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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The visfatin GT genotype may increase the risk of Alopecia Areata.

Certain gene variations may increase the risk of PCOS in South Indian women.

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

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

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Cashmere goats have a hair growth cycle with specific genes regulating growth, regression, and resting periods.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

Low biotin intake during pregnancy can affect biotin transport in mothers and fetuses.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

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

The EDAR gene greatly affects hair thickness in Asian populations.

Pregnancy increases certain GABA_A receptors in rat brains, influenced by steroid levels.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

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

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

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

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

Certain gene variations are not a major cause of male infertility in Nigerian men.

Finasteride affects prostate weights and pituitary activity differently with age.

CD10 and CD34 levels change during hair development and different hair growth stages, which could be important for hair regeneration treatments.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Mice with the naked gene have missing or abnormal hair cells.