Published in Biophys J on February 17, 2010
Aberrant repair and fibrosis development in skeletal muscle. Skelet Muscle (2011) 2.41
Differentiation of pluripotent stem cells to muscle fiber to model Duchenne muscular dystrophy. Nat Biotechnol (2015) 1.13
Quantitative evaluation of skeletal muscle defects in second harmonic generation images. J Biomed Opt (2013) 0.89
Molecular mechanism of sphingosine-1-phosphate action in Duchenne muscular dystrophy. Dis Model Mech (2013) 0.89
Imaging deep skeletal muscle structure using a high-sensitivity ultrathin side-viewing optical coherence tomography needle probe. Biomed Opt Express (2013) 0.87
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
Structural and functional evaluation of branched myofibers lacking intermediate filaments. Am J Physiol Cell Physiol (2012) 0.84
Second harmonic generation microscopy probes different states of motor protein interaction in myofibrils. Biophys J (2010) 0.84
Taking a deep look: modern microscopy technologies to optimize the design and functionality of biocompatible scaffolds for tissue engineering in regenerative medicine. J R Soc Interface (2013) 0.83
Theoretical and experimental SHG angular intensity patterns from healthy and proteolysed muscles. Biophys J (2013) 0.83
Impaired adaptive response to mechanical overloading in dystrophic skeletal muscle. PLoS One (2012) 0.82
Modeling of supramolecular centrosymmetry effect on sarcomeric SHG intensity pattern of skeletal muscles. Biophys J (2011) 0.81
Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice. Physiol Rep (2015) 0.81
Motor protein function in skeletal abdominal muscle of cachectic cancer patients. J Cell Mol Med (2013) 0.81
The heart in Duchenne muscular dystrophy: early detection of contractile performance alteration. J Cell Mol Med (2012) 0.78
Resolution and contrast enhancement of subtractive second harmonic generation microscopy with a circularly polarized vortex beam. Sci Rep (2015) 0.77
Myofibrillar misalignment correlated to triad disappearance of mdx mouse gastrocnemius muscle probed by SHG microscopy. Biomed Opt Express (2014) 0.77
Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development. Front Physiol (2014) 0.76
Altered nuclear dynamics in MDX myofibers. J Appl Physiol (1985) (2016) 0.75
Determination of the source of SHG verniers in zebrafish skeletal muscle. Sci Rep (2015) 0.75
Multimodal SHG-2PF Imaging of Microdomain Ca2+-Contraction Coupling in Live Cardiac Myocytes. Circ Res (2015) 0.75
Local activation of striated muscle fibres. J Physiol (1958) 15.87
Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle. Nat Med (2009) 3.27
Characterization of the myosin-based source for second-harmonic generation from muscle sarcomeres. Biophys J (2005) 3.01
Interplay of IKK/NF-kappaB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy. J Clin Invest (2007) 2.99
Minimally invasive high-speed imaging of sarcomere contractile dynamics in mice and humans. Nature (2008) 2.56
Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old. J Physiol (2001) 2.31
Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma. FASEB J (2007) 2.22
Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury. J Muscle Res Cell Motil (2001) 2.06
mdx mice show progressive weakness and muscle deterioration with age. J Neurol Sci (1995) 2.06
Age-associated changes in the response of skeletal muscle cells to exercise and regeneration. Ann N Y Acad Sci (1998) 1.99
Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse. Acta Neuropathol (1986) 1.97
Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle. J Cell Biol (1997) 1.94
Smooth, cardiac and skeletal muscle myosin force and motion generation assessed by cross-bridge mechanical interactions in vitro. J Muscle Res Cell Motil (1994) 1.85
Muscle damage in mdx (dystrophic) mice: role of calcium and reactive oxygen species. Clin Exp Pharmacol Physiol (2006) 1.79
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies. Curr Top Dev Biol (2008) 1.62
Abnormalities in structure and function of limb skeletal muscle fibres of dystrophic mdx mice. Proc Biol Sci (1992) 1.56
Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes. J Physiol (2007) 1.55
Loss of dystrophin causes aberrant mechanotransduction in skeletal muscle fibers. FASEB J (2004) 1.50
Matrix metalloproteinase-9 inhibition ameliorates pathogenesis and improves skeletal muscle regeneration in muscular dystrophy. Hum Mol Genet (2009) 1.44
Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx mouse muscle fibres. J Physiol (2005) 1.43
TRPC1 binds to caveolin-3 and is regulated by Src kinase - role in Duchenne muscular dystrophy. J Cell Sci (2008) 1.42
Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1. J Pharmacol Exp Ther (2003) 1.41
Expansion of revertant fibers in dystrophic mdx muscles reflects activity of muscle precursor cells and serves as an index of muscle regeneration. J Cell Sci (2006) 1.34
Measurement of muscle disease by quantitative second-harmonic generation imaging. J Biomed Opt (2008) 1.32
Common pathological mechanisms in mouse models for muscular dystrophies. FASEB J (2005) 1.31
Alteration in calcium handling at the subcellular level in mdx myotubes. J Biol Chem (2000) 1.30
New aspects of calcium signaling in skeletal muscle cells: implications in Duchenne muscular dystrophy. Biochim Biophys Acta (2002) 1.26
Susceptibility to sarcomere injury induced by single stretches of maximally activated muscles of mdx mice. J Appl Physiol (1985) (2004) 1.25
L-arginine decreases inflammation and modulates the nuclear factor-kappaB/matrix metalloproteinase cascade in mdx muscle fibers. Am J Pathol (2008) 1.25
Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice. Am J Pathol (2006) 1.24
Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling. Am J Physiol Cell Physiol (2009) 1.21
AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype. Mol Ther (2004) 1.21
In situ measurements of calpain activity in isolated muscle fibres from normal and dystrophin-lacking mdx mice. J Physiol (2007) 1.21
Gadolinium reduces short-term stretch-induced muscle damage in isolated mdx mouse muscle fibres. J Physiol (2003) 1.14
Branched fibers in dystrophic mdx muscle are associated with a loss of force following lengthening contractions. Am J Physiol Cell Physiol (2007) 1.13
Properties of enzymatically isolated skeletal fibres from mice with muscular dystrophy. J Physiol (1990) 1.13
Dystrophic skeletal muscle fibers display alterations at the level of calcium microdomains. Proc Natl Acad Sci U S A (2008) 1.12
Second harmonic imaging of intrinsic signals in muscle fibers in situ. J Biomed Opt (2004) 1.11
Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression. PLoS One (2008) 1.08
Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice. J Physiol (2003) 1.08
Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation. Dis Model Mech (2009) 1.08
Skeletal muscle diseases, inflammation, and NF-kappaB signaling: insights and opportunities for therapeutic intervention. Int Rev Immunol (2008) 1.07
Detection and imaging of non-contractile inclusions and sarcomeric anomalies in skeletal muscle by second harmonic generation combined with two-photon excited fluorescence. J Struct Biol (2008) 1.02
Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes. J Physiol (2001) 0.97
Actomyosin interactions in a novel single muscle fiber in vitro motility assay. J Muscle Res Cell Motil (2000) 0.97
Contractile properties of skinned muscle fibres from young and adult normal and dystrophic (mdx) mice. J Physiol (1993) 0.97
L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle. PLoS One (2008) 0.92
Skeletal muscle fiber splitting with weight-lifting exercise in rats. Am J Anat (1980) 0.90
New techniques in linear and non-linear laser optics in muscle research. J Muscle Res Cell Motil (2006) 0.88
Mini-dystrophin gene transfer in mdx4cv diaphragm muscle fibers increases sarcolemmal stability. Gene Ther (1997) 0.87
Unloaded speed of shortening in voltage-clamped intact skeletal muscle fibers from wt, mdx, and transgenic minidystrophin mice using a novel high-speed acquisition system. Biophys J (2008) 0.85
Bupivacaine-induced regeneration of rat soleus muscle: ultrastructural and immunohistochemical aspects. Ultrastruct Pathol (2006) 0.82
