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A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Genetic differences affect COVID-19 severity and treatment effectiveness.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Targeting 5α-reductase type 1 may help manage Tourette-like symptoms.

Isolation stress in rats reduces brain enzyme levels, affecting dopamine function.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Hair loss gene linked to prostate issues.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.