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Molecular Medicine Peer-reviewed scientific journal

Found: 128

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

EXPRESSION OF AORTA ENDOTHELIUM SIGNALING MOLECULES IN AGEING AND ATHEROSCLEROSIS

Introduction. Atherosclerosis proves to be age-dependent and social significant pathology. Knowledge of the role of signaling molecules in its development, and the elaboration on this basis molecular markers of restenosis after stenting of arteries remains to …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

MOLECULAR ASPECTS OF IN VITRO VESSELS AGING

Introduction. Understanding of molecular and cellular mechanisms of vessels aging is the base of new approach creating of drugs for cardio-vascular pathology treatment. The goal of this work is the investigation of molecular and cellular mechanisms of vessels …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

CONCENTRATION OF INTERLEUKINES IN BLOOD PLASMA IN PATIENTS WITH CHRONIC CEREBRAL ISCHEMIA – CARRIERS OF ANTI-INFLAMMATORY CYTOKINES GENES POLYMORPHISMS

Introduction. There were examined 195 patients with chronic сerebrovasсular pathology and 149 healthy residents of the Zabaykalsky region. The aim of the study. Detection of genetic polymorphism in cytokines IL4-589С>T, IL10-1082G>A, IL10-819C>T, IL10-592C>A, …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

PREDICTION THE RISK OF ISCHEMIC STROKE ON THE BASE ON GENETIC [APOE (Ε2, Ε3, Ε4), ACE (I / D), MTHFR (677S> T)] AND NON-GENETIC FACTORS WITH THE USE OF MODERN METHODS OF THE THEORY OF RECOGNITION BY PRECEDENTS

Introduction. Ischemic stroke (IS) is a multifactorial disease, resulting from a complex interaction of genetic and environmental factors. Individual cause of the disease, multiple factors and symptoms require advanced mathematical methods of predicting IS ris…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

CLINICAL AND GENETIC CHARACTERISTICS OF RUSSIAN PATIENTS WITH LYNCH SYNDROME

Aim. Lynch Syndrome, which is caused by a defect in one of the mismatch repair (MMR) genes, is the most common among all hereditary colorectal cancer syndromes. Patients with Lynch syndrome in different populations are inherent in both genetic and clinical fea…

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Research article2014

METHYLATION INVOLVEMENT IN REGULATION OF EXPRESSION OF FUNCTIONALLY SIGNIFICANT GENES ON CHROMOSOME 3: RHOA, GPX1, USP4, DAG1, NKIRAS1 IN BREAST CANCER

Introduction. Epigenetic changes caused by methylation in promoter CpG-islands are a fine and dynamic mechanism of gene expression regulation in tumors. Increased and decreased expression and alterations in the methylation status of the gene are considered to …

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Research article2014

APPLICATION OF NGS METHOD FOR ACVR2A GENE SEQUENCING IN WOMEN WITH PREECLAMPSIA

Introduction. Preeclampsia is one of the most frequent complications of pregnancy. Disease is based on the pathology of the vascular system of a pregnant woman. One of the candidate genes of preeclampsia is a gene encoding a protein receptor type 2A to activin…

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Research article2014

HOW TO TEACH A PHYSICIAN-PATHOLOGIST? PATHOPHYSIOLOGY TRANSFORMS INTO SYSTEMS PATHOBIOLOGY SERVING AN INTRODUCTION INTO TRANSLATIONAL MEDICINE

Pathophysiology as a science and curriculum discipline stands in front of the biggest challenge in its history. It extended farbeyond the limits of its historical name and embedded aspects of Pathochemistry, Immunopathology, Pathobiophysics and Pathoinformatic…

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Research article2014

EFFECT OF VAL66MET BDNF ALLELIC POLYMORPHISM ON DYNAMICS OF THE BDNF SERUM LEVEL AND PERFORMANCEOF THE RAVEN’S TEST IN PATIENTS WITH STROKE

Introduction.Study of the influence of molecular and genetic predisposition to forecast neurorehabilitation patients with stroke is of great scientific and practical importance. The aim of the study.Determining the impact of allelic polymorphism Val66Met BDNF …

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Research article2014

MUTATIONS IN ONCOGENES GNAQ AND GNA11 IN UVEAL MELANOMA PATIENTS

Introduction.Uveal melanoma (UM) is one of the most frequent intraocular tumors. Mutations in new oncogenes GNAQ and GNA11 are found in more than 50% of UM. GNAQ gene and its homologue GNA11 are coding the alpha subunit of heterotrimeric G-protein with GTPase …

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Research article2013

Val66Met BDNF POLYMORPHISM IN PATIENTS WITH A HIGH RISKOF MORTALITY DUE TO STROKE AND SEVERE TRAUMATIC BRAIN INJURY

We have studied BDNF gene Val66Met polymorphism in patients with a high risk of mortality due to stroke or severe head injury. Genotype ValVal rate was higher than that of in the control group in the total sample of subjects (75,5% and 63,6%; χ2=4,63; df=1; p=…

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Research article2013

ANALYSIS OF GENETIC POLYMORPHISMS IN ESTROGENMETABOLIZING ENZYMES IN OVARIAN CANCER PATIENTS IN THE SIBERIA REGION

Early diagnosis of ovarian cancer (OC) remains to be the actual problem in modern oncology due to the high mortality rate, asymptomatic course of the disease in the early stages and its aggressiveness. The aim was to study the genetic polymorphism of pathogene…

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Research article2013

THE OBESITY: THE MOLECULAR MECHANISMS AND THE OPTIMIZATION OF TARGET THERAPY

The article reviews modern data on the participation of signaling molecules in the pathogenesis of obesity. This review provides the detailed description of the functional morphology of adipose tissue as the major endocrine and immune organ. The imbalance in p…

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