Ruemmele P - Search Results

1

Frequency of activating mutations in FGFR2 exon 7 in bladder tumors from patients with early-onset and regular-onset disease.

Spiegelberg C, Giedl J, Gaisa NT, Rogler A, Riener MO, Filbeck T, Burger M, Ruemmele P, Hartmann A, Stoehr R. Spiegelberg C, et al. Among authors: ruemmele p. Int J Clin Exp Pathol. 2014 Mar 15;7(4):1708-13. eCollection 2014. Int J Clin Exp Pathol. 2014. PMID: 24817968 Free PMC article.

2

Lack of evidence for frequent MED12 p.L1224F mutation in prostate tumours from Caucasian patients.

Stoehr R, Taubert H, Gaisa NT, Smeets D, Kneitz B, Giedl J, Ruemmele P, Wieland WF, Rau TT, Hartmann A. Stoehr R, et al. Among authors: ruemmele p. J Pathol. 2013 Aug;230(4):453-6. doi: 10.1002/path.4208. J Pathol. 2013. PMID: 23661306

3

Low frequency of HNPCC-associated microsatellite instability and aberrant MMR protein expression in early-onset bladder cancer.

Giedl J, Schneckenpointner R, Filbeck T, Ruemmele P, Hofstaedter F, Burger M, Hartmann A, Stoehr R. Giedl J, et al. Among authors: ruemmele p. Am J Clin Pathol. 2014 Nov;142(5):634-9. doi: 10.1309/AJCPVTCJ4VU5HKVZ. Am J Clin Pathol. 2014. PMID: 25319978

4

Frequency of TERT Promoter Mutations in Prostate Cancer.

Stoehr R, Taubert H, Zinnall U, Giedl J, Gaisa NT, Burger M, Ruemmele P, Hurst CD, Knowles MA, Wullich B, Hartmann A. Stoehr R, et al. Among authors: ruemmele p. Pathobiology. 2015;82(2):53-7. doi: 10.1159/000381903. Epub 2015 May 21. Pathobiology. 2015. PMID: 25997473 Free article.

5

Mdm2 SNP309 G-variant is associated with invasive growth of human urinary bladder cancer.

Hitzenbichler F, Stoehr CG, Rogenhofer M, Wieland WF, Ruemmele P, Hartmann A, Stoehr R. Hitzenbichler F, et al. Among authors: ruemmele p. Pathobiology. 2014;81(2):53-9. doi: 10.1159/000355976. Epub 2013 Nov 9. Pathobiology. 2014. PMID: 24217660

6

Gene expression profiling of colorectal cancer and metastases divides tumours according to their clinicopathological stage.

Koehler A, Bataille F, Schmid C, Ruemmele P, Waldeck A, Blaszyk H, Hartmann A, Hofstaedter F, Dietmaier W. Koehler A, et al. Among authors: ruemmele p. J Pathol. 2004 Sep;204(1):65-74. doi: 10.1002/path.1606. J Pathol. 2004. PMID: 15307139

7

Mismatch repair proteins hMLH1 and hMSH2 are differently expressed in the three main subtypes of sporadic renal cell carcinoma.

Stoehr C, Burger M, Stoehr R, Bertz S, Ruemmele P, Hofstaedter F, Denzinger S, Wieland WF, Hartmann A, Walter B. Stoehr C, et al. Among authors: ruemmele p. Pathobiology. 2012;79(3):162-8. doi: 10.1159/000335642. Epub 2012 Feb 22. Pathobiology. 2012. PMID: 22378480

8

p53 Codon 72 polymorphism, loss of heterozygosity and high-risk human papillomavirus infection in a low-incidence German esophageal squamous cell carcinoma patient cohort.

Pantelis A, Pantelis D, Ruemmele P, Hartmann A, Hofstaedter F, Buettner R, Bootz F, Stoehr R. Pantelis A, et al. Among authors: ruemmele p. Oncol Rep. 2007 May;17(5):1243-8. Oncol Rep. 2007. PMID: 17390072

9

Distinction of hereditary nonpolyposis colorectal cancer and sporadic microsatellite-unstable colorectal cancer through quantification of MLH1 methylation by real-time PCR.

Bettstetter M, Dechant S, Ruemmele P, Grabowski M, Keller G, Holinski-Feder E, Hartmann A, Hofstaedter F, Dietmaier W. Bettstetter M, et al. Among authors: ruemmele p. Clin Cancer Res. 2007 Jun 1;13(11):3221-8. doi: 10.1158/1078-0432.CCR-06-3064. Clin Cancer Res. 2007. PMID: 17545526

10

EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice.

Gahr S, Stoehr R, Geissinger E, Ficker JH, Brueckl WM, Gschwendtner A, Gattenloehner S, Fuchs FS, Schulz C, Rieker RJ, Hartmann A, Ruemmele P, Dietmaier W. Gahr S, et al. Among authors: ruemmele p. Br J Cancer. 2013 Oct 1;109(7):1821-8. doi: 10.1038/bjc.2013.511. Epub 2013 Sep 3. Br J Cancer. 2013. PMID: 24002608 Free PMC article.

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