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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The EDAR gene greatly affects hair thickness in Asian populations.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

Targeting IL-15 may help treat Alopecia Areata.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

A genetic marker linked to a type of hair loss was found in most patients studied.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

The ACE1 gene variant doesn't affect long-COVID symptoms.

The N gene affects the protein makeup of mouse hair.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

Hair greying is mainly influenced by age, with genetics playing a smaller role.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

OR2AT4 helps reduce aging and cell damage in human skin cells.

The research found key RNA networks that may control hair growth in cashmere goats.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.