsight.

Press Contact:Liz Squirepress@ambrygen.com (202) 617-4662

View original content:http://www.prnewswire.com/news-releases/new-data-from-ambry-genetics-showed-concurrent-rna-and-dna-testing-identified-more-patients-with-hereditary-breast-cancer-than-dna-testing-alone-300972165.html

SOURCE Ambry Genetics

See the original post here:
New Data from Ambry Genetics Showed Concurrent RNA and DNA Testing Identified More Patients with Hereditary Breast Cancer than DNA Testing Alone -...

The Swedish Royal Family Wore Dazzling Tiaras to the Nobel Prize Ceremony – TownandCountrymag.com

JONATHAN NACKSTRANDGetty Images

Every year, members of the Swedish royal family gather for Nobel Prize Award Ceremony and banquet, honoring the 2019 Nobel laureates awarded the prizes in physics, chemistry, physiology or medicine, and literature in Stockholm, Sweden. (The Nobel Peace Prize is awarded in Oslo, Norway, and the Norwegian royal family hosts that ceremony).

The Swedish royal family goes all-out for the occasion with King Carl XVI Gustaf and Queen Silvia in attendance, along with Crown Princess Victoria and her husband Prince Daniel, Princess Madeleine, and Prince Carl Philip with Princess Sofia. The royal ladies traditionally wear sparkling tiaras and formal gowns fo the event, for added dazzle.

Last year, Silvia wore one of her favorite tiaras, the stunning Queen Sophia tiara, with a diamond and emerald necklace that perfectly coordinated with her green gown. Crown Princess Victoria, who is the heir to the Swedish throne, made a statement in the Connaught 'Forget-me-not" tiara, a diamond topper with circular detailing. Sofia went with pearls for her jewelry look, wearing the diamond and pearl Palmette tiara with a matching pearl choker.

Here, we've rounded up the standout tiaras as seen at the Nobel Prize Award Ceremony in Stockholm today:

Advertisement - Continue Reading Below

Queen Silvia and Crown Princess Victoria

Silvia chose a gown with intricate gold detailing, while Victoria opted for a black off-the-shoulder style. Both royals wore tiaras.

Queen Silvia

Silvia wore one of her favorite tiaras, the Queen Sophia tiara, which is also called the Nine Prong tiara,. Silvia also wore it to last year's Nobel Prize ceremony.

Crown Princess Victoria

Victoria wore the sparkling Baden fringe diamond tiara, paired with a diamond necklace and the Braganza Rose diamond brooch.

Princess Sofia and Princess Madeleine

Princess Sofia arrives at the ceremony with Princess Madeleine. Madeleine, who did not attend the Nobel Prize ceremony last year, wore a pink gown and an aquamarine tiara.

Princess Sofia

Sofia went for an all-blue ensemble, wearing a blue off-the-shoulder gown with her diamond wedding tiara, which was accented by new blue stones. The stones appear to be turquoises.

Princess Sofia

On her wedding day, Sofia's tiara was set with emeralds, but she has swapped out those stones on a few occasions. The Princess has replaced the stones with pearls in the past, like at the Nobel Prize ceremony in 2017 and 2018.

Princess Sofia

Another look at Sofia's tiara.

Princess Madeleine

Madeleine chose the Swedish Aquamarine Kokoshnik tiara, which once belonged to Princess Margaretha. The stunning diamond piece has been worn by Madeleine before, and by Crown Princess Victoria wore the tiara to the 2017 Nobel Prize Awards, per the Court Jeweller.

Princess Madeleine

A full look at her pink ensemble.

Princess Madeleine

Madeleine also wore dazzling diamond earrings and a matching bracelet with her tiara and sash.

Princess Madeleine

Another view of Madeleine's tiara at the Nobel Prize banquet.

Queen Silvia

Silvia's stunning brooch is on display as she arrives at the Nobel Prize banquet.

Princess Sofia

A look at Sofia's coordinating turquoise earrings, which perfectly match her tiara.

Princess Sofia

The new blue stones on the top of Sofia's diamond tiara were front and center as the royal sat during the Nobel Prize banquet.

