Published in Sci Signal on August 07, 2012
The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy. J Cell Biol (2013) 1.45
Ca2+-dependent proteolysis of junctophilin-1 and junctophilin-2 in skeletal and cardiac muscle. J Physiol (2012) 1.29
Src-dependent impairment of autophagy by oxidative stress in a mouse model of Duchenne muscular dystrophy. Nat Commun (2014) 1.21
Microtubules that form the stationary lattice of muscle fibers are dynamic and nucleated at Golgi elements. J Cell Biol (2013) 1.18
Real-time imaging of NADPH oxidase activity in living cells using a novel fluorescent protein reporter. PLoS One (2013) 1.04
A new therapeutic effect of simvastatin revealed by functional improvement in muscular dystrophy. Proc Natl Acad Sci U S A (2015) 1.04
X-ROS signaling in the heart and skeletal muscle: stretch-dependent local ROS regulates [Ca²⁺]i. J Mol Cell Cardiol (2012) 1.03
Microtubule binding distinguishes dystrophin from utrophin. Proc Natl Acad Sci U S A (2014) 0.98
Investigating cell mechanics with atomic force microscopy. J R Soc Interface (2015) 0.98
Reactive oxygen/nitrogen species and contractile function in skeletal muscle during fatigue and recovery. J Physiol (2016) 0.93
Mechanical stretch-induced activation of ROS/RNS signaling in striated muscle. Antioxid Redox Signal (2014) 0.92
X-ROS signalling is enhanced and graded by cyclic cardiomyocyte stretch. Cardiovasc Res (2013) 0.91
Human skeletal muscle xenograft as a new preclinical model for muscle disorders. Hum Mol Genet (2014) 0.90
Eccentric exercise in aging and diseased skeletal muscle: good or bad? J Appl Physiol (1985) (2013) 0.89
Mitochondria in the middle: exercise preconditioning protection of striated muscle. J Physiol (2016) 0.88
Dystrobrevin increases dystrophin's binding to the dystrophin-glycoprotein complex and provides protection during cardiac stress. J Mol Cell Cardiol (2014) 0.88
EUK-134 ameliorates nNOSμ translocation and skeletal muscle fiber atrophy during short-term mechanical unloading. Am J Physiol Regul Integr Comp Physiol (2014) 0.87
CL316,243, a β3-adrenergic receptor agonist, induces muscle hypertrophy and increased strength. Sci Rep (2016) 0.86
Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. Physiol Rev (2016) 0.85
Detyrosinated microtubules modulate mechanotransduction in heart and skeletal muscle. Nat Commun (2015) 0.85
Taurine: the appeal of a safe amino acid for skeletal muscle disorders. J Transl Med (2015) 0.85
Microtubule Actin Cross-linking Factor 1 regulates cardiomyocyte microtubule distribution and adaptation to hemodynamic overload. PLoS One (2013) 0.84
Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury. Cell Mol Life Sci (2014) 0.83
Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy. Cell Death Differ (2015) 0.81
Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice. Physiol Rep (2015) 0.81
NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress. Antioxid Redox Signal (2014) 0.81
Mechanotransduction in the endothelium: role of membrane proteins and reactive oxygen species in sensing, transduction, and transmission of the signal with altered blood flow. Antioxid Redox Signal (2014) 0.81
Acute failure of action potential conduction in mdx muscle reveals new mechanism of contraction-induced force loss. J Physiol (2013) 0.80
ROS Production via P2Y1-PKC-NOX2 Is Triggered by Extracellular ATP after Electrical Stimulation of Skeletal Muscle Cells. PLoS One (2015) 0.80
Reactive oxygen species generation is not different during isometric and lengthening contractions of mouse muscle. Am J Physiol Regul Integr Comp Physiol (2013) 0.80
Mechanisms of Myofascial Pain. Int Sch Res Notices (2014) 0.79
A new directionality tool for assessing microtubule pattern alterations. Cytoskeleton (Hoboken) (2014) 0.79
NADPH oxidase-2 inhibition restores contractility and intracellular calcium handling and reduces arrhythmogenicity in dystrophic cardiomyopathy. Am J Physiol Heart Circ Physiol (2014) 0.79
Diapocynin, a dimer of the NADPH oxidase inhibitor apocynin, reduces ROS production and prevents force loss in eccentrically contracting dystrophic muscle. PLoS One (2014) 0.78
