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

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Researchers found a gene mutation responsible for a rare hair loss condition.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

CYP11A1 is crucial for skin health and disease by producing important steroids.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

MPA increases cancer spread by boosting Eph A2 activity.

Early sunburn treatment with certain inhibitors may reduce skin cancer risk.

A rare gene variant causes hair and nail issues in a family.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Mutations in keratin genes cause skin disorders, but new treatments show promise.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A genetic variant in the KRT25 gene causes tightly curled hair.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.