au.\*:("SCHULMANN, Karsten")
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Colonic cancer and polypsSCHULMANN, Karsten; REISER, Markus; SCHMIEGEL, Wolff et al.Baillière's best practice & research. Clinical gastroenterology. 2002, Vol 16, Num 1, pp 91-114, issn 1521-6918Article
Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancersSALLOCH, Heidi; REINACHER-SCHICK, Anke; SCHMIEGEL, Wolff et al.International journal of colorectal disease (Print). 2010, Vol 25, Num 1, pp 97-107, issn 0179-1958, 11 p.Article
Mutational and LOH analyses of the chromosome 4q region in esophageal adenocarcinomaSTERIAN, Anca; KAN, Takatsugu; HAMILTON, James P et al.Oncology. 2006, Vol 70, Num 3, pp 168-172, issn 0030-2414, 5 p.Article
TFAP2E-DKK4 and Chemoresistance in Colorectal CancerEBERT, Matthias P. A; TÄNZER, Marc; SCHULMANN, Karsten et al.The New England journal of medicine. 2012, Vol 366, Num 1, pp 44-53, issn 0028-4793, 10 p.Article
Genotype-phenotype comparison of german MLH1 and MSH2 mutation carriers clinically affected with lynch syndrome : A report by the german hnpcc consortiumGOECKE, Timm; SCHULMANN, Karsten; DIETMAIER, Wolfgang et al.Journal of clinical oncology. 2006, Vol 24, Num 26, pp 4285-4292, issn 0732-183X, 8 p.Article
Inactivation of p16, RUNX3, and HPP1 occurs early in Barrett's-associated neoplastic progression and predicts progression riskSCHULMANN, Karsten; STERIAN, Anca; HAMILTON, James et al.Oncogene (Basingstoke). 2005, Vol 24, Num 25, pp 4138-4148, issn 0950-9232, 11 p.Article
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 german families suspected of hereditary nonpolyposis colorectal cancerMANGOLD, Elisabeth; PAGENSTECHER, Constanze; SCHACKERT, Hans K et al.International journal of cancer. 2005, Vol 116, Num 5, pp 692-702, issn 0020-7136, 11 p.Article
Prevalence of familial pancreatic cancer in GermanyBARTSCH, Detlef K; KRESS, Ralf; WITZIGMANN, Helmut et al.International journal of cancer. 2004, Vol 110, Num 6, pp 902-906, issn 0020-7136, 5 p.Article
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibilityLASCORZ, Jesús; FÖRSTI, Asta; SCHULMANN, Karsten et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 9, pp 1612-1619, issn 0143-3334, 8 p.Article
Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCCMORAK, Monika; SCHACKERT, Hans Konrad; KELLER, Gisela et al.European journal of human genetics. 2008, Vol 16, Num 7, pp 804-811, issn 1018-4813, 8 p.Article
Feasibility and diagnostic utility of video capsule endoscopy for the detection of small bowel polyps in patients with hereditary polyposis syndromesSCHULMANN, Karsten; HOLLERBACH, Stephan; KRAUS, Katja et al.The American journal of gastroenterology. 2005, Vol 100, Num 1, pp 27-37, issn 0002-9270, 11 p.Article
Identification of genes uniquely involved in frequent microsatellite instability colon carcinogenesis by expression profiling combined with epigenetic scanningMORI, Yuriko; JING YIN; DEACU, Elena et al.Cancer research (Baltimore). 2004, Vol 64, Num 7, pp 2434-2438, issn 0008-5472, 5 p.Article
Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriersFRIEDL, Waltraut; UHLHAAS, Siegfried; WEBER, Ruthild G et al.Human genetics. 2002, Vol 111, Num 1, pp 108-111, issn 0340-6717Article