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The myosin alkali light chain proteins and their genesAMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatmentStructural characterization of the human fast skeletal muscle troponin I gene (TNNI2)Close physical linkage of human troponin genes: organization, sequence, and expression of the locus encoding cardiac troponin I and slow skeletal troponin THyperubiquitination of proteins in dilated cardiomyopathyDetermination of the 5' exon structure of the human cardiac alpha-myosin heavy chain geneTelethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heartMyocardial expression of the arginine:glycine amidinotransferase gene is elevated in heart failure and normalized after recovery: potential implications for local creatine synthesisAssignment of the human cardiac/slow skeletal muscle troponin C gene (TNNC1) between D3S3118 and GCT4B10 on the short arm of chromosome 3 by somatic cell hybrid analysisTroponin I gene expression during human cardiac development and in end-stage heart failureIsolation and characterization of the human cardiac troponin I gene (TNNI3)A skeletal muscle-specific enhancer regulated by factors binding to E and CArG boxes is present in the promoter of the mouse myosin light-chain 1A geneEffect of AMP-deaminase 3 knock-out in mice on enzyme activity in heart and other organsReview and Updates in Regenerative and Personalized Medicine, Preclinical Animal Models, and Clinical Care in Cardiovascular Medicine.Advances in induced pluripotent stem cells, genomics, biomarkers, and antiplatelet therapy highlights of the year in JCTR 2013.Identification of a new target of miR-16, Vacuolar Protein Sorting 4a.Titin-truncating variants affect heart function in disease cohorts and the general population.Heterogeneic nature of adult cardiac side population cells.Choice of cell-delivery route for skeletal myoblast transplantation for treating post-infarction chronic heart failure in rat.Chronic treatment with clenbuterol modulates endothelial progenitor cells and circulating factors in a murine model of cardiomyopathy.RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing.Truncations of titin causing dilated cardiomyopathy.Localization of the acetylcholine receptor gamma subunit gene to human chromosome 2q32----qter.Possible regulatory roles of promoter g-quadruplexes in cardiac function-related genes - human TnIc as a model.Effect of adenosine monophosphate deaminase-1 C34T allele on the requirement for donor inotropic support and on the incidence of early graft dysfunction after cardiac transplantation.Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencersRegulated inositol-requiring protein 1-dependent decay as a mechanism of corin RNA and protein deficiency in advanced human systolic heart failure.Structure and regulation of human troponin genes.Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseClinical, molecular, and genomic changes in response to a left ventricular assist deviceGenetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?Developmental regulation of myosin gene expression in mouse cardiac muscleDevelopment of a Comprehensive Sequencing Assay for Inherited Cardiac Condition GenesFine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.Left ventricular assist device-induced molecular changes in the failing myocardium.Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11.FineSplice, enhanced splice junction detection and quantification: a novel pipeline based on the assessment of diverse RNA-Seq alignment solutions.Myocardial insulin-like growth factor-I gene expression during recovery from heart failure after combined left ventricular assist device and clenbuterol therapy.Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes.Expression of human membrane skeleton protein genes for protein 4.1 and betaIISigma2-spectrin assayed by real-time RT-PCR.
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Paul J Barton
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Paul J Barton
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Paul J Barton
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Paul J Barton
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Paul J Barton
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باول جي بارتون
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type
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Paul J Barton
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Paul J Barton
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Paul J Barton
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Paul J Barton
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Paul J Barton
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باول جي بارتون
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prefLabel
Paul J Barton
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Paul J Barton
@en
Paul J Barton
@es
Paul J Barton
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Paul J Barton
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باول جي بارتون
@ar
P106
P21
P31
P496
0000-0002-1165-7767