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Sunlight simulation causes skin inflammation, with different skin types reacting at different levels of exposure.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

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A specific gene mutation causes Olmsted syndrome.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

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