Anna Kostareva

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: EXPERIMENTAL CELL RESEARCH. 2024;442(1):114174
Flnc expression impacts mitochondrial function, autophagy, and calcium handling in C2C12 cells
Klimenko ES; Sukhareva KS; Vlasova YA; Smolina NA; Fomicheva YV; Knyazeva A; Muravyev AS; Sorokina MY; Gavrilova LS; Boldyreva LV; Medvedeva SS; Sejersen T; Kostareva AA
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2024;11:1321005
Molecular effects of cardiac contractility modulation in patients with heart failure of ischemic aetiology uncovered by transcriptome analysis
Lyasnikova E; Sukhareva K; Vander M; Zaitsev K; Firulyova M; Sergushichev A; Sorokina M; Trukshina M; Galenko V; Lelyavina T; Mitrofanova L; Simonova K; Abramov M; Faggian G; Luciani GB; Lebedev DS; Mikhaylov EN; Sitnikova M; Kostareva A
Article: CELL AND TISSUE RESEARCH. 2023;393(2):357-375
Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner
Sukhareva KS; Smolina NA; Churkina AI; Kalugina KK; Zhuk SV; Khudiakov AA; Khodot AA; Faggian G; Luciani GB; Sejersen T; Kostareva AA
Article: METHODS IN MOLECULAR BIOLOGY. 2023;2644:3-14
Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness.
Smolina N; Khudiakov A; Kostareva A
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2023;10:1216976
The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population
Kofeynikova O; Alekseeva D; Vershinina T; Fetisova S; Peregudina O; Kovalchuk T; Yakovleva E; Sokolnikova P; Klyushina A; Chueva K; Kostareva A; Pervunina T; Vasichkina E
Article: PLOS ONE. 2023;18(12):e0295974
In silico analysis of TRPM4 variants of unknown clinical significance
Tarnovskaya SI; Kostareva AA; Zhorov BS
Article: ORPHANET JOURNAL OF RARE DISEASES. 2022;17(1):358
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
Muravyev A; Vershinina T; Tesner P; Sjoberg G; Fomicheva Y; Cajbikova NN; Kozyreva A; Zhuk S; Mamaeva E; Tarnovskaya S; Jornholt J; Sokolnikova P; Pervunina T; Vasichkina E; Sejersen T; Kostareva A
Article: BIOCHEMISTRY AND BIOPHYSICS REPORTS. 2022;30:101249
Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome
Zaytseva AK; Kiselev AM; Boitsov AS; Fomicheva YV; Pavlov GS; Zhorov BS; Kostareva AA
Article: GENES. 2022;13(5):920
A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing
Gibitova EA; Dobrynin PV; Pomerantseva EA; Musatova EV; Kostareva A; Evsyukov I; Rychkov SY; Zhukova OV; Naumova OY; Grigorenko EL
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2022;9:932956
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
Perepelina K; Zaytseva A; Khudiakov A; Neganova I; Vasichkina E; Malashicheva A; Kostareva A
Article: FRONTIERS IN GENETICS. 2022;13:718853
Case Report: Loss-of-Function ABCC9 Genetic Variant Associated With Ventricular Fibrillation
Zaytseva A; Tulintseva T; Fomicheva Y; Mikhailova V; Treshkur T; Kostareva A
Article: FRONTIERS IN GENETICS. 2022;13:743472
Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63-Compound Heterozygous Variant
Andreeva S; Chumakova O; Karelkina E; Lebedeva V; Lubimtseva T; Semenov A; Nikitin A; Speshilov G; Kozyreva A; Sokolnikova P; Zhuk S; Fomicheva Y; Moiseeva O; Kostareva A
Article: CARDIOLOGY. 2022;147(1):35-46
Functional Analysis of SCN5A Genetic Variants Associated with Brugada Syndrome
Mikhailova VB; Karpushev AV; Vavilova VD; Klimenko ES; Tulintseva T; Yudina YS; Vasichkina ES; Zhorov BS; Kostareva A
Article: RESUSCITATION. 2021;168:176-185