Velocity of actomyosin sliding in vitro is reduced in dystrophic mouse diaphragm. Am J Respir Crit Care Med (2002) 0.81
Characterization of ultrastructural and contractile activation properties of crustacean (Cherax destructor) muscle fibres during claw regeneration and moulting. J Muscle Res Cell Motil (1995) 0.78
Velocity distributions of single F-actin trajectories from a fluorescence image series using trajectory reconstruction and optical flow mapping. J Biomed Opt (2008) 0.77
Actin sliding velocity on pure myosin isoforms from dystrophic mouse muscles. Muscle Nerve (2009) 0.77
Investigations of ultrastructure of damaged and regenerated skeletal muscle fibers. Ann Univ Mariae Curie Sklodowska Med (2004) 0.76
Transport of hemolysin across the outer membrane of Escherichia coli requires two functions. J Bacteriol (1983) 4.27
RANTES deposition by platelets triggers monocyte arrest on inflamed and atherosclerotic endothelium. Circulation (2001) 3.86
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J Cell Biol (1997) 3.32
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nat Genet (1996) 3.26
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature (1995) 2.92
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet (1997) 2.77
Transient limb ischemia induces remote ischemic preconditioning in vivo. Circulation (2002) 2.67
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature (1993) 2.63
Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblasts. Mol Cell Biol (1986) 2.47
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice. Hum Mol Genet (1995) 2.40
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form. Nat Genet (1995) 2.33
Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old. J Physiol (2001) 2.31
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation (1993) 2.30
Dermcidin: a novel human antibiotic peptide secreted by sweat glands. Nat Immunol (2001) 2.29
The chemokine KC, but not monocyte chemoattractant protein-1, triggers monocyte arrest on early atherosclerotic endothelium. J Clin Invest (2001) 2.26
Transcatheter closure as standard treatment for most interatrial defects: experience in 200 patients treated with the Amplatzer Septal Occluder. Cardiol Young (1999) 2.26
Human xeroderma pigmentosum group D gene encodes a DNA helicase. Nature (1993) 2.25
Human melanoma progression in skin reconstructs : biological significance of bFGF. Am J Pathol (2000) 2.23
Disk electrophoresis of wheat flour proteins with a modified apparatus utilizing gels of rectangular cross section. Anal Biochem (1965) 2.19
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene. Am J Hum Genet (1989) 2.12
The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: a potential mechanism for hepatic adverse reactions. Clin Pharmacol Ther (2001) 2.10
Scombroid poisoning. Ann Emerg Med (1996) 2.10
Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury. J Muscle Res Cell Motil (2001) 2.06
Mutations affecting activity and transport of haemolysin in Escherichia coli. Mol Gen Genet (1987) 2.01
Sepsis and the heart. Circulation (2007) 1.98
Comparison of results and complications of surgical and Amplatzer device closure of atrial septal defects. J Thorac Cardiovasc Surg (1999) 1.97
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet (1991) 1.93
Oncogenic GNAQ mutations are not correlated with disease-free survival in uveal melanoma. Br J Cancer (2009) 1.93
Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. J Cell Biol (2000) 1.92
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies. Neurology (1989) 1.88
Pulmonary regurgitation is an important determinant of right ventricular contractile dysfunction in patients with surgically repaired tetralogy of Fallot. Circulation (2004) 1.87
Incidence of atrial flutter/fibrillation in adults with atrial septal defect before and after surgery. Ann Thorac Surg (1999) 1.84
Human Bordetella bronchiseptica infection related to contact with infected animals: persistence of bacteria in host. J Clin Microbiol (1995) 1.84
