Gebert J - Search Results

1

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium.

Goecke T, Schulmann K, Engel C, Holinski-Feder E, Pagenstecher C, Schackert HK, Kloor M, Kunstmann E, Vogelsang H, Keller G, Dietmaier W, Mangold E, Friedrichs N, Propping P, Krüger S, Gebert J, Schmiegel W, Rueschoff J, Loeffler M, Moeslein G; German HNPCC Consortium. Goecke T, et al. Among authors: gebert j. J Clin Oncol. 2006 Sep 10;24(26):4285-92. doi: 10.1200/JCO.2005.03.7333. Epub 2006 Aug 14. J Clin Oncol. 2006. PMID: 16908935

2

Identification of a novel germline mutation in a FAP family.

Gebert JF, Hahn M, Kadmon M, Herfarth C, Schackert HK. Gebert JF, et al. Hum Mol Genet. 1994 Jul;3(7):1167-8. doi: 10.1093/hmg/3.7.1167. Hum Mol Genet. 1994. PMID: 7981688 No abstract available.

3

Monitoring gene therapy with cytosine deaminase: in vitro studies using tritiated-5-fluorocytosine.

Haberkorn U, Oberdorfer F, Gebert J, Morr I, Haack K, Weber K, Lindauer M, van Kaick G, Schackert HK. Haberkorn U, et al. Among authors: gebert j. J Nucl Med. 1996 Jan;37(1):87-94. J Nucl Med. 1996. PMID: 8544010 Free article.

4

Cytosine deaminase gene as a potential tool for the genetic therapy of colorectal cancer.

Rowley S, Lindauer M, Gebert JF, Haberkorn U, Oberdorfer F, Moebius U, Herfarth C, Schackert HK. Rowley S, et al. Among authors: gebert jf. J Surg Oncol. 1996 Jan;61(1):42-8. doi: 10.1002/(SICI)1096-9098(199601)61:1<42::AID-JSO10>3.0.CO;2-Z. J Surg Oncol. 1996. PMID: 8544459

5

Microsatellite instability analysis: a multicenter study for reliability and quality control.

Bocker T, Diermann J, Friedl W, Gebert J, Holinski-Feder E, Karner-Hanusch J, von Knebel-Doeberitz M, Koelble K, Moeslein G, Schackert HK, Wirtz HC, Fishel R, Rüschoff J. Bocker T, et al. Among authors: gebert j. Cancer Res. 1997 Nov 1;57(21):4739-43. Cancer Res. 1997. PMID: 9354434

6

Combined molecular and clinical approaches for the identification of families with familial adenomatous polyposis coli.

Gebert JF, Dupon C, Kadmon M, Hahn M, Herfarth C, von Knebel Doeberitz M, Schackert HK. Gebert JF, et al. Ann Surg. 1999 Mar;229(3):350-61. doi: 10.1097/00000658-199903000-00008. Ann Surg. 1999. PMID: 10077047 Free PMC article.

7

Molecular profiling of sporadic colorectal tumors by microsatellite analysis.

Gebert J, Sun M, Ridder R, Hinz U, Lehnert T, Möller P, Schackert HK, Herfarth C, von Knebel Doeberitz M. Gebert J, et al. Int J Oncol. 2000 Jan;16(1):169-79. Int J Oncol. 2000. PMID: 10601563

8

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P. Friedl W, et al. Among authors: gebert j. Gut. 2001 Apr;48(4):515-21. doi: 10.1136/gut.48.4.515. Gut. 2001. PMID: 11247896 Free PMC article.

9

Pathogenesis of DNA repair-deficient cancers: a statistical meta-analysis of putative Real Common Target genes.

Woerner SM, Benner A, Sutter C, Schiller M, Yuan YP, Keller G, Bork P, Doeberitz Mv, Gebert JF. Woerner SM, et al. Oncogene. 2003 Apr 17;22(15):2226-35. doi: 10.1038/sj.onc.1206421. Oncogene. 2003. PMID: 12700659

10

Molecular analysis of endometrial hyperplasia in HNPCC-suspicious patients may predict progression to endometrial carcinoma.

Sutter C, Dallenbach-Hellweg G, Schmidt D, Baehring J, Bielau S, von Knebel Doeberitz M, Gebert J. Sutter C, et al. Among authors: gebert j. Int J Gynecol Pathol. 2004 Jan;23(1):18-25. doi: 10.1097/01.pgp.0000101085.35393.4a. Int J Gynecol Pathol. 2004. PMID: 14668545

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