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SOX2 helps reduce wound size and pressure ulcer formation by suppressing oxidative stress and increasing antioxidant activity in mice.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

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

SSO helps in skin protection and keratinization.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

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

The side gland of Suncus murinus is a good model for studying human sebaceous glands.

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

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

rwSALT provides precise hair regrowth measurement from scalp photos.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Tanning ability is linked to specific DNA changes in skin genes.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

Loss of TET2 increases the risk of skin and oral cancer.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The PP2A-B55α protein is essential for brain and skin development in embryos.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.