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Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

CD26+ fibroblasts improve skin healing and integration better than CD26− fibroblasts.

Researchers developed a mouse model that successfully mimics the bladder damage seen in humans after radiation therapy.

Zfp462 deficiency in mice causes anxiety-like behaviors and excessive self-grooming.

Skin cancer often starts from Lgr5+ progenitor cells.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

MRL/MpJ mice's skin wounds heal with scars, unlike their ear wounds which can regenerate.

Chamaecyparis obtusa oil promotes hair growth in mice.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Human cathepsin V can replace mouse cathepsin L to maintain normal skin and hair in mice.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Hairless mice lose hair by 3-4 weeks, develop thicker, folded skin, and show pigmentation differences.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

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

The dataset includes detailed genetic information from mouse skin cells before and after injury.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.