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1دورية أكاديمية
المؤلفون: Andesdottir, Arna Kristin, Einarsson, Haukur, Jonsdottir, Hildur, Jónasson, Jón Gunnlaugur, Björnsson, Einar Stefán, Haraldsdóttir, Sigurdís
المساهمون: Faculty of Medicine, Other departments
مصطلحات موضوعية: Meltingarlæknisfræði, Meinafræði, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Colorectal Neoplasms/genetics, DNA Mismatch Repair, Germ-Line Mutation, Humans, Iceland/epidemiology, Mismatch Repair Endonuclease PMS2/genetics, MutL Protein Homolog 1/genetics, MutS Homolog 2 Protein/genetics, Gastroenterology, Hepatology
وصف الملف: 1314-1316.e1
العلاقة: Gastroenterology; 164(7); http://www.scopus.com/inward/record.url?scp=85153928925&partnerID=8YFLogxKTest; Andesdottir , A K , Einarsson , H , Jonsdottir , H , Jónasson , J G , Björnsson , E S & Haraldsdóttir , S 2023 , ' Metachronous Colorectal Cancer in Icelandic MSH6 and PMS2 Lynch Syndrome Carriers in 1955-2017 : A Population-based Study ' , Gastroenterology , vol. 164 , no. 7 , pp. 1314-1316.e1 . https://doi.org/10.1053/j.gastro.2023.02.007Test; 123563317; 42e7775c-6f54-4445-b9c2-b4cafd4f9b7e; 85153928925; unpaywall: 10.1053/j.gastro.2023.02.007; https://hdl.handle.net/20.500.11815/4170Test
الإتاحة: https://doi.org/20.500.11815/4170Test
https://doi.org/10.1053/j.gastro.2023.02.007Test
https://hdl.handle.net/20.500.11815/4170Test -
2دورية أكاديمية
المؤلفون: Salikhanov, Islam, Heinimann, Karl, Chappuis, Pierre, Buerki, Nicole, Graffeo, Rossella, Heinzelmann, Viola, Rabaglio, Manuela, Taborelli, Monica, Wieser, Simon, Katapodi, Maria C
المصدر: ISSN: 0022-2593 ; Journal of medical genetics, vol. 59, no. 9 (2022) p. 924-930.
مصطلحات موضوعية: info:eu-repo/classification/ddc/616, Costs and cost analysis, Gastrointestinal diseases, Genetic counseling, Genetic testing, Health care economics and organizations, Colorectal Neoplasms / diagnosis, Colorectal Neoplasms / epidemiology, Colorectal Neoplasms / genetics, Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis, Hereditary Nonpolyposis / epidemiology, Hereditary Nonpolyposis / genetics, Cost-Benefit Analysis, Early Detection of Cancer, Genetic Testing / methods, Humans, Switzerland / epidemiology
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34782441; https://archive-ouverte.unige.ch/unige:169014Test; unige:169014
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3دورية أكاديمية
المؤلفون: Allen, Jawara, Rosendahl Huber, Axel, Pleguezuelos-Manzano, Cayetano, Puschhof, Jens, Wu, Shaoguang, Wu, Xinqun, Boot, Charelle, Saftien, Aurelia, O'Hagan, Heather M, Wang, Hao, van Boxtel, Ruben, Clevers, Hans, Sears, Cynthia L
المصدر: Allen , J , Rosendahl Huber , A , Pleguezuelos-Manzano , C , Puschhof , J , Wu , S , Wu , X , Boot , C , Saftien , A , O'Hagan , H M , Wang , H , van Boxtel , R , Clevers , H & Sears , C L 2022 , ' Colon Tumors in Enterotoxigenic Bacteroides fragilis (ETBF)-Colonized Mice Do Not Display a Unique Mutational Signature but Instead Possess Host-Dependent Alterations in the APC Gene ' , Microbiology spectrum , vol. 10 , no. 3 , pp. e0105522 . https://doi.org/10.1128/spectrum.01055-22Test
