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The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Some people have a genetic variation that makes them less effective at breaking down drugs.

A specific gene variant may increase the risk of developing Alopecia Areata.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

5αR inhibitors help slow early prostate cancer cell growth, suggesting combined treatments are needed.

Blocking certain brain processes reduces mating behavior in female rats.

Certain derivatives are more effective 5α-reductase type 2 inhibitors than finasteride.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

5α-reductases increase epitestosterone's effect on androgen receptors.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

5alpha-reductase 2 is crucial for proper male brain development and sexual differentiation.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

A rabbit gene important for hair development was identified and detailed.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

A KRT32 gene variant causes loose anagen hair syndrome.

The B2 genes are crucial for hair growth in rats.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A missing mK6irs1 gene causes hair loss in mice.

Suppressing very long chain fatty acids is linked to skin cancer.