Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lene Byriel"'
Autor:
Torben Hansen, Jan Lindebjerg, John Pløen, Anders Jakobsen, Lise Nottelmann, Eva Fernebro, Lene Byriel, Lars Henrik Jensen, Rikke F. Andersen
Publikováno v:
Jensen, L H, Andersen, R F, Byriel, L, Fernebro, E, Jakobsen, A, Lindebjerg, J, Nottelmann, L, Ploen, J & Hansen, T F 2020, ' Phase II study of gemcitabine, oxaliplatin and capecitabine in patients with KRAS exon 2 mutated biliary tract cancers ', Acta oncologica (Stockholm, Sweden), vol. 59, no. 3, pp. 298-301 . https://doi.org/10.1080/0284186X.2019.1701201
Background: Molecular markers may identify subgroups of patients with clinically distinct behavior and response to treatment. In some gastrointestinal tumors, KRAS has prognostic value and negative predictive value. This is the first prospective stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3de678a70b042a92af30048dc421aea
Autor:
Dorthe G. Crüger, Anders Jakobsen, Jan Lindebjerg, Kathleen D. Danenberg, Hidekazu Kuramochi, Lene Byriel, Lars Henrik Jensen, Peter V. Danenberg, Anders Aamann Rasmussen
Publikováno v:
Jensen, L H, Rasmussen, A A, Byriel, L, Kuramochi, H, Crüger, D G, Lindebjerg, J, Danenberg, P V, Jakobsen, A & Danenberg, K 2013, ' Regulation of MLH1 mRNA and protein expression by promoter methylation in primary colorectal cancer : a descriptive and prognostic cancer marker study ', Cellular Oncology, vol. 36, no. 5, pp. 411-419 . https://doi.org/10.1007/s13402-013-0148-2
Background In colorectal cancer MLH1 deficiency causes microsatellite instability, which is relevant for the patient's prognosis and treatment, and its putative heredity. Dysfunction of MLH1 is caused by sporadic gene promoter hypermethylation or by
Autor:
Gert Bruun Petersen, Bent Nørgaard-Pedersen, Ivan Brandslund, Torben Larsen, Jens Flensted Lassen, Lene Byriel
Publikováno v:
Larsen, T B, Lassen, J F, Brandslund, I, Byriel, L, Petersen, G B & Nørgaard-Pedersen, B 1998, ' The Arg506Gln mutation (FV Leiden) among a cohort of 4188 unselected Danish newborns ', Thrombosis Research, vol. 89, no. 5, pp. 211-215 . https://doi.org/10.1016/S0049-3848(98)00010-3
Resistance to activated protein C (APC) is the most prevalent single phenomenon associated with thromboembolic disease. It is caused by a single point mutation in the factor V gene (Arg506Gln or FV Leiden), replacing an Arg506 with a Gin at the APC-c
Publikováno v:
Jensen, L H, Lindebjerg, J, Byriel, L, Kølvrå, S & Crüger, D G 2007, ' Strategy in clinical practice for classification of unselected colorectal tumours based on mismatch repair deficiency ', Colorectal Disease, vol. 10, no. 5, pp. 490-497 . https://doi.org/10.1111/j.1463-1318.2007.01378.x
Udgivelsesdato: 2007-Sep-14 Objective Deficiency of DNA mismatch repair (MMR) causes microsatellite instability (MSI) in a subset of colorectal cancers. Patients with these tumours have a better prognosis and may have an altered response to chemother
Publikováno v:
Jensen, L H, Lindebjerg, J, Byriel, L, Kølvrå, S & Crüger, D G 2007, ' Classification of mismatch repair deficiency in primary colorectal cancer ', Insight. Congress 2007, Yokohama, Japan, 24/08/2010 .
University of Southern Denmark
University of Southern Denmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::786ad8d414409d724752d4924a2b8b69
https://portal.findresearcher.sdu.dk/da/publications/789ada90-00e8-11dd-9e03-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/789ada90-00e8-11dd-9e03-000ea68e967b
Autor:
Inge Bernstein, Lillian Bomme Ousager, Anders Bojesen, Katrine Urth Hansen, Michael Hardt-Madsen, Lars Henrik Jensen, Lene Byriel, Christian Ladefoged, Jan Lindebjerg, Tine Plato Hansen
Publikováno v:
Web of Science
6600 Background: A myriad of molecular markers has been proposed and tested with the promise of improving cancer care. Few have been validated and even fewer have been implemented in daily clinic. The most common hereditary colorectal cancer entity,
Autor:
Lene Byriel, Lars Dysager, Steen Kølvraa, Jan Lindebjerg, Lars Henrik Jensen, Dorthe G. Crüger
Publikováno v:
Journal of Clinical Oncology. 27:4113-4113
4113 Background: The single most common cause of hereditary colorectal cancer is the Lynch syndrome, which is associated with deficiency of the mismatch repair genes MLH1, MSH2, or MSH6. Most MLH1 negative tumors are sporadic in origin, and they can
Autor:
Lars Henrik Jensen, Jan Lindebjerg, Lene Byriel, Gert Bruun-Petersen, Steen Kølvrå, Anders Jakobsen, Crüger, Dorthe G.
Publikováno v:
University of Southern Denmark
Jensen, L H, Lindebjerg, J, Byriel, L, Bruun-Petersen, G, Kølvrå, S, Jakobsen, A & Crüger, D G 2007, ' Classification of mismatch repair deficiency in primary colorectal cancer ', Dansk Selskab for Klinisk Onkologi, Årsmøde 2007, Vejle, Denmark, 24/08/2010 .
Jensen, L H, Lindebjerg, J, Byriel, L, Bruun-Petersen, G, Kølvrå, S, Jakobsen, A & Crüger, D G 2007, ' Classification of mismatch repair deficiency in primary colorectal cancer ', Dansk Selskab for Klinisk Onkologi, Årsmøde 2007, Vejle, Denmark, 24/08/2010 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4e061242871b06ede4961c1de112cbe4
https://portal.findresearcher.sdu.dk/en/publications/acc36750-00e9-11dd-9e03-000ea68e967b
https://portal.findresearcher.sdu.dk/en/publications/acc36750-00e9-11dd-9e03-000ea68e967b