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PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

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People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

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LIPH mutations cause woolly hair in some Chinese people.

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

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

The new synthetic retinoid RO 13-6298 effectively treated severe psoriasis at low doses with manageable side effects.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

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

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HSD11b1 affects skin nerves and increases non-histaminergic itch.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The MTR gene affects wool quality and production in Chinese Merino sheep.

A specific gene mutation causes a severe skin disorder in a family.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.