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

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A new mouse model effectively mimics vitiligo for research and drug testing.

Fatp4 is crucial for healthy skin development and function.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Iron deficiency in mothers causes hair loss in their baby mice.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Alopecia in VDR knockout mice is due to impaired hair cycle initiation, not keratinocyte issues.

Deleting TNFα gene reduces skin cancer risk in certain mice.

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

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

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Phospholipase C-δ1 is crucial for normal hair development.

FoxN1 overexpression in young mice harms immune cell and skin development.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

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

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

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