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sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

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

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

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

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

A new mouse mutation causes skin and hair defects due to a gene change.

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

TMPRSS2 affects COVID-19 severity and treatment options.

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

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

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

rwSALT provides precise hair regrowth measurement from scalp photos.

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

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

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

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

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

SFRP2 and PTGDS may be key factors in female hair loss.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

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

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

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