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The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

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

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

Ift20 is essential for hair follicle function and skin cell movement.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Researchers developed a method to measure different forms of a drug that could help treat prostate issues and hair loss, and found how these forms behave in animals.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

A specific gene mutation causes complete hair loss without other health issues.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Hereditary factors affect acne duration, not severity, and late-onset acne in females has different causes.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

A genetic variant in the KRT25 gene causes tightly curled hair.

The vector successfully directed specific gene expression in hair follicles.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

A new gene, JMJD1C, may affect testosterone levels in men.

The enzyme system in hair follicles is similar to the liver's and is inhibited by certain substances.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.