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المؤلفون: Platonov FA; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Tyryshkin K; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, K7L 3N6, Canada., Tikhonov DG; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Neustroyeva TS; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Sivtseva TM; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Yakovleva NV; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Nikolaev VP; Institute of Health, M.K. Ammosov North-Eastern Federal University, Yakutsk, 677010, The Russian Federation., Sidorova OG; Center for Integrated Medical Research, Academy of Medical Sciences, Yakutsk, 677010, The Russian Federation., Kononova SK; Center for Integrated Medical Research, Academy of Medical Sciences, Yakutsk, 677010, The Russian Federation., Goldfarb LG; National Institute of Neurological Disorder and Stoke, NIH, Bethesda, MD, 20892, USA. GoldfarbL@ninds.nih.gov., Renwick NM; Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, K7L 3N6, Canada.

المصدر: Neurogenetics [Neurogenetics] 2016 Jul; Vol. 17 (3), pp. 179-85. Date of Electronic Publication: 2016 Apr 22.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Intramural

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Fitness* , Selection, Genetic*, Ataxin-1/*genetics , Spinocerebellar Ataxias/*epidemiology , Spinocerebellar Ataxias/*genetics, Adult ; Aged ; Aged, 80 and over ; Birth Rate ; Cohort Studies ; Female ; Heterozygote ; Humans ; Incidence ; Male ; Middle Aged ; Mutation ; Siberia/epidemiology

المؤلفون: Barashkov NA; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Pshennikova VG; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Posukh OL; Laboratory of Human Molecular Genetics, Federal Research Center, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation.; Novosibirsk State University, Novosibirsk, Russian Federation., Teryutin FM; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Solovyev AV; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Klarov LA; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Department of Radiology, Republican Hospital # 2 -Center of Emergency Medicine, Ministry of Public Health of the Sakha Republic, Yakutsk, Russian Federation., Romanov GP; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Gotovtsev NN; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Kozhevnikov AA; Republican Centre of Professional Pathology, Republican Hospital # 2 -Center of Emergency Medicine, Ministry of Public Health of the Sakha Republic, Yakutsk, Russian Federation., Kirillina EV; Institute of Foreign Philology and Regional Studies, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Sidorova OG; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation., Vasilyevа LM; Audiology-Logopaedic Centre, Republican Hospital #1- National Medical Centre, Ministry of Public Health of the Sakha Republic, Yakutsk, Russian Federation., Fedotova EE; Audiology-Logopaedic Centre, Republican Hospital #1- National Medical Centre, Ministry of Public Health of the Sakha Republic, Yakutsk, Russian Federation., Morozov IV; Novosibirsk State University, Novosibirsk, Russian Federation.; SB RAS Genomics Core Facility, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation., Bondar AA; SB RAS Genomics Core Facility, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation., Solovyevа NA; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Kononova SK; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Rafailov AM; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Sazonov NN; Department of Biochemistry and Biotechnology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation., Alekseev AN; Institute of Humanitarian Research and Indigenous Peoples of the North, Siberian Branch of the Russian Academy of Sciences, Yakutsk, Russian Federation., Tomsky MI; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation., Dzhemileva LU; Laboratory of Human Molecular Genetics, Institute of Biochemistry and Genetics, Ufa Scientific Centre, Russian Academy of Sciences, Ufa, Russian Federation.; Department of Immunology and Human Reproductive Health, Bashkir State Medical University, Ufa, Russian Federation., Khusnutdinova EK; Laboratory of Human Molecular Genetics, Institute of Biochemistry and Genetics, Ufa Scientific Centre, Russian Academy of Sciences, Ufa, Russian Federation.; Department of Genetics and Fundamental Medicine, Bashkir State University, Ufa, Russian Federation., Fedorova SA; Department of Molecular Genetics, Federal State Budgetary Scientific Institution 'Yakut Science Centre of Complex Medical Problems,' Yakutsk, Russian Federation.; Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation.

المصدر: PloS one [PLoS One] 2016 May 25; Vol. 11 (5), pp. e0156300. Date of Electronic Publication: 2016 May 25 (Print Publication: 2016).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Connexins/*genetics , Hearing Loss/*genetics , Sequence Analysis, DNA/*methods, Adolescent ; Adult ; Arctic Regions ; Connexin 26 ; Exons ; Female ; Gene Frequency ; Hearing Loss/ethnology ; Humans ; Male ; Russia/ethnology ; Young Adult

المؤلفون: Kononova SK; Yakutsk Scientific Center of Complex Medical Problems, Siberian Branch of the Russian Academy of Medical Sciences, Yakutsk, Russia ; Institute of Natural Sciences, M. K. Ammosov North-Eastern Federal University, Yakutsk, Russia., Sidorova OG; Yakutsk Scientific Center of Complex Medical Problems, Siberian Branch of the Russian Academy of Medical Sciences, Yakutsk, Russia., Fedorova SA; Yakutsk Scientific Center of Complex Medical Problems, Siberian Branch of the Russian Academy of Medical Sciences, Yakutsk, Russia ; Institute of Natural Sciences, M. K. Ammosov North-Eastern Federal University, Yakutsk, Russia., Platonov FA; Institute of Natural Sciences, M. K. Ammosov North-Eastern Federal University, Yakutsk, Russia., Izhevskaya VL; Research Centre for Medical Genetics of the Russian Academy of Medical Sciences, Moscow, Russia., Khusnutdinova EK; Institute for Biochemistry and Genetics, Ufa Scientific Centre of the Russian Academy of Sciences, Ufa, Russia.

المصدر: International journal of circumpolar health [Int J Circumpolar Health] 2014 Jul 24; Vol. 73, pp. 25062. Date of Electronic Publication: 2014 Jul 24 (Print Publication: 2014).

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 9713056 Publication Model: eCollection Cited Medium: Internet ISSN: 2242-3982 (Electronic) Linking ISSN: 12399736 NLM ISO Abbreviation: Int J Circumpolar Health Subsets: MEDLINE

مواضيع طبية MeSH: Heterozygote*, Genetic Diseases, Inborn/*prevention & control , Genetic Testing/*ethics , Prenatal Diagnosis/*ethics, Adult ; Bioethical Issues ; Female ; Genetic Counseling ; Genetic Diseases, Inborn/diagnosis ; Health Knowledge, Attitudes, Practice ; Humans ; Middle Aged ; Pregnancy ; Registries ; Risk Assessment ; Siberia