Ncats.nih.gov

National Center for Advancing Translational Sciences

WebOur focus is to advance the science of translation, which is the process of turning observations into interventions to improve health. We work with researchers, the public and other stakeholder groups to design new …

Actived: 2 days ago

URL: ncats.nih.gov

About NCATS National Center for Advancing …

(7 days ago) WebAbout NCATS. The National Center for Advancing Translational Sciences (NCATS) — one of 27 Institutes and Centers at the National Institutes of Health (NIH) — was established to transform the …

Category: Health Go Now

Translational Science Spectrum National Center for …

(2 days ago) WebThe translational science spectrum represents each stage of research along the path from the biological basis of health and disease …

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Rare Diseases Research and Resources National …

(5 days ago) WebRare Diseases Research and Resources. NCATS is committed to using research to address the public health crisis presented by rare diseases. Speeding development of treatments for patients …

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Translational Science Principles National Center for Advancing

(3 days ago) WebNCATS’ mission is to turn biomedical research discoveries into health solution — including diagnostics, treatments, and interventions — through the application …

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A Translational Approach to Addressing COVID‑19

(2 days ago) WebDuring public health emergencies, science — and the process of turning observations into new therapies — must move faster than ever. That is where …

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Research National Center for Advancing Translational …

(Just Now) WebResearch. NCATS research addresses scientific and operational challenges that slow the development of the new interventions to improve human health. The Center aims to make translational …

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Genetic and Rare Diseases (GARD) Information Center

(7 days ago) WebThe Genetic and Rare Diseases (GARD) Information Center is a public health resource for people living with a rare disease and their families. It provides free access to …

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NCATS Staff Profiles

(7 days ago) WebNCATS Staff Profiles. Translation is a team sport. Click on the names below to learn more about NCATS staff members and their work in support of the Center’s …

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Staff Profile: Ken L. Wiley, Jr. National Center for Advancing

(5 days ago) WebBiography. Ken L. Wiley, Jr., is the chief of the Clinical Research Resources Section in the Clinical Affairs Branch within NCATS’ Division of Clinical Innovation, where …

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Patient/Community Engagement & Health Information

(2 days ago) WebThe Genetic and Rare Diseases Information Center provides up-to-date health information about numerous rare and genetic diseases. Patient-Focused Therapy …

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Study Suggests People with Rare Diseases Likely Face Higher …

(9 days ago) WebAbout 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. …

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Rare Diseases Community Resources National Center for …

(6 days ago) WebFor Patients. Access resources through NCATS’ Genetic and Rare Diseases (GARD) Information Center: Call the GARD Information Center at 1-888-205-2331 to …

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National COVID Cohort Collaborative (N3C) National Center for

(5 days ago) WebThe N3C offers one of the largest collections of secure and deidentified clinical data in the United States for COVID-19 research. Its ever-growing size and …

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Biomedical Research and Public Health Collaborations with NASA

(6 days ago) WebRead about why we would consider doing space-based biomedical research from former NCATS Director Christopher P. Austin.. NIH-NASA Collaboration. NIH and …

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Rare Diseases Registry Program (RaDaR) National Center for …

(7 days ago) WebNCATS launched the Rare Diseases Registry Program (RaDaR) website to provide the rare diseases community with easily accessible guidance on how to set up …

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Patient Registries

(1 days ago) WebPatient Registries. A registry is a systematic collection of standardized data about a group of individuals. Two primary types of registries are relevant to translational …

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Scientists Identify Characteristics to Better Define Long COVID

(4 days ago) WebA research team supported by the National Institutes of Health has identified characteristics of people with long COVID and those likely to have it. Scientists, using …

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About the National COVID Cohort Collaborative

(2 days ago) WebThe National COVID Cohort Collaborative (N3C) maintains one of the largest collections of clinical data related to COVID-19 symptoms and patient outcomes in the …

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Patient Registries

(5 days ago) WebPatient Registries. In the context of therapy development, a patient registry (also called a disease registry) is a database that collects and stores information about patients …

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Study Finds Immune Dysfunction Is a Significant Risk Factor for …

(1 days ago) WebThe N3C currently contains electronic health record data from more than 13 million people. Using these data, researchers quickly determined trends based on …

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Unmet medical need

(8 days ago) WebUnmet medical need. An unmet medical need is a condition or symptom whose treatment or diagnosis is not addressed adequately by available therapy. An unmet medical need …

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