Published in Cell Motil Cytoskeleton on January 01, 2008
Molecular regulation of contractile smooth muscle cell phenotype: implications for vascular tissue engineering. Tissue Eng Part B Rev (2010) 1.76
New insights into the regulation of the actin cytoskeleton by tropomyosin. Int Rev Cell Mol Biol (2010) 1.28
Cytoplasmic gamma-actin and tropomodulin isoforms link to the sarcoplasmic reticulum in skeletal muscle fibers. J Cell Biol (2011) 1.06
Cytoskeletal tropomyosins: choreographers of actin filament functional diversity. J Muscle Res Cell Motil (2013) 1.05
Tropomodulin capping of actin filaments in striated muscle development and physiology. J Biomed Biotechnol (2011) 0.98
Cytoskeletal tropomyosin Tm5NM1 is required for normal excitation-contraction coupling in skeletal muscle. Mol Biol Cell (2008) 0.96
An actin filament population defined by the tropomyosin Tpm3.1 regulates glucose uptake. Traffic (2015) 0.91
Myofibril-inducing RNA (MIR) is essential for tropomyosin expression and myofibrillogenesis in axolotl hearts. J Biomed Sci (2009) 0.90
Transcriptional adaptations following exercise in thoroughbred horse skeletal muscle highlights molecular mechanisms that lead to muscle hypertrophy. BMC Genomics (2009) 0.88
Research Resource: Hormones, Genes, and Athleticism: Effect of Androgens on the Avian Muscular Transcriptome. Mol Endocrinol (2016) 0.79
Localization and function of Xinα in mouse skeletal muscle. Am J Physiol Cell Physiol (2013) 0.78
Functional effects of mutations in the tropomyosin-binding sites of tropomodulin1 and tropomodulin3. Cytoskeleton (Hoboken) (2014) 0.78
Cytoskeletal remodelling proteins identified in fetal-maternal interface in pregnant women and rhesus monkeys. J Mol Histol (2011) 0.75
Lighting up microtubule cytoskeleton dynamics in skeletal muscle. Intravital (2014) 0.75
Distinctive patterns of microRNA expression in primary muscular disorders. Proc Natl Acad Sci U S A (2007) 3.72
Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans. Nat Genet (2007) 2.96
Multimodal analgesia and intravenous nutrition preserves total body protein following major upper gastrointestinal surgery. Reg Anesth Pain Med (2002) 2.60
Tropomyosin isoforms: divining rods for actin cytoskeleton function. Trends Cell Biol (2005) 2.45
A molecular pathway for myosin II recruitment to stress fibers. Curr Biol (2011) 2.25
The nature and frequency of cognitive deficits in children with neurofibromatosis type 1. Neurology (2005) 1.98
MURC/Cavin-4 and cavin family members form tissue-specific caveolar complexes. J Cell Biol (2009) 1.87
A systematic nomenclature for mammalian tropomyosin isoforms. J Muscle Res Cell Motil (2014) 1.77
Alterations in gamma-actin and tubulin-targeted drug resistance in childhood leukemia. J Natl Cancer Inst (2006) 1.76
Decreased bone mineral density in neurofibromatosis type 1: results from a pediatric cohort. J Pediatr Orthop (2007) 1.64
An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performance. Hum Mol Genet (2008) 1.62
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
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet (2004) 1.51
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia. Am J Hum Genet (2013) 1.51
Specification of actin filament function and molecular composition by tropomyosin isoforms. Mol Biol Cell (2003) 1.51
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. Am J Hum Genet (2013) 1.50
Four and a half LIM protein 1 binds myosin-binding protein C and regulates myosin filament formation and sarcomere assembly. J Biol Chem (2006) 1.50
Relationship between cognitive dysfunction, gait, and motor impairment in children and adolescents with neurofibromatosis type 1. Dev Med Child Neurol (2014) 1.50
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy. Am J Hum Genet (2013) 1.46
Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledge. Am J Med Genet A (2013) 1.43
Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder. Dev Med Child Neurol (2006) 1.42
Dysfunction induced by ischemia versus edema: does edema matter? J Thorac Cardiovasc Surg (2009) 1.42
A gene for speed? The evolution and function of alpha-actinin-3. Bioessays (2004) 1.42
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
Tropomyosin isoforms and reagents. Bioarchitecture (2011) 1.37
SEPN1: associated with congenital fiber-type disproportion and insulin resistance. Ann Neurol (2006) 1.32
Genes and human elite athletic performance. Hum Genet (2005) 1.28
