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Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

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

Mature hair surfaces are formed by keratinized cells with developed layers, not just modified plasma membranes.

A unique case of skin cancer showed unusual calcification, possibly linked to calcium-binding proteins.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Researchers found a non-functional sheep keratin gene due to mutations.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Enzyme presence in hair sheath cells decreases over time, affecting forensic analysis.

ACBP is crucial for healthy skin in mice.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

The cyst had unusual keratin spherules and resembled bone marrow.

Cathepsin E is crucial for normal skin cell differentiation and development.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

The southern elephant seal's skin layer helps waterproof the skin by being tightly connected to hair shafts.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.

Ceramide synthase 4 is essential for maintaining skin barrier health.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

Eyelid cells share signaling components but differ in pathway activity.

Epimorphin helps shape and develop epithelial cells, like those in hair follicles.

PEA-ENL improves skin delivery and reduces inflammation without side effects.

Keratin-75 is secreted by ameloblasts in a unique way without a signal peptide.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Keratinized wool cells still have some organelles like lysosomes and mitochondria.

EFFC might be common but underreported.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.