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T25 repeat in the 3' untranslated region of the CASP2 gene : A sensitive and specific marker for microsatellite instability in colorectal cancerFINDEISEN, Peter; KLOOR, Matthias; WAGNER, Rudolf et al.Cancer research (Baltimore). 2005, Vol 65, Num 18, pp 8072-8078, issn 0008-5472, 7 p.Article

Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriersDICK, Michelle G; VERSMOLD, Beatrix; KAST, Karin et al.International journal of cancer (Print). 2012, Vol 130, Num 6, pp 1314-1318, issn 0020-7136, 5 p.Article

A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal womenTCHATCHOU, Sandrine; JUNG, Anke; DITSCH, Nina et al.Carcinogenesis (New York. Print). 2009, Vol 30, Num 1, pp 59-64, issn 0143-3334, 6 p.Article

Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer riskFRANK, Bernd; BERMEJO, Justo Lorenzo; BURWINKEL, Barbara et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 7, pp 1442-1445, issn 0143-3334, 4 p.Article

Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 geneRATH, Michelle G; FATHALI-ZADEH, Farnoosh; BURGEMEISTER, Anna-Lena et al.Breast cancer research and treatment. 2012, Vol 133, Num 2, pp 725-734, issn 0167-6806, 10 p.Article

Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer riskYANG, Rongxi; BOWANG CHEN; MEINDL, Alfons et al.Breast cancer research and treatment. 2009, Vol 118, Num 2, pp 407-413, issn 0167-6806, 7 p.Article

Systematic identification of genes with coding microsatellites mutated in DNA mismatch repair-deficient cancer cellsWOERNER, Stefan M; GEBERT, Johannes; YUAN, Yan P et al.International journal of cancer. 2001, Vol 93, Num 1, pp 12-19, issn 0020-7136Article

A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer riskRONGXI YANG; SCHLEHE, Bettina; ARNOLD, Norbert et al.Breast cancer research and treatment. 2010, Vol 121, Num 3, pp 693-702, issn 0167-6806, 10 p.Article

Association of a Common AKAP9 Variant With Breast Cancer Risk : A Collaborative AnalysisFRANK, Bernd; WIESTLER, Miriam; MEINDL, Alfons et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 6, pp 437-442, issn 0027-8874, 6 p.Article

SNPs in ultraconserved elements and familial breast cancer riskRONGXI YANG; FRANK, Bernd; WEBER, Bernhard H. F et al.Carcinogenesis (New York. Print). 2008, Vol 29, Num 2, pp 351-355, issn 0143-3334, 5 p.Article

Pathogenesis of DNA repair-deficient cancers: a statistical meta-analysis of putative Real Common Target genesWOERNER, Stefan M; BENNER, Axel; SUTTER, Christian et al.Oncogene (Basingstoke). 2003, Vol 22, Num 15, pp 2226-2235, issn 0950-9232, 10 p.Article

Genetic variants within miR-126 and miR-335 are not associated with breast cancer riskRONGXI YANG; DICK, Michelle; SCHOTT, Sarah et al.Breast cancer research and treatment. 2011, Vol 127, Num 2, pp 549-554, issn 0167-6806, 6 p.Article

Periungual fibroma (Koenen tumors) as isolated sign of tuberous sclerosis complex with tuberous sclerosis complex 1 germline mutationQUIST, Sven R; FRANKE, Ingolf; SUTTER, Christian et al.Journal of the American Academy of Dermatology. 2010, Vol 62, Num 1, pp 159-161, issn 0190-9622, 3 p.Article

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers : A consortium of investigators of modifiers of BRCA1/2 studyCOUCH, Fergus J; SINILNIKOVA, Olga; PEOCK, Susan et al.Cancer epidemiology, biomarkers & prevention. 2007, Vol 16, Num 7, pp 1416-1421, issn 1055-9965, 6 p.Article

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancerWIRTENBERGER, Michael; TCHATCHOU, Sandrine; WEBER, Bernhard H. F et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 11, pp 2201-2208, issn 0143-3334, 8 p.Article

Acceptance of and attitude toward genetic testing for hereditary nonpolyposis colorectal cancer: A comparison of participants and nonparticipants in genetic counselingKELLER, Monika; JOST, Ralf; BÜCHLER, Markus W et al.Diseases of the colon & rectum. 2004, Vol 47, Num 2, pp 153-162, issn 0012-3706, 10 p.Article

A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 (NPAS2) is not associated with breast cancer riskFURU WANG; ZHIBIN HU; MEINDL, Alfons et al.Breast cancer research and treatment. 2011, Vol 127, Num 3, pp 769-775, issn 0167-6806, 7 p.Article

Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersENGEL, Christoph; VERSMOLD, Beatrix; GARETH EVANS, D et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 11, pp 2859-2868, issn 1055-9965, 10 p.Article

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation CarriersANTONIOU, Antonis C; SPURDLE, Amanda B; HOFMANN, Wera et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 937-948, issn 0002-9297, 12 p.Article

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancerWIRTENBERGER, Michael; SCHMUTZHARD, Julia; NIEDERACHER, Dieter et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 2, pp 423-426, issn 0143-3334, 4 p.Article

Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer riskVACLAVICEK, Annika; LORENZO BERMEJO, Justo; HEMMINKI, Kari et al.Breast cancer research and treatment. 2007, Vol 106, Num 2, pp 205-213, issn 0167-6806, 9 p.Article

Molecular analysis of Endometrial hyperplasia in HNPCC-suspicious patients may predict progression to Endometrial carcinomaSUTTER, Christian; DALLENBACH-HELLWEG, Gisela; SCHMIDT, Dietmar et al.International journal of gynecological pathology. 2004, Vol 23, Num 1, pp 18-27, issn 0277-1691, 10 p.Article

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry-based detection of microsatellite instabilities in coding DNA sequences: A novel approach to identify DNA-mismatch repair-deficient cancer cellsBONK, Thomas; HUMENY, Andreas; GEBERT, Johannes et al.Clinical chemistry (Baltimore, Md.). 2003, Vol 49, Num 4, pp 552-561, issn 0009-9147, 10 p.Article

Somatic mutations in familial adenomatous polyps: Nuclear translocation of β-catenin requires more than biallelic APC inactivationBLÄKER, Hendrik; SCHOLTEN, Martin; SUTTER, Christian et al.American journal of clinical pathology. 2003, Vol 120, Num 3, pp 418-423, issn 0002-9173, 6 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

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