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| Issue |
Title |
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| Vol 24, No 5 (2025) |
RET gene mutations and their importance in targeted therapy of medullary thyroid cancer |
Abstract
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N. Kim, A. A. Budaeva, V. V. Zakharov, S. U. Shuipova, I. R. Dishnaev, E. A. Medzhidov, A. A. Zakharenko, M. E. Boriskova, V. D. Nazarov, M. A. Omarov |
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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
PDF (Rus)
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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
PDF (Rus)
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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
PDF (Rus)
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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) |
GENETICS OF VESTIBULAR SYSTEM |
Abstract
PDF (Rus)
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V. A. Mglinets |
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| Vol 12, No 1 (2013) |
NEXT GENERATION SEQUENCING TECHNOLOGIES IN MEDICAL GENETIC STUDIES |
Abstract
PDF (Rus)
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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 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 14, No 11 (2015) |
Folate cycle: review and practical recommendations for the interpretation of genetic tests |
Abstract
PDF (Rus)
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N. V. Kokh, A. A. Slepukhina, G. I. Lifshits |
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| Vol 16, No 4 (2017) |
Genetically determined disorders of epoxygenase pathway of epoxyeicosatrienoic acids as a pathogenetic basis for the development of cardiovascular diseases |
Abstract
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A. V. Kharchenko, A. V. Polonikov |
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| Vol 17, No 3 (2018) |
Transcription of satellite DNA in human embryogenesis: review of literature and own data |
Abstract
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I. L. Trofimova, N. I. Enukashvily, T. V. Kuznetzova, V. S. Baranov |
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| Vol 18, No 10 (2019) |
Genetically associated breast cancer. Prevention and treatment |
Abstract
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A. D. Zikyrahodzhayev, E. K. Saribekyan, A. S. Sukhotko, A. V. Tregubova |
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| Vol 20, No 6 (2021) |
Modern ideas about the clinic, diagnosis and therapy of Fabry disease |
Abstract
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N. N. Mazanova, A. Yu. Asanov, M. I. Bakanov, I. G. Chebelyaev, K. V. Savostyanov |
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| Vol 14, No 12 (2015) |
Mechanisms of fetal adverse drug effects and importance of pharmacogenetics for safe medication use in pregnancy |
Abstract
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K. A. Zagorodnikova, A. T. Burbello, M. V. Pokladova |
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| Vol 16, No 4 (2017) |
Epigenetics of acute myeloid leukemia in adults and children |
Abstract
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V. V. Rudenko, A. S. Tanas, A. V. Popa, D. V. Zaletaev, V. V. Strelnikov |
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| Vol 17, No 4 (2018) |
The role of genetic factors in the development of gastric cancer |
Abstract
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L. F. Yusupova, A. Kh. Nurgalieva, R. I. Khusainova, D. D. Sakaeva, E. K. Khusnutdinova |
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| Vol 18, No 11 (2019) |
The hereditary ovarian cancer: role of candidate genes in disease pathogenesis |
Abstract
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R. R. Faiskhanova, D. S. Prokofieva, E. K. Khusnutdinova, D. D. Sakaeva, M. G. Gordiev |
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| Vol 20, No 6 (2021) |
Clinical and genetic parallels of the classification and diagnosis of Ehlers-Danlos syndrome |
Abstract
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D. D. Nadyrshina, A. V. Tyrin, E. K. Khusnutdinova, R. I. Khusainova |
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| Vol 14, No 12 (2015) |
The possibilities rendered by clinical pharmacogenetics for the personalized application of antibacterial drugs |
Abstract
PDF (Rus)
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E. I. Kondratieva, O. G. Novoselov, N. V. Petrova, R. A. Zinchenko, N. N. Chakova, V. I. Bobrovnichy |
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| Vol 16, No 5 (2017) |
Эволюция предиктивной медицины. Старые идеи, новые понятия |
Abstract
PDF (Rus)
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V. S. Baranov |
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| Vol 17, No 4 (2018) |
New approaches for diagnosis of Niemann-Pick disease type C |
Abstract
PDF (Rus)
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A. V. Degtyareva, S. V. Mikhailova, E. Y. Zakharova, T. Y. Proshlyakova, D. Y. Amirkhanova, M. S. Gautier |
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| Vol 18, No 12 (2019) |
Modern opportunities and indications for genetic diagnosis of male infertility |
Abstract
PDF (Rus)
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T. M. Sorokina, O. A. Solovova, V. B. Chernykh |
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| Vol 20, No 9 (2021) |
Characteristics of cortical tubers in tuberous sclerosis |
Abstract
PDF (Rus)
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E. V. Bychkova, M. Iu. Dorofeeva, V. V. Strelnikov, K. I. Anoshkin |
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| Vol 15, No 1 (2016) |
Genetics of migraine |
Abstract
PDF (Rus)
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N. S. Kondratieva, A. A. Anuchina, Z. G. Kokaeva, E. A. Naumova, J. E. Azimova, A. V. Sergeev, K. V. Skorobogatykh, G. R. Tabeeva, E. A. Klimov |
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| Vol 16, No 5 (2017) |
Possible genetic modifiers of spinal muscular atrophy |
Abstract
PDF (Rus)
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M. A. Maretina, A. V. Kiselev, V. S. Baranov |
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| Vol 17, No 5 (2018) |
Therapeutic approaches of the CRISPR/Cas genome editing system for genetic diseases in humans and model animals |
Abstract
PDF (Rus)
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V. A. Mglinets |
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| Vol 20, No 10 (2021) |
Clinical and molecular genetic features of neurofibromatosis type |
Abstract
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K. O. Karandasheva, E. S. Makashova, A. A. Martyanova, K. I. Anoshkin, S. V. Zolotova, V. V. Strelnikov |
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| Vol 15, No 2 (2016) |
Genetic heterogeneity of Mendelian disorders and DNA-diagnostics |
Abstract
PDF (Rus)
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A. V. Polyakov, O. A. Shchagina |
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| Vol 16, No 5 (2017) |
Epigenetic reprogramming in human gametes and preimplantation embryos |
Abstract
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A. V. Tikhonov, O. A. Efimova, A. A. Pendina, V. S. Baranov |
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| Vol 17, No 8 (2018) |
Hereditary spastic paraplegias in the era of next generation sequencing: genetic diversity, epidemiology, classification |
Abstract
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G. E. Rudenskaya, V. A. Kadnikova, O. P. Ryzhkova |
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| Vol 19, No 9 (2020) |
MicroRNA role in hereditary genetic diseases |
Abstract
PDF (Rus)
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O. M. Plotnikova, M. Yu. Skoblov |
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| Vol 20, No 12 (2021) |
The state of the reproductive system and fertility in men with trisomy 21 |
Abstract
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M. V. Andreeva, V. B. Chernykh, L. F. Kurilo |
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| Vol 15, No 3 (2016) |
Familial mediterranean fever: current view |
Abstract
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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
PDF (Rus)
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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
PDF (Rus)
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S. A. Smirnikhina, A. V. Lavrov |
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