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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

PAD type III enzyme is specific to rat skin and hair follicles.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Two new gene mutations cause a rare hair disorder.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Lack of cystatin M/E causes thin hair and dry skin.

Mesenchymal MEIS2 is essential for whisker development without needing sensory nerves.

A new method speeds up insulin amyloid fibril growth, useful for studying diseases.

Keratin gene clusters in humans and marsupials are similarly organized.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

Keratins are crucial proteins for hair and nails, with a structure that helps teach protein principles.

Spider joint hair sensilla are adapted to sense movement during walking.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

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.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.