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| Issue |
Title |
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| Vol 22, No 2 (2023) |
The use of antisense molecules for splicing modulation as a treatment for genetic disorders |
Abstract
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A. S. Galushkin, A. Yu. Nekrasov |
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| Vol 22, No 1 (2023) |
Wolf–Hirschhorn syndrome: etiology, pathogenesis, clinic, features of symptomatic therapy and anesthesia, prenatal diagnosis (review) |
Abstract
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E. I. Kosinova, Т. I. Zubtsova, O. B. Polshvedkina, Yu. G. Kolesnikova |
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| Vol 19, No 1 (2020) |
Formation of inverted duplication contiguous to a terminal deletion of short arm of chromosome 8 |
Abstract
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D. A. Yurchenko, E. L. Dadali, N. V. Shilova |
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| Vol 17, No 7 (2018) |
GENETIC BASIS OF OSTEOPOROSIS |
Abstract
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R. Ya. Mirgaliyeva, E. K. Khusnutdinova, R. I. Khusainova |
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| Vol 12, No 4 (2013) |
DECANALIZATION OF IMMUNE RESPONSE DURING THE DISPERSION OF MODERN HUMANS: THE RELATIONSHIPS OF GENETIC DIVERSITY IN IMMUNE SYSTEM GENES AND CLIMATIC AND GEOGRAPHIC FACTORS |
Abstract
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V. A. Stepanov, P. Candelaria, S. Khoo, G. Zhang, E. A. Trifonova, K. V. Simonova, A. V. Bocharova, I. A. Laing, C. Hayden, V. Backer, P. Bjerregaard, N. Lynch, I. Hagel, A. W. Musk, A. Bittles, J. Goldblatt, P. Le Souef |
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| Vol 12, No 2 (2013) |
GENETIC DISORDERS OF VESTIBULAR SYSTEM |
Abstract
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V. A. Mglinets |
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| Vol 12, No 2 (2013) |
THE INFLUENCE OF HUMAN GENETIC FACTORS ON HAART |
Abstract
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A. S. Tumanov |
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| Vol 12, No 4 (2013) |
HEMIPLEGIC MIGRAINE |
Abstract
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J. E. Azimova, Е. А. Klimov, K. V. Skorobogatykh, А. V. Sergeev, Z. G. Kokaeva, G. R. Tabeeva |
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| Vol 12, No 3 (2013) |
MODERN VIEWS ON THE PATHOGENESIS AND GENETICS OF OSTEOARTHRITIS |
Abstract
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A. V. Tyurin, R. I. Khusainova, R. A. Davletshin, E. K. Khusnutdinova |
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| Vol 12, No 3 (2013) |
GENETIC ASPECTS OF SUICIDAL BEHAVIOR |
Abstract
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A. G. Zainullina, Z. L. Khalilova, E. K. Khusnutdinova |
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| Vol 12, No 3 (2013) |
NEOPLASTIC TRANSFORMATION OF MULTIPOTENT MESENCHYMAL STROMAL CELLS IN VITRO |
Abstract
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A. A. Rzhaninova, D. O. Omelchenko, I. A. Fedunina |
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| Vol 13, No 11 (2014) |
MOLECULAR GENETIC ASPECTS OF PEPTIC ULCER DISEASE |
Abstract
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E. Kh. Shaymardanova, A. Kh. Nurgalieva, D. D. Nadyrshina, E. Kh. Khusnutdinova |
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| Vol 12, No 1 (2013) |
NEXT GENERATION SEQUENCING TECHNOLOGIES IN MEDICAL GENETIC STUDIES |
Abstract
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S. V. Toshchakov, I. N. Dominova, M. V. Patrushev |
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| Vol 12, No 1 (2013) |
MOLECULAR KARYOTYPING (ACGH) AS MODERN APPROACH FOR INVESTIGATIONS OF MISCARRIAGE CAUSES |
Abstract
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T. V. Nikitina, А. А. Kashevarova, N. А. Skryabin, N. N. Chechetkina, А. А. Melnikov, I. N. Lebedev |
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| Vol 12, No 1 (2013) |
GENETICS OF VESTIBULAR SYSTEM |
Abstract
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V. A. Mglinets |
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| Vol 14, No 5 (2015) |
POSSIBILITY OF THE ESTIMATION OF THE GENETIC COUNSELING EFFICIENCY: REVIEW |
Abstract
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E. E. Baranova, L. Yu. Ivanova, I. V. Zhuravleva, V. L. Izhevskaya, E. K. Ginter |