Experimental paper The emergency medical service has a crucial role to unravel the genetics of sudden cardiac arrest in young, out of hospital resuscitated patients Interim data from the MAP-IT study
Tiesmeier J; Gaertner A; Homm S; Jakob T; Stanasiuk C; Bachmann-Mennenga B; Henzler D; Grautoff S; Veit G; Hori E; Kellner U; Gummert JF; Hitz MP; Kostareva A; Klingel K; Paluszkiewicz L; Laser KT; Pfeiffer H; Fox H; Milting H
Article: MEMBRANES. 2021;11(8):599
L-Type Calcium Channel: Predicting Pathogenic/Likely Pathogenic Status for Variants of Uncertain Clinical Significance
Tarnovskaya SI; Kostareva AA; Zhorov BS
Article: BIOMOLECULES. 2021;11(6):769
Regulatory Action of Plasma from Patients with Obesity and Diabetes towards Muscle Cells Differentiation and Bioenergetics Revealed by the C2C12 Cell Model and MicroRNA Analysis
Khromova NV; Fedorov AV; Ma Y; Kondratov KA; Prikhodko SS; Ignatieva EV; Artemyeva MS; Anopova AD; Neimark AE; Kostareva AA; Babenko AY; Dmitrieva RI
Article: GENES. 2021;12(1):94
RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart
Vakhrushev Y; Kozyreva A; Semenov A; Sokolnikova P; Lubimtseva T; Lebedev D; Smolina N; Zhuk S; Mitrofanova L; Vasichkina E; Kostareva A
Article: FRONTIERS IN PHARMACOLOGY. 2021;12:756415
Intersegment Contacts of Potentially Damaging Variants of Cardiac Sodium Channel
Korkosh VS; Zaytseva AK; Kostareva AA; Zhorov BS
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2021;8:647812
Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation
Khudiakov AA; Panshin DD; Fomicheva YV; Knyazeva AA; Simonova KA; Lebedev DS; Mikhaylov EN; Kostareva AA
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2021;8:668231
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children
Kovalchuk T; Yakovleva E; Fetisova S; Vershinina T; Lebedeva V; Lyubimtseva T; Lebedev D; Mitrofanova L; Ryzhkov A; Sokolnikova P; Fomicheva Y; Kozyreva A; Zhuk S; Smolina N; Zlotina A; Pervunina T; Kostareva A; Vasichkina E
Article: FRONTIERS IN PHARMACOLOGY. 2021;12:742508
Possible Interactions of Extracellular Loop IVP2-S6 With Voltage-Sensing Domain III in Cardiac Sodium Channel
Zaytseva AK; Boitsov AS; Kostareva AA; Zhorov BS
Article: BMC MEDICAL GENOMICS. 2020;13(1):175
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report
Zlotina A; Melnik O; Fomicheva Y; Skitchenko R; Sergushichev A; Shagimardanova E; Gusev O; Gazizova G; Loevets T; Vershinina T; Kozyrev I; Gordeev M; Vasichkina E; Pervunina T; Kostareva A
Article: GENES. 2020;11(11):E1343-1343
FLNC Expression Level Influences the Activity of TEAD-YAP/TAZ Signaling
Knyazeva A; Khudiakov A; Vaz R; Muravyev A; Sukhareva K; Sejersen T; Kostareva A
Article: BIOCHIMICA ET BIOPHYSICA ACTA - MOLECULAR BASIS OF DISEASE. 2020;1866(11):165915
Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene
Khudiakov A; Zaytseva A; Perepelina K; Smolina N; Pervunina T; Vasichkina E; Karpushev A; Tomilin A; Malashicheva A; Kostareva A
Article: GENES. 2020;11(10):E1201-1201
Two New Cases of Hypertrophic Cardiomyopathy and Skeletal Muscle Features Associated with ALPK3 Homozygous and Compound Heterozygous Variants
Jorholt J; Formicheva Y; Vershinina T; Kiselev A; Muravyev A; Demchenko E; Fedotov P; Zlotina A; Rygkov A; Vasichkina E; Sejersen T; Kostareva A
Article: CELLULAR PHYSIOLOGY AND BIOCHEMISTRY. 2020;54(4):696-706
Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes.
