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Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

Hair follicle stem cells can change their role to ensure proper hair development.

A specific molecular switch, driven by MAPK/ERK signaling, helps spiny mice heal wounds by regenerating skin instead of forming scars.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

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

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

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

Kdm6b is crucial for skin cell differentiation.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Lack of Evi in skin causes psoriasis-like symptoms in mice.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Researchers found two new genetic variants linked to Alzheimer's disease.

Controlling Tslp can improve health in AEC syndrome patients.

Vitamin D receptor knockout mice have significant motor impairments but no cognitive deficits.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.