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ab15277 has been referenced in 61 publications.

  • Vanhoutte D  et al. Thrombospondin expression in myofibers stabilizes muscle membranes. Elife 5:N/A (2016). IHC-P ; Mouse . PubMed: 27669143
  • Baradaran-Heravi A  et al. Novel small molecules potentiate premature termination codon readthrough by aminoglycosides. Nucleic Acids Res 44:6583-98 (2016). PubMed: 27407112
  • Eftestøl E  et al. Increased hypertrophic response with increased mechanical load in skeletal muscles receiving identical activity patterns. Am J Physiol Cell Physiol 311:C616-C629 (2016). PubMed: 27488660
  • Jørgensen A  et al. Eccentric exercise 48 h prior to simulated diving has no effect on vascular bubble formation in rats. Eur J Appl Physiol 115:597-605 (2015). PubMed: 25394809
  • Xu J  et al. Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy. Skelet Muscle 5:43 (2015). WB, IF . PubMed: 26693275
  • Xu L  et al. CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice. Mol Ther N/A:N/A (2015). WB, IF . PubMed: 26449883
  • Yang Z  et al. Options for tracking GFP-Labeled transplanted myoblasts using in vivo fluorescence imaging: implications for tracking stem cell fate. BMC Biotechnol 14:55 (2014). Mouse . PubMed: 24919771
  • Hirt MN  et al. Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation. J Mol Cell Cardiol 74:151-61 (2014). IHC - Wholemount ; Rat, Human . PubMed: 24852842
  • Biesemann N  et al. Myostatin regulates energy homeostasis in the heart and prevents heart failure. Circ Res 115:296-310 (2014). IHC-Fr ; Mouse . PubMed: 24807786
  • Dandapat A  et al. Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene. Cell Rep 8:1484-96 (2014). ICC/IF ; Mouse . PubMed: 25176645
  • D'Arcy C  et al. X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene. J Child Neurol N/A:N/A (2014). IHC-Fr ; Human . PubMed: 25246303
  • Wein N  et al. Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med 20:992-1000 (2014). PubMed: 25108525
  • Beekman C  et al. A sensitive, reproducible and objective immunofluorescence analysis method of dystrophin in individual fibers in samples from patients with duchenne muscular dystrophy. PLoS One 9:e107494 (2014). IHC-Fr ; Human . PubMed: 25244123
  • Katz MY  et al. Three-dimensional myocardial scarring along myofibers after coronary ischemia-reperfusion revealed by computerized images of histological assays. Physiol Rep 2:N/A (2014). IHC-P ; Mouse . PubMed: 25347856
  • Yang Z  et al. Mononuclear cells from dedifferentiation of mouse myotubes display remarkable regenerative capability. Stem Cells 32:2492-501 (2014). WB ; Mouse . PubMed: 24916688
  • Anthony K  et al. Dystrophin quantification: Biological and translational research implications. Neurology 83:2062-9 (2014). IHC ; Human . PubMed: 25355828
  • Demonbreun AR  et al. Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. Am J Pathol 184:248-59 (2014). Mouse . PubMed: 24177035
  • Childers MK  et al. Gene therapy prolongs survival and restores function in murine and canine models of myotubular myopathy. Sci Transl Med 6:220ra10 (2014). PubMed: 24452262
  • Zhao C  et al. Recombinase-mediated reprogramming and dystrophin gene addition in mdx mouse induced pluripotent stem cells. PLoS One 9:e96279 (2014). IHC-Fr ; Mouse . PubMed: 24781921
  • Paulsen G  et al. Vitamin C and E supplementation hampers cellular adaptation to endurance training in humans: a double-blind, randomised, controlled trial. J Physiol 592:1887-901 (2014). Human . PubMed: 24492839
  • Yang L  et al. Effective exon skipping and dystrophin restoration by 2'-o-methoxyethyl antisense oligonucleotide in dystrophin-deficient mice. PLoS One 8:e61584 (2013). IHC-Fr ; Mouse . PubMed: 23658612
