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

Hair loss gene linked to prostate issues.

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.

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

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

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.

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.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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.

Mutation in hairless gene may increase hair loss risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A genetic marker linked to a type of hair loss was found in most patients studied.

Certain gene variations might be linked to severe acne in women but not in men.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.