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

المؤلفون: Thorunn Rafnar, Viorel Jinga, Stefan Rascu, Viorica Radoi, Daniel Badescu, Stefania Benonisdottir, Bjarni V. Halldorsson, Angelica Voinoiu, Radu Ursu, Hannes P. Eggertsson, Bjarni Gunnarsson, Paul D. Iordache, Razvan Danau, Cătălin Alexandru Staicu, Irma Eva Csiki, Mariana Jinga, Violeta Calota, Dana Mates, Nicoleta Suciu, Patrick Sulem, Daniel Radavoi, Gabriel Rosoga, Kari Stefansson, Sorin Cristian Sima, Andrei Manolescu, Júlíus Guðmundsson

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), School of Health Sciences (UI), Heilbrigðisvísindasvið (HÍ), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland

المصدر: Journal of Cellular and Molecular Medicine

مصطلحات موضوعية: 0301 basic medicine, Male, Erfðagreining, Genome-wide association study, unscreened population, Unscreened population, Genome-wide association studies, Prostate cancer, Gene Frequency, GWAS, genome‐wide association study, Oligonucleotide Array Sequence Analysis, Genetics, Prostate cancer risk, Aged, 80 and over, education.field_of_study, Middle Aged, prostate cancer, 3. Good health, Molecular Medicine, Population study, Original Article, Risk, Population, Single-nucleotide polymorphism, Blöðruhálskirtilskrabbamein, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, medicine, Biomarkers, Tumor, SNP, Erfðafræði, Humans, Genetic Predisposition to Disease, 1000 Genomes Project, education, Alleles, Aged, Neoplasm Staging, Romania, Genome, Human, Gene Expression Profiling, Prostatic Neoplasms, Cell Biology, Rannsóknir, Original Articles, Prostate-Specific Antigen, medicine.disease, 030104 developmental biology, Genetic Loci, Case-Control Studies, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e347f6d1ee2040725e35a42a4f8dc28dTest
http://europepmc.org/articles/PMC5824401Test