Pyrrolidine dithiocarbamate inhibits NF-kappa B mobilization and TNF production in human monocytes. J Immunol (1993) 1.84
Simultaneous determination of tissue tocopherols, tocotrienols, ubiquinols, and ubiquinones. J Lipid Res (1996) 1.81
Expression of CCR2 by endothelial cells : implications for MCP-1 mediated wound injury repair and In vivo inflammatory activation of endothelium. Arterioscler Thromb Vasc Biol (1999) 1.80
Awareness and early detection of cutaneous melanoma: an analysis of factors related to delay in treatment. Br J Dermatol (1999) 1.79
Forced expression of dystrophin deletion constructs reveals structure-function correlations. J Cell Biol (1996) 1.79
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms. Hum Mol Genet (1996) 1.74
Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted. J Virol (1998) 1.72
Metastatic pathways and time courses in the orderly progression of cutaneous melanoma. Br J Dermatol (2002) 1.71
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. Nat Genet (1994) 1.70
Problems in defining cutoff points of continuous prognostic factors: example of tumor thickness in primary cutaneous melanoma. J Clin Epidemiol (1997) 1.69
Differential expression of dystrophin isoforms in strains of mdx mice with different mutations. Hum Mol Genet (1996) 1.69
Identification and characterization of the dystrophin anchoring site on beta-dystroglycan. J Biol Chem (1995) 1.67
The dermatoscopic pattern of clear-cell acanthoma resembles psoriasis vulgaris. Dermatology (2001) 1.66
Increase of melanocytic nevus counts in children during 5 years of follow-up and analysis of associated factors. Arch Dermatol (1996) 1.65
Targeted overexpression of parathyroid hormone-related protein (PTHrP) to vascular smooth muscle in transgenic mice lowers blood pressure and alters vascular contractility. Endocrinology (1999) 1.64
Direct mapping of nuclear shell effects in the heaviest elements. Science (2012) 1.63
Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product. Gene Ther (2002) 1.62
Structure and content of the Entamoeba histolytica genome. Adv Parasitol (2007) 1.62
Regulation of creatine kinase induction in differentiating mouse myoblasts. Mol Cell Biol (1985) 1.59
Metastatic melanoma of unknown primary origin shows prognostic similarities to regional metastatic melanoma: recommendations for initial staging examinations. Cancer (1997) 1.59
Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells. Hum Mol Genet (1996) 1.56
Detection of melanoma cells in sentinel lymph nodes, bone marrow and peripheral blood by a reverse transcription-polymerase chain reaction assay in patients with primary cutaneous melanoma: association with Breslow's tumour thickness. Br J Dermatol (2001) 1.56
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy. J Exp Med (1996) 1.56
Human papillomaviruses are commonly found in normal skin of immunocompetent hosts. J Invest Dermatol (1998) 1.54
Conservation of the rifamycin sensitivity of transcription during T4 development. Nature (1969) 1.53
Trabecular bone pattern factor--a new parameter for simple quantification of bone microarchitecture. Bone (1992) 1.53
Deoxycholate induces mitochondrial oxidative stress and activates NF-kappaB through multiple mechanisms in HCT-116 colon epithelial cells. Carcinogenesis (2006) 1.50
Dermoscopic classification of atypical melanocytic nevi (Clark nevi). Arch Dermatol (2001) 1.49
Combined targeting of MAPK and AKT signalling pathways is a promising strategy for melanoma treatment. Br J Dermatol (2007) 1.49
Renal function after cardiopulmonary bypass surgery in cyanotic congenital heart disease. Int J Cardiol (2000) 1.47
Epidemiologic evidence for the role of melanocytic nevi as risk markers and direct precursors of cutaneous malignant melanoma. Results of a case control study in melanoma patients and nonmelanoma control subjects. J Am Acad Dermatol (1992) 1.47
ERCC1 and ERCC2 expression in malignant tissues from ovarian cancer patients. J Natl Cancer Inst (1992) 1.46
The mdx-amplification-resistant mutation system assay, a simple and rapid polymerase chain reaction-based detection of the mdx allele. Muscle Nerve (1996) 1.46
