Published in J Proteome Res on April 05, 2010
Profiling the Aspergillus fumigatus proteome in response to caspofungin. Antimicrob Agents Chemother (2010) 0.90
Cardioproteomics: advancing the discovery of signaling mechanisms involved in cardiovascular diseases. Am J Cardiovasc Dis (2011) 0.80
Decreased myocardial injury and improved contractility after administration of a peptide derived against the alpha-interacting domain of the L-type calcium channel. J Am Heart Assoc (2014) 0.76
The L-type Ca(2+) channel: A mediator of hypertrophic cardiomyopathy. Channels (Austin) (2016) 0.75
Glutathionylation of the L-type Ca2+ channel in oxidative stress-induced pathology of the heart. Int J Mol Sci (2014) 0.75
Identification of Proteins Implicated in the Increased Heart Rate in ShenSongYangXin-Treated Bradycardia Rabbits by iTRAQ-Based Quantitative Proteomics. Evid Based Complement Alternat Med (2015) 0.75
Evidence for redox sensing by a human cardiac calcium channel. Sci Rep (2016) 0.75
High fructose causes cardiac hypertrophy via mitochondrial signaling pathway. Am J Transl Res (2016) 0.75
Comparative mRNA and MicroRNA Profiling during Acute Myocardial Infarction Induced by Coronary Occlusion and Ablation Radio-Frequency Currents. Front Physiol (2016) 0.75
Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2. Neuromuscul Disord (2007) 2.00
Role of NAD(P)H oxidase in the regulation of cardiac L-type Ca2+ channel function during acute hypoxia. Cardiovasc Res (2005) 1.77
Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2. Am J Hum Genet (2006) 1.73
The exon 55 deletion in the nebulin gene--one single founder mutation with world-wide occurrence. Neuromuscul Disord (2009) 1.70
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. Am J Hum Genet (2008) 1.65
Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. Hum Mutat (2006) 1.61
Liar, a novel Lyn-binding nuclear/cytoplasmic shuttling protein that influences erythropoietin-induced differentiation. Blood (2008) 1.60
Segregation of a missense variant in enteric smooth muscle actin γ-2 with autosomal dominant familial visceral myopathy. Gastroenterology (2012) 1.57
Myosin storage (hyaline body) myopathy: a case report. Neuromuscul Disord (2006) 1.55
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin. Neuromuscul Disord (2004) 1.52
Deranged sodium to sudden death. J Physiol (2015) 1.51
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1). Am J Hum Genet (2004) 1.50
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy. Am J Hum Genet (2013) 1.46
Actin-related myopathy without any missense mutation in the ACTA1 gene. J Child Neurol (2004) 1.42
Nemaline myopathies. Semin Pediatr Neurol (2011) 1.40
Mutations in TPM3 are a common cause of congenital fiber type disproportion. Ann Neurol (2008) 1.39
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores. Am J Hum Genet (2010) 1.38
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. J Clin Invest (2014) 1.24
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1). Neuromuscul Disord (2003) 1.23
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy. Am J Hum Genet (2013) 1.20
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations. Ann Neurol (2004) 1.13
KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy. J Clin Invest (2014) 1.13
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Neuromuscul Disord (2004) 1.10
Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy. Am J Hum Genet (2011) 1.09
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms. Hum Mol Genet (2004) 1.08
Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies. Brain (2011) 1.08
The photoyellowing of stilbene-derived fluorescent whitening agents--mass spectrometric characterization of yellow photoproducts. Photochem Photobiol (2008) 1.07
Myopathy mutations in alpha-skeletal-muscle actin cause a range of molecular defects. J Cell Sci (2004) 1.06
Mutation update: the spectra of nebulin variants and associated myopathies. Hum Mutat (2014) 1.06
Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms. Acta Neuropathol (2012) 1.05
Dissociated flexor digitorum brevis myofiber culture system--a more mature muscle culture system. Cell Motil Cytoskeleton (2007) 1.04
Distal myopathies. Curr Opin Neurol (2005) 1.04
Nemaline myopathy caused by absence of alpha-skeletal muscle actin. Ann Neurol (2007) 1.02
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity. Cardiovasc Res (2013) 1.02
Evidence for regulation of mitochondrial function by the L-type Ca2+ channel in ventricular myocytes. J Mol Cell Cardiol (2009) 1.01
Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin. J Cell Biol (2009) 0.99
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin. Eur J Hum Genet (2008) 0.99
Differential regulation of SOCS genes in normal and transformed erythroid cells. Oncogene (2003) 0.97
Fetal akinesia: review of the genetics of the neuromuscular causes. J Med Genet (2011) 0.96
