Einträge von Keller, Gisela auf dem Publikationsserver

Heinrichs, Sophie K. M., Hess, Timo, Becker, Jessica, Hamann, Lutz, Vashist, Yogesh K., Butterbach, Katja, Schmidt, Thomas, Alakus, Hakan, Krasniuk, Iurii, Höblinger, Aksana, Lingohr, Philipp, Ludwig, Monika, Hagel, Alexander F., Schildberg, Claus W., Veits, Lothar, Gyvyte, Ugne, Weise, Katharina, Schüller, Vitalia, Böhmer, Anne C., Schröder, Julia, Gehlen, Jan, Kreuser, Nicole, Hofer, Sebastian, Lang, Hauke, Lordick, Florian, Malfertheiner, Peter, Moehler, Markus, Pech, Oliver, Vassos, Nikolaos, Rodermann, Ernst, Izbicki, Jakob R., Kruschewski, Martin, Ott, Katja, Schumann, Ralf R., Vieth, Michael, Mangold, Elisabeth, Gasenko, Evita, Kupcinskas, Limas, Brenner, Hermann, Grimminger, Peter, Bujanda, Luis, Sopeña, Federico, Espinel, Jesús, Thomson, Concha, Pérez-Aísa, Ángeles, Campo, Rafael, Geijo, Fernando, Collette, Daniela, Bruns, Christiane, Messerle, Katharina, Gockel, Ines, Nöthen, Markus M., Lippert, Hans, Ridwelski, Karsten, Lanas, Angel, Keller, Gisela, Knapp, Michael, Leja, Marcis, Kupcinskas, Juozas, García-González, Maria A., Venerito, Marino und Schumacher, Johannes (2018) Evidence for PTGER4 ,PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level. Cancer Medicine 7 (10), S. 5057-5065. Volltext nicht vorhanden.

Luber, Birgit, Deplazes, Joëlle, Keller, Gisela, Walch, Axel , Rauser, Sandra, Eichmann, Martin , Langer, Rupert , Höfler, Heinz, Hegewisch-Becker, Susanna, Folprecht, Gunnar , Wöll, Ewald, Decker, Thomas, Endlicher, Esther, Lorenzen, Sylvie, Fend, Falko, Peschel, Christian und Lordick, Florian (2011) Biomarker analysis of cetuximab plus oxaliplatin/leucovorin/5-fluorouracil in first-line metastatic gastric and oesophago-gastric junction cancer: results from a phase II trial of the Arbeitsgemeinschaft Internistische Onkologie (AIO). BMC Cancer 11 (1). Volltext nicht vorhanden.

Morak, Monika, Schackert, Hans Konrad, Rahner, Nils, Betz, Beate, Ebert, Matthias, Walldorf, Constanze, Royer-Pokora, Brigitte, Schulmann, Karsten, von Knebel-Doeberitz, Magnus, Dietmaier, Wolfgang, Keller, Gisela, Kerker, Brigitte, Leitner, Gertraud und Holinski-Feder, Elke (2008) Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC. European Journal of Human Genetics 16 (7), S. 804-811. Volltext nicht vorhanden.

Bettstetter, Marcus, Dechant, Stefan, Ruemmele, Petra, Vogel, Corinna, Kurz, Katrin, Morak, Monika, Keller, Gisela, Holinski-Feder, Elke, Hofstaedter, Ferdinand und Dietmaier, Wolfgang (2008) MethyQESD, a robust and fast method for quantitative methylation analyses in HNPCC diagnostics using formalin-fixed and paraffin-embedded tissue samples. Laboratory investigation 88 (12), S. 1367-1375. Volltext nicht vorhanden.

Steinke, Verena, Rahner, Nils, Morak, Monika, Keller, Gisela, Schackert, Hans K, Görgens, Heike, Schmiegel, Wolff, Royer-Pokora, Brigitte, Dietmaier, Wolfgang, Kloor, Matthias, Engel, Christoph , Propping, Peter und Aretz, Stefan (2008) No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. European Journal of Human Genetics 16 (5), S. 587-592. Volltext nicht vorhanden.

Bettstetter, Marcus, Dechant, Stephan, Ruemmele, Petra, Grabowski, Monika, Keller, Gisela, Holinski-Feder, Elke, Hartmann, Arndt, Hofstaedter, Ferdinand und Dietmaier, Wolfgang (2007) Distinction of Hereditary Nonpolyposis Colorectal Cancer and Sporadic Microsatellite-Unstable Colorectal Cancer through Quantification of MLH1 Methylation by Real-time PCR. Clinical Cancer Research 13 (11), S. 3221-3228. Volltext nicht vorhanden.

Goecke, Timm, Schulmann, Karsten, Engel, Christoph , Holinski-Feder, Elke, Pagenstecher, Constanze, Schackert, Hans K., Kloor, Matthias, Kunstmann, Erdmute, Vogelsang, Holger, Keller, Gisela, Dietmaier, Wolfgang, Mangold, Elisabeth, Friedrichs, Nicolaus, Propping, Peter, Krüger, Stefan, Gebert, Johannes, Schmiegel, Wolff, Rueschoff, Josef, Loeffler, Markus und Moeslein, Gabriela (2006) Genotype-Phenotype Comparison of German MLH1 and MSH2 Mutation Carriers Clinically Affected With Lynch Syndrome: A Report by the German HNPCC Consortium. Journal of Clinical Oncology 24 (26), S. 4285-4292. Volltext nicht vorhanden.

Engel, Christoph , Forberg, Jochen, Holinski‐Feder, Elke, Pagenstecher, Constanze, Plaschke, Jens, Kloor, Matthias, Poremba, Christopher, Pox, Christian P., Rüschoff, Josef, Keller, Gisela, Dietmaier, Wolfgang, Rümmele, Petra, Friedrichs, Nicolaus, Mangold, Elisabeth, Buettner, Reinhard, Schackert, Hans K., Kienle, Peter, Stemmler, Susanne, Moeslein, Gabriela und Loeffler, Markus (2006) Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. International Journal of Cancer 118 (1), S. 115-122. Volltext nicht vorhanden.

Müller, Annegret, Beckmann, Carmen, Westphal, Gabriela, Bocker Edmonston, Tina, Friedrichs, Nicolaus, Dietmaier, Wolfgang, Brasch, Frank E., Kloor, Matthias, Poremba, Christoph, Keller, Gisela, Aust, Daniela E., Faß, Jürgen, Büttner, Reinhard, Becker, Heinz und Rüschoff, Josef (2006) Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study. International Journal of Colorectal Disease 21 (7), S. 632-641. Volltext nicht vorhanden.

Grabowski, Monika, Mueller-Koch, Yvonne, Grasbon-Frodl, Eva, Koehler, Udo, Keller, Gisela, Vogelsang, Holger, Dietmaier, Wolfgang, Kopp, Reinhard, Siebers, Ulrike, Schmitt, Wolfgang, Neitzel, Birgit, Gruber, Maria, Doerner, Christa, Kerker, Brigitte, Ruemmele, Petra, Henke, Gabriele und Holinski-Feder, Elke (2005) Deletions Account for 17% of Pathogenic Germline Alterations in MLH1 and MSH2 in Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Families. Genetic Testing 9 (2), S. 138-146. Volltext nicht vorhanden.

Keller, Gisela, Hartmann, Arndt, Mueller, James und Höfler, Heinz (2001) Denaturing High Pressure Liquid Chromatography (DHPLC) for the Analysis of Somatic p53 Mutations. Laboratory Investigation 81 (12), S. 1735-1737. Volltext nicht vorhanden.