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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.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Multiomics is revolutionizing biology by enabling breakthroughs in research and disease diagnosis.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

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

Understanding tissue regeneration in animals can improve regenerative medicine.

A gene mutation causes monilethrix in a Chinese family.

Individuals with this condition often develop male traits and identities at puberty despite being raised as females.

Two new gene mutations cause a rare hair disorder.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

EDA2R gene linked to hair loss.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Dual wavelength LEDs may help reduce hair loss by lowering DHT levels.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

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

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

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

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.