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UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

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

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

A gene variation is linked to hair thickness in Asians.

Certain gene changes and hormone levels are linked to female hair loss.

A specific gene mutation causes Olmsted syndrome.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

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

Certain gene variations may increase the risk of PCOS in South Indian women.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

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

Sun exposure and genetics increase skin cancer risk from precancerous lesions.