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Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Disrupting Bcl-xL in mice reduces skin cancer risk.

BMI1 is essential for preventing hair greying and maintaining hair color.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

Olive oil helps Malassezia globosa overgrow, worsening atopic dermatitis in mice.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

Thymus-derived Tregs, not peripherally-derived Tregs, primarily regulate type 1 diabetes in the NOD mouse model.

Two-photon microscopy effectively tracks live stem cell activity in mouse skin with minimal harm and clear images.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Stem cell therapy affects 15 key genes in rats with diabetes-related erectile dysfunction.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

A specific gene mutation causes sparse, brittle hair in a family.

Type 2 diabetic stem cells can still help heal wounds effectively.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The Celsr1 gene is crucial for normal hair patterning in mice.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Bovine milk fats applied to mouse skin can promote hair growth similar to known hair growth treatments.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

MCHR2 gene duplications may be linked to alopecia areata.

FGFR2 signaling controls Merkel cell formation in different skin regions.