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Finasteride side effects in young men may be linked to specific gene variations.

Haplogroup X found in Altaian population supports Amerindian origin.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

A specific gene mutation causes Olmsted syndrome.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A gene mutation causes woolly hair in a Syrian patient.

Night shift work disrupts the body's natural clock genes.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A new mouse mutation causes skin and hair defects due to a gene change.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Fox genes are important for hair growth and development in cashmere goats.

Hair loss gene linked to prostate issues.

Eating collagen peptides may help with skin and hair growth.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Longer CAG repeats in gene linked to more severe hair loss in females.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Topical minoxidil can cause excessive hair growth in children, so use it carefully.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A gene called BMAL1 plays a role in controlling hair growth.

MC4R gene variants not linked to female hair loss.

Certain gene variations are linked to better memory in healthy Chinese women.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.