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An AI device for skin cancer was successfully integrated into the NHS, improving diagnosis accuracy and service capacity.

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ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Microfluidic models improve testing for aging, wound healing, and oral tissue, reducing animal testing.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

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miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Four new FGF5 gene variants cause long hair in dogs.

The Eda gene helps regulate the hair cycle in goats.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Hair samples can be used to create stem cells easily and non-invasively.

MCP@G improves diabetic wound healing by reducing stress and promoting tissue repair.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The combined treatment with engineered bacteria and yellow LED light improved wound healing in mice.

Using a combination of AMD3100 and FK506 can speed up and improve wound healing in diabetic rats.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

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

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

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Somatic BHD mutations are rare in Japanese renal tumors.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.