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

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

Mice with human chymase had a higher death rate when exposed to a toxin compared to normal mice.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Ornithine decarboxylase is crucial for hair growth regulation in mice.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Dual TCR Treg cells are common in mouse tissues and vary by location.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Diet changes can protect against harmful environmental effects on fetal development.

CDP is crucial for lung and hair follicle cell development.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Blocking a specific protein signal can make hair grow on mouse nipples.

A new mutation in mice causes crooked whiskers and messy hair.

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

Overexpressing follistatin in mice delays wound healing and reduces scar size.

The technique successfully promoted hair growth and skin renewal in mice.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

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

Key genes linked to hair growth and cancer were identified in hairless mice.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.