Found: 137
Research article2014
Romanova S.V., Vidmanova T.А., Zhukova E.А., Mayanskaya I.V., Stepanenko S.F., Timchenko I.A.
Introduction. One of the important tasks of hepatology is the prognosis of viral hepatitides. The prognosis is based on the analysis of genetic determination of the functioning of antiviral immunity, particularly, of the cytokine system. The aim of the study w…
Research article2014
Glotov A.S., Vashukova E.S., Danilova M.M., Pakin V.S., Masharsky A.E., Fedotov P.V., Zainulina M.S., Arzhanova O.N., Mozgovaya E.V., Baranov V.S.
Introduction. Preeclampsia is one of the most frequent complications of pregnancy. Disease is based on the pathology of the vascular system of a pregnant woman. One of the candidate genes of preeclampsia is a gene encoding a protein receptor type 2A to activin…
Research article2014
Chukhlovin A.B., Totolian Areg A.
The aim of our review article was to analyze different biological effects associated with functional allelic variants of certain genes upon the incidence and clinical course of uterine leiomyoma (UL) and some other hyperplastic uterine disorders. Based on a nu…
Research article2014
Dribnokhodova O.P., Mironov K.O., Dunaeva E.A., Shipulin G.A.
Introduction.The rs8175347 ((TA)5/6/7/8) in the UGT1A1 gene polymorphism is associated with the expression of UDP glucuronosyltransferase 1A1 enzyme. The low enzyme activity in patients with (TA)7 and (TA)8 alleles is associated with the risk of Gilbert syndro…
Research article2014
Yurov Yu.B., Vorsanova S.G., Iourov I.Yu.
Genomic and molecular genetic studies of autism can identify new biological markers to determine the etiology and the molecular and cellular mechanisms of the pathogenesis of this disease. In addition to the fundamental importance of this research the laborato…
Research article2014
Shuev G.N., Sychev D.A., Khokhlov A.A., Grachev A.V., Beloshitskaya T.A.
Introduction.SLCO1B1 encodes the organic anion–transporting polypeptide which has been shown to regulate the hepatic uptake of statins. SLCO1B1*5 genetic variant is associated with statin-induced myopathy. The aim of the study. Aim of the study is to research …
Research article2013
Shklovsky V.M., Vilyanov V.B., Fukalov Yu.A., Remennik A.Yu., Skipetrova L.A., Kobozev G.N., Orlov I.Yu., Petruschevsky A.G., Kudryashov A.V., Kokoreva M.E.
We have studied BDNF gene Val66Met polymorphism in patients with a high risk of mortality due to stroke or severe head injury. Genotype ValVal rate was higher than that of in the control group in the total sample of subjects (75,5% and 63,6%; χ2=4,63; df=1; p=…
Research article2013
Aim. To study a method of risk assessment neovascular age-related macular degeneration (AMD) with the genetic and clinical risk factors. Methods. The study included 255 patients with neovascular AMD (NVAMD) and 119 subjects in control group. Diagnosis and stag…
Research article2013
Yurieva E.A., Sukhorukov V.S., Tsaregorodtsev A.D., Vozdvizhenskaya E.S., Kharabadze M.N., Novikova N.N., Kovalchuk M.V.
The enhancement of ligand properties of protein molecules treated by toxic reagents has been revealed in model experiments in vitro on ordered protein films. In patients with endogenous intoxication caused by metabolic disorders there were also detected protei…
Research article2013
Afanasyeva N.A., Khvostova E.P., Pustyl’nyak V.O., Chasovnikova O.B., Krasil’nikov S.E., Gulyaeva L.F.
Early diagnosis of ovarian cancer (OC) remains to be the actual problem in modern oncology due to the high mortality rate, asymptomatic course of the disease in the early stages and its aggressiveness. The aim was to study the genetic polymorphism of pathogene…
Research article2012
Demin V.F., Belushkina N.N., Paltsev M.A.
An approach to the development of methodology for health risk assessment (HRA) for the effects of new environmental factors: nanoparticles and nanobiomaterials (NP/NBM) – products of modern nano-, nanobiotechnology has been proposed. The experience from develo…
Research article2012
Nazarenko M.S., Botkina O.Yu., Puzyrev V.P.
In the current study the association of the endothelial nitric oxide synthase (NOS3) gene G894T and VNTR polymorphisms with the risk of miscarriage in ethnically homogeneous population has been investigated. The frequency of A/B VNTR genotype was revealed to p…
Research article2012
Burdennyy A.M., Kazubskaya T.P., Braga E.A., Nosikov V.V., Loginov V.I.
The association of +/– polymorphic markers of GSTM1 and GSTT1 genes and Ile105Val polymorphic marker of GSTP1 gene with the risk of development of breast cancer (BC) and its histological subtypes was studied. We have showed an association of null genotypes of …
Research article2012
Gnatenko D.A., Kostyushev D.S., Andreeva A.V., Filatova G.A., Notkins A., M. von Herrath, Paltsev M.A., Suchkov S.V.
In autoimmune diabetes mellitus (IDDM), clinical manifestation is typically preceded by several years of latent autoimmune insulitis. The autoimmune process arises only in genetically predisposed people,and is usually provoked by an infectious pathogen. Dagnos…
Research article2012
Atkarskaya M.V., Zavarykina T.M., Zhizhina G.P., Burlakova E.B.
The associations of polymorphic markers of the xenobiotics – metabolizing genes (GSTТI, GSTМI, GSTPI), cell cycle regulation genes (ТР53,CDKNI) and of the gene XRCCI repairing damaged DNA bases in 54 healthy subjects and 50 patients with upper respiratory trac…
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ
Evsyukova I.I., Polyakova V.O., Kleimenova T.S., Kvetnoy I.M., Paltzev M.A.
Introduction. Buccal epithelium (BE), in which cells the expression of signal molecules reflecting the state of homeostasis of the body in normal and pathological conditions is verified, is used as a diagnostic material for a number of diseases in adults. The …
ОБЗОР
Takha E.A., Shuralev E.A., Renaudineau Y., Arleevskaya M.I.
Introduction. Rheumatoid arthritis, like other multifactorial diseases, develops as a result of an inadequate response of a predisposed organism to environmental challenges. Material and methods. A review of the literature on the molecular mechanisms of the ef…