Princess Madeleine

Another look at Madeleine's tiara.

Crown Princess Victoria

Victoria dazzled in the Baden fringe tiara.

Advertisement - Continue Reading Below

Originally posted here:
The Swedish Royal Family Wore Dazzling Tiaras to the Nobel Prize Ceremony - TownandCountrymag.com

Is the end of animal testing in sight? – E&T Magazine

Images of monkeys undergoing experiments in a German laboratory stirred a wave of public outrage recently, prompting questions whether such barbaric procedures are necessary in the 21st century. Technology exists today that could replace animal testing in the future, but how far is it from practical use?

In 2018, a team of Oxford University researchers announced that their computer models of human heart cells were able to predict side effects of various medications on the heart more accurately than animal studies.

While studies done on animals assessed the risk of arrythmias in human users with the accuracy of 75-85 per cent, the computer model of actual human heart cells made a correct prediction in 89-96 per cent of cases. That means that drugs could pass the animal tests but still later cause dangerous heart problems in patients, while this risk is lower when using computer models.

We took 62 drugs such as painkillers, antihistamines or antibiotics, many of which are on the market, and we looked for biomarkers indicating the risk of arrhythmias in our simulations, says Elisa Passini, a senior researcher in the Computational Cardiovascular Science team at the University of Oxford and the lead author of the paper published in the journal Frontiers in Physiology. Then we compared our results with what is known about these drugs. For example, there are reports of patients who have had a cardiac episode while taking these drugs. We compared our results with these reports and thats how we calculated the accuracy.

Passini says the difference in favour of the human heart cells computer model might arise because animal cells and organs, while having been widely used in drug development for decades, are in many ways similar to but by no means identical to human organs and cells.

Sometimes you dont see an effect in animals and then, if you give the drug to a human being, you will see an adverse effect on the heart, she adds.

In fact, according to a 2009 paper by Yale University epidemiologist Michael B Bracken, which was published in the Journal of the Royal Society of Medicine, there have been many cases in the past when drugs deemed safe in animal studies in fact caused serious harm once introduced to humans.

For example, thalidomide, a drug sold in the late 1950s and early 1960s as a sedative and treatment for morning sickness for pregnant women caused the foetuses to develop serious defects. Such side effects were not observed in animal studies.

A 2006 UK-based phase I clinical study of am immunomodulatory drug called TGN1412 (theralizumab), designed to alleviate symptoms of autoimmune diseases, caused life-threatening side-effects to all of the six previously healthy human volunteers enrolled in the study who were given the drug. Although they received doses 500 times lower than what had been found safe in animal studies, the human subjects quickly developed multi-organ failures and required lengthy hospitalisation. The drug had previously successfully passed tests not only in mice but also in rhesus monkeys, which up until then had been considered very similar to humans in their physiology.

Hazel Screen, a professor of biomedical engineering at Queen Mary University of London (QMUL), says that despite decades of use and refinement, the success rate in drug development based on the current animal models is extremely low.

Today, if something goes into clinical trials because it worked in animal models, the likelihood of it coming off is terrible, says Screen, who co-leads a project developing organ-on-a-chip technology another alternative that could replace animal tests in the future.

It currently takes approximately 14 years to develop a drug and only about 5 per cent of drugs actually end up being used to treat patients, she says.

Screen agrees with Passinis statement that one of the reasons for such a poor outcome is the fact that the cells, bodies and physiological processes of animals, while in many ways similar, simply do not perfectly match those of humans.

Screens colleague Professor Martin Knight says big pharma companies, hoping to improve this abysmal success rate, are looking for alternative technologies to at least partially replace animal tests.

Big pharma companies are primarily interested in increasing profits by getting better benefits for patients, rather than reducing animal testing per se, Knight says. They want to be able to predict more accurately whether these drugs are going to work and make sure that they progress more efficiently through the development pipeline.

According to the UK Home Office, 3.52 million scientific procedures were carried out in 2018 in the UK involving living animals, with mice, rats and fish making up 93 per cent of the total number.

