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Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

A gene mutation causes curly hair and hair loss in rats.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

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

New genetic mutations causing hair loss were found in a Chinese family.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Longer CAG repeats in gene linked to more severe hair loss in females.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Hsc70 protein may influence hair growth by responding to androgens.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

A gene mutation causes woolly hair in a Syrian patient.

Certain gene variations increase the risk of alopecia areata in Koreans.