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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.

A new gene mutation causes a rare type of hair loss.

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

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

FOXA1 and CCL2 genes are more active in women with PCOS, varying by phenotype.

A new method accurately measures clobetasol propionate in hair and skin.

MEF2C is crucial for normal hair cycle progression.

A specific gene change in APCDD1 increases the risk of hair loss.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

The testes significantly contribute to vitamin D metabolism and may affect male reproductive health and conditions like hair loss.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Nexin 1 may help control hair growth.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

TMPRSS2 affects COVID-19 severity and treatment options.

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

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.