The amount, the Home Office said, decreased by 7 per cent compared to 2017. Of the total amount, 1.80 million procedures were for experimental purposes, focusing on basic research, the development of new treatments, safety testing of pharmaceuticals, surgical training and education. The rest focused on the creation and breeding of genetically altered animals.

The cost of these experiments is substantial, especially since regulators, pressured by the 21st-century animal-rights-conscious public, require the scientists to improve conditions and minimise pain and suffering of the creatures used.

Many pharma companies are interested in the in-silico simulations of the Oxford University team, according to Passini. The team, which is part of the EU-funded Compbiomed initiative, has developed a software called Virtual Assay, which can run on a regular laptop and complete a simulation of 100 human heart cells interacting with a certain drug in about five minutes.

Our models are built on data from human patients, says Passini. Its usually patients that have gone through some surgery during which the doctors removed some cells, which were further studied. We also use data from healthy hearts that were not suitable for transplantations. The models are based on a large number of equations that represent what we know about the cardiac cells, their behaviour, their membranes, and the transport of ions in and out of cells.

These models, Passini says, are now quite ready to replace the early stage so-called in-vitro experiments experiments conducted on animal cells or small tissue samples.

We hope that our technology could in the not so distant future replace most of the in-vitro experiments, she adds. That would already make a huge difference because very large numbers of animals are used for these early stage experiments. The scientists kill the animals and take their cells. A much smaller number of animals is used for the later-stage in-vivo experiments.

The Oxford team can already run 3D simulations of an entire human heart. The availability of computational power, or lack thereof, is, however, the major stumbling block for this type of complex simulation.

We have access to some of the most powerful supercomputers in Europe, but it still takes hours to simulate a single heartbeat in 3D, Passini adds. We can afford to do this for scientific purposes, but the availability of such computer power is still limiting the use of these simulations by the industry. We are exploring alternatives, such as GPUs, which might make it more affordable in the future.

The Compbiomed project, which has recently concluded its first stage, has the ultimate goal of creating the entire human organism in silico that could be used for drug testing and simulations of various health conditions.

QMULs Knight says that the organ-on-a-chip technology could in the future reduce the number of mice, the most commonly used animal species in medical research, needed at certain stages of the drug development process. But for that to happen, the alternative technologies have to be validated and proved as reliable (if not more) as the currently used animal models.

The regulatory authorities are understandably going to be nervous about accepting results entirely from a completely new technology compared to using a set of well-established, if not always very accurate, animal models, Knight declares.

For them to accept new technologies, such as organ-on-a-chip, you have to prove that your liver, lung or gut model works in every imaginable set-up. Thats a lot of science and validation and confirmation before you reach that point.

Organ-on-a-chip systems use living human cells in a 3D device to mimic how human organs function. These devices can be used to test both the safety and efficacy of new medicines and other products, reducing the dependency on animal experiments. Usually the size of a 50-pence coin, chips already exist simulating human liver, lung and intestine.

Creating an environment that would simulate, as closely as possible, the environment in which the cells exist in the human body is the greatest engineering challenge facing the researchers.

Its become clear recently that mechanical forces have a huge impact on cell biology and therefore on how drugs behave, says Knight. Therefore, we need to make sure that the model systems that are being developed incorporate the right mechanical forces that the different tissues experience. For example, a model of the lung has to incorporate stretching as you inflate your lung; it has to incorporate the flow of air over the surface of the cells of the lung and the flow of blood in the blood vessels. And only by incorporating these key mechanical stimuli can we hope to generate a model that is truly predictive of how a drug is to behave in a body.

Last year, QMUL received a grant from Research Councils UK to lead a network that aims to bring together the UK research community in order to advance organ-on-a-chip development and cooperate with regulators and industry on validating the technology so that it can be rolled out on a larger scale.

While the complete end of animal experiments in medical science may be decades away, the researchers are positive that with the introduction of already existing technologies, their validation and further improvement, the numbers of animals required for the advancement of science will be gradually but significantly reduced over the coming decades.

Sign up to the E&T News e-mail to get great stories like this delivered to your inbox every day.

