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Center for Genetic Medicine Research
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Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.
Human molecular genetics Jul, 2013 | Pubmed ID: 23535822
The proton pump inhibitor lansoprazole improves the skeletal phenotype in dystrophin deficient mdx mice.
PloS one , 2013 | Pubmed ID: 23843959
VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects.
EMBO molecular medicine Oct, 2013 | Pubmed ID: 24014378
Effects of Dantrolene Therapy on Disease Phenotype in Dystrophin Deficient mdx Mice.
PLoS currents , 2013 | Pubmed ID: 24270550
The protein phosphatase 2A B56γ regulatory subunit is required for heart development.
Developmental dynamics : an official publication of the American Association of Anatomists Jun, 2014 | Pubmed ID: 24425002
Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophy.
Human molecular genetics Jun, 2014 | Pubmed ID: 24463621
Children's National Medical Center
Kathleen S. Tatem1,
James L. Quinn1,
Aditi Phadke1,
Qing Yu1,
Heather Gordish-Dressman1,2,
Kanneboyina Nagaraju1,2
1Center for Genetic Medicine Research, Children's National Medical Center,
2Department of Integrative Systems Biology, George Washington University School of Medicine and Health Sciences
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