Entries of Kloor, Matthias on the publication server

Rahner, Nils, Brockschmidt, Felix F., Steinke, Verena, Kahl, Philip, Becker, Tim, Vasen, Hans F. A. , Wijnen, Juul T., Tops, Carli J. M., Holinski-Feder, Elke, Ligtenberg, Marjolijn J. L. , Spruijt, Liesbeth, Görgens, Heike, Stemmler, Susanne, Kloor, Matthias, Dietmaier, Wolfgang, Schumacher, Johannes , Nöthen, Markus M. and Propping, Peter (2012) Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors. Familial Cancer 11 (1), pp. 19-26. Fulltext not available.

Engel, Christoph , Rahner, Nils, Schulmann, Karsten, Holinski–Feder, Elke, Goecke, Timm O., Schackert, Hans K., Kloor, Matthias, Steinke, Verena, Vogelsang, Holger, Möslein, Gabriela, Görgens, Heike, Dechant, Stefan, von Knebel Doeberitz, Magnus, Rüschoff, Josef, Friedrichs, Nicolaus, Büttner, Reinhard, Loeffler, Markus, Propping, Peter and Schmiegel, Wolff (2010) Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer. Clinical Gastroenterology and Hepatology 8 (2), pp. 174-182. Fulltext not available.

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 and Aretz, Stefan (2008) No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. European Journal of Human Genetics 16 (5), pp. 587-592. Fulltext not available.

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 and 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), pp. 4285-4292. Fulltext not available.

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 and 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), pp. 115-122. Fulltext not available.

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 and 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), pp. 632-641. Fulltext not available.

Giuffrè, Giuseppe, Müller, Annegret, Brodegger, Thomas, Bocker-Edmonston, Tina, Gebert, Johannes, Kloor, Matthias, Dietmaier, Wolfgang, Kullmann, Frank, Büttner, Reinhard, Tuccari, Giovanni and Rüschoff, Josef (2005) Microsatellite Analysis of Hereditary Nonpolyposis Colorectal Cancer-Associated Colorectal Adenomas by Laser-Assisted Microdissection. The Journal of Molecular Diagnostics 7 (2), pp. 160-170. Fulltext not available.