View post:
Is the end of animal testing in sight? - E&T Magazine

UVA, UVA-Wise Land Three Professors Among State’s Top 12 for 2020 – University of Virginia

The three University of Virginia professors named 2020 Outstanding Faculty Award winners Friday by the State Council of Higher Education for Virginia push the boundaries of the typical classroom and of their academic disciplines, employing hands-on experiences for students and conducting game-changing scholarship to aid humanity.

Arthur Weltman, professor and founding chair of the Department of Kinesiology in the Curry School of Education and Human Development, also holds UVAs 2019-21 Cavaliers Distinguished Teaching Professorship. Kirsten Gelsdorf, a professor of practice in the Frank Batten School of Leadership and Public Policy, came to UVA after working for the United Nations for two decades. Ryan Huish, an associate professor of biology at UVAs College at Wise, takes students of all ages outside, making the surrounding natural world their classroom and market.

Since 1987, the SCHEV awards have recognized faculty at Virginias institutions of higher learning who exemplify the highest standards of teaching, scholarship and service.Among the 12 awardees from Virginias colleges and universities, UVAs trio will be recognized for exemplifying the highest standards of teaching, scholarship and service at a March 9 ceremony in Richmond. Each will receive $7,500 from Dominion Energy, co-sponsor of the faculty awards.

A closer look at the awardees:

Gelsdorf was one of two professors SCHEV recognized as a Rising Star for early career achievements. Although she has only been on UVAs faculty for 3 years, she has already won teaching awards from Batten and from the University, as well as received perfect course-evaluation ratings from students.

The demand for her class, Global Humanitarian Crises, a 40-student seminar, skyrocketed to more than 200 students. She also piloted Battens first remote synchronous learning course to include students from UVAs College at Wise.

One student mentioned that Gelsdorfs weekend-long humanitarian crisis simulation required a higher level of thinking than any other college assignment he had undertaken. This experience encapsulates Professor Gelsdorfs desire to push us as students, to help bridge the gap between the theoretical and the practical, the student wrote.

As a professor of practice, Gelsdorf brings two decades of professional experience in United Nations programs to the University to bridge the academic-practitioner divide and influence policy change, activities that have operated on isolated tracks for too long, she wrote.

The field of global humanitarian aid, which has defined my lifes work, rests on the principle of the humanitarian imperative that people have the right to give and receive aid, she wrote. Through her scholarship and teaching, Gelsdorf aims to help expand and strengthen research and partnerships on Grounds and around the world that can influence policy change.

It is my clear responsibility to bring the questions of global humanity to this next generation.

- Kirsten Gelsdorf

The world will increasingly face unanswered questions and intractable challenges that result from conflict and disasters happening around the world. That is why I am so thankful that Batten and its leadership and public policy mission give me the unique opportunity to combine research and policy engagement into a portfolio where I can build partnerships between incredible faculty, students and external organizations to work on the humanitarian issues I care so deeply about, Gelsdorf wrote in an email after hearing she had won the award.

As Battens director of humanitarian policy, she has undertaken numerous high-level research and policy projects with organizations like the Red Cross, Global Emergency Groupand United Nations.

Together with other Batten faculty, she is now launching a series of research and policy labs that include work on early childhood education in crisis contexts and predictive analytics for migration that are being launched this month in London and at the Global Refugee Forum in Geneva.

This year, she also published with Daniel G. Maxwell, a colleague at Tufts University, Understanding the Humanitarian World, a book that traces the development of the modern humanitarian aid system and has already been adopted by numerous universities and international organizations.

An associate professor of biology at UVAs College at Wise, Huish specifically focuses on ethnobotany, the study of human-plant interactions.

He encourages student-centered learning in the classroom in novel ways. For example, in his General Botany course, he has asked his students to choreograph and perform an interpretive dance on the process of photosynthesis, one of the most important biochemical reactions to life on Earth, yet a very complex and difficult process to grasp.

Writing about his love for plants, which he links to his earliest memories, Huish wrote in a teaching statement, The beautiful complexity of photosynthetic organisms is what originally filled our early atmosphere with life-sustaining oxygen by splitting water molecules; sparked the dawn of modern human civilization in the Fertile Crescent with agriculture; initiated globalization with the spice trade; solicited trade wars; manufactured compounds that humans converted to pharmaceuticals and the list of connections goes on.