مصطلحات موضوعية: Adenomatous Polyposis Coli/genetics, Animals, Bacterial Infections/pathology, Bacteroides fragilis/genetics, Colon/microbiology, Colonic Neoplasms/genetics, Colorectal Neoplasms/microbiology, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Disease Models, Animal, Escherichia coli/genetics, Genes, APC, Mice, Mutation
الإتاحة: https://doi.org/10.1128/spectrum.01055-22Test
https://doi.org/20.500.11755/613fd9c5-80b0-4501-ad0e-fe486dce0256Test
https://pure.knaw.nl/portal/en/publications/613fd9c5-80b0-4501-ad0e-fe486dce0256Test
https://hdl.handle.net/20.500.11755/613fd9c5-80b0-4501-ad0e-fe486dce0256Test -
4دورية أكاديمية
المساهمون: Yoon Young Choi, Su-Jin Shin, Jae Eun Lee, Lisa Madlensky, Seung-Tae Lee, Ji Soo Park, Jeong-Hyeon Jo, Hyunki Kim, Daniela Nachmanson, Xiaojun Xu, Sung Hoon Noh, Jae-Ho Cheong, Olivier Harismendy, Kim, Hyunki
مصطلحات موضوعية: Adult, Age of Onset, Aged, Biomarkers, Tumor / genetics, Colorectal Neoplasms / genetics, Colorectal Neoplasms, Hereditary Nonpolyposis / genetics, Endometrial Neoplasms / genetics, Female, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Loss of Function Mutation, Male, Microsatellite Instability, Middle Aged, Prevalence, Retrospective Studies, Stomach Neoplasms / genetics, Whole Exome Sequencing
وصف الملف: application/pdf
العلاقة: SCIENTIFIC REPORTS; J02646; OAK-2021-09745; https://ir.ymlib.yonsei.ac.kr/handle/22282913/187574Test; T202124877; SCIENTIFIC REPORTS, Vol.11(1) : 14807, 2021-07
الإتاحة: https://doi.org/10.1038/s41598-021-94292-4Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/187574Test -
5دورية أكاديمية
المؤلفون: Seppälä, Toni T, Dominguez-Valentin, Mev, Crosbie, Emma J, Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria G, Cavestro, Giulia M, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A, Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauß, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Vida, Joan B, Kariv, Revital, Rosner, Guy, Piñero, Tamara A, Pavicic, Walter, Kalfayan, Pablo, Ten Broeke, Sanne W, Jenkins, Mark A, Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, de Vos Tot Nederveen Cappel, Wouter H, Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Büttner, Reinhard, Görgens, Heike, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, von Knebel Doeberitz, Magnus, Loeffler, Markus, Redler, Silke, Weitz, Jürgen, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Hopper, John L, Win, Aung K, Lindor, Noralane M, Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A, Figueiredo, Jane C, Thibodeau, Stephen N, Therkildsen, Christina, Wadt, Karin A W, Mourits, Marian J E, Ketabi, Zohreh, Denton, Oliver G, Rødland, Einar A, Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Möslein, Gabriela, Rokkones, Erik, Sampson, Julian R, Evans, D G, Møller, Pål
المصدر: Seppälä , T T , Dominguez-Valentin , M , Crosbie , E J , Engel , C , Aretz , S , Macrae , F , Winship , I , Capella , G , Hovig , E , Nielsen , M , Sijmons , R H , Bertario , L , Bonanni , B , Tibiletti , M G , Cavestro , G M , Mints , M , Gluck , N , Katz , L , Heinimann , K , Vaccaro , C A , Green , K , Lalloo , F , Hill , J , Schmiegel ....
