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1دورية أكاديمية
المؤلفون: Tilea, Monica, Ólafsdóttir, Sigríður, Duță, Oana-Adriana
المساهمون: School of education (UI), Menntavísindasvið (HÍ), Háskóli Íslands, University of Iceland
مصطلحات موضوعية: Menntakerfi, Viðhorf, Rúmenía, Ísland, Nemendur, Educational system, Romanian learners, Icelandic learners, Comparative research, Samanburðarrannsóknir, Opinion polls
وصف الملف: 129-143
العلاقة: Social Sciences and Education Research Review;7(1); https://sserr.roTest; Tilea, M., Duță, O & Ólafsdóttir, S. (2020). A Romanian and Icelandic student's profile from the perspective of education for democratic citizenship. Social Sciences and Education Research Review, 7(1), 129-143.; https://hdl.handle.net/20.500.11815/2056Test; Social Sciences and Education Research Review
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2دورية أكاديمية
المؤلفون: Iordache, Paul, Mates, Dana, Gunnarsson, Bjarni, Eggertsson, Hannes, sulem, patrick, Benonisdottir, Stefania, Csiki, Irma Eva, Rascu, Stefan, Radavoi, Daniel, Ursu, Radu, Staicu, Catalin, Calota, Violeta, Voinoiu, Angelica, Jinga, Mariana, Rosoga, Gabriel, Danau, Razvan, Sima, Sorin Cristian, Badescu, Daniel, Suciu, Nicoleta, Radoi, Viorica, Mates, Ioan Nicolae, Dobra, Mihai, Nicolae, Camelia, Kristjansdottir, Sigrun, Jónasson, Jón G., Manolescu, Andrei, Arnadottir, Gudny, Jensson, Brynjar Örn, Jonasdottir, Aslaug, Sigurdsson, Asgeir, le Roux, Louise, Johannsdottir, Hrefna, Rafnar, Thorunn, Halldórsson, Bjarni, Jinga, Viorel, Stefansson, Kari
المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland
مصطلحات موضوعية: Colorectal cancer, Lynch syndrome, Romania, Endaþarmskrabbamein, Lynch heilkenni, Rúmenía
وصف الملف: 6068-6076
العلاقة: info:eu-repo/grantAgreement/EC/FP7/202059; Journal of Cellular and Molecular Medicine;22(12); Iordache, PD, Mates, D, Gunnarsson, B, et al. Identification of Lynch syndrome risk variants in the Romanian population. J Cell Mol Med. 2018; 22: 6068– 6076. https://doi.org/10.1111/jcmm.13881Test; 1582-4934 (eISSN); https://hdl.handle.net/20.500.11815/1301Test; Journal of Cellular and Molecular Medicine
الإتاحة: https://doi.org/20.500.11815/1301Test
https://doi.org/10.1111/jcmm.13881Test
https://hdl.handle.net/20.500.11815/1301Test -
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المؤلفون: Bjarni Gunnarsson, Viorel Jinga, Angelica Voinoiu, Hrefna Johannsdottir, Stefan Rascu, Stefania Benonisdottir, Violeta Calota, Sorin Cristian Sima, Jon G. Jonasson, Razvan Danau, Dana Mates, Viorica Radoi, Daniel Badescu, Radu Ursu, Camelia Nicolae, Gudny A. Arnadottir, Cătălin Alexandru Staicu, Bjarni V. Halldorsson, Thorunn Rafnar, Paul D. Iordache, Aslaug Jonasdottir, Asgeir Sigurdsson, Kari Stefansson, Mihai Dobra, Irma Eva Csiki, Hannes P. Eggertsson, Sigrun Kristjansdottir, Ioan Nicolae Mates, Mariana Jinga, Louise le Roux, Andrei Manolescu, Brynjar O. Jensson, Nicoleta Suciu, Daniel Radavoi, Gabriel Rosoga, Patrick Sulem
المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland
المصدر: Journal of Cellular and Molecular Medicine
مصطلحات موضوعية: Male, 0301 basic medicine, Rúmenía, DNA Mismatch Repair, DNA Glycosylases, Risk Factors, PMS2, Mismatch Repair Endonuclease PMS2, Genetics, education.field_of_study, Middle Aged, Lynch syndrome, 3. Good health, DNA-Binding Proteins, MutS Homolog 2 Protein, Adenomatous Polyposis Coli, Molecular Medicine, Female, Original Article, MutL Protein Homolog 1, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Lynch heilkenni, Population, Biology, MLH1, Familial adenomatous polyposis, 03 medical and health sciences, MUTYH, medicine, Humans, Genetic Predisposition to Disease, MLH1,MSH2,MSH6, MUTYH,PMS2, education, neoplasms, Aged, Endaþarmskrabbamein, Romania, nutritional and metabolic diseases, Original Articles, Cell Biology, DNA Methylation, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal cancer, digestive system diseases, MSH6, 030104 developmental biology, MSH2, Mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb71a9cd3010c7f038a6df677219bc6Test
https://doi.org/10.1111/jcmm.13881Test -
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