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Zfp157 is active in many mouse tissues during development and in specific adult cells.

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

Actin filaments help stabilize and reshape cell membranes.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

ODC transgenic mice can model human hair loss with skin lesions.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

miR-144 affects hair growth by interacting with Lhx2.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Defects in certain proteins cause major heart abnormalities during early development.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Sostdc1 controls the size and number of hair and mammary gland structures.

Krtap11-1 is important for hair strength and structure.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

Antizyme slows skin tumor growth by reducing cell growth in mice.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.