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Nail-matrical fibroblasts can make non-nail cells produce hard keratin, useful for nail repair.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Keratins are key to developing and regenerating hair follicles for treating hair loss.

Keratin 79 cells help form and regenerate hair canals.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

Scientists developed a system to study human hair growth using skin cells, which could help understand hair development and improve skin substitutes for medical use.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Overactive signaling in hair follicles can lead to skin cancer.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

Epithelial proliferation and hyperkeratosis are linked to gastric ulcers in pigs.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Progerin affects cell shape but not hair or skin in mice.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Trichohyalin, a protein from pig tongue, was purified and found to have a filamentous structure.

HPV8 causes skin cancer by expanding specific skin stem cells.

Alkylation of human hair keratin allows for adjustable drug release rates in hydrogels for medical use.

Monilethrix is linked to a gene cluster on chromosome 12.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

K15 and Id3 are important in hair follicle regeneration, with K15 increasing in early stages and Id3 responding later.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Glycoproteins are present in the cell membranes of various keratin fibers.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Human hair proteins can help blood clot when mixed in equal parts.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.