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Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Hair-follicle nerves in cats' spinal cords can be inhibited by GABA-related connections.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

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

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Keratin 17 is crucial for early hair strength and cell survival.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

K6hf is a unique protein found only in a specific layer of hair follicles.

Keratin structure changes during keratinization, but the exact model remains uncertain.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Disulfide bonds are crucial for hair structure during keratinization.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

A special receptor in sensory nerve endings helps control how they respond to stretching.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

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

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.