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Intralesional triamcinolone acetonide effectively treats alopecia areata, as shown by significant improvements in hair regrowth and dermoscopic indicators.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new method quickly extracts and identifies proteins from hair and other keratin sources.

Cystatin M/E helps in the final stages of hair and nail formation by controlling certain enzymes.

Curved human hair has different structures on its convex and concave sides.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

The unit area trichogram is a reliable method to assess hair loss and treatment response in people with androgenic alopecia by measuring hair density and thickness.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Trichoscopy effectively detects early hair follicle changes before visible baldness in men under 40.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

Mice without certain skin proteins had abnormal skin and hair development.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Trichoscopy effectively helps diagnose different types of hair loss in women.

Hair and wool have diverse keratins and keratin-associated proteins.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

A 15-year-old girl with hypothyroidism had excess hair and skin issues due to blocked hair follicles.

Yellow dots were the most common sign of alopecia areata found using trichoscopy.

Different bovine tissues show varying types of cytokeratins.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

Keratin expression reflects cell organization and differentiation, not causes it.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Capitate trichomes have more endoplasmic reticulum and vacuoles, while peltate trichomes have more plastids and larger subcuticular spaces.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Ubiquitin, a protein, is found in hair, nails, and skin.

A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

Different human hair keratin types have unique structures that affect how they dissolve and can be used to create self-tendons.