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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

Ghrelin and its receptors likely aren't risk factors for PCOS.

TGM3 is important for skin and hair structure and may help diagnose cancer.

AH-001 could be a safer and more effective treatment for hair loss.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

Scientists found a gene in mice that causes early hearing loss.

Trichohyalin is also found in the outer layers of normal human skin.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Hairless protein can block vitamin D activation in skin cells.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

LhGH promotes hair growth and prevents hair loss in mice.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

Rac1 is essential for proper hair structure and color.

RNase L hinders hair follicle regeneration by altering immune signals.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

PAR-1 may play a role in hair growth regulation in human hair follicles.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Mutations in the hHb6 gene cause the hair disorder monilethrix.