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Autologous cell-based therapies, especially SVF, effectively and safely improve atrophic acne scars.

The STRIAA tool helps doctors quickly and effectively assess the severity of Alopecia Areata.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

The device applies substances directly to body tissues, improving cell transplant and treatment processes.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Testosterone reduces knee movement, while flutamide and finasteride increase it.

Intravital imaging advances help study bone and dental stem cells in real-time, despite technical challenges.

Clascoterone cream could be used for other skin conditions affected by hormones.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

BAF200 is essential for proper heart and coronary artery formation.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The study introduced a new imaging technology to track skin healing and bone marrow cell activity over time.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

A new patch can deliver stable antibodies over time for potential HIV treatment.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

The treatment with valproate, acetylcarnitine, folic acid, and vitamin B12 may improve muscle strength in children with SMA without significant side effects.

Deucravacitinib led to full hair regrowth in a severe alopecia areata patient.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.