Submissions are open for the upcoming issue.

Molecular Medicine Peer-reviewed scientific journal

Found: 102

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOCIATION OF ADRENERGIC RECEPTORS GENES POLYMORPHISMS (ADRA2A, ADRB3) WITH OBESITY IN TATARS WOMEN

Association of adrenergic receptors gene polymorphisms in overweight persons has been shown by Gagnon J. et al. in 1996. For the locus Trp64Arg (rs4994) β3-adrenoceptor gene was shown to be associated with the risk of obesity, confirmed by the works of a numbe…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOCIATION OF INFECTIVE ENDOCARDITIS WITH GENE POLYMORPHISMS OF THE PHASE II XENOBIOTIC DETOXICATION SYSTEM ENZYMES

Introduction. Pathogenesis of infective endocarditis (IE) is not quite clear till now. In last years research of variants of the genes connected with pathogenesis of IE was performed. The aim. The investigation of IE association with gene single-nucleotide pol…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

POLYMORPHISM VARIANTS IN NOTCH1 AS PREDICTORS OF AORTIC INSUFFICIENCY IN PATIENTS WITH BICUSPID AORTIC VALVE

The aim of the study was to establish the contribution of NOTCH1 polymorphisms on the development of a combined bicuspid aortic valve and aortic coarctation. Design and Patients. The study included 34 patients, the control group consisted of 200 cases without …

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

THE PROFILE OF MICRORNA EXPRESSION IN LIVER IN CHRONIC HEPATITIS C PATIENTS AND THEIR ASSOCIATION WITH CLINICAL PARAMETERS

Introduction. Hepatitis C virus (HCV) is a major risk factor for chronic hepatitis, liver cirrhosis and hepatocellular carcinoma. Molecular mechanisms of fibrogenesis are associated with the activation or inhibition of signaling pathways, which are controlling…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOCIATION OF TREM-1 GENE POLYMORPHISMS WITH RISK OF CORONARY ARTERY DISEASE IN RUSSIAN POPULATION

Introduction. Atherosclerosis, manifesting itself as acute coronary syndrome, stroke, and peripheral artery disease, is a chronic progressive inflammatory disease driven by both innate and adaptive immunity. As Triggering Receptor Expressed on Myeloid Cells-1 …

Details ↗
ОБЗОР2017

EFFECT OF HUMAN MICROBIOTA ON THE CARDIOVASCULAR SYSTEM

In the presented review a new potential risk factor for atherosclerosis and cardiovascular disease such as microflora of the human gastrointestinal tract is considered. The modern concept of lipid metabolism and its effects on human health outlining the basic …

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ABERRANT METHYLATION OF PROMOTER REGIONS OF SOX7, P15INK4B AND WNT PATHWAY ANTAGONIST GENES IN PATIENTS WITH MYELODYSPLASTIC SYNDROME

Introduction. Hypermethylation of CpG islands in tumor-suppressor genes are supposed to be a key mechanism of the development of the myelodysplastic syndrome (MDS) The aim of the study. To determine the association between methylation status of SOX7, p15INK4b,…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

A SEARCH FOR MARKERS OF GENETIC SUSCEPTIBILITY TO THE DEVELOPMENT OF JOINT HYPERMOBILITY AND OSTEOARTHRITIS IN PATIENTS FROM THE BASHKORTOSTAN REPUBLIC

Introduction. Osteoartitis (OA) is the polyetiological disease pathogenesis of which is not fully understood. One of the risk factors for osteoarthritis may be connective tissue dysplasia, which is based on genetic defects of cartilage structures. The aim is t…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

MOLECULAR GENETIC AND PHENOTYPIC CHARACTERISTICS OF PATIENTS WITH LUNG ADENOCARCINOMA AMONG INHABITANTS OF THE SOUTH OF RUSSIA

Introduction. EGFR mutation and EML4-ALK fusion are the most clinically significant genetic alterations in non-small cell lung cancer. Numerous studies have been devoted to EGFR mutations and their association with phenotypic clinical and pathological characte…

Details ↗
ОБЗОР2016

PHARMACOGENETIC ASPECTS OF THE EFFICACY AND SAFETY OF HALOPERIDOL IN PATIENTS WITH ADDICTIVE DISORDERS

The use of haloperidol in clinical practice is often accompanied by the development of severe unwanted adverse side effects from the side of various organs and systems. In the narcological practice the use of antipsychotic drugs is not seldom complicated by ex…

Details ↗
ОБЗОР2016

COMMON DISEASE: ROLE OF GENETIC FACTORS AND NUTRIENTS

In this brief review there are considered possible reasons for the spread of disease of the multifactorial nature in modern populations from standpoints of the discordance between evolutionary formed genetic diversity and rapidly changing environmental factors…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

ASSOCIATIONS OF CANDIDATE GENES IN THE FORMATION OF UTERINE FIBROIDS

Introduction. Uterine fibroids – a benign tumor, growing from immature muscle cells of the vascular wall of the uterus. It ranked first among the benign tumors of the genital organs, with one in ten suffers from gynecological patients with uterine myoma. The a…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

MOLECULAR GENETIC MARKERS IN EVALUATING RISK OF OCCUPATIONAL DISEASES AMONG WORKERS IN THE CHEMICAL PRODUCTIONS

Introduction. Determination of the role of genetic markers in the formation of individual susceptibility to the effects of harmful chemicals both opens up new possibilities for assessing the risk of occupational and production-related diseases and address prev…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

GENERAL AND SPECIFIC IN THE GENOME OF PATIENTS WITH TYPE 1 AND TYPE 2 DIABETES

Introduction. Diabetes mellitus type 1 and type 2 are having a number similar etiological factors and certain resemblance in the mechanisms of the disease. Therefore it is important to try to estimate the role of common genetic component in the genesis and for…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

GENETIC AND MORPHOLOGICAL MARKERS OF NON-DEVELEPING PREGNANCY

Introduction. High rate of non-developing pregnancy in the structure of reproductive loss dictates the need to identify the etiological factors of this disease at different levels of organization of alive matter. The aim of the study. The search for associatio…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

ASSOCIATION BETWEEN XRCC1 ARG399GLN AND P53 ARG72PRO POLYMORPHIC MARKERS AND THE RISK OF BREAST CANCER RISK IN KYRGYZ WOMEN

Aim. To investigate the possible association between XRCC1 Arg399Gln and p53 Arg72Pro polymorphism and the risk of breast cancer (BC) risk in Kyrgyz women. Methods. The XRCC1 Arg399Gln and p53 Arg72Pro genotypes were determined with the use of the polymerase c…

Details ↗

Article search and quick navigation

Navigation