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Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

CD2 might be a new treatment target for patchy alopecia areata.

A mutation in the Sgkl gene causes defective hair growth in mice.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Flavin prevents cataracts in young rats.

Nelfb is essential for dermal fat development and survival.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

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

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

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

5% topical minoxidil improves hair density and quality in monilethrix patients.

An artificial lipid barrier can restore hair growth in cases of SCD1 deficiency.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

Finasteride helps female-pattern hair loss.

Vitamin D receptor gene changes don't affect alopecia areata risk.

A mutation in the human hairless gene causes alopecia universalis.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.