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Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

Iron deficiency in mothers causes hair loss in their baby mice.

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

Increased energy use in Pik3r1-related insulin resistance isn't due to Ucp1 thermogenesis.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Hoxc13 gene is essential for hair, nail, and papilla development.

The LTF gene may help predict and manage nonspecific orbital inflammation.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

AIMP1 can boost hair growth by increasing stem cell activity.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Noggin promotes skin tumors by activating certain cell signaling pathways.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

FOL-005 peptide can reduce human hair growth by lowering FGF7 levels.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

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

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Spt4 and Spt6 are essential for fat cell development.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Researchers found a non-functional sheep keratin gene due to mutations.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.