List of works - Anna Kostareva

Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubes

scientific article published on 10 August 2014

Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness

scientific article

Autotransplantation of cryopreserved ovarian tissue--effective method of fertility preservation in cancer patients.

scientific article published on October 2014

Beta-catenin in schizophrenia: Possibly deleterious novel mutation.

scientific article

Chicken rRNA Gene Cluster Structure

scientific article

Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.

scientific article

De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy

scientific article published on 17 June 2018

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.

scientific article published on 14 November 2007

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

scientific article

Desmin mutations in a St. Petersburg cohort of cardiomyopathies

scientific article published on 01 December 2006

Different Notch signaling in cells from calcified bicuspid and tricuspid aortic valves

scientific article published on 20 November 2017

Early changes of gene expression profiles in the rat model of arterial injury

scientific article published on 06 February 2014

Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.

scientific article published on 7 March 2006

Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene.

scientific article

Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene

scientific article

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing

scientific article

Genetic spectrum of cardiomyopathies with neuromuscular phenotype.

scientific article published on January 2013

Heparinase treatment of heparin-contaminated plasma from coronary artery bypass grafting patients enables reliable quantification of microRNAs

scientific article published on 8 April 2016

Heterogeneity of the nucleic acid repertoire of plasma extracellular vesicles demonstrated using high-sensitivity fluorescence-activated sorting

scientific article published on 30 March 2020

Mechanisms of Smooth Muscle Cell Differentiation Are Distinctly Altered in Thoracic Aortic Aneurysms Associated with Bicuspid or Tricuspid Aortic Valves

scientific article published on 25 July 2017

Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria

scientific article published on 19 June 2008

Modulation of insulin degrading enzyme activity and liver cell proliferation

scientific article

NOTCH1 Mutations in Aortic Stenosis: Association with Osteoprotegerin/RANK/RANKL.

scientific article published on 26 January 2017

Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes.

scientific article published on 24 February 2015

Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve

scientific article published on 10 February 2016

Phenotypic and Functional Changes of Endothelial and Smooth Muscle Cells in Thoracic Aortic Aneurysms

scientific article published on 19 January 2016

Polymorphisms of β 1-adrenoreceptor gene and cardiovascular complications in patients with thyrotoxicosis

scientific article

Primary Murine Myotubes as a Model for Investigating Muscular Dystrophy

scientific article

Progressive cardiac conduction disease associated with a DSP gene mutation.

scientific article

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

scientific article published in 2022

Regulation of nutrition-associated receptors in blood monocytes of normal weight and obese humans.

scientific article published on 22 January 2015

Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects.

scientific article published on 18 February 2016

Seventy years after the siege of Leningrad: does early life famine still affect cardiovascular risk and aging?

scientific article

Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy

scientific article published on 22 August 2017

Synthesis of some CC chemokines and their receptors in the synovium in rheumatoid arthritis

scientific article published on 29 November 2014

Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification.

scientific article published on 14 September 2017

Variable pathogenic potentials of mutations located in the desmin alpha-helical domain.

scientific article published on September 2006

Variants in the NOTCH1 gene in patients with aortic coarctation.

scientific article

Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner

scientific article published on 6 May 2015

List of works by Anna Kostareva

Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubes

Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness

Autotransplantation of cryopreserved ovarian tissue--effective method of fertility preservation in cancer patients.

Beta-catenin in schizophrenia: Possibly deleterious novel mutation.

Chicken rRNA Gene Cluster Structure

Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.

De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

Desmin mutations in a St. Petersburg cohort of cardiomyopathies

Different Notch signaling in cells from calcified bicuspid and tricuspid aortic valves

Early changes of gene expression profiles in the rat model of arterial injury

Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.

Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene.

Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing

Genetic spectrum of cardiomyopathies with neuromuscular phenotype.

Heparinase treatment of heparin-contaminated plasma from coronary artery bypass grafting patients enables reliable quantification of microRNAs

Heterogeneity of the nucleic acid repertoire of plasma extracellular vesicles demonstrated using high-sensitivity fluorescence-activated sorting

Mechanisms of Smooth Muscle Cell Differentiation Are Distinctly Altered in Thoracic Aortic Aneurysms Associated with Bicuspid or Tricuspid Aortic Valves

Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria

Modulation of insulin degrading enzyme activity and liver cell proliferation

NOTCH1 Mutations in Aortic Stenosis: Association with Osteoprotegerin/RANK/RANKL.

Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes.

Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve

Phenotypic and Functional Changes of Endothelial and Smooth Muscle Cells in Thoracic Aortic Aneurysms

Polymorphisms of β 1-adrenoreceptor gene and cardiovascular complications in patients with thyrotoxicosis

Primary Murine Myotubes as a Model for Investigating Muscular Dystrophy

Progressive cardiac conduction disease associated with a DSP gene mutation.

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

Regulation of nutrition-associated receptors in blood monocytes of normal weight and obese humans.

Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects.

Seventy years after the siege of Leningrad: does early life famine still affect cardiovascular risk and aging?

Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy

Synthesis of some CC chemokines and their receptors in the synovium in rheumatoid arthritis

Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification.

Variable pathogenic potentials of mutations located in the desmin alpha-helical domain.

Variants in the NOTCH1 gene in patients with aortic coarctation.

Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner