А. А. Морозов

ORCID: 0000-0001-9350-8804
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About
Contact & Profiles
Research Areas
  • Congenital Heart Disease Studies
  • Pulmonary Hypertension Research and Treatments
  • Vascular anomalies and interventions
  • Cardiovascular and Diving-Related Complications
  • Cancer Cells and Metastasis
  • Venous Thromboembolism Diagnosis and Management
  • Congenital Diaphragmatic Hernia Studies
  • Congenital heart defects research
  • Medical and Biological Sciences
  • Hip and Femur Fractures
  • Cardiomyopathy and Myosin Studies
  • Protease and Inhibitor Mechanisms
  • Sarcoma Diagnosis and Treatment
  • Pleural and Pulmonary Diseases
  • Chronic Kidney Disease and Diabetes
  • Atomic and Subatomic Physics Research
  • Cardiac Valve Diseases and Treatments
  • Neurogenetic and Muscular Disorders Research
  • RNA modifications and cancer
  • Dermatologic Treatments and Research
  • Viral-associated cancers and disorders
  • Urinary and Genital Oncology Studies
  • Graphene and Nanomaterials Applications
  • Cancer Research and Treatments
  • Cardiac Structural Anomalies and Repair

Federal Almazov North-West Medical Research Centre
2017-2023

City Children's Hospital No. 22
2021-2023

Ministry of Health of the Russian Federation
2023

Federal State Budgetary Institution "Federal Center For Cardiovascular Surgery" Ministry of Health of The Russian Federation
2021

Moscow State University of Medicine and Dentistry
2017

Eli Lilly (United States)
2012

Memorial Sloan Kettering Cancer Center
2010

Kettering University
2009-2010

Matrix metalloproteinases (MMPs) are a family of zinc-containing endopeptidases that catalyze the degradation reactions extracellular matrix components. In humans, 23 enzymes this known, which subdivided into 6 groups based on their structure and substrate types: collagenases, gelatinases, stromelysins, matrilizines, MMP membrane type other MMPs. functions diverse, an imbalance activity may be one etiological factors various diseases. The review considers classification, regulation genetic...

10.18786/2072-0505-2017-45-4-266-279 article EN cc-by Almanac of Clinical Medicine 2017-01-01

Abstract Purpose: Recent evidence suggests that at least some sarcomas arise through aberrant differentiation of mesenchymal stromal cells (MSCs), but MSCs have never been isolated directly from human sarcoma specimens. Experimental Design: We examined cell lines and primary adherent cultures derived surgical samples for features MSCs. further characterized as either benign or malignant by the presence tumor-defining genetic lesions tumor formation in immunocompromised mice. Results: show a...

10.1158/1078-0432.ccr-09-2886 article EN Clinical Cancer Research 2010-12-01

Матриксные металлопротеиназы (ММП) - ферменты класса гидролаз, осуществляющие ферментативный катализ с помощью связанного в активном центре иона цинка. Функции ММП разнообразны, и нарушение баланса их активности может быть одним из этиологических факторов различных заболеваний. В данном обзоре рассмотрена классификация человека, особенности структуры регуляции, а также роль физиологических патологических процессах организме человека. Приведен перечень наиболее изученных на настоящий момент...

10.25557/gm.2017.2.7297 article RU Nauchno-prakticheskii zhurnal «Patogenez» 2017-10-02

5012 Background: VEGF receptor-mediated-signaling contributes to ovarian cancer pathogenesis. Elevated expression and serum levels are associated with poor clinical outcomes. We investigated RAM, a fully human VEGFR-2 antagonist antibody, in patients (pts) persistent or recurrent EOC/FTC/PPC. Methods: Adult women EOC/FTC/PPC who had completed ≥1 platinum (P)-based chemotherapeutic (ct) regimen P-free interval (PFI) of <12 months (m), progression on, disease after P-based therapy were...

10.1200/jco.2012.30.15_suppl.5012 article EN Journal of Clinical Oncology 2012-05-20

Introduction . TAPVC is a condition that requires diagnosis and surgical treatment in short period of time. As the result an absence direct connection between pulmonary veins left atrium, systemic venous return drainage to right heart with volume pressure overload. At same time, preload depending on atrial septal defect. The hemodynamic features create conditions for abnormal spread electric impulses, whereas necessity reconstruction level — reasons rhythm conduction disturbance...

10.18705/2782-3806-2023-3-2-23-30 article EN cc-by Russian Journal for Personalized Medicine 2023-05-19

Clinical data of a 39-year-old patient with corrected transposition the great arteries, combined complete atrioventricular block and conduction along an accessory pathway, are presented. The features changes in structure system, rhythm characteristic this rare congenital heart disease discussed.

10.35336/va-2023-2-14 article EN cc-by Journal of Arrhythmology 2023-06-27

Abstract Introduction: Mesothelioma is an aggressive malignancy which spreads via local invasion. We have observed fine, long, non-adherent cable-like structures connecting mesothelioma cells in vitro are consistent with tunneling nanotubes, entity recently described malignant as well neuronal and immune cells. hypothesized that nanotubes facilitate intercellular communication between distant neighboring transfer of intracellular components. Materials Methods: Biphasic sarcomatoid cells,...

