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A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

Sericin from silk cocoons could be a promising drug delivery tool, but stability and consistency need improvement.

Consider rare forms of CAH for accurate diagnosis and treatment.

MTS24 marks a new type of skin cell that helps hair growth and repair.

Keratin 75 might be important in oral cancer progression.

Ganoderma lucidum extract may help treat stress-related hair loss.

The optimal concentration for caffeine release in gel form is 0.2% caffeine and 2.3% chitosan.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

pCLCA2 protein may help maintain skin structure and function.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A 25-year-old man had an unusual case of benign skin tumors and hair loss.

The patient had paraneoplastic pemphigus without mucosal involvement.

The Spherical Skin Model improves drug and cosmetic testing by accurately mimicking human skin for efficient compound screening.

Sonidegib effectively treated basal cell carcinoma in a patient with lupus without worsening lupus symptoms.

Reduced CD44 expression may cause abnormal hyaluronate buildup in cutaneous myxoma.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

Glycylglycine makes hair softer by improving alignment and changing hair's internal properties.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

A new gene mutation causes insulin resistance in a girl and her mother.

Cyclosporin A promotes hair growth in mice and increases a protein linked to hair growth, but it may not work the same way in humans.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.

Women with PCOS and hair loss have lower levels of the protein gelsolin in their blood.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.