  • van den Bergen JC  et al. Dystrophin levels and clinical severity in Becker muscular dystrophy patients. J Neurol Neurosurg Psychiatry N/A:N/A (2013). Human . PubMed: 24292997
  • Chun JL  et al. Injection of vessel-derived stem cells prevents dilated cardiomyopathy and promotes angiogenesis and endogenous cardiac stem cell proliferation in mdx/utrn-/- but not aged mdx mouse models for duchenne muscular dystrophy. Stem Cells Transl Med 2:68-80 (2013). ICC/IF ; Mouse, Rat . PubMed: 23283493
  • Lavasani M  et al. The microenvironment-specific transformation of adult stem cells models malignant triton tumors. PLoS One 8:e82173 (2013). IHC-Fr ; Mouse . PubMed: 24349213
  • van den Bergen JC  et al. Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy. J Neurol Neurosurg Psychiatry N/A:N/A (2013). Human . PubMed: 23667215
  • Mu X  et al. Regeneration of soft tissues is promoted by MMP1 treatment after digit amputation in mice. PLoS One 8:e59105 (2013). IHC-P ; Mouse . PubMed: 23527099
  • Roberts TC  et al. Extracellular microRNAs are dynamic non-vesicular biomarkers of muscle turnover. Nucleic Acids Res N/A:N/A (2013). Mouse . PubMed: 23945935
  • Yin H  et al. Context Dependent Effects of Chimeric Peptide Morpholino Conjugates Contribute to Dystrophin Exon-skipping Efficiency. Mol Ther Nucleic Acids 2:e124 (2013). IHC ; Mouse . PubMed: 24064708
  • Kim JE  et al. Status Epilepticus Induces Vasogenic Edema via Tumor Necrosis Factor-a/ Endothelin-1-Mediated Two Different Pathways. PLoS One 8:e74458 (2013). WB, ICC/IF ; Rat . PubMed: 24040253
  • Paez-Colasante X  et al. Improvement of Neuromuscular Synaptic Phenotypes without Enhanced Survival and Motor Function in Severe Spinal Muscular Atrophy Mice Selectively Rescued in Motor Neurons. PLoS One 8:e75866 (2013). PubMed: 24086650
  • D'Arcy CE  et al. Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. Hum Mol Genet N/A:N/A (2013). PubMed: 24087791
  • Masubuchi N  et al. Subcellular localization of dystrophin isoforms in cardiomyocytes and phenotypic analysis of dystrophin-deficient mice reveal cardiac myopathy is predominantly caused by a deficiency in full-length dystrophin. Exp Anim 62:211-7 (2013). WB ; Mouse . PubMed: 23903056
  • Beckman SA  et al. Beneficial effect of mechanical stimulation on the regenerative potential of muscle-derived stem cells is lost by inhibiting vascular endothelial growth factor. Arterioscler Thromb Vasc Biol 33:2004-12 (2013). IHC ; Mouse . PubMed: 23723372
  • Barbash IM  et al. MRI roadmap-guided transendocardial delivery of exon-skipping recombinant adeno-associated virus restores dystrophin expression in a canine model of Duchenne muscular dystrophy. Gene Ther : (2012). WB, ICC/IF ; Dog . PubMed: 22551778
  • Lawlor MW  et al. Inhibition of activin receptor type IIB increases strength and lifespan in myotubularin-deficient mice. Am J Pathol 178:784-93 (2011). IHC-Fr ; Mouse . PubMed: 21281811
  • Kumar A  et al. Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A. Hum Mol Genet 20:2333-43 (2011). IHC ; Mouse . PubMed: 21441569
  • Jeudy S  et al. Bcl-2 Inhibits the Innate Immune Response during Early Pathogenesis of Murine Congenital Muscular Dystrophy. PLoS One 6:e22369 (2011). IHC (PFA fixed) ; Mouse . PubMed: 21850221
  • Townsend D  et al. Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs. J Clin Invest 120:1140-50 (2010). WB ; Dog . PubMed: 20234088
  • Tanaka KK  et al. Syndecan-4-expressing muscle progenitor cells in the SP engraft as satellite cells during muscle regeneration. Cell Stem Cell 4:217-25 (2009). IHC-FoFr ; Mouse . PubMed: 19265661
