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A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The gene GJA1 is important for regulating coarse hair density in goats.

Changing CDK4 levels affects the number of stem cells in mouse hair follicles.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Most mouse hair keratin genes are on chromosomes 11 and 15.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

ILC1-like cells can cause alopecia areata by themselves.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

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

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

STEAP3 protein might help treat hair loss, but more testing is needed.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Four new genes related to sheep wool were discovered, showing genetic diversity.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Platelet factor 4 slows down hair growth and could make hair loss treatments more effective if removed.

Certain gene variations are found in people with polycystic ovary syndrome.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

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

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Certain genetic markers may increase or decrease prostate cancer risk.