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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The scraggly mutation causes hair loss and skin defects in mice.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

A specific gene mutation causes long hair in Angora rabbits.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

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

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Abnormal gene expression related to keratin causes hair loss in certain mice.

A KRT32 gene variant causes loose anagen hair syndrome.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The Gsdma3 gene is essential for normal hair development in mice.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

A new method can detect mutations in mice by observing changes in hair follicle cells.

The gene Prss53 affects hair shape and bone development in rabbits.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

A mutation in the KRT74 gene causes tightly curled hair.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Mutations in the SNRPE gene cause hereditary hair loss.