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Blocking EGFR in mice causes hair loss and skin changes.

HuR is essential for Treg function and preventing autoimmunity.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

CTCF protein is essential for skin and hair follicle development in mice.

The scraggly mutation causes hair loss and skin defects in 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.

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

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

RXRα is crucial for proper immune response and links diet to immune function.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

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

Ovariectomized mice mimic postmenopausal hair loss, and estradiol helps maintain hair density.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

New mouse models help study melanocytic cells for melanoma research.

ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes that lead to more hair follicles entering resting phases.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Retinoic acid affects male and female muscle energy use and function differently.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

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

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

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

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