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| Vol 14, No 5 (2015) |
THE ROLE OF GENETIC MARKERS AND NUTRIENTS IN THE DEVELOPMENT OF COMMON DISEASES |
Abstract
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A. N. Kucher |
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| Vol 15, No 3 (2016) |
Familial mediterranean fever: current view |
Abstract
PDF (Rus)
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S. A. Atoyan |
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| Vol 16, No 5 (2017) |
Application of high-resolution DNA melting analysis in diagnostics of hereditary diseases |
Abstract
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D. I. Nikitina, M. A. Maretina, A. A. Egorova, A. B. Maslennikov, A. V. Kiselev |
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| Vol 19, No 10 (2020) |
Evaluation of the clinical and economic effectiveness of newborn screening programs for inborn errors of metabolism |
Abstract
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N. L. Pechatnikova, E. Y. Zakharova, V. L. Izhevskaya |
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| Vol 15, No 7 (2016) |
Biomarkers in diagnosis and treatment monitoring for the cell organelles diseases |
Abstract
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T. D. Krylova, T. Y. Proshlyakova, G. V. Baydakova, Y. S. Itkis, M. V. Kurkina, E. Y. Zakharova |
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| Vol 16, No 6 (2017) |
Association of opioid receptors gene OPRM1 polymorphism and phenotypic diversity of chronic pain syndrome of oncological genesis |
Abstract
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O. P. Bobrova, N. A. Shnayder, S. K. Zyryanov, A. A. Modestov |
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| Vol 17, No 9 (2018) |
Intestinal organoids and their application for personalized diagnostics and treatment of cystic fibrosis |
Abstract
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A. S. Efremova, T. B. Bukharova, N. Y. Kashirskaya, D. V. Goldshtein |
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| Vol 19, No 11 (2020) |
Familial Mediterranean Fever (FMF) and Pregnancy: Literature Review |
Abstract
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P. O. Sotskiy |
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| Vol 15, No 9 (2016) |
Gene therapy of hereditary diseases by CRISRP/Cas9 technology in vivo |
Abstract
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S. A. Smirnikhina, A. V. Lavrov |
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| Vol 16, No 7 (2017) |
Molecular-genetic characteristics of Wilson`s disease |
Abstract
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G. M. Baiazutdinova, O. A. Shchagina, A. V. Poliakov |
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| Vol 17, No 10 (2018) |
Sex chromosomes abnormalities and CNVs, and their diagnosis |
Abstract
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V. B. Chernykh |
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| Vol 19, No 11 (2020) |
Current problems of providing medical care for patients with orphan diseases in the Russian Federation |
Abstract
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A. I. Gayduk, Ya. V. Vlasov, E. Yu. Zakharova |
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| Vol 15, No 9 (2016) |
Генетические аспекты расстройств аутистического спектра |
Abstract
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N. A. Semenova |
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| Vol 16, No 8 (2017) |
Non-invasive prenatal tests: european and american recomendations |
Abstract
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E. E. Baranova, M. S. Belenikin, L. A. Zhuchenko, V. L. Izhevskaya |
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| Vol 17, No 10 (2018) |
Interpretation of pathogenic copy number variations |
Abstract
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N. V. Shilova, M. E. Minzhenkova |
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| Vol 19, No 12 (2020) |
Molecular bases of primary monogenic dyslipidemia |
Abstract
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O. N. Ivanova, P. A. Vasiliev, E. Yu. Zakharova |
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| Vol 15, No 11 (2016) |
Neocentromeres |
Abstract
PDF (Rus)
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N. V. Shilova |
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| Vol 16, No 9 (2017) |
Clinical and genetic characteristics of hereditary diseases and syndromes with glaucoma |