  • Pilichou K  et al. Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy. J Exp Med 206:1787-802 (2009). IHC-Fr ; Mouse . PubMed: 19635863
  • Paulsen G  et al. Subcellular movement and expression of HSP27, alphaB-crystallin, and HSP70 after two bouts of eccentric exercise in humans. J Appl Physiol 107:570-82 (2009). PubMed: 19498098
  • Sáinz N  et al. Leptin administration favors muscle mass accretion by decreasing FoxO3a and increasing PGC-1alpha in ob/ob mice. PLoS One 4:e6808 (2009). IHC-P ; Mouse . PubMed: 19730740
  • Jia Y  et al. Erythropoietin signaling promotes transplanted progenitor cell survival. FASEB J 23:3089-99 (2009). IHC-P ; Mouse . PubMed: 19417086
  • Jazedje T  et al. Human fallopian tube: a new source of multipotent adult mesenchymal stem cells discarded in surgical procedures. J Transl Med 7:46 (2009). WB, ICC/IF ; Human . PubMed: 19538712
  • Williams JH  et al. Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice. BMC Biotechnol 8:35 (2008). IHC-Fr ; Mouse . PubMed: 18384691
  • Sirsi SR  et al. Functionalized PEG-PEI copolymers complexed to exon-skipping oligonucleotides improve dystrophin expression in mdx mice. Hum Gene Ther 19:795-806 (2008). IHC-Fr ; Mouse . PubMed: 18647087
  • Vitiello L  et al. In vivo delivery of naked antisense oligos in aged mdx mice: Analysis of dystrophin restoration in skeletal and cardiac muscle. Neuromuscul Disord 18:597-605 (2008). PubMed: 18602263
  • Crisan M  et al. A perivascular origin for mesenchymal stem cells in multiple human organs. Cell Stem Cell 3:301-13 (2008). IHC-Fr ; Human . PubMed: 18786417
  • Cowling BS  et al. Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy. J Cell Biol 183:1033-48 (2008). IHC-Fr ; Mouse . PubMed: 19075112
  • Schessl J  et al. Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. J Clin Invest 118:904-12 (2008). ICC/IF ; Human . PubMed: 18274675
  • Wang B  et al. A canine minidystrophin is functional and therapeutic in mdx mice. Gene Ther : (2008). PubMed: 18432277
  • Mackey AL  et al. Evidence of skeletal muscle damage following electrically stimulated isometric muscle contractions in humans. J Appl Physiol 105:1620-7 (2008). IHC-Fr ; Human . PubMed: 18801957
  • Abedi M  et al. Haematopoietic stem cells participate in muscle regeneration. Br J Haematol 138:792-801 (2007). PubMed: 17672885
  • Welch EM  et al. PTC124 targets genetic disorders caused by nonsense mutations. Nature 447:87-91 (2007). PubMed: 17450125
  • Zheng B  et al. Prospective identification of myogenic endothelial cells in human skeletal muscle. Nat Biotechnol 25:1025-34 (2007). PubMed: 17767154
  • Galeano B  et al. Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine. J Clin Invest 117:1585-94 (2007). IHC-P ; Mouse . PubMed: 17549255
  • Deasy BM  et al. A role for cell sex in stem cell-mediated skeletal muscle regeneration: female cells have higher muscle regeneration efficiency. J Cell Biol 177:73-86 (2007). IHC-Fr ; Mouse . PubMed: 17420291
  • Mackey AL  et al. The influence of anti-inflammatory medication on exercise-induced myogenic precursor cell responses in humans. J Appl Physiol 103:425-31 (2007). PubMed: 17463304
  • Liadaki K  et al. Co-detection of GFP and dystrophin in skeletal muscle tissue sections. Biotechniques 42:699-700 (2007). ICC/IF ; Mouse . PubMed: 17612290
  • Di Rocco G  et al. Myogenic potential of adipose-tissue-derived cells. J Cell Sci 119:2945-52 (2006). IHC-P ; Mouse . PubMed: 16825428
  • Lechner BE  et al. Developmental regulation of biglycan expression in muscle and tendon. Muscle Nerve 34:347-55 (2006). PubMed: 16810681

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