Altered ROS production, NF-κB activation and interleukin-6 gene expression induced by electrical stimulation in dystrophic mdx skeletal muscle cells. Biochim Biophys Acta (2015) 0.78
Modeling Local X-ROS and Calcium Signaling in the Heart. Biophys J (2015) 0.78
Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice. Hum Mol Genet (2014) 0.78
Mechano-chemo transduction tunes the heartstrings. Sci Signal (2014) 0.77
The Dystrophin Complex: Structure, Function, and Implications for Therapy. Compr Physiol (2015) 0.77
NOX2 Inhibition Impairs Early Muscle Gene Expression Induced by a Single Exercise Bout. Front Physiol (2016) 0.77
Regulation of NADPH oxidases in skeletal muscle. Free Radic Biol Med (2016) 0.77
Inhibition of iPLA2 β and of stretch-activated channels by doxorubicin alters dystrophic muscle function. Br J Pharmacol (2013) 0.76
Loss of CENP-F results in distinct microtubule-related defects without chromosomal abnormalities. Mol Biol Cell (2016) 0.76
A beginner's guide to atomic force microscopy probing for cell mechanics. Microsc Res Tech (2016) 0.76
ROS and RNS signaling in skeletal muscle: critical signals and therapeutic targets. Annu Rev Nurs Res (2013) 0.76
GsMTx4-D is a cardioprotectant against myocardial infarction during ischemia and reperfusion. J Mol Cell Cardiol (2016) 0.76
Simvastatin offers new prospects for the treatment of Duchenne muscular dystrophy. Rare Dis (2016) 0.75
2015 William Allan Award. Am J Hum Genet (2016) 0.75
Lighting up microtubule cytoskeleton dynamics in skeletal muscle. Intravital (2014) 0.75
Mechanical transduction by ion channels: A cautionary tale. World J Neurol (2015) 0.75
Abnormalities in brain structure and biochemistry associated with mdx mice measured by in vivo MRI and high resolution localized (1)H MRS. Neuromuscul Disord (2015) 0.75
Age-related alterations in the sarcolemmal environment are attenuated by lifelong caloric restriction and voluntary exercise. Exp Gerontol (2016) 0.75
Altered nuclear dynamics in MDX myofibers. J Appl Physiol (1985) (2016) 0.75
Differential Expression of NADPH Oxidases Depends on Skeletal Muscle Fiber Type in Rats. Oxid Med Cell Longev (2016) 0.75
Utrophin suppresses low frequency oscillations and coupled gating of mechanosensitive ion channels in dystrophic skeletal muscle. Channels (Austin) (2015) 0.75
Calcium Sparks in the Heart: Dynamics and Regulation. Res Rep Biol (2015) 0.75
Differential expression analysis for sequence count data. Genome Biol (2010) 64.56
Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell (1987) 20.27
Mechanotransduction across the cell surface and through the cytoskeleton. Science (1993) 14.01
Gene ontology analysis for RNA-seq: accounting for selection bias. Genome Biol (2010) 9.15
Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels. Science (2010) 6.29
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states. Nat Med (2007) 5.25
Mechanical behavior in living cells consistent with the tensegrity model. Proc Natl Acad Sci U S A (2001) 3.47
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy. Neurology (2010) 3.37
Novel competitive inhibitor of NAD(P)H oxidase assembly attenuates vascular O(2)(-) and systolic blood pressure in mice. Circ Res (2001) 3.24
Characteristics of the inhibition of NADPH oxidase activation in neutrophils by apocynin, a methoxy-substituted catechol. Am J Respir Cell Mol Biol (1994) 3.23
X-ROS signaling: rapid mechano-chemo transduction in heart. Science (2011) 3.20
Uncontrolled calcium sparks act as a dystrophic signal for mammalian skeletal muscle. Nat Cell Biol (2005) 3.14
Bilayer-dependent inhibition of mechanosensitive channels by neuroactive peptide enantiomers. Nature (2004) 3.12
Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophy. Neurology (2005) 2.53
Axial stretch of rat single ventricular cardiomyocytes causes an acute and transient increase in Ca2+ spark rate. Circ Res (2009) 2.35
Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse. J Physiol (2004) 2.17
