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Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Researchers found a new mutation causing total hair loss from birth.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

FGF13 gene changes cause excessive hair growth in a rare condition.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

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

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

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

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The improved genome of the African spiny mouse helps study its tissue regeneration.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.