10.1158/1538-7445.am10-4814 article EN Cancer Research 2010-04-01

The clinical experience of performing ventriculoatrial shunting in children with hydrocephalus tumor etiology the Department Neurosurgery Children Almazov National Medical Research Centre is presented. Intraoperative and postoperative echocardiographic monitoring suggested as main method distal (atrial) catheter system.

10.18705/2311-4495-2018-5-1-36-43 article EN cc-by Translational Medicine 2018-05-12

Aim. Description of three clinical cases pediatric patients with dilated cardiomyopathy (DCMP) and an analysis their genetic causes. Material methods . Using the method targeted sequencing, data were obtained on presence pathogenic variants RBM20 gene in DCMP. Results. Three childhood DCMP development, associated structural disorders gene, are particularly described. It is known that involved splicing mRNA TTN encoding titin protein. A disorder can lead to a change biomechanical signaling...

10.15829/1560-4071-2019-10-92-99 article EN cc-by Russian Journal of Cardiology 2019-11-03

<h3>ЦЕЛЬ ИССЛЕДОВАНИЯ</h3> Представить результаты анатомической коррекции транспозиции магистральных артерий (ТМА) за период с 1992 по 2021 г. <h3>МАТЕРИАЛ И МЕТОДЫ</h3> Исследование включало 504 ребенка ТМА, из них у 120 (23,8%) больных порок был ассоциирован дефектом межжелудочковой перегородки (ДМЖП), 60 (11,9%) пациентов сочетался ДМЖП и обструкцией дуги аорты. Всем детям была выполнена одномоментная коррекция ТМА методом артериального переключения, а также сопутствующих внутрисердечных...

10.17116/kardio202215041361 article RU Russian Journal of Cardiology and Cardiovascular Surgery 2022-01-01

O bjective. Pulmonary hypertension is one of the typical complications congenital heart defects with pulmonary overload circulation. Hemodynamic status circulation critically important for patients univentricular anatomy and determines opportunities results surgical treatment. Case report. We present a case report superior vena cava syndrome feigning thrombosis anastomosis in patient after Glenn procedure. Clear clinical picture, hemodynamic instability inability to exclude dysfunction were...

10.18705/1607-419x-2015-21-1-89-92 article EN Arterial’naya Gipertenziya (Arterial Hypertension) 2015-01-01

Pulmonary atresia with defect of interventricular septum and collateral pulmonary blood flow refers to complicated congenital malformation the heart. Surgical treatment represents itself as very difficult task because anatomical variability this abnormality. The main problem surgery is a definitive repair including correction maldistributions arterial bed (unifocalization flow), reconstruction outflow tract right ventricle closing defect. performance could be successful in patients case...

10.24884/0042-4625-2015-174-4-9-12 article EN cc-by Grekov s Bulletin of Surgery 2015-08-28

Some cancers carry massive genomic rearrangements, confined to one chromosomal region, that are thought arise in a single event.

10.1126/scitranslmed.3002126 article EN Science Translational Medicine 2011-01-19

The article presents a rare case of combination Ebstein’s anomaly and primary cardiomyopathy in 14-year-old teenager. clinical demonstrates diagnostic difficulties due to an unusual picture, as well interpretation choice treatment tactics.

10.18705/2782-3806-2023-3-2139-147 article EN cc-by Russian Journal for Personalized Medicine 2023-05-20

Neonatal lupus is a rare disease associated with the circulation in mother’s blood of one or more autoantibodies to soluble intracellular ribonucleoproteins Ro/SS-A and La/SS-B. This extremely often manifested by congenital heart block, which can progress even after birth child. We have described case fibrosis, calcification cartilaginous metaplasia atrioventricular node zone, caused complete block child who died from neonatal lupus.

10.35336/va-2023-2-10 article EN cc-by Journal of Arrhythmology 2023-06-27

Whole-genome sequencing will soon become easily available, but many challenges lie ahead.

10.1126/scitranslmed.3001227 article EN Science Translational Medicine 2010-05-05

Abstract Background: Mesenchymal Stem Cells (MSCs) have been proposed as the cell of origin sarcoma. In soft tissues, microvascular pericyte has recently shown to MSC properties (Crisan et al, Cell 3:301). We previously reported isolation benign mesenchymal cultures from sarcoma surgical samples. These cells immunophenotype (CD45-CD31- CD73+CD105+CD90+) and in vitro differentiation potential characteristic MSCs. hypothesized that these sarcoma-associated MSCs (SA-MSCs) are derived pericytes...

10.1158/1535-7163.targ-09-c250 article EN Molecular Cancer Therapeutics 2009-12-01

Collagen-secreting cells in kidney fibrosis may be derived from microvascular pericytes the stroma rather than through an epithelial-to-mesenchymal transition.

10.1126/scitranslmed.3001078 article EN Science Translational Medicine 2010-03-24
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