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Markers help differentiate between apocrine and eccrine sweat glands to identify sweat gland tumors.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Y27632 increases cell growth through EGFR signaling, not ROCK1/2.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

The EDAR V370A allele in East Asians likely evolved due to reliance on aquatic resources providing essential nutrients.

The EDAR V370A allele in East Asians likely evolved due to reliance on aquatic resources providing essential nutrients.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Referral rates for anaphylaxis patients improved significantly after implementing guidelines.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

Higher IL-31 levels are linked to worse itching in chronic kidney disease patients.

Cepharanthine shows promise as a potential lung cancer treatment by effectively killing cancer cells.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

Restoring phenylalanine levels improved skin and hair symptoms in a PKU infant.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Cepharanthine effectively reduces Herpes Simplex Virus Type 1 by blocking certain cell pathways and promoting cell death.

Wnt7a helps corneal cells grow and stick together, aiding in repair.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Epiregulin can help hair grow and may be useful for treating hair loss.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Epidermal growth factor increases extra hair cells in newborn rat ears.