مصطلحات موضوعية: Adult, Aged, Biomarkers, Tumor/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Cross-Sectional Studies, DNA Mismatch Repair, Databases, Factual, Female, Follow-Up Studies, Genital Neoplasms, Female/prevention & control, Heterozygote, Humans, Hysterectomy/methods, Middle Aged, Mutation, Prognosis, Prospective Studies, Salpingo-oophorectomy/methods, ResearchInstitutes_Networks_Beacons/mcrc, Manchester Cancer Research Centre
الإتاحة: https://doi.org/10.1016/j.ejca.2021.02.022Test
https://research.manchester.ac.uk/en/publications/b69d6946-2d71-4de2-8b39-ca0c6023d2d0Test -
6دورية أكاديمية
المؤلفون: Evans, D Gareth
المصدر: Evans , D G & et al. 2020 , ' Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study : a double-blind, randomised, placebo-controlled trial ' , Lancet , vol. 395 , no. 10240 , pp. 1855-1863 . https://doi.org/10.1016/S0140-6736Test(20)30366-4
مصطلحات موضوعية: Anti-Inflammatory Agents, Non-Steroidal/adverse effects, Aspirin/adverse effects, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Double-Blind Method, Follow-Up Studies, Heterozygote, Humans, Intention to Treat Analysis, Life Tables, Medication Adherence, Proportional Hazards Models
الإتاحة: https://doi.org/10.1016/S0140-6736Test(20)30366-4
https://research.manchester.ac.uk/en/publications/c1e90071-1be0-4ce2-8a26-69f991bc8f4cTest
http://www.scopus.com/inward/record.url?scp=85086110417&partnerID=8YFLogxKTest -
7دورية أكاديمية
المؤلفون: Gallon, Richard, Phelps, Rachel, Hayes, Christine, Brugieres, Laurence, Guerrini-Rousseau, Léa, Colas, Chrystelle, Muleris, Martine, Ryan, Neil A J, Evans, D Gareth, Grice, Hannah, Jessop, Emily, Kunzemann-Martinez, Annabel, Marshall, Lilla, Schamschula, Esther, Oberhuber, Klaus, Azizi, Amedeo A, Baris Feldman, Hagit, Beilken, Andreas, Brauer, Nina, Brozou, Triantafyllia, Dahan, Karin, Demirsoy, Ugur, Florkin, Benoit, Foulkes, William, Januszkiewicz-Lewandowska, Danuta, Jones, Kristi J, Kratz, Christian P, Lobitz, Stephan, Meade, Julia, Nathrath, Michaela, Pander, Hans-Jürgen, Perne, Claudia, Ragab, Iman, Ripperger, Tim, Rosenbaum, Thorsten, Rueda, Daniel, Sarosiek, Tomasz, Sehested, Astrid, Spier, Isabel, Suerink, Manon, Zimmermann, Stefanie-Yvonne, Zschocke, Johannes, Borthwick, Gillian M, Wimmer, Katharina, Burn, John, Jackson, Michael S, Santibanez-Koref, Mauro
المصدر: Gastroenterology, 164 (4), 579 - 592.e8 (2023)
مصطلحات موضوعية: Constitutional Mutation Burden, Functional Test, Pediatric Cancer, Replication Error Repair, Mismatch Repair Endonuclease PMS2, Humans, Microsatellite Instability, Genotype, DNA Mismatch Repair/genetics, Mismatch Repair Endonuclease PMS2/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Neoplastic Syndromes, Hereditary/diagnosis, Hereditary/genetics, Colorectal Neoplasms/genetics, Colorectal Neoplasms/diagnosis, Brain Neoplasms/diagnosis, Brain Neoplasms, Hereditary Nonpolyposis, DNA Mismatch Repair, Hereditary, Hepatology, Gastroenterology, Life sciences, Genetics & genetic processes, Human health sciences, Pediatrics, Oncology, Sciences du vivant
العلاقة: https://api.elsevier.com/content/article/PII:S0016508522014445?httpAccept=text/xmlTest; urn:issn:0016-5085; urn:issn:1528-0012; https://orbi.uliege.be/handle/2268/314387Test; info:hdl:2268/314387; scopus-id:2-s2.0-85148051094; info:pmid:36586540
الإتاحة: https://doi.org/10.1053/j.gastro.2022.12.017Test
https://orbi.uliege.be/handle/2268/314387Test -
8دورية أكاديمية
المؤلفون: Ryan, N A J, Glaire, M A, Blake, D, Cabrera-Dandy, M, Evans, D G, Crosbie, E J
