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The DLQI is a key tool for measuring quality of life in dermatology.

A rare combination of hair loss and excessive fine hair growth was found in celiac disease patients.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The combined treatment with engineered bacteria and yellow LED light improved wound healing in mice.

RNase L hinders hair follicle regeneration by altering immune signals.

A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

A new method accurately measures a drug in skin for cancer therapy research.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

CTP-543 is generally safe for treating alopecia areata.

Low-dose chemotherapy is safer, more effective, and cost-effective than surgery for treating bone lesions in children.

A new compound slows cancer cell growth and causes cell death by blocking cell cycle progression and increasing cell-damaging molecules.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

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

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

A man was diagnosed with a rare form of lupus after showing unique skin symptoms that responded well to treatment.

Long non-coding RNAs play a key role in yak hair growth cycles.

Notch1 helps skin heal by attracting cells that aid repair.

The treatment showed high response rates and was well-tolerated, potentially extending patient survival.

Defects in certain proteins cause major heart abnormalities during early development.

Cardiomyocyte-derived media can inhibit lung cancer cell growth and movement.

RNase L hinders hair growth by altering immune signals.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.