Plaschke J - Search Results

1

Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability.

Plaschke J, Schwanebeck U, Pistorius S, Saeger HD, Schackert HK. Plaschke J, et al. Cancer Lett. 2003 Mar 10;191(2):179-85. doi: 10.1016/s0304-3835(02)00633-x. Cancer Lett. 2003. PMID: 12618331

2

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.

Plaschke J, Krüger S, Pistorius S, Theissig F, Saeger HD, Schackert HK. Plaschke J, et al. Int J Cancer. 2002 Feb 10;97(5):643-8. doi: 10.1002/ijc.10097. Int J Cancer. 2002. PMID: 11807791

3

Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression.

Plaschke J, Krüger S, Jeske B, Theissig F, Kreuz FR, Pistorius S, Saeger HD, Iaccarino I, Marra G, Schackert HK. Plaschke J, et al. Cancer Res. 2004 Feb 1;64(3):864-70. doi: 10.1158/0008-5472.can-03-2807. Cancer Res. 2004. PMID: 14871813

4

Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients.

Pistorius S, Kruger S, Hohl R, Plaschke J, Distler W, Saeger HD, Schackert HK. Pistorius S, et al. Among authors: plaschke j. Gynecol Oncol. 2006 Aug;102(2):189-94. doi: 10.1016/j.ygyno.2005.12.032. Epub 2006 Feb 14. Gynecol Oncol. 2006. PMID: 16476474

5

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.

Krüger S, Engel C, Bier A, Mangold E, Pagenstecher C, Doeberitz Mv, Holinski-Feder E, Moeslein G, Keller G, Kunstmann E, Friedl W, Plaschke J, Rüschoff J, Schackert HK; German HNPCC-Consortium. Krüger S, et al. Among authors: plaschke j. Cancer Lett. 2006 May 18;236(2):191-7. doi: 10.1016/j.canlet.2005.05.013. Cancer Lett. 2006. PMID: 16832876

6

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.

Pistorius S, Görgens H, Plaschke J, Hoehl R, Krüger S, Engel C, Saeger HD, Schackert HK. Pistorius S, et al. Among authors: plaschke j. Cancer Lett. 2007 Apr 8;248(1):89-95. doi: 10.1016/j.canlet.2006.06.002. Epub 2006 Jul 11. Cancer Lett. 2007. PMID: 16837128

7

Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability.

Plaschke J, Preußler M, Ziegler A, Schackert HK. Plaschke J, et al. Int J Colorectal Dis. 2012 Jul;27(7):911-9. doi: 10.1007/s00384-011-1408-0. Epub 2012 Jan 10. Int J Colorectal Dis. 2012. PMID: 22249440

8

An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer.

Goessl C, Plaschke J, Pistorius S, Hahn M, Frank S, Hampl M, Görgens H, Koch R, Saeger HD, Schackert HK. Goessl C, et al. Among authors: plaschke j. Eur J Cancer. 1997 Oct;33(11):1869-74. doi: 10.1016/s0959-8049(97)00219-0. Eur J Cancer. 1997. PMID: 9470849

9

Quantitative differences between aberrant transcripts which occur as common isoforms and due to mutation-based exon skipping of the mismatch repair gene hMLH1.

Plaschke J, Bulitta C, Saeger HD, Schackert HK. Plaschke J, et al. Clin Chem Lab Med. 1999 Sep;37(9):883-7. doi: 10.1515/CCLM.1999.131. Clin Chem Lab Med. 1999. PMID: 10596954

10

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.

Plaschke J, Kruppa C, Tischler R, Bocker T, Pistorius S, Dralle H, Rüschoff J, Saeger HD, Fishel R, Schackert HK. Plaschke J, et al. Int J Cancer. 2000 Mar 1;85(5):606-13. doi: 10.1002/(sici)1097-0215(20000301)85:5<606::aid-ijc2>3.0.co;2-b. Int J Cancer. 2000. PMID: 10699937

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