about
Primary Murine Myotubes as a Model for Investigating Muscular DystrophyPolymorphisms of β 1-adrenoreceptor gene and cardiovascular complications in patients with thyrotoxicosisCongenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.Chicken rRNA Gene Cluster StructureGenetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation SequencingModulation of insulin degrading enzyme activity and liver cell proliferationRing chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects.NOTCH1 Mutations in Aortic Stenosis: Association with Osteoprotegerin/RANK/RANKL.Genetic spectrum of cardiomyopathies with neuromuscular phenotype.Autotransplantation of cryopreserved ovarian tissue--effective method of fertility preservation in cancer patients.Phenotypic and Functional Changes of Endothelial and Smooth Muscle Cells in Thoracic Aortic Aneurysms.Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.Variable pathogenic potentials of mutations located in the desmin alpha-helical domain.Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.Progressive cardiac conduction disease associated with a DSP gene mutation.Mechanisms of Smooth Muscle Cell Differentiation Are Distinctly Altered in Thoracic Aortic Aneurysms Associated with Bicuspid or Tricuspid Aortic ValvesSeventy years after the siege of Leningrad: does early life famine still affect cardiovascular risk and aging?Heparinase treatment of heparin-contaminated plasma from coronary artery bypass grafting patients enables reliable quantification of microRNAsValve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification.Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness.Variants in the NOTCH1 gene in patients with aortic coarctation.Regulation of nutrition-associated receptors in blood monocytes of normal weight and obese humans.Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene.Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene.Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy.Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.Beta-catenin in schizophrenia: Possibly deleterious novel mutation.Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes.Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner.Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubesMice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondriaDesmin mutations in a St. Petersburg cohort of cardiomyopathiesSynthesis of some CC chemokines and their receptors in the synovium in rheumatoid arthritisEarly changes of gene expression profiles in the rat model of arterial injuryNotch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valveDe novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathyDifferent Notch signaling in cells from calcified bicuspid and tricuspid aortic valvesHeterogeneity of the nucleic acid repertoire of plasma extracellular vesicles demonstrated using high-sensitivity fluorescence-activated sorting
P50
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P50
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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Anna Kostareva
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0000-0002-9349-6257