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A new DSG4 gene mutation causes hair defects in a young girl.

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

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

PDGFA helps activate hair growth in cashmere goats.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

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

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

Patched1 helps prevent tumors by controlling cell growth.

TRPS1 is crucial for bone, kidney, and hair follicle development.

LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Ultra-high molecular weight poly-γ-glutamic acid may help promote hair growth.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Proteoglycans are vital for tissue growth and healing, with potential as treatment targets.