Gusev K; Khudiakov A; Zaytseva A; Perepelina K; Makeenok S; Kaznacheyeva E; Kostareva A
Article: STEM CELL RESEARCH. 2020;47:101895
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln
Perepelina K; Kostina A; Klauzen P; Khudiakov A; Rabino M; Crasto S; Zlotina A; Fomicheva Y; Sergushichev A; Oganesian M; Dmitriev A; Kostareva A; Di Pasquale E; Malashicheva A
Article: BIOCHIMICA ET BIOPHYSICA ACTA - MOLECULAR BASIS OF DISEASE. 2020;1866(6):165745
Desmin mutations result in mitochondrial dysfunction regardless of their aggregation properties
Smolina N; Khudiakov A; Knyazeva A; Zlotina A; Sukhareva K; Kondratov K; Gogvadze V; Zhivotovsky B; Sejersen T; Kostareva A
Article: JOURNAL OF EXTRACELLULAR VESICLES. 2020;9(1):1743139
Heterogeneity of the nucleic acid repertoire of plasma extracellular vesicles demonstrated using high-sensitivity fluorescence-activated sorting
Kondratov K; Nikitin Y; Fedorov A; Kostareva A; Mikhailovskii V; Isakov D; Ivanov A; Golovkin A
Article: CARDIOLOGY. 2020;145(11):746-756
Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients
Vershinina T; Fomicheva Y; Muravyev A; Jorholt J; Kozyreva A; Kiselev A; Gordeev M; Vasichkina E; Segrushichev A; Pervunina T; Sjoberg G; Skyttner-Rahmani S; Sejersen T; Kostareva A
Article: PLOS ONE. 2020;15(3):e0229227
Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments
Cimiotti D; Fujita-Becker S; Moehner D; Smolina N; Budde H; Wies A; Morgenstern L; Gudkova A; Sejersen T; Sjoeberg G; Muegge A; Nowaczyk MM; Reusch P; Pfitzer G; Stehle R; Schroder RR; Mannherz HG; Kostareva A; Jaquet K
Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2019;20(21):E5514-5514
Clinical Response to Personalized Exercise Therapy in Heart Failure Patients with Reduced Ejection Fraction Is Accompanied by Skeletal Muscle Histological Alterations
Lelyavina TA; Galenko VL; Ivanova OA; Komarova MY; Ignatieva EV; Bortsova MA; Yukina GY; Khromova NV; Sitnikova MY; Kostareva AA; Sergushichev A; Dmitrieva RI
Article: SCIENTIFIC REPORTS. 2019;9(1):12934
Interstitial cells in calcified aortic valves have reduced differentiation potential and stem cell-like properties
Bogdanova M; Zabirnyk A; Malashicheva A; Enayati KZ; Karlsen TA; Kaljusto M-L; Kvitting J-PE; Dissen E; Sullivan GJ; Kostareva A; Stenslokken K-O; Rutkovskiy A; Vaage J
Article: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 2019;516(3):777-783
Characterization of a novel SCN5A genetic variant A1294G associated with mixed clinical phenotype
Zaytseva AK; Karpushev AV; Kiselev AM; Mikhaylov EN; Lebedev DS; Zhorov BS; Kostareva AA
Article: FRONTIERS IN GENETICS. 2019;10:608
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy
Kiselev A; Vaz R; Knyazeva A; Sergushichev A; Dmitrieva R; Khudiakov A; Jorholt J; Smolina N; Sukhareva K; Fomicheva Y; Mikhaylov E; Mitrofanova L; Predeusu A; Sjoberg G; Rudenko D; Sejersen T; Lindstrand A; Kostareva A
Article: FRONTIERS IN PHYSIOLOGY. 2019;10:335
Atomic Mechanisms of Timothy Syndrome-Associated Mutations in Calcium Channel Cav1.2
Korkosh VS; Kiselev AM; Mikhaylov EN; Kostareva AA; Zhorov BS
Article: HUMAN MUTATION. 2018;39(9):1161-1172
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy
Kiselev A; Vaz R; Knyazeva A; Khudiakov A; Tarnovskaya S; Liu J; Sergushichev A; Kazakov S; Frishman D; Smolina N; Pervunina T; Jorholt J; Sjoberg G; Vershinina T; Rudenko D; Arner A; Sejersen T; Lindstrand A; Kostareva A
Article: ATHEROSCLEROSIS SUPPLEMENTS. 2018;35:e6-e13
Notch, BMP and WNT/β-catenin network is impaired in endothelial cells of the patients with thoracic aortic aneurysm
Kostina A; Bjork H; Ignatieva E; Irtyuga O; Uspensky V; Semenova D; Maleki S; Tomilin A; Moiseeva O; Franco-Cereceda A; Gordeev M; Faggian G; Kostareva A; Eriksson P; Malashicheva A
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2018;102(5):760-775
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.
