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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

The Hippo signaling pathway helps control organ size during regeneration by regulating gene expression.

HLA can be linked to autoimmune hepatitis.

Hairless gene not strongly linked to baldness.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Somatic BHD mutations are rare in Japanese renal tumors.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Hoxc13 is essential for hair growth and follicle development.

Sox10 is important for hair follicle development and hair growth cycles.

The olfactory epithelium can regenerate throughout life, aided by specific cells, genes, and new research methods.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

p2y5, now called LPA6, is a receptor important for human hair growth.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

FOXN1 duplication can cause excessive hair growth.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

Lamins are vital for cell survival, organ development, and preventing premature aging.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.