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

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

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

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

A new mouse model for vitiligo helps study immune responses and potential treatments.

cgVEGF164 boosts hair follicle growth in mice.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Scientists turned mouse skin cells into hair-inducing cells using chemicals, which could help treat hair loss.

Zinc made mice's coarse hair turn into fine hair without affecting skin structure.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

Activating β-catenin can turn skin cells into hair follicles.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

The Itpr3 gene causes a specific hair pattern in mice.

A new gene causes hairlessness and skin cysts in rats.

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Dormant melanoma cells in mice interact minimally with memory T cells due to a suppressive tumor environment.

A mutation in the Sgkl gene causes defective hair growth in mice.