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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

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

A gene deletion causes the "hairless" trait in Iffa Credo rats.

New mutations in the DSG4 gene cause a rare hair condition.

Two gene areas linked to male pattern baldness found, more research needed.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

AR gene not major factor in female hair loss; different from male hair loss.

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

A mouse gene mutation increases the risk of skin cancer.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

Scientists discovered two versions of a new human hair keratin gene.

Mice with the naked gene have missing or abnormal hair cells.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

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

Changing light periods synchronized wool growth cycles in sheep.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

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.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.