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Trichocytic cytokeratins are found in hair, nails, tongue, and thymus cells, showing complex regulation in tissue development.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Keratin 79 cells help form and regenerate hair canals.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Canine claws have complex structures with different keratin types, similar to hair and nails.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Marsupial hair structure and keratin distribution are similar to placental mammals.

Keratin expression reflects cell organization and differentiation, not causes it.

Mutations in keratin genes can cause skin and mucosa disorders.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

Krtap11-1 is important for hair strength and structure.

Human and bovine hair follicles have distinct cytokeratins specific to hair-forming cells.

Human skin cells with stem-like features can help create new hair follicles and sebaceous glands when combined with other cells.

Keratin 15 helps maintain tissue integrity and is reduced in activated keratinocytes.

PAR-1 may play a role in hair growth regulation in human hair follicles.

The patient had paraneoplastic pemphigus without mucosal involvement.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Most patients had less hair growth in affected areas after treatment.

The new keratin film without KAPs stains better and could help study keratin functions.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.