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Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

STIM1 is essential for sweat secretion.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

The new test can measure very small amounts of testosterone in hair, and grinding the hair up first gives more accurate results.

New protein changes may be involved in the immune attack on hair follicles in alopecia areata.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Keratin proteins are crucial for hair growth and structure.

Immortalized rat dermal papilla cells can still induce hair growth.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Mutation in hairless gene may increase hair loss risk.

GPR40 agonists help hair growth through the protein ANGPTL4.

Mutation in hairless gene may increase hair loss risk.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

p2y5, now called LPA6, is a receptor important for human hair growth.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

Serotonin helps wounds heal faster.

Higher levels of certain nerve-related proteins are linked to hair loss in women with scalp pain.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A specific gene mutation causes woolly hair and hair loss.

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

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A new compound shows promise as a topical treatment for hair loss.