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PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

A female dog with mixed male and female traits was treated successfully with surgery.

circCFAP20DC helps goat ovarian cells grow, aiding follicle development.

Early diagnosis and treatment of congenital adrenal hyperplasia are crucial to manage symptoms and prevent complications.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.

NKCC1 transporters help control neuron excitability and inhibition.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

Basonuclin is crucial for hair follicle development and cycling in mice.

Cidea is essential for proper lipid storage and secretion in sebaceous glands, affecting skin and hair health.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Cinchonine Nanostructured Lipid Carriers serum safely and effectively stimulates hair growth and increases the number and size of hair follicles.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Confocal Laser Scanning Microscopy (CLSM) is a useful tool for studying how drugs interact with skin and diagnosing skin disorders, despite some limitations.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Increasing XIAP and DDRGK1 can help prevent hearing loss from loud noise.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Different PADI isoforms help cells develop diverse functions.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.