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ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

CD44 variant changes start alopecia areata, but don't maintain it.

Folate receptor β helps suppress the immune system in macrophages and affects cancer growth and hair health.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

The improved surgical method increases success and reduces fetal loss in fetal mouse models for scarless skin healing.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

QLT0267 stops hair follicle cell growth and movement.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The new rodent model successfully mimics non-lean human PCOS symptoms.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

TGF-alpha affects skin thickness, hair growth, and may contribute to psoriasis and papilloma formation.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.