Mitochondrial single-stranded DNA-binding protein is required for mitochondrial DNA replication and development in Drosophila melanogaster. Mol Biol Cell (2001) 1.44
Basal cell carcinoma: histological classification and body-site distribution. Br J Dermatol (2006) 1.43
Inflammatory role and prognostic value of platelet chemokines in acute coronary syndrome. Thromb Haemost (2014) 1.42
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin. Nat Genet (1993) 1.42
The chemokine receptor CXCR3 mediates rapid and shear-resistant adhesion-induction of effector T lymphocytes by the chemokines IP10 and Mig. Eur J Immunol (1998) 1.41
[Morphologic studies of the placentas of HIV-positive mothers]. Pathologe (1988) 1.41
Low-grade non-Hodgkin's lymphoma after high-grade non-Hodgkin's lymphoma in a child with ataxia telangiectasia. Cancer (1994) 1.40
[Elective lymph node dissection in primary malignant melanoma]. Hautarzt (1996) 1.39
[Assessment of the capability of performance of patients with psychic and psychosomatic diseases--a diagnostic model]. Versicherungsmedizin (2011) 1.39
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY: ABNORMAL SPLITTING OF ETHYL GROUPS DUE TO MOLECULAR ASSYMETRY. Proc Natl Acad Sci U S A (1961) 1.38
Oral hairy leukoplakia in 71 HIV-seropositive patients: clinical symptoms, relation to immunologic status, and prognostic significance. J Am Acad Dermatol (1996) 1.38
[Merkel cell tumor of the skin]. Dtsch Med Wochenschr (1997) 1.38
Determinants of survival in patients with brain metastases from cutaneous melanoma. Br J Cancer (2010) 1.37
Expression of the iap gene coding for protein p60 of Listeria monocytogenes is controlled on the posttranscriptional level. J Bacteriol (1991) 1.36
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors. Mol Ther (2000) 1.36
Undecalcified preparation of bone tissue: report of technical experience and development of new methods. Virchows Arch A Pathol Anat Histopathol (1991) 1.34
Lack of efficacy of rituximab in Wegener's granulomatosis with refractory granulomatous manifestations. Ann Rheum Dis (2005) 1.33
Quantification of stromal thinning, epithelial thickness, and corneal haze after photorefractive keratectomy using in vivo confocal microscopy. Ophthalmology (1997) 1.33
Induction of cancer cell apoptosis by alpha-tocopheryl succinate: molecular pathways and structural requirements. FASEB J (2001) 1.33
mdx muscle pathology is independent of nNOS perturbation. Hum Mol Genet (1998) 1.32
Differential immobilization and hierarchical involvement of chemokines in monocyte arrest and transmigration on inflamed endothelium in shear flow. Eur J Immunol (1999) 1.32
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform. Hum Mol Genet (1994) 1.32
Selective cancer cell killing by alpha-tocopheryl succinate. Br J Cancer (2001) 1.32
Aorto-iliac multidetector-row CT angiography with low kV settings: improved vessel enhancement and simultaneous reduction of radiation dose. Eur Radiol (2004) 1.31
Precision top-quark mass measurement at CDF. Phys Rev Lett (2012) 1.30
Acral cutaneous melanoma in caucasians: clinical features, histopathology and prognosis in 112 patients. Br J Dermatol (2000) 1.29
Met-RANTES reduces vascular and tubular damage during acute renal transplant rejection: blocking monocyte arrest and recruitment. FASEB J (1999) 1.28
Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy. Hum Mol Genet (2000) 1.27
Melanocytes in nevi and melanomas synthesize basement membrane and basement membrane-like material. An immunohistochemical and electron microscopic study including immunoelectron microscopy. J Cutan Pathol (2000) 1.27
Cellular mechanisms of depressed atrial contractility in patients with chronic atrial fibrillation. Circulation (2001) 1.27
Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin. J Biol Chem (1995) 1.26
Contraction-induced injury to single permeabilized muscle fibers from mdx, transgenic mdx, and control mice. Am J Physiol Cell Physiol (2000) 1.26
Expression and regulation of the plasmid-encoded hemolysin determinant of Escherichia coli. Mol Gen Genet (1984) 1.25