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Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

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

Human hair follicle stem cells can help heal wounds faster.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Ferroportin in macrophages is crucial for hair growth and skin healing by managing iron distribution.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Interferon α‐2b can temporarily reduce hepatitis C virus and normalize liver enzyme levels.

The marker 5-hmC changes in hair follicle stem cells when they start to grow.

ECM1-modified stem cells can effectively treat liver cirrhosis.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Testosterone increases cell growth and reduces IL-6 in gum cells.

ARHGEF3 is essential for proper hair follicle development in mice.

EGF signaling affects gene expression in skin cells, influencing hair growth and potentially cancer.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

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

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

VEGF165 influences hair follicle cell growth and movement through VEGFR-2 activation.

Hair follicles could be used to noninvasively monitor our body's internal clock and help identify risks for related diseases.

HEY2+ cells help regenerate skin during wound healing.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.