Abstract
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O. V. Khlebnikova, E. L. Dadali |
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| Vol 17, No 11 (2018) |
Molecular mechanisms of disturbance of imprinted genes in pathology of pre-and postnatal development |
Abstract
PDF (Rus)
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E. A. Sazhenova, I. N. Lebedev |
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| Vol 19, No 12 (2020) |
The utility of exome sequencing in diagnosis of hereditary diseases |
Abstract
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E. G. Okuneva, A. A. Kozina, N. V. Baryshnikova, A. Yu. Krasnenko, O. I. Klimchuk, I. F. Stetsenko, N. A. Plotnikov, E. I. Surkova, V. V. Ilinsky |
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| Vol 15, No 12 (2016) |
Genetic factors in development of intracranial arterial aneurisms |
Abstract
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O. B. Belousova, V. A. Gorozhanin |
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| Vol 16, No 10 (2017) |
Newborn screening for inherited metabolic diseases: key issues |
Abstract
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E. Yu. Zakharova, V. L. Izhevskaya, G. V. Baydakova, T. A. Ivanova, O. V. Chumakova, S. I. Kutsev |
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| Vol 17, No 12 (2018) |
Clinical and genetic aspects of cardiomyopathy |
Abstract
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K. I. Minniakhmetova, R. I. Khusainova, I. E. Nikolaeva, I. R. Minniakhmetov, E. K. Khusnutdinova |
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| Vol 20, No 1 (2021) |
Familial Mediterranean Fever (FMF), Female and Male Fertility: Literature Review |
Abstract
PDF (Rus)
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P. O. Sotskiy |
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| Vol 15, No 10 (2016) |
Current approaches for treatment of muscular dystrophies |
Abstract
PDF (Rus)
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J. V. Vyakhireva, N. V. Zernov, A. V. Marakhonov, A. A. Guskova, M. Yu. Skoblov |
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| Vol 16, No 11 (2017) |
Whole genome amplification as a method for analysis of single cells |
Abstract
PDF (Rus)
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A. A. Tveleneva, E. V. Musatova, N. V. Shilova |
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| Vol 18, No 3 (2019) |
Preimplantation genetic testing for aneuploidy: state of the art, trends and perspectives |
Abstract
PDF (Rus)
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I. N. Lebedev |
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| Vol 20, No 1 (2021) |
Alpha-1-antitrypsin deficiency: diagnosis and treatment (literature review) |
Abstract
PDF (Rus)
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E. A. Larshina, N. V. Milovanova, E. A. Kamenets |
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| Vol 16, No 2 (2017) |
Recent advances in genetics of osteoarthritis |
Abstract
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D. A. Shapovalova, A. V. Tyurin, E. K. Khusnutdinova, R. I. Khusainova |
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| Vol 16, No 12 (2017) |
Genome variability of somatic cells in human complex diseases |
Abstract
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M. S. Nazarenko, A. A. Sleptcov, A. V. Markov, V. P. Puzyrev |
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| Vol 18, No 3 (2019) |
Preimplantation genetic diagnosis (testing) for monogenic disorders: indications and ethics |
Abstract
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E. V. Solovyova, L. P. Nazarenko, L. I. Minaycheva, A. V. Svetlakov |
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| Vol 20, No 2 (2021) |
Genetics of mental retardation |
Abstract
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I. V. Anisimova |
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| Vol 16, No 2 (2017) |
Lynch syndrome: current status |
Abstract
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A. S. Tsukanov, Y. A. Shelygin, D. A. Semenov, D. Y. Pikunov, A. V. Polyakov |
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| Vol 17, No 1 (2018) |
Cytogenetic and expression markers of individual human radiosensitivity |
Abstract
PDF (Rus)
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S. A. Vasilyev, I. N. Lebedev |
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