Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

The scraggly mutation causes hair loss and skin defects in mice.

Drug repurposing offers a faster, cheaper way to find treatments for rare diseases.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

CRISPR-Cas9 can successfully edit genes in large mammals like Cashmere goats.

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

Targeting CD169+ skin macrophages may help treat psoriasis.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

GI198745 is more potent and longer-lasting than finasteride, potentially better for treating hair loss.

miR-486 may help prevent hair loss in alopecia areata.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

There's a red birthmark on the scalp.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

A new treatment using a DNA aptamer can promote hair growth by targeting a specific receptor.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Russelia equisetiformis may help promote hair growth.