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The nanocomposite hydrogels can repair themselves, change shape, reduce inflammation, protect against oxidation, kill bacteria, stop bleeding, and help heal diabetic wounds while allowing for wound monitoring.

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

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

The hydrogel speeds up skin wound healing effectively.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

The new sprayable wound mask helps heal wounds without scars.

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

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

The hydrogel helps skin heal by encouraging new blood vessel growth.

PHAs are promising biodegradable materials for medical and dental uses.

Hair structure forms the same way inside and outside the body.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

Mice without certain skin proteins had abnormal skin and hair development.