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Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Certain gene variations may increase the risk and severity of alopecia areata.

Gene variations may increase oxidative stress in male pattern baldness.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

New genetic mutations linked to rare skin disorders were found in three newborns.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

miR-182 may help treat hallux valgus by targeting FGF9.

FOXN1 gene variants cause low T cells and immune issues from birth.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Seven new genetic risk areas for prostate cancer were found.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Researchers found 15 new genetic links to skin traits in Japanese women.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Hair follicles can be used to study gene mutations in Stargardt disease.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.