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LX-38 is a safer drug option for treating prostate issues and hair loss without hormonal side effects.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

Combination therapy, including JAK inhibitors, effectively regrows hair and reduces severity in Black children with stubborn Alopecia Areata.

Zingiber junceum Gagnep. is now found in Vietnam and contains various bioactive compounds.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

Eurycoma longifolia extract may help increase testosterone levels and reduce andropause symptoms.

YH0618 granules may help prevent hair loss in breast cancer patients undergoing chemotherapy.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

VYN201 shows promise as a safe and effective treatment for non-segmental vitiligo.

Abrocitinib at 100 mg and 200 mg daily may significantly improve moderate-to-severe atopic dermatitis in patients 12 years and older.

A quick method was developed to detect banned substances in urine for doping control.

The nanocomposite effectively targets lung cancer cells without harming normal cells.

Two new gene mutations cause a rare hair disorder.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new mutation in mice causes crooked whiskers and messy hair.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.