His passion for plants and dedication to teaching everyone to love and respect plants was so inspiring it changed my whole career path, wrote Jenni Gilliam, a former student whos an intern at the Center for Appalachian Studies.

He doesnt just teach the biology of plants to undergraduate students; he also teaches younger students and adult community members about local edible plants, plus medicinal or economic possibilities with plants.

He learns from them, too, and is currently interviewing community members to preserve not only Appalachian traditional uses and folklore, but also to work toward preserving the native plants and their habitats.

He has conducted medical botany research in the South Pacific Islands, working with local people of the Tonga islands. In addition, he leads a UVA-Wise team working with a Tongan plant that potentially could prevent the effects of MRSA, an antibiotic-resistant super bug becoming more common in hospitals.

My passion is to help others comprehend at even some small level, the vast beauty, potential and complexity of these humble yet magnificent organisms.

- Ryan Huish

Closer to home, Huish is also researching the potential of hemp to replace tobacco farming and the development of maple syrup as a product. He and his students share their knowledge with the community, and he has led a tour of his own farm to show methods of woodland management. He is collaborating with the regional nonprofit organization Appalachian Sustainable Development and Virginia Tech in the Appalachian Beginning Forest Farmer Coalition.

I am grateful and honored to have received this award, Huish wrote in an email. I feel that this award reflects the greater good and the strengths of UVA-Wise, which espouses the liberal arts paradigm of applying deep interdisciplinary collaboration and societal connections to problem-solving. I am proud that we emphasize the well-rounded development of these skills in our students and faculty for real and meaningful progress.

Arthur Weltman was awarded the 2019-21 Cavaliers Distinguished Teaching Professorship earlier this year, an endowed chair that recognizes an eminent scholar for outstanding and enduring excellence in the teaching of undergraduates.

During his 35 years at UVAs Curry School of Education and Human Development, he has led its exercise physiology program. Curry School Dean Robert Pianta appointed him the founding chair of the new Department of Kinesiology in 2013.

He also founded and directs the Exercise Physiology Core Laboratory, funded by the National Institutes of Health for 30 years, and holds a joint appointment in the School of Medicine. Weltmans research focuses on the role of intense and regular exercise in health and disease. He and his collaborators have contributed to understanding how exercise affects individuals from children to older adults.

Through his exercise physiology courses, he has influenced thousands of graduate and undergraduate students and trained scientists in exercise intervention. His students engage in the exercise research as participants as well as investigators. They have written about how much they learn in his challenging classes and how much they appreciate his laid-back approach and availability.

Weltman also helped to initiate both peer and alumni mentoring programs, and he continues to serve as a resource for students long after they graduate. Many have gone on to academic careers and point to his mentorship for influencing their success.

Recognized by the Seven Society and the Z Society for his passion and devotion to teaching at the University, Weltman wrote that the opportunity to teach and learn from students in and outside of the classroom is one of the joys of my job and among the most rewarding experiences of my career.

The opportunity to teach and learn from students in and outside of the classroom is one of the joys of my job and among the most rewarding experiences of my career.

- Arthur Weltman

He added that he is both honored and humbled to be named a recipient of this prestigious award. From my perspective, this award is a testament to the talented students, faculty and staff who I have had the pleasure of working with over the last 35 years at UVA, he wrote in an email about the SCHEV award.

His research is known nationally and internationally. The NIH has funded his research projects, many with cross-disciplinary collaborators and students, for more than 30 years. He has published 246 papers in refereed journals at last count, many with student co-authors, and his work has an exceptionally high rate of citation by other researchers.

Some of the topics he and colleagues have studied include whether strength training is safe and effective for prepubescent children, and how high-intensity exercise affects growth hormone release or cardiometabolic risk in older adults.

He has served as an exercise physiology adviser for the Department of Athletics at UVA since 1990, as well as for a number of professional sports teams.

Go here to see the original:
UVA, UVA-Wise Land Three Professors Among State's Top 12 for 2020 - University of Virginia