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A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

A new gene mutation causes a rare type of hair loss.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

A new mutation in the HR gene causes hair loss in a specific family.

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

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A specific gene mutation causes sparse, brittle hair in a family.

Variation in the TCHH gene affects wool curliness in sheep.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hox genes control hair follicle stem cell regeneration in different body regions.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Hoxc13 is essential for hair growth and follicle development.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Lgr5+ stem cells do not cause skin tumors.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.