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GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

A unique gene mutation was found in a family with monilethrix.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

AUC and APL are distinct conditions needing careful clinical assessment.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Higher CRBP1 levels are linked to more severe alopecia areata.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A mutation in the human hairless gene causes alopecia universalis.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Hair follicles play a crucial role in regulating skin barrier function.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

A new genetic mutation was found causing hair and eye issues in a boy.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Certain genes are linked to the risk of developing Alopecia Areata.

AKR1C3 could be a treatment target for metabolic issues in PCOS.