The mechanosensitive ion channel Piezo1 is inhibited by the peptide GsMTx4. Biochemistry (2011) 1.93
Tensegrity-based mechanosensing from macro to micro. Prog Biophys Mol Biol (2008) 1.90
Muscle damage in mdx (dystrophic) mice: role of calcium and reactive oxygen species. Clin Exp Pharmacol Physiol (2006) 1.79
Fulvene-5 potently inhibits NADPH oxidase 4 and blocks the growth of endothelial tumors in mice. J Clin Invest (2009) 1.68
A transverse tubule NADPH oxidase activity stimulates calcium release from isolated triads via ryanodine receptor type 1 S -glutathionylation. J Biol Chem (2006) 1.65
Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity. J Clin Invest (1997) 1.61
Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism. Proc Natl Acad Sci U S A (2009) 1.58
Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes. J Physiol (2007) 1.55
Mechanotransduction: the role of mechanical stress, myocyte shape, and cytoskeletal architecture on cardiac function. Pflugers Arch (2011) 1.52
Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers. J Physiol (1999) 1.47
Differential redox regulation of ORAI ion channels: a mechanism to tune cellular calcium signaling. Sci Signal (2010) 1.44
Cell prestress. II. Contribution of microtubules. Am J Physiol Cell Physiol (2002) 1.43
Fast-twitch skeletal muscles of dystrophic mouse pups are resistant to injury from acute mechanical stress. Am J Physiol Cell Physiol (2002) 1.40
Dystrophin is a microtubule-associated protein. J Cell Biol (2009) 1.38
Mitochondrial redox state and Ca2+ sparks in permeabilized mammalian skeletal muscle. J Physiol (2005) 1.37
Calcium and the damage pathways in muscular dystrophy. Can J Physiol Pharmacol (2010) 1.37
Intramembrane charge movement and L-type calcium current in skeletal muscle fibers isolated from control and mdx mice. Biophys J (2003) 1.32
The Ras-related GTPase Rac1 binds tubulin. J Biol Chem (1996) 1.29
Skeletal muscle NADPH oxidase is increased and triggers stretch-induced damage in the mdx mouse. PLoS One (2010) 1.29
Streptomycin reduces stretch-induced membrane permeability in muscles from mdx mice. Neuromuscul Disord (2006) 1.25
Myotube depolarization generates reactive oxygen species through NAD(P)H oxidase; ROS-elicited Ca2+ stimulates ERK, CREB, early genes. J Cell Physiol (2006) 1.22
Skeletal muscle function: role of ionic changes in fatigue, damage and disease. Clin Exp Pharmacol Physiol (2004) 1.19
Poloxamer 188 reduces the contraction-induced force decline in lumbrical muscles from mdx mice. Am J Physiol Cell Physiol (2008) 1.19
Akt activation prevents the force drop induced by eccentric contractions in dystrophin-deficient skeletal muscle. Hum Mol Genet (2008) 1.19
Proteolysis results in altered leak channel kinetics and elevated free calcium in mdx muscle. J Membr Biol (1993) 1.18
Metabolic regulation of Ca2+ release in permeabilized mammalian skeletal muscle fibres. J Physiol (2003) 1.15
Redox regulation of calcium ion channels: chemical and physiological aspects. Cell Calcium (2011) 1.13
rAAV6-microdystrophin rescues aberrant Golgi complex organization in mdx skeletal muscles. Traffic (2007) 1.13
Passive mechanical properties of maturing extensor digitorum longus are not affected by lack of dystrophin. Muscle Nerve (2006) 1.12
Mice lacking Homer 1 exhibit a skeletal myopathy characterized by abnormal transient receptor potential channel activity. Mol Cell Biol (2008) 1.12
Quantitative measurement of Ca²(+) in the sarcoplasmic reticulum lumen of mammalian skeletal muscle. Biophys J (2010) 1.09
How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes. Trends Cardiovasc Med (2000) 1.08
Imaging and elasticity measurements of the sarcolemma of fully differentiated skeletal muscle fibres. Microsc Res Tech (2005) 1.07
Fibroblast cytoskeletal remodeling contributes to connective tissue tension. J Cell Physiol (2011) 1.07
Non-invasive optical imaging of muscle pathology in mdx mice using cathepsin caged near-infrared imaging. Mol Imaging Biol (2011) 1.00
Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy. J Cardiol (2008) 0.99
Tensegrity and mechanotransduction. J Bodyw Mov Ther (2008) 0.95
