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Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Lack of TrkC receptor delays hair follicle development.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

Four specific genes are linked to keloid formation and could be potential treatment targets.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

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

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

The vector successfully directed specific gene expression in hair follicles.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

A new keratin gene was found in mice, explaining hair growth.

A truncated protein linked to breast cancer may change cell adhesion.

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

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

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A specific gene mutation causes a severe skin disorder in a family.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.