With all the types of RNA we know about today, it might be easy to take some of them for granted! RNA was first discovered in the 1880s, but for over a century, many important types of RNA remained unknown. That's why scientists Victor Ambros at UMass Chan Medical School and Gary Ruvkun at Massachusetts General Hospital have been awarded the 2024 Noble Prize in Physiology for their discovery of microRNAs! These tiny RNAs play a huge role in regulating genes, which is very important for our health. They can also be biomarkers for certain diseases, and scientists are also studying their potential to be used in new therapies. Learn more about microRNAs and other types of RNA in our fact sheet: https://lnkd.in/eS-8AKPh
National Human Genome Research Institute (NHGRI)
Research
Bethesda, MD 46,030 followers
The Forefront of Genomics®
About us
NHGRI is the driving force for advancing genomics research at the National Institutes of Health. By conducting and funding world-class genomics research, training the next generation of genomics experts, and collaborating with diverse communities, NHGRI accelerates scientific and medical breakthroughs that improve human health. Learn more at http://genome.gov.
- Website
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http://www.genome.gov
External link for National Human Genome Research Institute (NHGRI)
- Industry
- Research
- Company size
- 201-500 employees
- Headquarters
- Bethesda, MD
- Type
- Government Agency
- Founded
- 1989
- Specialties
- human genome, genetics, genomics, ethical, legal and social issues , scientific research, clinical research, community outreach, policy, and healthcare
Locations
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Primary
31 Center Dr.
Building 31, Room 4B09
Bethesda, MD 20892-2125, US
Employees at National Human Genome Research Institute (NHGRI)
Updates
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National Human Genome Research Institute (NHGRI) reposted this
Genomics is constantly evolving and advancing, including the regular development of new experimental technologies and data-analysis methods. Such advances are readily applicable to ongoing efforts to develop new and more inclusive sets of reference human genome sequences and improve the ability to detect all variants in each newly sequenced human genome. The long-term goal is to have sufficient knowledge about genomic variation in all human populations, ensuring equity in the benefits of genomic medicine. I encourage you to learn more in our Genomic Variation factsheet: https://lnkd.in/egQfcBP4.
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Join NHGRI on October 15 at 10 a.m. ET for our webinar, “Ancient Genetic Clues into Modern Human Disease.” Researchers are working to uncover the genetic architecture of human diseases and traits — and one way they can do this is by studying ancient and historical DNA that is over 500 years old! This can help provide insights into the origins and biology of human disease. The webinar discussion will help NHGRI identify research gaps, responsible practices, and future opportunities as ancient and historical DNA is increasingly used to discern why certain diseases and traits vary across places and populations. Learn more and register! https://lnkd.in/eCmcedzz
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Excitement about a metaverse — a 3D virtual world with our avatars — has come and gone, but if it becomes more integrated into our everyday lives, it may change the way we interact with healthcare and medicine. For example, imagine your future avatar leaving the digital workplace to visit a physician in a virtual clinic space, followed by immersive, AI-guided physical therapy and later, an immersive virtual support group. While a “medical metaverse” like this doesn’t exist currently, each setting would require you to trust the provider and medical system and trust that your privacy is protected. NHGRI researcher Susan Persky, Ph.D., recently wrote a commentary on how building this medical metaverse with human psychology in mind can help us take full advantage of emerging technologies in a way that is psychologically and ethically sound. Read the commentary, published in the Journal of Medical Extended Reality, here: https://lnkd.in/eHYA-4-F
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Happy Mean Girls Day! We love October for many reasons, but one of the top ones is because it marks the start of the Human Genome Project! This was the first effort to completely decipher the sequences of the human genome as well as the genomes of a couple of other species that are commonly used in research, like the mouse and the fruit fly. The Human Genome Project brought together thousands of researchers from around the world and from many different disciplines to work on completing the first sequence of a human genome! Learn more in our HGP fact sheet: https://lnkd.in/ef_wpc8b
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Applications are now open for NHGRI and ASHG’s Genomics and Public Service Fellowship Program! This is an exciting opportunity for postbacs and post-grads to gain experience in public policy, education and #scicomm. Learn more and apply by Nov. 30! https://lnkd.in/eV4tu9Ak
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Sequencing helps us investigate the functions of genes! Researchers use genome sequencing to search for genomic variations that may play a role in the development or progression of a disease. Learn more in our DNA sequencing fact sheet! https://lnkd.in/dPkzPQb
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National Human Genome Research Institute (NHGRI) reposted this
Exciting opportunity alert! Applications are now open for the ASHG-National Human Genome Research Institute (NHGRI) & Public Service Fellowship Program from October 1 through January 5. 🌟 This partnership provides valuable training in public policy, science communication, and education, offering pathways for postbaccalaureate and graduate-level individuals to advance genomics. Interested in applying or learning more? Visit our webpage and submit your application to be part of a dynamic program driving the future of genomics: https://lnkd.in/gMHhRqWM #Genomics #ASHG #CareerDevelopment #Genetics
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National Human Genome Research Institute (NHGRI) reposted this
Acting Deputy Director, National Human Genome Research Institute, National Institutes of Health; Head of the Health Disparities Unit
In light of the changing treatment options for SCD, it is paramount that the community has access to information on clinical trials and new SCD gene therapies. The Democratizing Education for SCD Gene Therapy Project helps to explain the different steps of navigating clinical trials and information on FDA-approved gene therapy treatments. It is important to have open conversations with your healthcare team and ask questions before, during, and after every step. Click here to check out our updated information! https://lnkd.in/gAcn4QPT
Sickle cell disease gene therapy education project
genome.gov
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In light of the recent changes in treatment options for sickle cell disease, it’s crucial for patients and families to have access to information that will help them make informed decisions about their treatment. That is why Vence L. Bonham, Jr. J.D. and his group at NHGRI have put together important and actionable educational materials about gene therapy for patients and families in the sickle cell disease community. These resources have been updated to include the latest gene therapies to treat sickle cell disease. More than 50 scientists, physicians, patients, and community advocates worked together to develop content for the Democratizing Education for Sickle Cell Disease Gene Therapy Project. You can access these resources here: https://lnkd.in/ezquk4kA