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K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A girl had rickets due to a gene mutation affecting vitamin D response.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

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

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Ritlecitinib shows promise as a versatile treatment for various autoimmune and inflammatory diseases.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

BRG1 is essential for skin cells to move and heal wounds properly.

Disruptions in sleep-wake cycles can cause health problems like mental, metabolic, and heart diseases, and cancer.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

K42 and K124 keratins are only found in horse hoof lamellae.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

A specific gene mutation causes a severe skin disorder in a family.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

The inhibitor affects androgen metabolism but not ovarian function.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Ritlecitinib was generally well tolerated in children with alopecia areata.