Martin AR; Karczewski KJ; Kerminen S; Kurki MI; Sarin A-P; Artomov M; Eriksson JG; Esko T; Genovese G; Havulinna AS; Kaprio J; Konradi A; Korányi L; Kostareva A; Männikkö M; Metspalu A; Perola M; Prasad RB; Raitakari O; Rotar O; Salomaa V; Groop L; Palotie A; Neale BM; Ripatti S; Pirinen M; Daly MJ
Article: SCIENTIFIC REPORTS. 2018;8(1):2777
Altered DNA methylation indicates an oscillatory flow mediated epithelial-to-mesenchymal transition signature in ascending aorta of patients with bicuspid aortic valve
Bjorck HM; Du L; Pulignani S; Paloschi V; Lundstromer K; Kostina AS; Osterholm C; Malashicheva A; Kostareva A; Evangelista A; Teixido-Tura G; Maleki S; Franco-Cereceda A; Eriksson P
Article: FRONTIERS IN GENETICS. 2018;9:209
Rare Case of Ulnar-Mammary-Like Syndrome With Left Ventricular Tachycardia and Lack of TBX3 Mutation
Zlotina A; Kiselev A; Sergushichev A; Parmon E; Kostareva A
Article: FRONTIERS IN GENETICS. 2018;9:684
Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy
Knyazeva A; Krutikov A; Golovkin A; Mishanin A; Pavlov G; Smolina N; Hushkina A; Sejersen T; Sjoberg G; Galagudza M; Kostareva A
Article: FRONTIERS IN PHYSIOLOGY. 2018;9:1635
Inflammation and Mechanical Stress Stimulate Osteogenic Differentiation of Human Aortic Valve Interstitial Cells
Bogdanova M; Kostina A; Enayati KZ; Zabirnyk A; Malashicheva A; Stenslokken K-O; Sullivan GJ; Kaljusto M-L; Kvitting J-PE; Kostareva A; Vaage J; Rutkovskiy A
Article: AMINO ACIDS. 2017;49(11):1815-1829
Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy
Tarnovskaya S; Kiselev A; Kostareva A; Frishman D
Article: STEM CELL RESEARCH. 2017;24:85-88
Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene
Khudiakov A; Kostina D; Zlotina A; Yany N; Sergushichev A; Pervunina T; Tomilin A; Kostareva A; Malashicheva A
Article: STEM CELL RESEARCH. 2017;24:77-80
Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene
Khudiakov A; Kostina D; Zlotina A; Nikulina T; Sergushichev A; Gudkova A; Tomilin A; Malashicheva A; Kostareva A
Article: METHODS IN MOLECULAR BIOLOGY. 2017;1601:79-87
Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness.
Smolina N; Bruton J; Kostareva A; Sejersen T
Article: BIOMED RESEARCH INTERNATIONAL. 2017;2017:6917907-10
NOTCH1 Mutations in Aortic Stenosis: Association with Osteoprotegerin/RANK/RANKL
Irtyuga O; Malashicheva A; Zhiduleva E; Freylikhman O; Rotar O; Back M; Tarnovskaya S; Kostareva A; Moiseeva O
Article: BIOMOLECULAR DETECTION AND QUANTIFICATION. 2016;8:9-14
Heparinase treatment of heparin-contaminated plasma from coronary artery bypass grafting patients enables reliable quantification of microRNAs.
Kondratov K; Kurapeev D; Popov M; Sidorova M; Minasian S; Galagudza M; Kostareva A; Fedorov A
Article: PLOS ONE. 2016;11(9):e0163362
Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing
Kostareva A; Kiselev A; Gudkova A; Frishman G; Ruepp A; Frishman D; Smolina N; Tarnovskaya S; Nilsson D; Zlotina A; Khodyuchenko T; Vershinina T; Pervunina T; Klyushina A; Kozlenok A; Sjoberg G; Golovljova I; Sejersen T; Shlyakhto E
Article: MOLECULAR CYTOGENETICS. 2016;9:18
Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects
Zlotina A; Nikulina T; Yany N; Moiseeva O; Pervunina T; Grekhov E; Kostareva A
Article: MOLECULAR GENETICS AND METABOLISM. 2015;115(2-3):118-127
Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner
Malashicheva A; Bogdanova M; Zabirnyk A; Smolina N; Ignatieva E; Freilikhman O; Fedorov A; Dmitrieva R; Sjoberg G; Sejersen T; Kostareva A
Article: BIOMED RESEARCH INTERNATIONAL. 2015;2015:127807-3
Congenital Heart Defects Are Rarely Caused by Mutations in Cardiac and Smooth Muscle Actin Genes
Khodyuchenko T; Zlotina A; Pervunina T; Zverev D; Malashicheva A; Kostareva A
Article: BIOMED RESEARCH INTERNATIONAL. 2015;2015:594751-12
Primary Murine Myotubes as a Model for Investigating Muscular Dystrophy
Smolina N; Kostareva A; Bruton J; Karpushev A; Sjoberg G; Sejersen T
Article: CELL CALCIUM. 2014;56(4):269-275
Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubes
Smolina N; Bruton J; Sjoberg G; Kostareva A; Sejersen T
Article: CONGENITAL HEART DISEASE. 2014;9(5):391-396
Variants in the NOTCH1 Gene in Patients with Aortic Coarctation
Freylikhman O; Tatarinova T; Smolina N; Zhuk S; Klyushina A; Kiselev A; Moiseeva O; Sjoberg G; Malashicheva A; Kostareva A
Article: JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY. 2014;25(5):789-796.e7
Early Changes of Gene Expression Profiles in the Rat Model of Arterial Injury
Fedorov A; Kostareva A; Raud J; Roy J; Hedin U; Razuvaev A
Article: PEDIATRIC CARDIOLOGY. 2013;34(2):467-470
Diagnostic Challenge in Desmin Cardiomyopathy With Transformation of Clinical Phenotypes
Gudkova A; Kostareva A; Sjoberg G; Smolina N; Turalchuk M; Kuznetsova I; Rybakova M; Edstrom L; Shlyakhto E; Sejersen T
Article: ACTA MYOLOGICA. 2011;30(1):42-45
Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.