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred. Neuromuscul Disord (2006) 0.95
Myeloid Leukemia Factor 1 inhibits erythropoietin-induced differentiation, cell cycle exit and p27Kip1 accumulation. Oncogene (2004) 0.95
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy. Hum Mutat (2014) 0.95
Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia. Am J Hum Genet (2013) 0.94
Qo site of mitochondrial complex III is the source of increased superoxide after transient exposure to hydrogen peroxide. J Mol Cell Cardiol (2010) 0.93
Crystal structures of the Lyn protein tyrosine kinase domain in its Apo- and inhibitor-bound state. J Biol Chem (2008) 0.93
Myopathies resulting from mutations in sarcomeric proteins. Curr Opin Neurol (2004) 0.93
Erythroid defects in TRalpha-/- mice. Blood (2008) 0.92
Consensus statement on standard of care for congenital myopathies. J Child Neurol (2012) 0.92
Ca(v)1.2 calcium channel is glutathionylated during oxidative stress in guinea pig and ischemic human heart. Free Radic Biol Med (2011) 0.92
L-type Ca(2+) channel contributes to alterations in mitochondrial calcium handling in the mdx ventricular myocyte. Am J Physiol Heart Circ Physiol (2013) 0.91
An alphaTropomyosin mutation alters dimer preference in nemaline myopathy. Ann Neurol (2005) 0.91
Regulator of G-protein signaling 5 controls blood pressure homeostasis and vessel wall remodeling. Circ Res (2013) 0.90
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain (2013) 0.90
A functional genomics approach to dissect the mode of action of the Stagonospora nodorum effector protein SnToxA in wheat. Mol Plant Pathol (2011) 0.90
Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy. J Neuropathol Exp Neurol (2008) 0.89
A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscul Disord (2013) 0.89
MADM, a novel adaptor protein that mediates phosphorylation of the 14-3-3 binding site of myeloid leukemia factor 1. J Biol Chem (2002) 0.89
Nemaline myopathy type 6: clinical and myopathological features. Muscle Nerve (2010) 0.89
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies. Hum Mutat (2014) 0.88
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy. Biochem J (2012) 0.88
The role of the cysteine-rich domain and netrin-like domain of secreted frizzled-related protein 4 in angiogenesis inhibition in vitro. Oncol Res (2012) 0.87
Myeloperoxidase-derived oxidants inhibit sarco/endoplasmic reticulum Ca2+-ATPase activity and perturb Ca2+ homeostasis in human coronary artery endothelial cells. Free Radic Biol Med (2011) 0.87
NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24. Biochem Biophys Res Commun (2005) 0.87
Investigation of changes in skeletal muscle alpha-actin expression in normal and pathological human and mouse hearts. J Muscle Res Cell Motil (2010) 0.86
Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function. Acta Neuropathol (2015) 0.85
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1). Neuromuscul Disord (2006) 0.85
HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor. J Biol Chem (2003) 0.85
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred. Neuromuscul Disord (2006) 0.85
Novel application of flow cytometry: determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart. Cell Motil Cytoskeleton (2007) 0.84
Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression. PLoS One (2011) 0.84
Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases--quantification of striated alpha-actins by MRM-mass spectrometry. Neuromuscul Disord (2008) 0.84
Production of human skeletal alpha-actin proteins by the baculovirus expression system. Biochem Biophys Res Commun (2003) 0.83
Characterization of three myotonia-associated mutations of the CLCN1 chloride channel gene via heterologous expression. Hum Mutat (2004) 0.83
138th ENMC Workshop: nemaline myopathy, 20-22 May 2005, Naarden, The Netherlands. Neuromuscul Disord (2005) 0.83
Nemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weakness. PLoS One (2012) 0.82
Testin, a novel binding partner of the calcium-sensing receptor, enhances receptor-mediated Rho-kinase signalling. Biochem Biophys Res Commun (2011) 0.82
Actinopathies and myosinopathies. Brain Pathol (2009) 0.81
A proteomic analysis of the acute effects of high-intensity exercise on skeletal muscle proteins in fasted rats. Clin Exp Pharmacol Physiol (2006) 0.81
Skeletal muscle alpha-actin diseases. Adv Exp Med Biol (2008) 0.81
A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance. Neuromuscul Disord (2010) 0.81
Clinical utility gene card for: nemaline myopathy. Eur J Hum Genet (2012) 0.81
Myeloid leukemia factor 1 associates with a novel heterogeneous nuclear ribonucleoprotein U-like molecule. J Biol Chem (2006) 0.81
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. J Clin Invest (2015) 0.80
Targeting Lyn tyrosine kinase through protein fusions encompassing motifs of Cbp (Csk-binding protein) and the SOCS box of SOCS1. Biochem J (2012) 0.80