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Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Keratinocytes contribute to hidradenitis suppurativa by causing inflammation and worsening the condition.

A rabbit gene important for hair development was identified and detailed.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A rare gene variant causes hair and nail issues in a family.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

Activating Kras in mouse skin causes excess skin and hair loss.

A mutation in the KRT25 gene causes woolly hair and hair loss.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

A specific gene mutation causes sparse, brittle hair in a family.

Krtap11-1 is important for hair strength and structure.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Lipase H is important for hair follicle function and shaping hair fibers.

A new keratin gene was found in mice, explaining hair growth.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell 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.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Keratin proteins in hair are complex and come from multiple gene families.