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News Release
NIH researchers have discovered a rare and sometimes lethal inflammatory disease - otulipenia - that primarily affects young children.
… biological pathways to send and receive chemical cues in reaction to injury, infection or stress. Otulipenia is one of …
Genetic Disorders
Factor V Leiden thrombophilia is an inherited disorder of blood clotting.
About Genomics
In 2003, an accurate and complete human genome sequence was finished two years ahead of schedule and at a cost less than the original estimated budget.
Educational Resources
A ribosome is a cellular particle made of RNA and protein that serves as the site for protein synthesis in the cell.
Genetic Disorders
Wilson disease is a rare genetic condition that causes a person's body to store too much of the mineral copper, leading to organ damage that may cause death.
Educational Resources
Translation is the process of translating the sequence of a messenger RNA (mRNA) molecule to a sequence of amino acids during protein synthesis.
Genetic Disorders
Severe Combined Immunodeficiency is a severe, genetic condition of the immune system.
… of the lymphocyte receptor is called the "common" gamma chain, because it is a common component of lymphocyte …
Educational Resources
An amino acid is the fundamental molecule that serves as the building block for proteins.
For Health Professionals
Essential genomics competencies, practice guidelines, and curricular resources for a variety of health professions.
… mother, Dai  Pediatric Pharmacogenomics: Opioid adverse reaction management of an African American child: Stephanie  …