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ITGA4, ITGB7, TNFα, IL10 genes polymorphisms in the ethnic Buryat patients with ulcerative colitis
Zhilin I.V., Chashkova E.Y., Zhilina A.A., Tsyrempilova A.C.
Association of rs266729 and rs16861194 polymorphisms of the ADIPOQ gene with the risk of obesity in residents of the Moscow region
Pogozheva A.V., Sorokina E.Y.
Associations between obesity and vitamin D availability depending on the rs2228570 polymorphism of the VDR gene and rs9939609 polymorphism of the FTO gene in the midland and the Extreme North of Russia
Pogozheva A.V., Sorokina E.Y., Sokolnikov A.A.
Long-term survival of uveal melanoma patients after enucleation, depending on molecular genetic aberrations
Neroev V.V., Saakyan S.V., Amiryan A.G., Tsygankov A.Y., Burdennyy A.M., Loginov V.I., Khlgatyan M.R.
POLYMORPHISM OF CHRONIC GLOMERULONEPHRITIS ASSOCIATION WITH ADPRT1 GENE VAL762ALA
Kamyshova E.S., Shvetsov M.Y., Shestakov A.E., Kutyrina I.M., Nosikov V.V.
Polymorphism of the adiponutrin gene (PNPLA3) in the indigenous inhabitants of the Republic of Sakha (Yakutia) with type 2 diabetes mellitus
Kurtanov K.A., Sydykova L.A., Pavlova N.I., Filippova N.P., Dodokhov V.V., Apsolikhova G.A., Solov'eva N.A., D'yakonova A.T., Neustroeva L.M., Varlamova M.A., Borisova N.V.
INTERFAMILIAL POLYMORPHISM OF TYPE 1 DYSTONIA
Ostapchuk K.A., Kotov S.V., Sidorova O.P., Polyakov A.V., Galeeva N.M., Misikov V.K.
Evaluation of an association of the rs1801133 MTHFR gene polymorphism with folic acid deficiency in obese patients
Pogozheva A.V., Sorokina E.Y., Aristarkhova T.V.
THE DEVELOPMENT OF DIAGNOSTICS AND ALIMENTARY PREVENTION SYSTEM OF NON-COMMUNICABLE DISEASES
Pogozheva A.V., Sorokina E.Y., Baturin A.K., Peskova E.V., Makurina O.N., Levin L.G., Aristarkhova T.V., Korosteleva M.M., Denisova N.N., Solntseva T.N., Aleshina L.V., Toboleva M.A.
The contribution of the AGT, GNB3, MTHFR, MTRR, ApoE, and PPARα polymorphisms to the development of masked arterial hypertension in patients with low and moderate cardiovascular risk
Koziolova N.A., Chernyavina A.I.
Molecular and genetic diagnostics of inflammatory bowel diseases
Kuznetsova D.A., Razumov A.S., Merzlyakov M.V., Vavin G.V., Repnikova R.V.
Functional polymorphism of the serotonin reuptake transporter SLC6A4 gene in various clinical variants of irritable bowel syndrome
Pushkina A.V., Avalueva A.B., Bakulin I.G., Topanova A.A., Murzina A.A., Sitkin S.I., Lapinsky I.V., Skazyvaeva E.V.
Predicting the rate of liver fibrosis in patients with chronic hepatitis C virus infection based on the combination of genetic and environmental factors
Taratina O.V., Samokhodskaia L.M., Krasnova T.N., Mukhin N.A.
The role of TNF-alpha gene (-238G/A and -308G/A) polymorphisms in the etiology and pathogenesis of inflammatory bowel diseases in various ethnic groups
Zhilin I.V., Chashkova E.Y., Zhilina A.A., Pushkarev B.S., Korotaeva N.S.
Classification, regulation of activity, and genetic polymorphism of matrix metalloproteinases in health and disease
Shadrina A.S., Plieva Y.Z., Kushlinskiy D.N., Morozov A.A., Filipenko M.L., Chang V.L., Kushlinskii N.E.
EVALUATION OF AN ASSOCIATION BETWEEN RS5219 POLYMORPHISM OF KCNJ11 GENE AND THE RISK OF TYPE 2 DIABETES MELLITUS
Sorokina E.Y., Pogozheva A.V., Peskova E.V., Makurina O.N., Baturin A.K.
Association of celiac disease genetic markers with reproduction disorders
Minaycheva L.I., Bragina E.Y., Zhalsanova I.Z., Chesnokova N.A., Marusin A.V.
Association of gene polymorphisms of the reninangiotensin system and endothelial dysfunction with development and severity of portal hypertension in patients with chronic hepatitis C
Taratina O.V., Samokhodskaya L.M., Krasnova T.N., Mukhin N.A.
1 - 18 of 18 Items

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