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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Spt4 and Spt6 are essential for fat cell development.

HPV8 causes skin cancer by expanding specific skin stem cells.

The UHS promoter is specific to mouse hair follicles.

Raptor and Rictor have stable expression in hair cycles, with Raptor marking stem cells and Rictor involved in hair shaft formation.

K6hf is a unique protein found only in a specific layer of hair follicles.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Mrp3 helps in wound healing and hair growth.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.