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Molecular Medicine Peer-reviewed scientific journal

Found: 202

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

BONE AND MALIGNANT DISEASES OF UTERINE: PROFILE OF EXPRESSION OF GENES OF STEROID RECEPTORS AND TUMOR SUPPRESSOR PTEN

Introduction. Myoma occupies a leading place in the structure of gynecological diseases, reduces the fertility rate and living standardsin females of reproductive age. In 85% cases myoma is combined with adenomyosis, which complicates the treatment and increas…

10.29296/24999490-2018-03-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE ROLE OF P53 AND NOXA IN THE PATHOGENESIS OF EARLY MISCARRIAGES

Introduction. Missed and spontaneous abortions are one of the most important causes of the reproductive loss. The aim of the study: to study specialties of mRNA expression of p53 and proteins of its signaling pathway in the decidual tissue at 6–10 weeks of ges…

10.29296/24999490-2018-03-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE ANALYSIS OF RASSF1A AND SEMA3B TUMOR SUPRESSOR GENES CPG-ISLANDS METHYLATION STATUS IN UVEAL MELANOMA PATIENTS

Introduction. Uveal melanoma (UM) is a tumor of neuroectodermal origin developing from melanocytes of the uveal tract. The very common pathological characteristic of UM is its metastatic activity in liver, leading to the poor efficiency of the treatment. That`…

10.29296/24999490-2018-01-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

PROTEOMIC PROFILING OF ESCHERICHIA COLI, ISOLATED FROM CROHN’S DISEASE PATIENTS

Introduction. A possible pathogenesis for Crohn’s disease (CD) involves the provocation of uncontrollable immune response by intestinal microbiota. Escherichia coli is regarded as a candidate for possible pathogen, since its content is increased in intestine o…

10.29296/24999490-2018-01-04Details ↗
ПЕРЕДОВАЯ СТАТЬЯ2018

PHARMACOLOGICAL TREATMENT OF PARKINSON’S DISEASE: MOLECULAR ASPECTS AND PROSPECTS

Parkinson’s disease (PD) is a progressive, age-related, neuronal disorder that affects as much as 1% of the persons over 65 years. According to forecasts of the World Health Organization over the world about 9 million people will suffer from PD by 2030. So PD …

10.29296/24999490-2018-02-01Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ACTIVITY OF HIF PATHWAY IN EPIDERMIS AS CONTROL FACTOR FOR SKIN VASCULATURE

Introduction. The physiological state of the skin vasculature is largely determined by the influence of environmental factors, including the alteration of the oxygen partial pressure. Obviously, the epidermis, as the surface layer of the skin, should play a ke…

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ОБЗОР2017

THE ROLE OF MOLECULAR AND GENETIC FACTORS IN UVEAL MELANOMA PATHOGENESIS

Uveal melanoma (UM) is a rare, aggressive intraocular malignant tumor, leading to metastatic disease in more than 50% of patients. Cytogenetic and molecular studies have identified some genetic prognostic factors considered to be reliable to forecast the survi…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

NEW TRANSLATIONAL MODEL OF COGNITIVE DEFICIT IN SCHIZOPHRENIA

Introduction. Taken into account the literature data on the leading role of perceptual deficit in the pathogenesis of schizophrenia and the lack of experimental models of this impairment we proposed the novel test of instinctive aversion (TIA). The work was pe…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

TOLL-LIKE RECEPTOR-4 GENETIC POLYMORPHISM IN ERYSIPELAS PATIENTS

Introduction. Erysipelas is characterized by consistently high morbidity rate, pronounced tendency to recur, the frequent change of lymph circulation, formation of secondary elephantiasis and others symptoms. The prediction of the course of erysipelas is unres…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

CHARCTERISTICS OF CHANGES OF COLLGEN MAIN TYPES I–VI IN CALCIFIC AORTIC VALVE STENOSIS PATHOGENESIS

Introduction. The gain of elderly persons in the population of industrial countries provides a high actuality to investigations of pathogenesis of calcific aortic valve stenosis (CAVS). The aim of the study. To specify the quality and quantity pattern of colla…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

CLINICAL IMPLICATION OF SERUM INSULIN-LIKE GROWTH FACTORS (IGF) AND IGF BINDING PROTEINS IN COLORECTAL CANCER PATIENTS

Introduction. Insulin-like growth factor (IGF) signaling system plays a major role in development and progression of various malignant tumors including colorectal cancer (CRC), so far its components are considered as potential diagnostic and prognostic markers…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

CHARACTERISTICS OF DNA-METHYLATION IN UTERINE FIBROIDS

Introduction authors made an attempt to demonstrate the role of DNA-methylation in pathogenesis of uterine fibroids. The epigenetic aspects based on personal investigations and literary data have been reviewed. The research underlined a perspective of investig…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

EXPRESSION RATES OF THE CASPASE 3,6,8 AND 9 GENES IN PERIPHERAL BLOOD LEUKOCYTES IN HEALTHY DONORS AND PATIENTS WITH NONALCOHOLIC FATTY LIVER DISEASE IN THE ABSENCE OF HEPATOPROTECTIVE THERAPY AND AFTER THERAPY WITH URSODEOXYCHOLIC ACID

Introduction. The contribution of caspase-dependent apoptosis in the pathogenesis of nonalcoholic fatty liver disease (NAFLD) is not fully understood. One possible mechanism of hepatoprotective action of ursodeoxycholic acid (UDCA) is the suppression of apopto…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

MOLECULAR AND MORPHOLOGICAL EFFECTS OF PREOPERATIVE HYPOFRACTIONATION FOR RECTAL CANCER

Introduction. Radiotherapy becomes a standard of combination treatment of the rectal cancer. That is why the development of its pathogenetical bases is very impotent. The aim of the study. The purpose of the study was to analyze molecular and morphological eff…

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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…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

TWO NOVEL MUTATIONS IN THE SLC37A4 GENE IN A CHILD WITH GLYCOGEN STORAGE DISEASE TYPE IB

Introduction. Glycogen storage disease (GSD) type Ib is caused by mutations in the SLC37A4 gene. The aim of the study. To verify the diagnosis by molecular genetic studies. Patient. Child at the age of 5 years and 8 months with severe hepatomegaly, nephromegal…

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