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

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Hair is mostly made of three protein types: helical, high-sulfur, and high-tyrosine.

The research concluded that hyaluronic acid affects the formation and growth of hair follicle-like structures in a lab setting.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

A specific gene mutation causes sparse, brittle hair in a family.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

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

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

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

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Specific cross-linkages help make hair proteins stable and strong.