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Mice, Inbred mdx

Known as: mdx Mouse, Inbred mdx Mice, Inbred mdx Mouse 
A strain of mice arising from a spontaneous MUTATION (mdx) in inbred C57BL mice. This mutation is X chromosome-linked and produces viable homozygous… 
National Institutes of Health

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Related topics

5 relations
DystrophinIn BloodMicrobiologicalMuscular Dystrophy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
DISCONNECTION AND RESPONSIBILITY
In Causation and Responsibility, Michael Moore offers an integrated conception of the law, morality, and metaphysics, centered on… 
Highly Cited
2007
Highly Cited
2007
Flk-1+ adipose-derived mesenchymal stem cells differentiate into skeletal muscle satellite cells and ameliorate muscular dystrophy in mdx mice.
Duchenne muscular dystrophy (DMD) is a severe hereditary disease characterized by the absence of dystrophin on the sarcolemma of… 
Highly Cited
2007
Highly Cited
2007
T and B lymphocyte depletion has a marked effect on the fibrosis of dystrophic skeletal muscles in the scid/mdx mouse
Abnormal connective tissue proliferation following muscle degeneration is a major pathological feature of Duchenne muscular… 
Highly Cited
2004
Highly Cited
2004
Restoration of dystrophin expression in mdx mice by intravascular injection of naked DNA containing full-length dystrophin cDNA
Duchenne muscular dystrophy (DMD) is a lethal, X-linked, recessive disease caused by a defect in the dystrophin gene. No… 
Highly Cited
2003
Highly Cited
2003
CpG-A and B oligodeoxynucleotides enhance the efficacy of antibody therapy by activating different effector cell populations.
Immunostimulatory CpG oligodeoxynucleotides (ODNs) can enhance the therapeutic effect of monoclonal antibodies (mAbs) by… 
Highly Cited
2000
Highly Cited
2000
Deflazacort Increases Laminin Expression and Myogenic Repair, and Induces Early Persistent Functional Gain in mdx Mouse Muscular Dystrophy
Deflazacort slows the progress of Duchenne muscular dystrophy (DMD) with fewer side effects than prednisone. In mdx mice… 
Highly Cited
2000
Highly Cited
2000
Large-scale analysis of differential gene expression in the hindlimb muscles and diaphragm of mdx mouse.
Highly Cited
1998
Highly Cited
1998
Nuclear magnetic resonance spectroscopy study of muscle growth, mdx dystrophy and glucocorticoid treatments: correlation with repair
Proton nuclear magnetic resonance spectroscopy (1 H NMR) can be used to study skeletal muscle metabolism. The mdx mouse is a… 
Highly Cited
1995
Highly Cited
1995
Successful histocompatible myoblast transplantation in dystrophin- deficient mdx mouse despite the production of antibodies against dystrophin
Myoblast transplantation has been considered a potential treatment for some muscular disorders. It has proven very successful… 
Highly Cited
1995
Highly Cited
1995
Pretreatment of myoblast cultures with basic fibroblast growth factor increases the efficacy of their transplantation in mdx mice
The effect of pretreatment of cultures with basic fibroblast growth factor (bFGF) on myoblast allotransplantation to C57BL/10ScSn… 
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