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Restoration of absent in melanoma 2 (AIM2) induces G2/M cell cycle arrest and promotes invasion of colorectal cancer cellsPATSOS, Georgios; GERMANN, Anja; GEBERT, Johannes et al.International journal of cancer (Print). 2010, Vol 126, Num 8, pp 1838-1849, issn 0020-7136, 12 p.Article

Brush border myosin Ia inactivation in gastric but not endometrial tumorsMAZZOLINI, Rocco; RODRIGUES, Paulo; HERNANDEZ-LOSA, Javier et al.International journal of cancer (Print). 2013, Vol 132, Num 8, pp 1790-1799, issn 0020-7136, 10 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

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

Identification of differentially expressed genes in colorectal adenoma compared to normal tissue by suppression subtractive hybridizationWENTZENSEN, Nicolas; WILZ, Birgit; FINDEISEN, Peter et al.International journal of oncology. 2004, Vol 24, Num 4, pp 987-994, issn 1019-6439, 8 p.Article

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: The German Hereditary Nonpolyposis Colorectal Cancer ConsortiumPLASCHKE, Jens; ENGEL, Christoph; RÜSCHOFF, Jose et al.Journal of clinical oncology. 2004, Vol 22, Num 22, pp 4486-4494, issn 0732-183X, 9 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

Expression of an endogenous retroviral sequence from the HERV-H group in gastrointestinal cancersWENTZENSEN, Nicolas; COY, Johannes F; KNAEBEL, Hanns-Peter et al.International journal of cancer. 2007, Vol 121, Num 7, pp 1417-1423, issn 0020-7136, 7 p.Article

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumorPLASCHKE, Jens; LINNEBACHER, Michael; KLOOR, Matthias et al.European journal of human genetics. 2006, Vol 14, Num 5, pp 561-566, issn 1018-4813, 6 p.Article

Immunoselective pressure and human leukocyte antigen class I antigen machinery defects in microsatellite unstable colorectal cancersKLOOR, Matthias; BECKER, Christina; BENNER, Axel et al.Cancer research (Baltimore). 2005, Vol 65, Num 14, pp 6418-6424, issn 0008-5472, 7 p.Article

Identification of an HLA-A0201-restricted CTL epitope generated by a tumor-specific frameshift mutation in a coding microsatellite of the OGT geneRIPBERGER, Eva; LINNEBACHER, Michael; SCHWITALLE, Yvette et al.Journal of clinical immunology. 2003, Vol 23, Num 5, pp 415-423, issn 0271-9142, 9 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

A large MSH2 Alu insertion mutation causes HNPCC in a German kindredKLOOR, Matthias; SUFFER, Christian; WENTZENSEN, Nicolas et al.Human genetics. 2004, Vol 115, Num 5, pp 432-438, issn 0340-6717, 7 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

Evaluation of Bethesda guidelines in relation to microsatellite instabilityWÜLLENWEBER, Hans-Peter; SUTLER, Christian; GEBERT, Johannes et al.Diseases of the colon & rectum. 2001, Vol 44, Num 9, pp 1281-1289, issn 0012-3706Article

High Frequency of LMAN1 Abnormalities in Colorectal Tumors with Microsatellite InstabilityROECKEL, Nina; WOERNER, Stefan M; KLOOR, Matthias et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 1, pp 292-299, issn 0008-5472, 8 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

Frameshift peptide-derived T-cell epitopes: A source of novel tumor-specific antigensLINNEBACHER, Michael; GEBERT, Johannes; RUDY, Wolfgang et al.International journal of cancer. 2001, Vol 93, Num 1, pp 6-11, issn 0020-7136Article

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

Microsatellite instability of selective target genes in HNPCC-associated colon adenomasWOERNER, Stefan M; KLOOR, Matthias; PAGENSTECHER, Constanze et al.Oncogene (Basingstoke). 2005, Vol 24, Num 15, pp 2525-2535, issn 0950-9232, 11 p.Article

Mechanisms of inactivation of the receptor tyrosine kinase EPHB2 in colorectal tumorsALAZZOUZI, Hafid; DAVALOS, Veronica; IMAI, Kohzoh et al.Cancer research (Baltimore). 2005, Vol 65, Num 22, pp 10170-10173, issn 0008-5472, 4 p.Article

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