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QR678 and QR678 Neo treatments, combined with corticosteroid injections, work better for alopecia areata than corticosteroid injections alone.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

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

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Promising cancer treatments were found, but the manufacturer closed.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

RUM-loaded SLN shows promise for treating acne and hair loss topically.

K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

The treatments stopped hair regrowth in mice.

The new synthetic retinoid RO 13-6298 effectively treated severe psoriasis at low doses with manageable side effects.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

The 3D printed scaffold with SB216763 and copper helps heal wounds and regrow skin and hair.

Hex gene plays a crucial role in starting feather development in chick embryos.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

DRDE-07 shows promise for treating skin diseases due to its favorable properties.

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

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Low-penetration genes might help personalize colorectal cancer prevention.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.