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

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

Editing the FGF5 gene in sheep increases fine wool growth.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

High S100A4 levels worsen glioblastoma by promoting blood vessel growth.

A rare pituitary tumor in an 18-year-old male caused hormonal issues and vision loss, requiring surgery and further treatment.

TGF-β receptor 1 helps deer antlers grow by aiding skin and cartilage cell growth.

Somatostatin may help protect hair follicles from immune attacks.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Early dermatological referrals are important for women and girls with Turner syndrome to improve life quality.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

T cells affect skin cell genes in inflammatory diseases, and therapy can normalize these changes.

Mutations in the KRT16 gene can cause skin and nail disorders.

New genes and pathways are important for testosterone production and male sexual development.

Thymosin β4 and VEGF are important for blood vessel formation in many organs.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Gamma/delta T cells help defend skin against heavy metals.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.