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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

MC4R gene variants not linked to female hair loss.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Lack of Fgf21 slows hair growth by affecting gene interactions.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Igf1r helps regulate hair growth cycles.

ESR2 gene linked to female-pattern hair loss.

Mutations in specific llama genes may affect fiber quality for textiles.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

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

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Nestin-expressing hair follicle cells may be useful for nerve repair and regeneration.

Key genes for mink fur have been identified, aiding conservation efforts.

The fuzzy gene is crucial for controlling hair growth cycles.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

FGF signaling is crucial for starting feather development in chicken embryos.

CTIP2 may help in skin development and maintenance.