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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Blocking IL-17a can improve age-related smell loss in mice.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

ZDHHC17 methylation may help treat or identify facial skin aging.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Monilethrix is linked to a gene cluster on chromosome 12.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Blocking IL-17 can reduce joint inflammation in Ross River Virus infections.

A boy's hair turned red because of genetic mutations, not lack of zinc.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Specific keratin gene mutations can cause monilethrix.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Combining fractional CO₂ laser with type III collagen improves acne scar treatment.

FGF13 gene changes cause excessive hair growth in a rare condition.

Variation in the TCHH gene affects wool curliness in sheep.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.