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

Two new gene mutations cause a rare hair disorder.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

The B2 genes are crucial for hair growth in rats.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Disulfide bonds are crucial for hair structure during keratinization.

TGase 3 helps build hair structure by forming strong bonds between proteins.

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

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

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

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

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

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

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

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

Trichocyte filaments have a low-density core and may include proteins for hair structure.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

TCHHL1 is a protein important for hair growth, found in hair follicles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.