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Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

The rs1128977 gene variant may affect cholesterol and body measurements.

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

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

MC4R gene variants not linked to female hair loss.

Chinese medicine may help treat hair loss by affecting genes and enzyme activity.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

CAG repeat polymorphism and prostate zone volume are not reliable markers of long-term androgen sensitivity.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

The HCR gene contributes to psoriasis risk.

Certain genetic variants may increase the risk of developing PCOS.

Ceramide Synthase 4 is essential for normal hair growth and preventing hair loss.

Three genes linked to the development of trichilemmal cysts were found.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Finasteride treatment changes Cx43 in rat testes, possibly causing fertility issues.

Certain genes control the color of human hair by affecting pigment production.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.