Angiotensin II and NGF differentially influence microtubule proteins in PC12W cells: role of the AT2 receptor. Brain Res Mol Brain Res (1998) 0.93
Stretch-induced membrane damage in muscle: comparison of wild-type and mdx mice. Adv Exp Med Biol (2010) 0.91
Intramuscular renin-angiotensin system is activated in human muscular dystrophy. J Neurol Sci (2009) 0.90
A dominant negative form of Rac1 affects myogenesis of adult thoracic muscles in Drosophila. Dev Biol (2005) 0.88
Colchicine's other indication--effect of FDA action. N Engl J Med (2010) 0.86
Calcium homeostasis and cell death in Sol8 dystrophin-deficient cell line in culture. Cell Calcium (2001) 0.85
Genetic deletion of trkB.T1 increases neuromuscular function. Am J Physiol Cell Physiol (2011) 0.83
Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: col6a1-/- and mdx. J Biomed Biotechnol (2010) 0.83
Angiotensin II induces microtubule reorganization mediated by a deacetylase SIRT2 in endothelial cells. Hypertens Res (2011) 0.80
Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy. BMC Med Genet (2007) 0.79
Glucose restriction inhibits skeletal myoblast differentiation by activating SIRT1 through AMPK-mediated regulation of Nampt. Dev Cell (2008) 5.51
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states. Nat Med (2007) 5.25
Genomics, intellectual disability, and autism. N Engl J Med (2012) 3.74
The IGS Standard Operating Procedure for Automated Prokaryotic Annotation. Stand Genomic Sci (2011) 3.62
Elevated stearoyl-CoA desaturase-1 expression in skeletal muscle contributes to abnormal fatty acid partitioning in obese humans. Cell Metab (2005) 3.47
Termination of cardiac Ca(2+) sparks: an investigative mathematical model of calcium-induced calcium release. Biophys J (2002) 3.38
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1. Proc Natl Acad Sci U S A (2007) 3.32
X-ROS signaling: rapid mechano-chemo transduction in heart. Science (2011) 3.20
Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis. J Am Soc Nephrol (2008) 2.74
Ergatis: a web interface and scalable software system for bioinformatics workflows. Bioinformatics (2010) 2.69
An interactive power analysis tool for microarray hypothesis testing and generation. Bioinformatics (2006) 2.62
Ca2+ blinks: rapid nanoscopic store calcium signaling. Proc Natl Acad Sci U S A (2005) 2.56
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum Mol Genet (2003) 2.50
Axial stretch of rat single ventricular cardiomyocytes causes an acute and transient increase in Ca2+ spark rate. Circ Res (2009) 2.35
Sources of variability and effect of experimental approach on expression profiling data interpretation. BMC Bioinformatics (2002) 2.31
Mitofusin-2 maintains mitochondrial structure and contributes to stress-induced permeability transition in cardiac myocytes. Mol Cell Biol (2011) 2.23
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration. Brain (2006) 2.22
Dynamic elastic modulus of porcine articular cartilage determined at two different levels of tissue organization by indentation-type atomic force microscopy. Biophys J (2004) 2.20
Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures. Muscle Nerve (2009) 2.19
Early detection of aging cartilage and osteoarthritis in mice and patient samples using atomic force microscopy. Nat Nanotechnol (2009) 2.19
Staphylococcus aureus biofilms: properties, regulation, and roles in human disease. Virulence (2011) 2.14
Changes in ubiquitin proteasome pathway gene expression in skeletal muscle with exercise and statins. Arterioscler Thromb Vasc Biol (2005) 2.12
Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta. J Clin Invest (2009) 2.10
Gene profiling in spinal cord injury shows role of cell cycle in neuronal death. Ann Neurol (2003) 2.06
SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength. Diabetes (2013) 2.05
Calorie-related rapid onset of alveolar loss, regeneration, and changes in mouse lung gene expression. Am J Physiol Lung Cell Mol Physiol (2003) 2.04
Secreted proteome profiling in human RPE cell cultures derived from donors with age related macular degeneration and age matched healthy donors. J Proteome Res (2006) 2.04
Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin. Dev Cell (2004) 2.01
Interactively optimizing signal-to-noise ratios in expression profiling: project-specific algorithm selection and detection p-value weighting in Affymetrix microarrays. Bioinformatics (2004) 1.98
Variability in muscle size and strength gain after unilateral resistance training. Med Sci Sports Exerc (2005) 1.95
ACE ID genotype and the muscle strength and size response to unilateral resistance training. Med Sci Sports Exerc (2006) 1.86
Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration. Hum Mol Genet (2006) 1.85
Gene expression profiling in DQA1*0501+ children with untreated dermatomyositis: a novel model of pathogenesis. J Immunol (2002) 1.83
Tissue-specific alternative splicing of TCF7L2. Hum Mol Genet (2009) 1.80
The RNA helicases p68/p72 and the noncoding RNA SRA are coregulators of MyoD and skeletal muscle differentiation. Dev Cell (2006) 1.78
Constitutive activation of MAPK cascade in acute quadriplegic myopathy. Ann Neurol (2004) 1.77
Quarky calcium release in the heart. Circ Res (2010) 1.75
Protein kinase A phosphorylation of the cardiac calcium release channel (ryanodine receptor) in normal and failing hearts. Role of phosphatases and response to isoproterenol. J Biol Chem (2002) 1.73
AKAP150 is required for stuttering persistent Ca2+ sparklets and angiotensin II-induced hypertension. Circ Res (2008) 1.72
Golgi export of the Kir2.1 channel is driven by a trafficking signal located within its tertiary structure. Cell (2011) 1.71
GRB14, GPD1, and GDF8 as potential network collaborators in weight loss-induced improvements in insulin action in human skeletal muscle. Physiol Genomics (2006) 1.67
Activation of the endoplasmic reticulum stress response in autoimmune myositis: potential role in muscle fiber damage and dysfunction. Arthritis Rheum (2005) 1.67
Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B. Am J Pathol (2008) 1.65
In vivo restoration of physiological levels of truncated TrkB.T1 receptor rescues neuronal cell death in a trisomic mouse model. Neuron (2006) 1.64
ACTN3 genotype is associated with increases in muscle strength in response to resistance training in women. J Appl Physiol (1985) (2005) 1.57
Embryonic myogenesis pathways in muscle regeneration. Dev Dyn (2004) 1.57
Differential dependency network analysis to identify condition-specific topological changes in biological networks. Bioinformatics (2008) 1.56
Modulation of sarcoplasmic reticulum Ca2+ release in skeletal muscle expressing ryanodine receptor impaired in regulation by calmodulin and S100A1. Am J Physiol Cell Physiol (2011) 1.55
Alterations in mRNA expression and protein products following spinal cord injury in humans. J Physiol (2007) 1.55
Probe set algorithms: is there a rational best bet? BMC Bioinformatics (2006) 1.53
An analysis of anesthesia-controlled operating room time after propofol-based total intravenous anesthesia compared with desflurane anesthesia in ophthalmic surgery: a retrospective study. Anesth Analg (2014) 1.52
Dystrophin-deficient cardiomyopathy in mouse: expression of Nox4 and Lox are associated with fibrosis and altered functional parameters in the heart. Neuromuscul Disord (2008) 1.52
ACTN3 and MLCK genotype associations with exertional muscle damage. J Appl Physiol (1985) (2005) 1.52
Deranged sodium to sudden death. J Physiol (2015) 1.51
Functional characteristics of dystrophic skeletal muscle: insights from animal models. J Appl Physiol (1985) (2002) 1.50
Slug is a novel downstream target of MyoD. Temporal profiling in muscle regeneration. J Biol Chem (2002) 1.50
Functional polymorphisms associated with human muscle size and strength. Med Sci Sports Exerc (2004) 1.49
The cooperative international neuromuscular research group Duchenne natural history study--a longitudinal investigation in the era of glucocorticoid therapy: design of protocol and the methods used. Muscle Nerve (2013) 1.48
Differential gene expression in patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler (2011) 1.48
