C. Matsumura

发表

Identification of plasma interleukins as biomarkers for deflazacort and omega‐3 based Duchenne muscular dystrophy therapy

Samara Camaçarí de Carvalho, C. Matsumura, H. S. Neto, 2018, Cytokine.

Doxycycline ameliorates the dystrophic phenotype of skeletal and cardiac muscles in mdx mice

C. Matsumura, H. S. Neto, M. Marques, 2012, Muscle & nerve.

Prevention of muscle fibrosis and myonecrosis in mdx mice by suramin, a TGF‐β1 blocker

C. Matsumura, H. S. Neto, M. Marques, 2011, Muscle & nerve.

Laser de baixa intensidade favorece a regeneração muscular em modelo experimental desnutrido e recuperado

C. Matsumura, A. Pertille, Maisa Cardoso da Silva, 2018, Fisioterapia e Pesquisa.

Evaluation of skeletal muscle regeneration in experimental model after malnutrition.

C. Matsumura, A. Pertille, K. F. Moura, 2017, Brazilian journal of biology = Revista brasleira de biologia.

Mechanical, biochemical and morphometric alterations in the femur of mdx mice.

C. Matsumura, J. Camilli, C. Bertran, 2011, Bone.

Stretch-activated calcium channel protein TRPC1 is correlated with the different degrees of the dystrophic phenotype in mdx mice.

C. Matsumura, M. Marques, A. Taniguti, 2011, American journal of physiology. Cell physiology.

High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway

E. J. Caldeira, M. Conte, C. Matsumura, 2018, bioRxiv.

Understanding the beneficial effects of doxycycline on the dystrophic phenotype of the mdx mouse

Elaine Minatel, C. Matsumura, M. Marques, 2014, Muscle & nerve.

Suramin affects metalloproteinase‐9 activity and increases beta‐dystroglycan levels in the diaphragm of the dystrophin‐deficient mdx MOUSE

C. Matsumura, H. S. Neto, M. Marques, 2012, Muscle & nerve.

Diltiazem and verapamil protect dystrophin‐deficient muscle fibers of MDX mice from degeneration: A potential role in calcium buffering and sarcolemmal stability

C. Matsumura, M. Marques, A. Pertille, 2009, Muscle & nerve.

Suramin attenuates dystrophin‐deficient cardiomyopathy in the mdx mouse model of duchenne muscular dystrophy

C. Matsumura, H. S. Neto, M. Marques, 2013, Muscle & nerve.

Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.

C. Matsumura, V. Carmignac, M. Durbeej, 2011, Human molecular genetics.

Isobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of Dystrophy

C. Matsumura, M. Marques, M. Durbeej, 2013, PloS one.

Alterations in The Permeability of Dystrophic Fibers During Neuromuscular Junction Development

C. Matsumura, M. Marques, H. Santo Neto, 2007, Acta biologica Hungarica.

Quantitative Proteomic Analysis Reveals Metabolic Alterations, Calcium Dysregulation, and Increased Expression of Extracellular Matrix Proteins in Laminin α2 Chain–deficient Muscle*

C. Matsumura, M. Durbeej, K. Gawlik, 2014, Molecular & Cellular Proteomics.

Low-intensity laser favors muscle regeneration in a malnourished and recovered experimental model

C. Matsumura, A. Pertille, Maisa Cardoso da Silva, 2018 .