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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

HLD10 can include increased body hair and Mongolian spots.

PI3Kδ inhibition may effectively treat cutaneous chronic graft-versus-host disease.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Pigs are a good model for studying human hair growth and disorders.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Total glucosides of paeony may help treat alopecia areata by reducing inflammation and hair loss.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Mutations in the hairless gene cause a rare form of permanent hair loss.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

New genetic variants linked to albinism were found in Pakistani families.

Glypican-1 is important for blood vessel growth in hair follicles and could help treat hair loss.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Grasp protein helps maintain skin health after UVB exposure.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

New mouse models of Pemphigus show severe symptoms and need better treatments.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.