Tropomyosin isoform expression regulates the transition of adhesions to determine cell speed and direction. Mol Cell Biol (2009) 1.26
ACTN3: A genetic influence on muscle function and athletic performance. Exerc Sport Sci Rev (2007) 1.26
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. J Clin Invest (2014) 1.24
Single section Western blot: improving the molecular diagnosis of the muscular dystrophies. Neurology (2003) 1.22
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretch. J Neuropathol Exp Neurol (2011) 1.21
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy. J Cell Biol (2008) 1.21
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
Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy. Am J Hum Genet (2008) 1.20
Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis. Neuromuscul Disord (2007) 1.19
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. Hum Mutat (2010) 1.17
Tissue-specific tropomyosin isoform composition. J Histochem Cytochem (2005) 1.17
ETS factors regulate Vegf-dependent arterial specification. Dev Cell (2013) 1.16
Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair. Traffic (2011) 1.15
Molecular consequences of dominant Bethlem myopathy collagen VI mutations. Ann Neurol (2007) 1.15
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity. Ann Neurol (2008) 1.14
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3. Hum Mol Genet (2005) 1.14
A gene for speed: the emerging role of alpha-actinin-3 in muscle metabolism. Physiology (Bethesda) (2010) 1.13
Genes for elite power and sprint performance: ACTN3 leads the way. Sports Med (2013) 1.13
Targeting of a tropomyosin isoform to short microfilaments associated with the Golgi complex. Mol Biol Cell (2003) 1.08
ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling. J Clin Invest (2013) 1.08
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
Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene Expr Patterns (2006) 1.08
Congenital fiber type disproportion--30 years on. J Neuropathol Exp Neurol (2003) 1.07
Calpains, cleaved mini-dysferlinC72, and L-type channels underpin calcium-dependent muscle membrane repair. J Neurosci (2013) 1.07
Hand involvement in children with Charcot-Marie-Tooth disease type 1A. Neuromuscul Disord (2008) 1.07
Assessment of executive function and attention in children with neurofibromatosis type 1: relationships between cognitive measures and real-world behavior. Child Neuropsychol (2011) 1.06
Health-related quality of life in boys with Duchenne muscular dystrophy: agreement between parents and their sons. J Child Neurol (2010) 1.06
Mutation update: the spectra of nebulin variants and associated myopathies. Hum Mutat (2014) 1.06
Increased connective tissue growth factor associated with cardiac fibrosis in the mdx mouse model of dystrophic cardiomyopathy. Int J Exp Pathol (2010) 1.05
γ-Actin regulates cell migration and modulates the ROCK signaling pathway. FASEB J (2011) 1.05
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis. Neuromuscul Disord (2007) 1.05
Actin mutations are one cause of congenital fibre type disproportion. Ann Neurol (2004) 1.04
Sorting of a nonmuscle tropomyosin to a novel cytoskeletal compartment in skeletal muscle results in muscular dystrophy. J Cell Biol (2004) 1.03
Spatial localisation of actin filaments across developmental stages of the malaria parasite. PLoS One (2012) 1.03
The actin cytoskeleton as a sensor and mediator of apoptosis. Bioarchitecture (2012) 1.03
Age-related findings on MRI in neurofibromatosis type 1. Pediatr Radiol (2006) 1.01
Mechanisms underlying intranuclear rod formation. Brain (2007) 1.01
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy. Neuromuscul Disord (2010) 1.01
Association analysis of ACE and ACTN3 in elite Caucasian and East Asian swimmers. Med Sci Sports Exerc (2013) 1.00
Cognitive and psychological profile of males with Becker muscular dystrophy. J Child Neurol (2007) 0.99
Corpus callosum morphology and its relationship to cognitive function in neurofibromatosis type 1. J Child Neurol (2010) 0.99
Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins. BMC Evol Biol (2010) 0.99
Diverse roles of the actin cytoskeleton in striated muscle. J Muscle Res Cell Motil (2009) 0.99
Tropomyosins in skeletal muscle diseases. Adv Exp Med Biol (2008) 0.99
A novel class of anticancer compounds targets the actin cytoskeleton in tumor cells. Cancer Res (2013) 0.99
Brain structure and function in neurofibromatosis type 1: current concepts and future directions. J Neurol Neurosurg Psychiatry (2010) 0.98