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The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The Shh gene controls cell growth and death in cashmere goat hair follicles, affecting hair growth.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Researchers found four genes that could help diagnose severe alopecia areata early.

A mutation in the IL2RA gene increases the risk of alopecia areata.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Inhibiting prolactin reduces hair follicle activation in cashmere goats.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Removing SIX1 in fat cells reduces skin fibrosis.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Ginseng and Albizia extracts may help prevent age-related hair thinning.

SOX4 is crucial for the development of melanoma.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Researchers created human hair follicles using a new method that could help treat hair loss.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

All adults have Demodex mites, which vary by region.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

HOXC13 is essential for hair and nail development by regulating Foxn1.