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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A mutation in the KRTHB5 gene causes hair and nail issues.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Hair varies in size and features depending on body region.

No link found between new male baldness genes and female hair loss.

The rs4541843 variant is linked to higher risk and severity of alopecia areata.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Keratin gene clusters in humans and marsupials are similarly organized.

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

A genetic variant linked to hair thinning in Japanese women was found.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

New genetic locations explain much of hair color variation in Europeans.

MC4R gene variants not linked to female hair loss.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.