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Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Human hair proteins can be used to create scaffolds that support cell growth for tissue engineering.

Keratin proteins are consistent across different hair types from the same person.

Dermoscopy is useful for identifying skin lesions in dogs, with specific features distinguishing infundibular keratinising acanthomas from follicular cysts.

A new classification system for skin cysts was proposed to improve diagnosis.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

3D skin models better mimic human skin and melanoma progression than older methods.

Mutations in keratin genes cause skin disorders, but new treatments show promise.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Regenerated skin after calciphylaxis resembles scar tissue with fewer hairs.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Dermatologists can detect smaller hair density changes than previously thought.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The new bioreactor improves skin grafts by evenly stretching cells and monitoring conditions for better growth.

Nude mice with grafted human skin developed scars similar to human hypertrophic scars.

Dermoscopy is effective in diagnosing facial actinic keratosis using specific features.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

Intracorneal vacuoles are common in parakeratotic skin diseases in dogs, especially with more parakeratosis.

The kitten's skin condition improved significantly after 4 weeks of treatment.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.