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The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

Melatonin reduces BMP2 gene expression in goat hair follicles during the resting period.

5% topical minoxidil improves hair density and quality in monilethrix patients.

No significant link was found between the studied genes and female hair loss in the Polish population.

Gene differences affect finasteride side effects in men with hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

FGF5 gene mutations cause long hair in domestic cats.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

A gene mutation in mice causes skin defects and early death.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Reduced AR gene methylation may cause early pubic hair growth in girls.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

S100A3 protein is crucial for hair shaft formation in mice.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Signaling pathways are crucial for hair growth in goats.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.