Stimulated emission depletion live-cell super-resolution imaging shows proliferative remodeling of T-tubule membrane structures after myocardial infarction. Circ Res (2012) 1.47
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia. Sci Transl Med (2011) 1.46
Analysis of human skeletal muscle after 48 h immobilization reveals alterations in mRNA and protein for extracellular matrix components. J Appl Physiol (1985) (2006) 1.45
Proteomics and systems biology in exercise and sport sciences research. Exerc Sport Sci Rev (2007) 1.43
Inflammasome up-regulation and activation in dysferlin-deficient skeletal muscle. Am J Pathol (2010) 1.41
Patterns of global gene expression in rat skeletal muscle during unloading and low-intensity ambulatory activity. Physiol Genomics (2003) 1.41
The PEPR GeneChip data warehouse, and implementation of a dynamic time series query tool (SGQT) with graphical interface. Nucleic Acids Res (2004) 1.40
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy. Am J Hum Genet (2008) 1.39
Defective intracellular Ca(2+) signaling contributes to cardiomyopathy in Type 1 diabetic rats. Am J Physiol Heart Circ Physiol (2002) 1.38
A web-accessible complete transcriptome of normal human and DMD muscle. Neuromuscul Disord (2002) 1.38
Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense delivery. Proc Natl Acad Sci U S A (2012) 1.32
Skipping toward personalized molecular medicine. N Engl J Med (2007) 1.30
Response of rat muscle to acute resistance exercise defined by transcriptional and translational profiling. J Physiol (2002) 1.29
Paradoxical cellular Ca2+ signaling in severe but compensated canine left ventricular hypertrophy. Circ Res (2005) 1.29
Trypsin-induced proteome alteration during cell subculture in mammalian cells. J Biomed Sci (2010) 1.29
Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule. Hum Mutat (2008) 1.29
Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies. Mamm Genome (2012) 1.28
Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice. J Cardiovasc Pharmacol Ther (2011) 1.28
GeMInA, Genomic Metadata for Infectious Agents, a geospatial surveillance pathogen database. Nucleic Acids Res (2009) 1.27
Fgfr4 is required for effective muscle regeneration in vivo. Delineation of a MyoD-Tead2-Fgfr4 transcriptional pathway. J Biol Chem (2005) 1.27
Micro- and nanomechanical analysis of articular cartilage by indentation-type atomic force microscopy: validation with a gel-microfiber composite. Biophys J (2010) 1.26
A kinase-deficient TrkC receptor isoform activates Arf6-Rac1 signaling through the scaffold protein tamalin. J Cell Biol (2006) 1.24
Downregulation of myelination, energy, and translational genes in Menkes disease brain. Mol Genet Metab (2005) 1.24
S100A1 and calmodulin compete for the same binding site on ryanodine receptor. J Biol Chem (2008) 1.23
CYP3A4 genetic variant and disease-free survival among white and black men after radical prostatectomy. J Urol (2004) 1.23
VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects. EMBO Mol Med (2013) 1.22
Balancing muscle hypertrophy and atrophy. Nat Med (2004) 1.22
Novel CLCN1 mutations with unique clinical and electrophysiological consequences. Brain (2002) 1.22
Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling. Am J Physiol Cell Physiol (2009) 1.21
A randomized clinical trial to assess the effect of statins on skeletal muscle function and performance: rationale and study design. Prev Cardiol (2010) 1.21
Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane. Proc Natl Acad Sci U S A (2013) 1.21
In vivo and in vitro characterization of novel neuronal plasticity factors identified following spinal cord injury. J Biol Chem (2004) 1.20
Olfactory biopsies demonstrate a defect in neuronal development in Rett's syndrome. Ann Neurol (2003) 1.19
Gene expression profiling of experimental traumatic spinal cord injury as a function of distance from impact site and injury severity. Physiol Genomics (2005) 1.19
An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss. Genome Biol (2015) 1.19