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Blocking a specific enzyme in male rat fetuses leads to the development of nipples and feminized genitalia.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

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

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

Targeting 5α-reductase type 1 may help manage Tourette-like symptoms.

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

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Acute stress increases Y1 receptor gene expression in certain brain areas, but repeated stress does not.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

RORA may help regulate hair growth by affecting hair follicle stem cells.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

A new gene mutation causes insulin resistance in a girl and her mother.

Understanding snoRNA regulation may help slow skin aging.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Human bone cells mainly produce a type 1 enzyme that may help regulate bone health.

Finasteride may help improve certain brain function issues linked to dopamine.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

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

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

RNase L hinders hair growth by altering immune signals.

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

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

A new gene variant causes glucocorticoid resistance in a mother and son.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.