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New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

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

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

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

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

EDA2R gene linked to hair loss.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The new aptamer TAGX-0003 shows promise as an effective treatment for hair loss disorder alopecia areata.

Spt4 and Spt6 are essential for fat cell development.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

PPARs help regulate skin health and could be used to treat skin disorders.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Elastin-like recombinamers show promise for better wound healing and skin regeneration.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.