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Mutational landscape of prostate tumors revealed by whole-exome sequencing
Gilyazova I.R., Yankina M.A., Kunsbaeva G.B., Klimentova E.A., Izmaylov A.A., Pavlov V.N., Khusnutdinova E.K.
Genetic Control of Meiosis in Plants
Simanovsky S.A., Bogdanov Y.F.
Ethnic Features of Genetic Susceptibility to Breast Cancer
Bermisheva M.A., Bogdanova N.V., Gilyazova I.R., Zinnatullina G.F., Bisultanova Z.I., Khusnutdinova E.K.
Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia
Akhmetgaleyeva A.F., Khidiyatova I.M., Saifullina E.V., Idrisova R.F., Magzhanov R.V., Khusnutdinova E.K.
Insertion Mutations of the shaggy Gene, Encoding Protein Kinase GSK3, Extend Drosophila melanogaster Lifespan
Trostnikov M.V., Veselkina E.R., Krementsova A.V., Roshina N.V., Pasyukova E.G.
Sarcoglycanopathies: Clinical, Molecular and Genetic Characteristics, Epidemiology, Diagnostics and Treatment Options
Bulakh M.V., Ryzhkova O.P., Polyakov A.V.
Analysis of heteroplasmy in the major noncoding region of mitochondrial DNA in the blood and atherosclerotic plaques of carotid arteries
Golubenko M.V., Nazarenko M.S., Frolov A.V., Sleptsov A.A., Markov A.V., Glushkova M.E., Barbarash O.L., Puzyrev V.P.
Study of the Role of the Main Factors of Population Dynamics in the Mechanism of Differentiation and Formation of Diversity and Genetic Load of Hereditary Diseases in Subpopulations of the Karachay-Cherkess Republic
Zinchenko R.A., El’chinova G.I., Bikanov R.A., Marakhonov A.V., Kadyshev V.V., Kutsev S.I., Ginter E.K.
Sodium Channelopathies: From Molecular Physiology towards Medical Genetics
Marakhonov A.V., Varenikov G.G., Skoblov M.Y.
Heterozygosity for mutations affecting coat pigmentation in the American mink (Neovison vison) enhances structural stability of adrenal cortex under stress conditions
Trapezov O.V., Luzenko N.D., Trapezova L.I.
The Rate of Human Germline Mutations—Variable Factor of Evolution and Diseases
Uspenskaya N.Y., Akopov S.B., Snezhkov E.V., Sverdlov E.D.
Updating Diagnostic Spectrum of Recurring CFTR Mutations
Adyan T.A., Stepanova A.A., Krasovskiy S.A., Polyakov A.V.
Mutational analysis of hemophilia B in Russia: Molecular-genetic study
Surin V.L., Demidova E.Y., Selivanova D.S., Luchinina Y.A., Salomashkina V.V., Pshenichnikova O.S., Likhacheva E.A.
Mutations in the Insulin Signaling Pathway Genes Affect Carbohydrate Level under Heat Stress in Drosophila melanogaster Females
Eremina M.A., Karpova E.K., Rauschenbach I.Y., Pirozhkova D.S., Andreenkova O.V., Gruntenko N.E.
Mutations in RAS/BRAF genes in rectal tumors: From adenomas to early carcinomas
Shelygin Y.A., Maynovskaya O.A., Rybakov E.G., Shubin V.P., Chernyshov S.V., Frolov S.A., Kashnikov V.N., Pospekhova N.I.
Reliability of the search for 19 common mutations in the CFTR gene in Russian cystic fibrosis patients and the calculated frequency of the disease in Russian Federation
Stepanova A.A., Krasovsky S.A., Polyakov A.V.
PAX6 Gene Characteristic and Causative Role of PAX6 Mutations in Inherited Eye Pathologies
Vasilyeva T.A., Voskresenskaya A.A., Pozdeyeva N.A., Marakhonov A.V., Zinchenko R.A.
Mutations in the APC gene in Russian patients with classic form of familial adenomatous polyposis
Tsukanov A.S., Pospekhova N.I., Shubin V.P., Kuzminov A.M., Kashnikov V.N., Frolov S.A., Shelygin Y.A.
Bioactive effect of the preparation biostyl on the reproductive function of different genotypes of American mink
Trapezov O.V., Zemljanitskaja E.I., Rasputina O.V., Naumkin I.V., Trapezova L.I.
Heterogeneity in Colorectal Primary Tumor and Synchronous Liver Metastases
Shubin V.P., Ponomarenko A.A., Tsukanov A.S., Maynovskaya O.A., Rybakov E.G., Panina M.V., Kashnikov V.N., Frolov S.A., Shelygin Y.A.
The search for new candidate genes involved in ovarian cancer pathogenesis by exome sequencing
Prokofyeva D.S., Mingajeva E.T., Bogdanova N.V., Faiskhanova R.R., Sakaeva D.D., Dörk T., Khusnutdinova E.K.
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