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Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Keratin 17 is crucial for early hair strength and cell survival.

Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

A testosterone-induced hair loss model in mice was successfully created for future research and treatment testing.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Increasing m6A levels can improve skin cell growth and wound healing.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Proteolytic enzymes damaged hair follicle stem cells in transgenic mice.

Acid inside cells speeds up aging and turns on aging signs in mice.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Fatp4 is crucial for healthy skin development and function.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

Four new FGF5 gene variants cause long hair in dogs.

Overexpressing ovine β-catenin in mice skin increases hair follicle density and growth.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

A missing mK6irs1 gene causes hair loss in mice.

A mutation in the human hairless gene causes alopecia universalis.

Blocking EGFR in mice causes hair loss and skin changes.