Triple therapy for chronic hepatitis C: Practical Aspects by I G Bakulin, A V Kiseleva

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INFLUENCE OF SMOKING ON THE METHYLIZING STATUS OF DESOXYRIBONUCLEIC ACID by A. V. Kiseleva, A. A. Zharikova, A. N. Meshkov

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MEDICAL PROFESSIONAL DISCOURSE WITHIN THE COGNITIVE LINGUISTIC ANALYSIS FRAMEWORK by E. A. Vishnyakova, O. D. Vishnyakova, A. V. Kiseleva

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Role of Nitric Oxide in Neuronal Damages in Critical Conditions by A. V. Kiseleva, Yu. A. Churlyaev, Ye. V. Grigoryev

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Monitoring the Microcirculation in Critical Conditions: Possibilities and Limitations by T. O. Tokmakova, S. Yu. Permyakova, A. V. Kiseleva, D. L. Shukevich, E. V. Grigoryev

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Arterial calcification, atherosclerosis and osteoporosis: only clinical associations or a genetic platform? by I. A. Skripnikova, M. A. Kolchina, A. N. Meshkov, A. V. Kiseleva, O. M. Drapkina

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From biobanking to personalized prevention of obesity, diabetes and metabolic syndrome by A. I. Ershova, A. A. Ivanova, A. V. Kiseleva, E. A. Sotnikova, A. N. Meshkov, O. M. Drapkina

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Assessment of polygenic risk of hypertension by A. S. Limonova, A. I. Ershova, A. V. Kiseleva, V. E. Ramensky, Yu. V. Vyatkin, V. A. Kutsenko, A. N. Meshkov, O. M. Drapkina

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ASSOCIATION OF THE VARIANTS OF NUCLEOTIDE SEQUENCE OF THE GENE ADIPOQ WITH PLASMATIC LEVEL OF ADIPONECTIN, THE GRADE OF CORONARY ATHEROSCLEROSIS SEVERITY AND RATE OF CARDIOVASCULAR... by S. A. Smetnev, A. N. Meshkov, M. V. Klimushina, N. E. Gavrilova, A. I. Ershova, A. V. Kiseleva, V. A. Metelskaya, O. M. Drapkina

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Biobank data for studying the genetic architecture of osteoporosis and developing genetic risk scores by E. A. Sotnikova, A. V. Kiseleva, A. N. Meshkov, A. I. Ershova, A. A. Ivanova, M. A. Kolchina, V. A. Kutsenko, I. A. Skripnikova, O. M. Drapkina

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ANGPTL3, ANGPTL4, APOA5, APOB, APOC2, APOC3, LDLR, PCSK9, LPL gene variants and coronary artery disease risk by A. N. Meshkov, A. V. Kiseleva, A. I. Ershova, E. A. Sotnikova, S. A. Smetnev, A. S. Limonova, A. A. Zharikova, M. Zaychenoka, V. E. Ramensky, O. M. Drapkina

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Shelf life of whole blood samples in a biobank and the yield of deoxyribonucleic acid during genetic testing by O. P. Skirko, A. N. Meshkov, I. A. Efimova, V. A. Kutsenko, A. V. Kiseleva, M. S. Pokrovskaya, O. V. Kurilova, E. A. Sotnikova, M. V. Klimushina, O. M. Drapkina

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Variant of the <i>FLNC</i> gene nucleotide sequence in a family with different phenotypic manifestations of left ventricular non-compaction by O. V. Kulikova, R. P. Myasnikov, A. N. Meshkov, M. M. Kudryavtseva, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, M. S. Kharlap, S. N. Koretsky, V. E. Sinitsyn, O. M. Drapkina

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Pathogenic Variant Rs1471414348of the TTN Gene in the Patient with Familial Left Venticular Noncompaction Cardiomyopathy by O. V. Kulikova, A. N. Meshkov, R. P. Myasnikov, A. V. Kiseleva, S. N. Koretsky, A. A. Zharikova, M. S. Kharlap, E. A. Mershina, V. E. Sinitsyn, O. P. Skirko, I. A. Efimova, M. S. Pokrovskaya, S. A. Boytsov, O. M. Drapkina

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New Variant of <i>MYH7</i> Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course by R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, A. V. Kiseleva, A. O. Shumarina, S. N. Koretskiy, A. A. Zharikova, M. G. Divashuk, M. S. Kharlap, S. E. Serduk, E. A. Mershina, V. E. Sinitsyn, S. A. Boytsov, O. M. Drapkina

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The non-compacted myocardium in patients with hemochromatosis: a phenomenon or cardiopathy? The role of magnetic resonance imaging and molecular genetics in diagnosis by E. A. Mershina, O. V. Kulikova, R. P. Myasnikov, E. A. Lukina, A. N. Meshkov, A. V. Kiseleva, P. S. Pilyus, S. N. Koretsky, M. S. Kharlap, R. V. Ponomarev, N. V. Tsvetaeva, O. F. Nikulina, S. A. Boytsov, V. E. Sinitsyn, O. M. Drapkina

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RBM20 nucleotide sequence variant in a family with a dilated phenotype of left ventricular non-compaction by O. V. Kulikova, R. P. Myasnikov, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, E. A. Sotnikova, M. M. Kudryavtseva, M. S. Kharlap, M. G. Divashuk, A. A. Zharikova, R. K. Angarsky, S. N. Koretsky, D. А. Filatova, V. E. Sinitsyn, O. M. Drapkina

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Nucleotide sequence variant of the TPM1 gene in a family with different phenotypes of left ventricular non-compaction by M. M. Kudryavtseva, A. V. Kiseleva, R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, E. A. Mershina, R. K. Angarsky, Е. A. Sotnikova, M. G. Divashuk, A. A. Zharikova, S. N. Koretsky, D. A. Filatova, V. E. Sinitsyn, N. A. Sdvigova, V. I. Barsky, E. N. Basargina, O. M. Drapkina

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The combination of left ventricular non-compaction and hypertrophic cardiomyopathy in one family with a pathogenic variant in the MYBPC3 gene (rs397516037) by R. P. Myasnikov, A. V. Kulikova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. V. Klimushina, M. G. Divashuk, O. V. Kurilova, P. S. Pilyus, M. S. Kharlap, S. N. Koretsky, O. M. Larina, V. E. Sinitsyn, L. A. Gandaeva, V. I. Barsky, E. N. Basargina, S. A. Boytsov, O. M. Drapkina

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New variant of PRDM16 gene nucleotide sequence in a family with various phenotypic manifestations of the non-compacted myocardium by R. P. Myasnikov, A. A. Bukaeva, O. V. Kulikova, A. I. Ershova, A. V. Petukhova, E. D. Zotova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, P. S. Pilyus, M. S. Kharlap, V. M. Mikova, S. N. Koretsky, L. A. Gandaeva, V. E. Sinitsyn, E.. N. Basargina, S. A. Boytsov, E. A. Snigir, A. I. Akinshina, D. A. Kashtanova, V. V. Makarov, V. S. Yudin, O. M. Drapkina

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