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Molecular Medicine Peer-reviewed scientific journal

Found: 338

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

GIANT CELL TUMOR OF THE SACRUM: RADIOLOGICAL AND MORPHOLOGICAL CHARACTERISTICS

Introduction. Giant cell tumors (GCT) of bones are benign tumors with the potential for the aggressive course and ability to metastasize. GCT accounts for approximately 5% of all primary bone tumors. Materials and methods. The clinical case of the patient L., …

10.29296/24999490-2019-04-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

POLYMORPHISM AND SYNERGISM OF THE HEMOSTASIS SYSTEM GENES IN PATHOGENESIS OF INFECTIVE ENDOCARDITIS

Introduction. The genetically determined tendency of patients to thrombosis may be one of the etiopathophysiological factors of the infective endocarditis (IE). Aim. А search for variants of genes and their combinations in the hemostatic system, the carriage o…

10.29296/24999490-2019-04-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

THE ROLE AND INTERACTION OF POLYMORPHIC VARIANTS OF NON-ALLELIC GENES KCNJ11, ADIPOQ, ITLN1, LEP, TCF7L2, PPARG IN THE INCREASE IN THE RISK OF DIABETES TYPE 2 IN KYRGYZ REPUBLIC

Aim. To study the intergenic interaction and estimate the contribution of polymorphic loci p.K23E (rs5219, KCNJ11), g.15661G>T (rs1501299, ADIPOQ), p.V109D (rs2274907, ITLN1), g.2453G>A (rs7799039, LEP), g.53341C>T (rs7903146, TCF7L2), and p.P12A (rs1801282, P…

10.29296/24999490-2019-04-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ANALYSIS OF POLYMORPHISM OF GENES OF THE HEMOSTASIS SYSTEM IN PREGNANT WOMEN SUFFERING A MIGRAINE

Introduction. The study of the genetic mechanisms of migraines is based on the investigation of genes of possible susceptibility and analysis of the influence of gene polymorphism in combination with environmental factors that form the pathogenetic chain of th…

10.29296/24999490-2019-03-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

FREQUENCY OF THE TERT RS2853669 POLYMORPHISM IN MELANOMA PATIENTS RESIDING IN THE EASTERN SIBERIA REGION

Introduction. The telomerase reverse transcriptase gene (TERT) promoter region is frequently mutated in different types of cancer. Several studies have shown patients who carry the mutation –245T>C (rs2853669) to have a worse prognosis. The aim of the study is…

10.29296/24999490-2019-05-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

COMPARATIVE CHARACTERISTICS OF THE SUSCEPTIBILITY OF KUPFFER CELLS AND MACROPHAGES OF BONE-BACKGROUND ORIGIN TO ACTIVATION FACTORS

Introduction. In mammals, there are several populations of macrophages, developing from bone marrow progenitors and resident macrophages, developing from the embryonic precursors of the yolk. One of the reasons for the coexistence of several populations of mac…

10.29296/24999490-2019-03-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ALLELES AND GENOTYPES DISTRIBUTION OF XENOBIOTIC BIOTRANSFORMATION GENES IN MOTHERS OF CHILDREN WITH CONGENITAL HEART DISEASES

Introduction. In this research the frequency of variant alleles of genes for xenobiotic biotransformation in women living in a highly urbanized region of Western Siberia and having children with congenital heart diseases was studied. Materials and methods. Wom…

10.29296/24999490-2019-06-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

AGE FEATURES OF THE EXPRESSION OF SIGNAL MOLECULES – PROTEIN P53, COLLAGEN TYPE II, VEGF AND VEGFR IN BIOPTATES OF INTACT MYOMETRY IN UTERINE MYOMA

Introduction. Leiomyomas also called fibroids, is the most common benign gynecological tumor in premenopausal women. The complex pathogenesis shows multiple biogenetical and multifactorial aspects to influence the etiology and growth of leiomyomas. A clinical …

10.29296/24999490-2019-06-11Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

OPTIMIZATION OF THE METHOD OF THE MULTI-TARGET SINGLE-BASE ELONGATION FOR THE DETECTION OF SOMATIC MUTATIONS IN MALIGNANCIES

Background. Genotyping of the tumor samples is necessary for a personalized approach in the treatment of patients with malignancies. The identification of somatic mutations in EGFR and KRAS genes can help to predict the course of the disease and to individuali…

10.29296/24999490-2019-02-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ACTIVATING POINT MUTATION OF BRCA1/2 GENES IN AZERBAIJAN POPULATION

Introduction. Breast cancer is the leading cancer type among woman of Azerbaijan population. Hereditary mutations of the BRCA1/2 genes are considered as high risk for appeared breast and ovarian cancers. In Azerbaijan BRCA1/2-related breast and ovarian cancer …

10.29296/24999490-2019-02-05Details ↗
ОБЗОР2019

THE ROLE OF NF-κB AND von HIPPEL-LINDAU PROTEIN IN THE CREATION OF A MOLECULAR PORTRAIT OF KIDNEY CANCERS

The review presents data on the role of the nuclear factor NF-κB and the von Hippel-Lindau protein (VHL) in the development of kidney cancer. Chemo- and radioresistance, specific for renal cell carcinoma, represented a significant problem in the treatment of p…

10.29296/24999490-2019-03-03Details ↗
ОБЗОР2019

THE ROLE OF NEUROTROPHIC FACTORS OF PLACENTA IN DEVELOPMENT OF THE FETUS BRAIN IN HYPERHOMOCYSTEINEMIA

This review article focuses on modern ideas about the role of neurotrophic factors (BDNF, NGF, NRG1, etc.) in the formation of the placenta and their impact on the development of the fetal nervous system in early ontogenesis. Data on the common effect of neuro…

10.29296/24999490-2019-03-01Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

MOLECULAR GENETIC ASPECTS OF THE RISK FOR FAMILY ADENOMATOUS POLYPOSIS

Introduction. The origin of the genetic predisposition to family adenomatous polyposis is associated with functional disorders of the repair system. The molecular mechanism of this phenomenon is not sufficiently studied and need clarification. The aim of the s…

10.29296/24999490-2018-06-11Details ↗

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