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Molecular Medicine Peer-reviewed scientific journal

Found: 101

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2022

GENETIC PREDICTORS OF SPORADIC CONGENITAL HEART DEFECTS IN CHILDREN

Background. Congenital heart defects can be embryopathies formed due to an imbalance in the processes of differentiation and proliferation in cardiac progenitor cells. One of the reasons for these disorders may be genetically restricted signaling, including th…

10.29296/24999490-2022-01-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

INNATE AND ADAPTIVE IMMUNITY DURING INFECTION AND IMMUNIZATION WITH INACTIVATED TICK-BORNE ENCEPHALITIS VACCINE

Introduction. Viral infections induce cellular and humoral immunity that provide virus elimination. Extracellular presentation of antigens of formaldehyde-inactivated vaccines causes mainly humoral immune response with risk of persistent infection. The aim of …

10.29296/24999490-2021-06-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

THE ALTERATION OF MICRORNA EXPRESSION PROFILES IN CUTANEOUS MALIGNANT MELANOMA AND BENIGN MELANOCYTIC NEVI

Introduction. Early diagnostics of such oncological disease as cutaneous malignant melanoma is strictly important for the decrease of mortality. It is known that microRNA expression in melanoma cells and in bening melanocytic nevi is different, that can be use…

10.29296/24999490-2021-04-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

MOLECULAR AND GENETIC POTENTIAL OF THE VIRULENT EFFECTS OF ESCHERICHIA COLI ISOLATES TAKEN FROM ULCER COLITIS PATIENTS

Introduction. The human microbiota is part of the «human-microbiome» system and is actively involved in developing various pathological responses and conditions in the body. It is currently essential to study the pathogenesis of ulcerative colitis (UC), a poly…

10.29296/24999490-2021-04-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

Alterations in mRNA expression of rat astrocytes co-cultured with c6 glioma cells and impact of glioma-conditioned astrocytes on dendritic cell maturation

Introduction. Under the influence of glioma cells, peritumoral zone astrocytes may acquire tumorigenic phenotype, particularly due to the suppression of immunocompetent cells. The aim of the study. Investigate the changes in the gene expression profile of glio…

10.29296/24999490-2021-05-03Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

EFFECT OF PNPLA3, SERPINA1, AND HFE GENES POLYMORPHISMS ON THE COURSE OF NONALCOHOLIC FATTY LIVER DISEASE

Introduction: nonalcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide. But it remains unclear what factors influence the progression of the disease. It is interesting to study the influence of the genetic aspect on the course of NAF…

10.29296/24999490-2021-03-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

EXPRESSION OF GLIAL MARKERS, CYTOKINES AND MARKERS OF NEUROGENESIS IN THE MOUSE HIPPOCAMPUS DURING AGING AND IN RESPONSE TO LIPOPOLYSACCHARIDE

Introduction. Aging is associated with a decrease in the neuro- and synaptogenesis as well as hyperactivation of glial cells, which leads to changes in the morphofunctional state of the nervous tissue of the hippocampus and, as a consequence, a deterioration i…

10.29296/24999490-2021-03-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

FEATURES OF EXPRESSION OF β-AMYLOID IN CEREBRAL ENDOTHELIAL CELLS IN EXPERIMENTAL ALZHEIMER’S DISEASE

Introduction. The formation of neurofibrillary plexuses and the accumulation of senile plaques in the parenchyma and cerebral vessels are the key pathological signs of Alzheimer’s disease presenting a neurodegenerative disease. The main component of senile pla…

10.29296/24999490-2021-02-04Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

Features of local expression of mRNA, IL-1β, IL-18, CCL2/MCP-1 in modeling pigment epithelium atrophy and retinal degeneration in the experiment on rabbits

Introduction. Degenerative retinal diseases are considered as the leading cause of blindness and low vision worldwide. The last studies have provided convincing evidence of the involvement of immunological factors in the development and progression of the dise…

10.29296/24999490-2021-02-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

THE LEVEL OF EXPRESSION OF PROGESTERONE, ESTRADIOL AND VITAMIN D RECEPTORS IN MONONUCLEAR CELLS OF THE PERIPHERAL BLOOD OF PATIENTS WITH SURGICAL MENOPAUSE

Introduction. Patients with surgical menopause are at risk for an osteopenic syndrome. For adequate medical correction of osteoporosis, it is necessary to clarify the mechanisms of the pathogenesis of this condition. It is known that osteoclasts, the activatio…

10.29296/24999490-2020-01-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

EXPRESSION OF FACTORS ACTIVATED BY HYPOXIA, GROWTH FACTOR VEGF, ITS RECEPTOR, CARBOHYDRASE IX IN TISSUE IN PAPILLARY CANCERs AND METASTASES

Introduction. The molecular mechanisms of the development of tumor pathology of the thyroid gland are associated with the activation of angiogenesis and the development of hypoxia, which contributes to the proliferation, invasion, and progression of the diseas…

10.29296/24999490-2020-06-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

THE ASSOCIATION OF RS75555045 AND RS12904699 WITH SUDDEN CARDIAC DEATH

Introduction. The single-nucleotide polymorphisms rs75555045 and rs12904699 were found in the own genome-wide allelotyping as possible new molecular genetic markers of sudden cardiac death (SCD). The results obtained in such studies require verification in the…

10.29296/24999490-2020-05-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

Prediction of the blastulation onset in one day behind embryos by the expression profile of small non-coding RNAs

Introduction. Successful embryonic development immediately after fertilization depends on the maternal messenger RNAs (mRNAs) destruction and zygotic genome transcription activation during maternal to zygotic transition (MZT). Key regulators of MZP are small n…

10.29296/24999490-2020-05-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2020

STANDARDIZATION OF THE METHOD OF MULTI-TARGET SINGLE-NUCLEOTIDE ELONGATION FOR MOLECULAR GENETIC STUDY OF CYTOLOGICAL MATERIAL IN THYROID NEOPLASM

Introduction. Thyroid cancer (TC) is the most prevalent cancer among malignant neoplasms of the organs of the endocrine system. Cytological categories Bethesda III–V of TC are considered to be the most difficult for making a diagnosis. Molecular genetic tests …

10.29296/24999490-2020-06-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

THE LEVEL OF EXPRESSION OF PROGESTERONE, ESTRADIOL AND VITAMIN D RECEPTORS IN MONONUCLEAR CELLS OF THE PERIPHERAL BLOOD OF PATIENTS WITH SURGICAL MENOPAUSE

Introduction. Patients with surgical menopause are at risk for an osteopenic syndrome. For adequate medical correction of osteoporosis, it is necessary to clarify the mechanisms of the pathogenesis of this condition. It is known that osteoclasts, the activatio…

10.29296/24999490-2019-01-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

COMPLEX F8 GENE REARRANGEMENTS

Introduction. Hemophilia A is a frequent X-linked recessive disorder associated with the absence or functional defect of blood clotting factor VIII. Вoth point mutations and large structural rearrangements – deletions, duplications, and inversions were describ…

10.29296/24999490-2019-01-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

DBH GENE POLYMORPHISM IN PSORIASIS PATIENTS

Introduction. Psoriasis is a chronic inflammatory autoimmune disease with complex etiology including inheritable factors as well. Some scientists suggest psoriasis to be a systemic disease affecting not only skin. Thus, on the edge of dermatology and psychiatr…

10.29296/24999490-2019-04-09Details ↗
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

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 ↗

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