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Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Y27632 increases cell growth through EGFR signaling, not ROCK1/2.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A KRT32 gene variant causes loose anagen hair syndrome.

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

The hydrogel dressings speed up healing and reduce scarring.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The Gsdma3 gene is essential for normal hair development in mice.

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

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

IRS-specific genes in Tan sheep hair follicles peak at birth and may affect wool crimp.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A mutation in the KRT74 gene causes tightly curled hair.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Fish oil increased cell growth and macrophages in the skin but didn't affect COX-2 expression.