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hMSH5 : A human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesisBOCKER, T; BARUSEVICIUS, A; KOVATICH, A. J et al.Cancer research (Baltimore). 1999, Vol 59, Num 4, pp 816-822, issn 0008-5472Article

Transcription-coupled repair deficiency and mutations in human mismatch repair genesMELLON, I; RAJPAL, D. K; KOI, M et al.Science (Washington, D.C.). 1996, Vol 272, Num 5261, pp 557-560, issn 0036-8075Article

Prediction of MLH1 and MSH2 mutations in lynch syndromeBALMANA, Judith; STOCKWELL, David H; BURBIDGE, Lynn Anne et al.JAMA, the journal of the American Medical Association. 2006, Vol 296, Num 12, pp 1469-1478, issn 0098-7484, 10 p.Article

PCR-based random mutagenesis using manganese and reduced dNTP concentrationLIN-GOERKE, J. L; ROBBINS, D. J; BURCZAK, J. D et al.BioTechniques. 1997, Vol 23, Num 3, pp 409-412, issn 0736-6205Article

Role of MUTYH and MSH2 in the Control of Oxidative DNA Damage, Genetic Instability, and TumorigenesisRUSSO, Maria Teresa; DE LUCA, Gabriele; CASORELLI, Ida et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 10, pp 4372-4379, issn 0008-5472, 8 p.Article

Proliferating cell nuclear antigen and Msh2p-Msh6p interact to form an active mispair recognition complexFLORES-ROZAS, Hernan; CLARK, Delbert; KOLODNER, Richard D et al.Nature genetics. 2000, Vol 26, Num 3, pp 375-378, issn 1061-4036Article

An insight into the genetic pathway of adenocarcinoma of the small intestineWHEELER, J. M. D; WARREN, B. F; BODMER, W. F et al.Gut. 2002, Vol 50, Num 2, pp 218-223, issn 0017-5749Article

Additive roles of XPA and MSH2 genes in UVB-induced skin tumorigenesis in miceYOSHINO, Masafumi; NAKATSU, Yoshimichi; TE RIELE, Hein et al.DNA repair. 2002, Vol 1, Num 11, pp 935-940, issn 1568-7864, 6 p.Article

Msh-2 suppresses in vivo mutation in a gene dose and lesion dependent mannerSANSOM, Owen J; TOFT, Neil J; WINTON, Douglas J et al.Oncogene (Basingstoke). 2001, Vol 20, Num 27, pp 3580-3584, issn 0950-9232Article

Clinical implications of genetic testing of hereditary nonpolyposis colorectal cancerVASEN, H. F. A; WIJNEN, J.Cytogenetics and cell genetics. 1999, Vol 86, Num 2, pp 136-139, issn 0301-0171Article

The effect of Msh2 knockdown on methylating agent induced toxicity in DNA glycosylase deficient cellsCOOLEY, N; ELDER, R. H; POVEY, C et al.Toxicology (Amsterdam). 2010, Vol 268, Num 1-2, pp 111-117, issn 0300-483X, 7 p.Article

A founder mutation of the MSH2 gene and Hereditary nonpolyposis colorectal cancer in the United StatesLYNCH, Henry T; CORONEL, Stephanie M; WAGNER, Anja et al.JAMA, the journal of the American Medical Association. 2004, Vol 291, Num 6, pp 718-724, issn 0098-7484, 7 p.Article

Methylation of the hMLH1 promoter in familial gastric cancer with microsatellite instabilityYANAGISAWA, Y; AKIYAMA, Y; IIDA, S et al.International journal of cancer. 2000, Vol 85, Num 1, pp 50-53, issn 0020-7136Article

Genetic instability of microsatellites in hematological neoplasmsROBLEDO, M; MARTINEZ, B; ARRANZ, E et al.Leukemia. 1995, Vol 9, Num 6, pp 960-964, issn 0887-6924Article

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortiumBAKRY, Doua; ARONSON, Melyssa; CONSTANTINI, Shlomi et al.European journal of cancer (1990). 2014, Vol 50, Num 5, pp 987-996, issn 0959-8049, 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

Alterations of BAT-26 identify a subset of gastric cancer with distinct clinicopathologic features and better postoperative prognosisWU, Ming-Shiang; LEE, Chung-Wei; SHEU, Jin-Chuan et al.Hepato-gastroenterology. 2002, Vol 49, Num 43, pp 285-289, issn 0172-6390Article

Mutations in rad3, msh2, and RAD52 affect the rate of gene amplification in the yeast Saccharomyces cerevisiaePETERSON, Christopher; KORDICH, Jennifer; MILLIGAN, Laura et al.Environmental and molecular mutagenesis (Print). 2000, Vol 36, Num 4, pp 325-334, issn 0893-6692Article

Expression of the human mismatch repair gene hMSH2 : A potential marker for urothelial malignancyLEACH, F. S; HSIEH, J.-T; MOLBERG, K et al.Cancer. 2000, Vol 88, Num 10, pp 2333-2341, issn 0008-543XArticle

Binding of mismatched microsatellite DNA sequenes by the human MSH2 proteinFISHEL, R; EWEL, A; LEE, S et al.Science (Washington, D.C.). 1994, Vol 266, Num 5189, pp 1403-1405, issn 0036-8075Article

Exonic deletions of mismatch repair genes MLH1 and MSH2 correlate with prognosis and protein expression levels in malignant melanomasKORABIOWSKA, Monika; BRINCK, Ulrich; STACHURA, Jerzy et al.Anticancer research. 2006, Vol 26, Num 2A, pp 1231-1235, issn 0250-7005, 5 p.Article

Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6CAMPISI HEGAN, Denise; NARAYANAN, Latha; JIRIK, Frank R et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 12, pp 2402-2408, issn 0143-3334, 7 p.Article

Microsatellite instability is associated with genetic alteration but not with low levels of expression of the human mismatch repair proteins hMSH2 and hMLH1SHIN, K.-H; PARK, J.-G.European journal of cancer (1990). 2000, Vol 36, Num 7, pp 925-931, issn 0959-8049Article

Microsatellite instability and p53 mutations are associated with abnormal expression of the MSH2 gene in adult acute leukemiaZHU, Y.-M; DAS-GUPTA, E. P; RUSSELL, N. H et al.Blood. 1999, Vol 94, Num 2, pp 733-740, issn 0006-4971Article

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteriaBECK, N. E; TOMLINSON, I. P. M; HOMFRAY, T et al.Human genetics. 1997, Vol 99, Num 2, pp 219-224, issn 0340-6717Article

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