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Clinical features of the microRNA genes methylation in borderline ovarian tumors and depending on the histological structure in ovarian malignancies
Lukina S.S., Burdennyy A.M., Filippova E.A., Pronina I.V., Kazubskaya T.P., Kushlinsky D.N., Utkin D.O., Braga E.A., Loginov V.I., Kushlinskii N.E.
A clinical case of familial enteropathic acrodermatitis caused by a new genetic mutation in exon 10 of the SLC39A4 gene
Stadnikova A.S., Tamrazova O.B., Zakharova I.N., Dmitrieva Y.A., Taganov A.V., Yudina A.E., Bagramova G.E.
Association of VEGFA gene rs2010963 polymorphism with cervical cancer and its progression
Rogalev A.V., Kishenya M.S., Pishchulina S.V., Khomutov E.V.
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.
CYP2C19 gene polymorphism and its impact on the long-term prognosis after myocardial infarction
Solodun M.V., Yakushin S.S., Moseichuk K.A., Filippov E.V.
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.
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.
Characteristics of the mutation spectrum identified by comprehensive investigation of the CFTR gene in the Russian patients
Petrova N.V., Marakhonov A.Y., Vasilyeva T.A., Kashirskaya N.Y., Kondratyeva E.I., Zhekayte E.K., Voronkova A.Y., Sherman V.D., Galkina V.A., Ginter E.K., Kutsev S.I., Zinchenko R.A.
A case of late manifestation of primary adrenal insufficiency in the autoimmune polyglandular syndrome type 1
Troshina V.V., Grebennikova T.A., Belaya Z.E.
EXPRESSION PROFILES AND METHYLATION GENES IN CLEAR CELL RENAL CARCINOMA
Braga E.A., Zhinzhilo T.A., Kolpakov A.V., Mikhaylenko D.S., Kushlinskii N.E.
Efficiency of SpCas9 and AsCpf1 (Cas12a) programmable nucleases at genomic safe harbor loci in HEK293 cells
Pavlova S.V., Elisaphenko E.A., Shayakhmetova L.S., Medvedev S.P.
Challenges of the differential diagnosis between the subtypes of the junctional epidermolysis bullosa: presentation of two clinical cases
Kotalevskaya Y.Y., Marycheva N.M.
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 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.
The LGALS1 gene polymorphism is not associated with galectin-1 levels in tumor tissue and blood of colon cancer patients
Urazova O.I., Reyngardt G.V., Kolobovnikova Y.V., Kurnosenko A.V., Poletika V.S., Vasil'yeva O.A., Avgustinovich A.V.
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.
THE MOLECULAR PATHOGENESIS OF BLADDER CANCER
Nemtsova M.V., Kushlinskii N.E.
A clinical case of partial androgen resistance syndrome (Reifenstein syndrome)
Dzeranova L.K., Pigarova E.A., Ivannikova E.V., Kurilo L.F., Chernykh V.B., Polyakov A.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.
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 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.
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.
DEVELOPMENT OF A MULTIPLEX ALLELE-SPECIFIC REAL-TIME PCR METHOD FOR DETECTION OF PIK3CA GENE SOMATIC MUTATIONS AND ITS VALIDATION IN THE TUMORS OF BREAST CANCER PATIENTS
Filipenko M.L., Shamovskaya D.V., Oskina N.A., Oscorbin I.P., Khrapov E.A., Ovchinnikova L.K., Gershteyn E.S., Kushlinskii N.E.
Cardiomyopathies associated with the DES gene mutations: molecular pathogenesis and gene therapy approaches
Kochergin-Nikitsky K.S., Zaklyazminskaya E.V., Lavrov A.V., Smirnikhina S.A.
Molecular and genetic diagnostics of inflammatory bowel diseases
Kuznetsova D.A., Razumov A.S., Merzlyakov M.V., Vavin G.V., Repnikova R.V.
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.
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.
1 - 27 of 27 Items

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