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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 genetic mutation was found causing hair and eye issues in a boy.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

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

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

Researchers found a new mutation causing total hair loss from birth.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

Researchers created an efficient method to extract DNA from marmoset hair, avoiding blood chimerism.

Photobiomodulation did not significantly improve hair density in dogs with alopecia X.

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

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

ALRN-6924 may prevent hair loss caused by chemotherapy.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.