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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

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

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Deleting Twist1 in skin cells reduces UVB-induced skin cancer risk.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A new keratin gene was found in mice, explaining hair growth.

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

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A new gene mutation linked to a skin condition was found in a Spanish family.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Rac1 is crucial for normal hair structure and pigmentation.

A mutation in the human hairless gene causes alopecia universalis.

A gene mutation causes curly hair and hair loss in rats.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Using special RNA to target a mutant gene fixed hair problems in mice.

Hair loss in certain mice is linked to changes in keratin-related genes.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

A new gene variant causes curly coats in some dog breeds.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

CHI3L1 and CXCL5 proteins help promote hair growth.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.