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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Hoxc13 gene is essential for hair, nail, and papilla development.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Keratin patterns in hair follicles help understand hair growth and potential hair and nail disorders.

New mutations in the DSG4 gene cause a rare hair condition.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The ventral matrix is the main source of the nail plate.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

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

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

Actin filaments help stabilize and reshape cell membranes.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

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

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

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

New treatments targeting specific genes show promise for treating keratin disorders.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.