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Genetic Disorders
Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging.
Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging. … Progeria is an extremely rare genetic disease of childhood … The most severe form of the disease is Hutchinson-Gilford progeria syndrome, recognizing the efforts of Dr. Jonathan …
Educational Resources
Progeria is a rare disease characterized by accelerated aging.
ProgeriaProgeria is a rare disease characterized by accelerated … Cell, Gene Mutation, Nuclear Membrane, Nucleus, Protein … Progeria is a rare disease characterized by accelerated aging. The classic form of progeria is called Hutchinson-Gilford progeria syndrome …
News Release
The U.S. Food and Drug Administration has approved the first treatment for progeria, a rare and fatal pediatric disease, characterized by dramatic, rapid aging beginning in childhood.
… Drug Administration has approved the first treatment for progeria , a rare and fatal pediatric disease, characterized … is available to discuss his lab’s research activities on progeria, including its involvement in the discovery of the … demonstration that this drug class could provide benefit. Progeria, also known as Hutchinson-Gilford progeria syndrome, …
News Release
Using a recently developed DNA base-editing technique, researchers correct accelerating aging disorder.
… of mice with the genetic variation associated with progeria,  a rare genetic disease that causes extreme … browser does not support the video tag. Base editing for progeria treatment Progeria is caused by a mutation in the nuclear lamin A gene …
ProgeriaProgeria is a rare disease characterized by accelerated aging. The classic form of progeria is called Hutchinson-Gilford progeria syndrome (HGPS), named for the doctors who first …
Staff
Dr. Michael Erdos is an Associate Investigator in the Molecular Genetics Section of the Center for Precision Health Research.
… for the rare premature-aging disease, Hutchinson Gilford Progeria Syndrome (HGPS). Two of those treatment strategies … potential for therapeutic development. Hutchinson-Gilford Progeria Syndrome In the ultra-rare premature aging disorder … by 62%. Dr. Erdos and colleagues are now supporting the Progeria Research Foundation application with the FDA for …
Staff
Dr. Francis Collins is a senior investigator in Center for Precision Health Research.
… 2 diabetes, and the gene that causes Hutchinson-Gilford progeria syndrome, a rare condition that causes premature … lab's significant projects focuses on Hutchinson-Gilford progeria syndrome (HGPS), a rare genetic disorder … inhibitors (FTIs) might be beneficial in treatment of progeria, and cell culture experiments showed that FTIs could …
Partner with NHGRI
NHGRI's technologies, inventions and discoveries are available for licensing.
…   … Mouse Models Mouse Model of Hutchinson-Gilford Progeria Syndrome and Vascular Abnormalities DHHS Reference …
The Genomics Landscape
In the February 12, 2021 edition of The Genomics Landscape, Dr. Eric Green talks about the 20-year anniversary of the publications that reported the draft human genome sequence.
… DNA-editing method shows promise to treat mouse model of progeria In Broad Institute video, Dr. Collins describes new study using gene base editing to treat progeria What a year it was for science advances! Researchers …
Staff
Dr. Merideth is a staff clinician in the Office of the Clinical Director and program director for both the NHGRI Medical Biochemical Genetics Fellowship and NHGRI Clinical Biochemical Genetics Fellowship.
… the first Natural History Study in Hutchinson-Gilford Progeria Syndrome (HGPS), developing outcome parameters which … Introne WJ. Phenotype and course of Hutchinson-Gilford progeria syndrome . N Engl J Med 358:592-604, 2008. … …