Kostareva A; Sjoberg G; Gudkova A; Smolina N; Semernin E; Shlyakhto E; Sejersen T
Article: JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY. 2008;29(1):25-36
Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria
Kostareva A; Sjoberg G; Bruton J; Zhang S-J; Balogh J; Gudkova A; Hedberg B; Edstrom L; Westerblad H; Sejersen T
Article: ACTA MYOLOGICA. 2006;25(3):109-115
Desmin mutations in a St. Petersburg cohort of cardiomyopathies.
Kostareva A; Gudkova A; Sjoberg G; Kiselev I; Moiseeva O; Karelkina E; Goldfarb L; Schlyakhto E; Sejersen T
Article: HUMAN MUTATION. 2006;27(9):906-913
Variable pathogenic potentials of mutations located in the desmin alpha-helical domain
Goudeau B; Rodrigues-Lima F; Fischer D; Casteras-Simon M; Sambuughin N; de Visser M; Laforet P; Ferrer X; Chapon F; Sjoberg G; Kostareva A; Sejersen T; Dalakas MC; Goldfarb LG; Vicart P
Article: EXPERIMENTAL CELL RESEARCH. 2006;312(9):1554-1565
Forced expression of desmin and desmin mutants in cultured cells:: Impact of myopathic missense mutations in the central coiled-coil domain on network formation
Baer H; Kostareva A; Sjoeberg G; Sejersen T; Katus HA; Herrmann H
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2005;102(42):15099-15104
Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages
Bär H; Mücke N; Kostareva A; Sjöberg G; Aebi U; Herrmann H
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Review: PFLUGERS ARCHIV EUROPEAN JOURNAL OF PHYSIOLOGY. 2024;476(5):735-753
Biophysical mechanisms of myocardium sodium channelopathies
Zaytseva AK; Kulichik OE; Kostareva AA; Zhorov BS
Review: FRONTIERS IN PHARMACOLOGY. 2022;13:835825
Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
Bogdanova M; Zabirnyk A; Malashicheva A; Semenova D; Kvitting J-PE; Kaljusto M-L; Perez MDM; Kostareva A; Stenslokken K-O; Sullivan GJ; Rutkovskiy A; Vaage J
Review: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2021;22(14):7349
Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype
Ignatieva E; Smolina N; Kostareva A; Dmitrieva R
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2016;216:188-189
Progressive cardiac conduction disease associated with a DSP gene mutation
Kiselev A; Mikhaylov E; Parmon E; Sjoberg G; Sejersen T; Tarnovskaya S; Nugnyi P; Mitrofanova L; Lebedev D; Kostareva A
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2015;184:272-273
Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes
Pervunina T; Vershinina T; Kiselev A; Nikitina I; Grekhov E; Mitrofanova L; Sjoberg G; Kostareva A
Review: FRONTIERS IN BIOSCIENCE-SCHOLAR. 2013;5(1):325-340
Genetic spectrum of cardiomyopathies with neuromuscular phenotype.
Kostareva A; Sejersen T; Sjoberg G
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2009;131(3):410-412
Deletion in TNNI3 gene is associated with restrictive cardiomyopathy
Kostareva A; Gudkova A; Sjoberg G; Morner S; Semernin E; Krutikov A; Shlyakhto E; Sejersen T
Thesis / dissertation: 2007
Genetic and pathophysiological study of desmin derangements in cardiac disorders
Kostareva, Anna
Review: LAKARTIDNINGEN. 2005;102(11):845-853
[Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
Sjöberg G; Kostareva A; Sejersen T

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Anknuten till Forskning, Kvinnors och barns hälsa, Karolinska Institutet, 2024-2027

Examina och utbildning

MEDICINE DOKTORSEXAMEN, Institutionen för kvinnors och barns hälsa, Karolinska Institutet, 2007

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