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BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

Androgen receptors help prostate cancer cells grow and resist drugs.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Genetic variants affect minoxidil hair loss treatment success.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

MOF controls skin development by regulating genes for mitochondria and cilia.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A new easy-to-use biosensor was made to detect androgen receptor mRNA, which could help diagnose related conditions quickly.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

Keratin proteins in hair are complex and come from multiple gene families.

A specific genetic variation affects wool quality in sheep.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The document concludes that the androgen receptor's structure and function are complex, affecting how it regulates genes and is involved in diseases like prostate cancer.

SRD5A1 is crucial in advanced prostate cancer, and blocking both SRD5A1 and SRD5A2 is more effective than targeting SRD5A2 alone.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.