Recent research from Michigan Medicine takes aim at the a variant in gene SCN1B, which causes a severe form of developmental epileptic encephalopathy.

Researchers at Washington University School of Medicine in St. Louis have conducted a longitudinal study on an individual ...

A team led by University of Pittsburgh School of Public Health geneticists has shown, for the first time, that a gene ...

Black fur comes from a genetic mutation that was likely in domesticated dogs thousands of years ago. The dark fur is rare in Europe due to a reduced genetic diversity, but at least half of the ...

Researchers find a master epigenetic switch that activates silenced genes to compensate for their missing counterparts in a ...

Accumulation of fat molecules is detrimental to the cell. Researchers have made a breakthrough in understanding how our cells manage to stay healthy by recycling important fat molecules. Their study ...

nhgri.nih.gov Fraser syndrome is characterised by cryptophthalmos, cutaneous syndactyly, malformations of the larynx and genitourinary tract, craniofacial dysmorphism, orofacial clefting, mental ...

Feb. 6, 2025 — Despite new medication, cystic fibrosis often leads to permanent lung damage. Researchers have discovered that the disease causes changes in the immune system early in life ...