Submissions are open for the upcoming issue.

Molecular Medicine Peer-reviewed scientific journal

Found: 239

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

GENE EXPRESSION OF INTEGRIN RECEPTORS AND THEIR LIGANDS IN PAPILLARY THYROID CARCINOMA WITH DIFFERENT BRAF V600E MUTATION STATUS

Introduction. Papillary thyroid cancer (PTC) is the most common malignancy of the endocrine system. As the most frequent genetic alteration BRAF V600E mutation in PTC leads to changes in the activity of intracellular signaling pathways. As a result, expression…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

OVEREXPRESSION OF APOPTOTIC ENDONUCLEASE ENDOG INHIBITS TELOMERASE ACTIVITY IN HUMAN CD4+ T CELLS

Introduction. Alternative splicing of telomerase catalytic subunit hTERT (human Telomerase Reverse Transcriptase) regulates the telomerase activity. The increased expression of non-active spliced hTERT results in inhibition of telomerase. However, very little …

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

INFLUENCE OF SLCO1B1 GENE C.T521>C POLYMORPHISM ON THERAPY WITH SIMVASTATIN IN CORONARY HEART DISEASE PATIENTS

Introduction. Carrier protein OATP1B1, encoded by the SLCO1B1gene, is involved in the transport of simvastatin into liver cells. SLCO1B1 gene polymorphisms influence on the functionality of the transporter, which could reflect on the efficacy and safety of tre…

Details ↗
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…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

MATRIX METALLOPROTEINASE-2 IN BONE MARROW OF PATIENTS WITH ACUTE MYELOID LEUKEMIA AND MYELODISPLASTIC SYNDROME

Introduction. Search for correct markers for diagnosis, prognosis and evaluation of the effectiveness of chemotherapy is the most important problem of the modern oncohematology. The aim. To determine the clinical relevance of matrix metalloproteinase-2 (MMP-2)…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

EXPRESSION OF THE AGR2 GENE AND ITS ROLE IN THE CONTROL OF THE DEVELOPMENT AND SECRETORY FUNCTION OF MAMMALIAN EPITHELIAL TISSUES

ntroduction. Agr2protein belongs to the family of disulfide isomerases of the endoplasmic reticulum and contains active cysteine domains involved in the formation of disulfide bonds with mucins. It is expressed in goblet cells of the intestinal epithelium and …

Details ↗
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…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ANALYSIS OF THE INTERFERONS OF I, II AND III TYPES, IL23 AND ANTIVIRAL PROTEIN MXA FOR MULTIPLE SCLEROSIS

Introduction. A lot of factors of innate and specific immunity are involved in development of the autoimmune diseases – multiple sclerosis (MS) that cause the damages of myelin envelopes of nerve fibres with irreversible neurological consequences. To decrease …

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

PROTEOMIC AND METABOLOMIC MANIFESTATIONS OF DIFFERENT VARIANTS OF APOLIPOPROTEIN E GENES POLYMORPHISM IN OBESE PATIENTS

Introduction. Currently questions on the role of genes polymorphism that regulate metabolism and implicated in metabolic disorders are disputed. Objective. The study of proteomic and metabolomic manifestations of different variants of apolipoprotein E genes po…

Details ↗
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…

Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

AΒ42 – APROMISSING NON-INVASIVE MARKER FOR LIFE-TIME DIAGNOSIS OF ALZHEIMER’S DISEASE

Introduction. Alzheimer's disease (AD) is a socially important neurodegenerative disease. The prevalence rate of AD is increasing over recent years. According to the hypothesis concerning AD to be a systematic disease its manifestation can be detected in vario…

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 ↗
ОБЗОР2017

EXOSOMES FROM VARIOUS BIOLOGICAL FLUIDS: PATTERN AND FUNCTION

Exosomes are microscopic extracellular vesicles with diametr 30–100 nm, which are secreted by different types of cells and may be detected in normal (blood serum, saliva, urine, breast milk) and pathological (ascite) biological fluids. It was shown that exosom…

Details ↗
ПЕРЕДОВАЯ СТАТЬЯ2016

MOLECULAR AND CELLULAR MECHANISMS OF ALZHEIMER’S DISEASE

Alzheimer's disease being the socially significant neurodegenerative disease of the elderly, ranks 6th on the causes of death among somatic pathologies. The molecular mechanisms of Alzheimer's disease still remain unexplored until the end, and the efficacy of …

Details ↗

Article search and quick navigation

Navigation