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The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Potassium cyanide changes hair's disulfide bonds to monosulfide, affecting high-sulfur proteins more.

Created large amounts of grape seed compounds using a new method.

Washing permed hair after using thioglycolic acid helps reform strong bonds, making hair stronger.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

The serum reduces acne and improves skin clarity.

SEF cryogels effectively kill bacteria, stop bleeding, and speed up wound healing.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

EETs can delay seizures by affecting GABA activity, offering potential new treatments for seizures.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Three genes linked to the development of trichilemmal cysts were found.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Thiazole, a sulfur and nitrogen chemical, is useful in creating potential drugs for conditions like seizures, cancer, bacterial infections, tuberculosis, inflammation, malaria, viruses, Alzheimer's, diabetes, and A1-receptor issues.

Keratin-75 is secreted by ameloblasts in a unique way without a signal peptide.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Sheep hair follicle transglutaminases are calcium-dependent.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Two new types of eyelid cysts were identified, each with different treatment challenges.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

Human skin can make serotonin and melatonin.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.