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A mutation in mice causes hair loss and immune problems.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new mouse mutation causes skin and hair defects due to a gene change.

B6J mice live longer before 24 months, but B6N mice live longer after; both strains show weight gain, increased food and water intake, and health issues as they age.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Hair loss in certain mice is linked to changes in keratin-related genes.

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

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Adult spiny mice recover better from heart attacks than common lab mice.

A new method can detect mutations in mice by observing changes in hair follicle cells.

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

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

Dopamine affects coat color changes in agouti mice.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Spiny mice regenerate skin better than laboratory mice due to larger hair bulges, more stem cells, and different collagen ratios.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

Suppressing ODC activity reduces tumor growth in hair follicles.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.