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IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Scientists identified and cloned specific keratin proteins in mouse hair.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

MEF2C is crucial for normal hair cycle progression.

HoxC genes are crucial for normal hair and nail development.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A genetic variant in goats is linked to cashmere growth.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

KAP6 genes are conserved across species and active in hair follicles.

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

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

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Most mouse hair keratin genes are on chromosomes 11 and 15.

A new mouse mutation causes skin and hair defects due to a gene change.