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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

Researchers found a genetic region that influences the number of coat layers in dogs.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

WNT10A gene mutations cause short anagen hair syndrome.

Trps1 is essential for proper hair follicle development.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

Androgen receptors help prostate cancer cells grow and resist drugs.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A specific gene mutation causes woolly hair and hair loss.

The B2 genes are crucial for hair growth in rats.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.