Search Results - A. Zarubin

Comparison of Uncontrolled and Device-Induced Therapeutic Hypothermia in Newborn Infants with Hypoxic Ischemic Encephalopathy by A. A. Zarubin, E. S. Filippov, A. S. Vanyarkina, O. G. Ivanova, A. A. Shishkina

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The Effect of Severe Birth Asphyxia on the Hemostasis System in Newborns During the First Hour of Life by I. E. Golub, A. A. Zarubin, N. I. Micheeva, A. S. Vanyarkina, O. G. Ivanova

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The results of entomological monitoring West Nile fever on the territory of the Crimean peninsula in the 2022 season by N. A. Zarubin, N. V. Borodai, S. K. Udovichenko, A. Yu. Galkina, I. D. Kaysarov

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Changes in DNA methylation profile in liver tissue during progression of HCV-induced fibrosis to hepatocellular carcinoma by I. A. Goncharova, A. A. Zarubin, N. P. Babushkina, I. A. Koroleva, M. S. Nazarenko

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Mechanisms of oxygen-dependent microbicidal system of neutrophils in the prognosis of acute pancreatitis by M. A. Shevlyaeva, G. K. Karipidi, S. V. Avakimyan, V. A. Zarubin, E. G. Ermolenko

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Blocks identical by descent in the genomes of the indigenous population of Siberia demonstrate genetic links between populations by N. A. Kolesnikov, V. N. Kharkov, K. V. Vagaitseva, A. A. Zarubin, V. A. Stepanov

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HYPOXIC-ISCHEMIC ENCEPHALOPATHY IN NEONATES BORN TO SEVERE BIRTH ASPHYXIA by A. A. Zarubin, N. I. Mikheeva, E. S. Filippov, T. A. Belogorova, A. S. Vanyarkina, A. A. Shishkin

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The Forest and Tundra Nenets: differences in Y-chromosome haplogroups by V. N. Kharkov, L. V. Valikhova, D. S. Adamov, A. A. Zarubin, I. Yu. Khitrinskaya, V. A. Stepanov

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Structure and origin of Tuvan gene pool according to autosome SNP and Y-chromosome haplogroups by V. A. Stepanov, N. A. Kolesnikov, L. V. Valikhova, A. A. Zarubin, I. Yu. Khitrinskaya, V. N. Kharkov

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Traces of Paleolithic expansion in the Nivkh gene pool based on data on autosomal SNP and Y chromosome polymorphism by V. N. Kharkov, N. A. Kolesnikov, L. V. Valikhova, A. A. Zarubin, A. L. Sukhomyasova, I. Yu. Khitrinskaya, V. A. Stepanov

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Relationship of the gene pool of the Khants with the peoples of Western Siberia, Cis-Urals and the Altai-Sayan Region according to the data on the polymorphism of autosomic locus a... by V. N. Kharkov, N. A. Kolesnikov, L. V. Valikhova, A. A. Zarubin, M. G. Svarovskaya, A. V. Marusin, I. Yu. Khitrinskaya, V. A. Stepanov

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West Nile Fever in the Russian Federation in 2022, the Incidence Forecast for 2023 by E. V. Putintseva, S. K. Udovichenko, D. N. Nikitin, N. V. Boroday, A. A. Baturin, A. Yu. Machneva, A. S. Antonov, N. A. Zarubin, A. V. Toporkov

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New mutation of the TP53 gene associated with the hereditary breast cancer in a young Tuvinian woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ponomareva, N. N. Babyshkina, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

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Deoxyribonucleic acid methylation in the enhancer region of the CDKN2A/2B and CDKN2B-AS1 genes in blood vessels and cells in patients with carotid atherosclerosis by Yu. A. Koroleva, A. V. Markov, I. A. Goncharova, A. A. Sleptsov, N. P. Babushkina, N. R. Valiakhmetov, D. V. Sharysh, A. A. Zarubin, M. S. Kuznetsov, B. N. Kozlov, M. S. Nazarenko

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Rare missense substitutions in the mitochondrial DNA genes in patients with ventricular tachycardia by M. V. Golubenko, N. P. Babushkina, V. A. Korepanov, N. R. Valiakhmetov, T. A. Atabekov, K. N. Vitt, A. A. Zarubin, O. A. Makeeva, S. A. Afanasiev, R. E. Batalov, A. A. Garganeeva, M. S. Nazarenko, V. P. Puzyrev

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Results of reconnaissance epizootiological monitoring for West Nile fever in certain regions of European Russia and the Urals in 2024 by Natalia V. Borodai, Anna V. Nesgovorova, Aina K. Mendygalieva, Anna Yu. Koloskova, Svetlana K. Udovichenko, Nikolay A. Zarubin, Stanislav A. Kargashin, Yevgeny A. Gusev, Artem A. Baturin, Irina A. Khabarova, Elena V. Putintseva, Andrey V. Toporkov

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A novel germline mutation of the <i>PALB2</i> gene in a young Yakut breast cancer woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ivanova, D. G. Tikhonov, N. S. Kipriyanova, A. N. Egorov, L. D. Zhuikova, N. A. Shefer, E. B. Topolnitskiy, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies by E. A. Fonova, A. A. Kashevarova, M. E. Lopatkina, A. A. Sivtsev, A. A. Zarubin, V. V. Demeneva, G. N. Seitova, L. I. Minaycheva, O. A. Salyukova, S. V. Fadyushina, V. V. Petrova, E. O. Belyaeva, L. P. Nazarenko, I. N. Lebedev

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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability by A. A. Kashevarova, E. O. Belyaeva, E. A. Fonova, M. E. Lopatkina, O. Y. Vasilyeva, D. A. Fedotov, A. A. Zarubin, A. A. Sivtsev, V. V. Demeneva, O. A. Salyukova, V. V. Petrova, S. V. Fadiushina, L. I. Minaycheva, G. N. Seitova, L. P. Nazarenko, I. N. Lebedev

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Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1... by A. A. Kashevarova, M. E. Lopatkina, O. Yu. Vasilyeva, D. A. Fedotov, A. D. Lobanov, E. A. Fonova, I. Z. Zhalsanova, A. A. Zarubin, O. A. Salyukova, E. O. Belyaeva, V. V. Petrova, E. G. Ravzhaeva, A. A. Agafonova, A. D. Cheremnykh, N. B. Torkhova, S. L. Vovk, I. N. Lebedev

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