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Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

Bikunin is found on the cell boundaries of certain skin layers and may help regulate skin and hair functions.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Combining PRS with TAFR is promising for treating complex fistulas, with most patients achieving long-term healing.

Researchers created five new human scalp cell lines that could be useful for hair growth and loss research.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Kv1.3 blockers may help treat alopecia areata and promote hair regrowth.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Stat3 affects skin cancer development by altering keratinocyte stem cell behavior.

Shaykh Abbas Kuta Karang significantly advanced Malay medical knowledge with his detailed manuscript.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

Robertsonian translocation can cause recurrent miscarriages.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Human-hair keratin artificial tendons are biocompatible and degrade well in rabbits.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

The study revealed the detailed structure of a keratin dimer, aiding understanding of how intermediate filament proteins function.

A 14-year-old boy was diagnosed with a rare hair condition that may lead to hair thinning and has no known effective treatments.

Activating TRPV3 stops human hair growth.

Vitamin D protects skin cells from damage caused by captopril.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

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CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.