المصدر: Ryan , N A J , Glaire , M A , Blake , D , Cabrera-Dandy , M , Evans , D G & Crosbie , E J 2019 , ' The proportion of endometrial cancers associated with Lynch syndrome : a systematic review of the literature and meta-analysis ' , Genetics in Medicine , vol. 21 , no. 10 , pp. 2167-2180 . https://doi.org/10.1038/s41436-019-0536-8Test
مصطلحات موضوعية: Adult, Brain Neoplasms/genetics, Colorectal Neoplasms/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Comorbidity, DNA Mismatch Repair/genetics, Early Detection of Cancer, Endometrial Neoplasms/genetics, Female, Genetic Testing, Germ-Line Mutation, Humans, Immunohistochemistry, Microsatellite Instability, Middle Aged, Neoplastic Syndromes, Hereditary/genetics
وصف الملف: application/pdf
العلاقة: https://research-information.bris.ac.uk/en/publications/680bec92-f577-4867-9f60-673679d693e8Test
الإتاحة: https://doi.org/10.1038/s41436-019-0536-8Test
https://hdl.handle.net/1983/680bec92-f577-4867-9f60-673679d693e8Test
https://research-information.bris.ac.uk/en/publications/680bec92-f577-4867-9f60-673679d693e8Test
https://research-information.bris.ac.uk/ws/files/253697845/s41436_019_0536_8.pdfTest -
9
المؤلفون: Jawara Allen, Axel Rosendahl Huber, Cayetano Pleguezuelos-Manzano, Jens Puschhof, Shaoguang Wu, Xinqun Wu, Charelle Boot, Aurelia Saftien, Heather M. O’Hagan, Hao Wang, Ruben van Boxtel, Hans Clevers, Cynthia L. Sears
المساهمون: Hubrecht Institute for Developmental Biology and Stem Cell Research
المصدر: Microbiology spectrum, 10(3). American Society for Microbiology
مصطلحات موضوعية: Microbiology (medical), Genes, APC, Colon, Physiology, Bacteroides fragilis, Mice, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Escherichia coli, Genetics, Animals, Hereditary Nonpolyposis/genetics, General Immunology and Microbiology, Ecology, Animal, Colorectal Neoplasms/microbiology, Adenomatous Polyposis Coli/genetics, Bacteroides fragilis/genetics, Colonic Neoplasms/genetics, Bacterial Infections, Cell Biology, Colorectal Neoplasms, Hereditary Nonpolyposis, APC, Escherichia coli/genetics, Disease Models, Animal, Infectious Diseases, Genes, Adenomatous Polyposis Coli, Disease Models, Colonic Neoplasms, Mutation, Colon/microbiology, Colorectal Neoplasms, Bacterial Infections/pathology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::278afae4175af2db176a76e2686e0ac5Test
https://doi.org/10.1128/spectrum.01055-22Test -
10دورية أكاديمية
المؤلفون: Mur, Pilar, De Voer, Richarda M, Olivera-Salguero, Rubén, Rodríguez-Perales, Sandra, Pons, Tirso, Setién, Fernando, Aiza, Gemma, Valdés-Mas, Rafael, Bertini, Angelo, Pineda, Marta, Vreede, Lilian, Navarro, Matilde, Iglesias, Silvia, González, Sara, Brunet, Joan, Valencia, Alfonso, Esteller, Manel, Lázaro, Conxi, Kops, Geert J P L, Urioste, Miguel, Puente, Xose S, Capellá, Gabriel, Valle, Laura
المصدر: Mur , P , De Voer , R M , Olivera-Salguero , R , Rodríguez-Perales , S , Pons , T , Setién , F , Aiza , G , Valdés-Mas , R , Bertini , A , Pineda , M , Vreede , L , Navarro , M , Iglesias , S , González , S , Brunet , J , Valencia , A , Esteller , M , Lázaro , C , Kops , G J P L , Urioste , M , Puente , X S , Capellá , G & Valle , L 2018 , ....
مصطلحات موضوعية: Adenomatous Polyposis Coli/genetics, Cell Cycle Proteins/chemistry, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Germ-Line Mutation, Humans, Models, Molecular, Pedigree, Poly-ADP-Ribose Binding Proteins/chemistry, Protein Conformation, Protein-Serine-Threonine Kinases/chemistry, Spindle Apparatus/genetics
الإتاحة: https://doi.org/10.1186/s12943-018-0762-8Test
https://doi.org/20.500.11755/76ecf250-55e8-46e0-904b-ce50d8757d9eTest
https://pure.knaw.nl/portal/en/publications/76ecf250-55e8-46e0-904b-ce50d8757d9eTest
https://hdl.handle.net/20.500.11755/76ecf250-55e8-46e0-904b-ce50d8757d9eTest