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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Certain gene changes and hormone levels are linked to female hair loss.

A new method effectively detects toxic pyrrolizidine alkaloids in honey and flour.

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

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

Cepharanthine is a well-tolerated drug with multiple medical uses, including anti-inflammatory and anti-cancer properties.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Combining diphenylcyclopropenone with anthralin is more effective for hair regrowth in alopecia areata than using diphenylcyclopropenone alone, but may cause more side effects.

Topical DPCP is somewhat effective for hair loss in alopecia areata, but more research is needed.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

PC-associated alopecia has unique microscopic features.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

88% phenol is effective for treating alopecia areata.

Certain gene variations increase the risk of alopecia areata in Koreans.

Combining DPCP with PRP doesn't improve hair regrowth in alopecia areata.

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

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Topical alpha-terthienyl with UVA may safely treat psoriasis without cancer risk.

Similar treatments might work for different types of scarring hair loss.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.