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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Sgk3 is essential for normal hair follicle growth and maintenance.

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

The vector successfully directed specific gene expression in hair follicles.

Transglutaminase does not modify human hair.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

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

Pal-KCV peptide strengthens hair and reduces breakage by up to 52%.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Human hair keratin scaffold material degrades in muscles mainly through the ubiquitin system with lysosome help.