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A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Necrosulfonamide helps hair grow by blocking a protein linked to hair loss.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

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

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Phospholipase Cδ1 is crucial for normal skin and hair development.

A specific gene mutation causes different hair defects in Indian monilethrix families.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

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

Noggin is necessary to start the hair growth phase in skin after birth.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

NXC736 significantly reduced hair loss in mice with alopecia areata.

Keratins 6, 16, and 17 increase in damaged or diseased skin and may help diagnose skin issues.

Early treatment with immunoglobulin and aspirin reduces heart complications in children with Kawasaki disease.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

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

AKN is a chronic scalp condition in African-descended males, treated with topicals, antibiotics, steroids, and sometimes surgery or laser.

Vitamin D receptor is essential for hair growth signaling.

A new gene mutation linked to a skin condition was found in a Spanish family.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.