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The Exfoliate-Dissolve-Repair skincare approach may effectively treat keratosis pilaris and reduce the need for corticosteroids.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

PCL nanoscaffold-based liver spheroids are effective for drug screening and studying liver toxicity.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

L-cysteine slows down the breaking of bonds in hair due to electrostatic interactions.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

ESR2 gene linked to female-pattern hair loss.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

The nano-carrier makes etoposide safer and more effective against lung cancer.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

MSC-CM cream speeds up burn wound healing better than the control treatment.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Confocal Laser Scanning Microscopy (CLSM) is a useful tool for studying how drugs interact with skin and diagnosing skin disorders, despite some limitations.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Keratin-encapsulated liposomes effectively repair and protect UV-damaged hair.

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

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

The combination of the excimer lamp and liquor carbonis detergens is more effective for scalp psoriasis than the lamp alone.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.