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Molecular Medicine Peer-reviewed scientific journal

Found: 113

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 ↗
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 ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

ASSOCIATION OF GENETIC MARKERS WITH THE DEVELOPMENT OF ENDOCARDITIS OF NONINFECTIOUS AND INFECTIOUS ETIOLOGY

Introduction. New technologies of DNA genotyping and sequencing contribute to the rapid accumulation of our knowledge about human genomic variations and search for inherited determinants of complex genetic traits. There is a large amount of data on association…

10.29296/24999490-2018-06-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

PROTECTION OF NEURAL STEM CELLS FROM GENOTOXIC EFFECTS BY FACTORS SECRETED BY MESENCHYMAL STEM CELLS

Introduction. The brain injury induced during radiotherapy and chemotherapy is largely dependent on a disruption of neurogenesis in the subgranular zone of the dentate gyrus in the hippocampus as a result of the neural stem cells (NSCs) damage. The aim of the …

10.29296/24999490-2018-06-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

POLYMORPHISM OF VEGF-A GENES AND THE RISK OF THE DEVELOPMENT OF THE EXUDATIVE AGE-RELATED MACULAR DEGENERATION

Introduction. Age-related macular degeneration (AMD), in particular, its exudative form, has for many years held a leading position in the causes of the loss of visual acuity and leads to blindness in 90% of elderly cases. The loss of central vision is based o…

10.29296/24999490-2018-05-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE EXPRESSIVE METHOD OF DNA ISOLATION FROM FROZEN BLOOD

Introduction. Mass genotyping, aimed both at identifying of genetic characteristics of populations and the creation of genomic libraries, scientific research, was implemented on large samples, required the accumulation and/or conservation of samples of the bio…

10.29296/24999490-2018-05-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE NEW MOLECULAR GENETIC MARKERS OF THE SUDDEN CARDIAC DEATH IDENTIFIED BY NEXT-GENERATION SEQUENCING

The aim of the study is an investigation of the association between mutations A1744S of MYH7, 9928_9929insE of TTN, T171M of CACNA1C, A189T of JPH2, S434Y of VCL, H4552R of RYR2, Y1495X of SCN5A and the sudden cardiac death (SCD). Investigating mutations were …

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

EVALUATION OF THE ROLE OF POLYMORPHIC VARIANTS OF NO-SYNTHASES GENES OF IN PATHOGENESIS OF PSORIASIS

The aim of the study was to analyze two single nucleotide substitutions in the NOS2 (rs2779249, c-1290G>T, 5'-region) and NOS3 (rs2070744, c-813C>T, in tron 1) genes in psoriasis patients. Materials and methods. DNA samples from 88 psoriasis patients and 365 c…

10.29296/24999490-2018-04-11Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

PHARMACOGENETIC TESTING BY POLYMORPHIC MARKERS G1846A (CYP2D6*4) AND C100T (CYP2D6*10) CYP2D6 GENE IN CORONARY HEART DISEASEPATIENTS, TAKING BETA-BLOCKERS IN THE SAKHA REPUBLIC (YAKUTIA)

Introduction. The aim of this study to determine carrier frequencies of polymorphic markers G1846A (CYP2D6*4) and C100T (CYP2D6*10) of the CYP2D6 gene in coronary heart disease (CHD) patients in Russian and Yakut ethnic groups. The association between theadmin…

10.29296/24999490-2018-04-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE PREVALENCE OF CYP2C19*2, *3 POLYMORPHISMS AMONG RUSSIANS AND YAKUTS WITH PEPTIC ULCER DISEASE, LIVING IN SAKHA REPUBLIC (YAKUTIA)

Introduction. Proton pump inhibitors (PPI) are widely spread as antisecretory drugs for a treatment of acid diseases, such as the gastric ulcer. Most of the proton pump inhibitors are inactivated in the liver by cytochromes P450 2C19 (CYP2C19) to the form of i…

10.29296/24999490-2018-04-06Details ↗
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 ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

THE CYP2C19*2, CYP2C19*3 POLYMORPHISMS ASSOCIATED WITH THE RESISTANCE TO CLOPIDOGREL IN PATIENTS WITH ACUTE CORONARY SINDROME IN THE YAKUT AND RUSSIAN ETHNIC GROUPS

ntroduction. The aim of this study was to determine the prevalence rate of CYP2C19 alleles, associated with the risk of the resistance to clopidogrel and the development of thrombotic complications in patients with acute coronary syndrome (ACS) from Russian an…

10.29296/24999490-2018-02-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

«RISKY» COMBINATIONS OF CANDIDATE GENES FOR HYPERPLASTIC PROCESSES OF THE ENDOMETRIUM

Introduction. Endometrial hyperplasia represents a chronic progressive disease characterized by high prevalence among women in older age groups. The aim of the study. To study the involvement of combinations of candidate genes in the formation of hyperplastic …

10.29296/24999490-2018-02-09Details ↗
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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