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MSH6, GTBP (G/T mismatch-binding protein) gène de réparationSOUSSI, Thierry.Bulletin du cancer. 2006, Vol 93, Num 2, pp 151-152, issn 0007-4551, 2 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

Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in latviaIRMEJS, Arvids; BOROSENKO, Viktors; MELBARDE-GORKUSA, Inga et al.Anticancer research. 2007, Vol 27, Num 1B, pp 653-658, issn 0250-7005, 6 p.Article

Recently identified colon cancer predispositions : MYH and MSH6 mutationsKASTRINOS, Fay; SYNGAL, Sapna.Seminars in oncology. 2007, Vol 34, Num 5, pp 418-424, issn 0093-7754, 7 p.Article

Cloning of rat MLH1 and expression analysis of MSH2, MSH3, MSH6, and MLH1 during spermatogenesisVANI, R. G; VARGHESE, C. M; RAO, M. R. S et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 3, pp 460-467, issn 0888-7543Article

Msh6 Protects Mature B Cells from Lymphoma by Preserving Genomic StabilityPELED, Jonathan U; SELLERS, Rani S; IGLESIAS-USSEL, Maria D et al.The American journal of pathology. 2010, Vol 177, Num 5, pp 2597-2608, issn 0002-9440, 12 p.Article

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

The associated contributions of p53 and the DNA mismatch repair protein msh6 to spontaneous tumorigenesisYOUNG, Leah C; KEULING, Angela M; LAI, Raymond et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 10, pp 2131-2138, issn 0143-3334, 8 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

The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppressionEDELMANN, W; UMAR, A; CROUSE, G et al.Cancer research (Baltimore). 2000, Vol 60, Num 4, pp 803-807, issn 0008-5472Article

Constitutional mismatch repair deficiency and childhood leukemia/lymphoma - report on a novel biallelic MSH6 mutationRIPPERGER, Tim; BEGER, Carmela; RAHNER, Nils et al.Haematologica (Roma). 2010, Vol 95, Num 5, pp 841-844, issn 0390-6078, 4 p.Article

The distinct spectra of tumor-associated Apc mutations in mismatch repair-deficient Apc1638N mice define the roles of MSH3 and MSH6 in DNA repair and intestinal tumorigenesisKURAGUCHI, Mari; KAN YANG; WONG, Edmund et al.Cancer research (Baltimore). 2001, Vol 61, Num 21, pp 7934-7942, issn 0008-5472Article

Mutations of the human MUT S homologue 6 gene in ampullary carcinoma and gastric cancerIMAI, Y; INOUE, T; ISHIKAWA, T et al.International journal of cancer. 1998, Vol 78, Num 5, pp 576-580, issn 0020-7136Article

MSH6 Mutations Arise in Glioblastomas during Temozolomide Therapy and Mediate Temozolomide ResistanceYIP, Stephen; JIANGYONG MIAO; CAHILL, Daniel P et al.Clinical cancer research (Print). 2009, Vol 15, Num 14, pp 4622-4629, issn 1078-0432, 8 p.Article

MSH2 -118T>C and MSH6 -159C>T promoter polymorphisms and the risk of colorectal cancerMRKONJIC, Miralem; RAPTIS, Stavroula; KNIGHT, Julia A et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 12, pp 2575-2580, issn 0143-3334, 6 p.Article

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyHUNTER, Chris; SMITH, Raffaella; O'MEARA, Sarah et al.Cancer research (Baltimore). 2006, Vol 66, Num 8, pp 3987-3991, issn 0008-5472, 5 p.Article

Loss of the mismatch repair protein MSH6 in human Glioblastomas is associated with tumor progression during temozolomide treatmentCAHILL, Daniel P; LEVINE, Kymberly K; LAFRATE, A. John et al.Clinical cancer research. 2007, Vol 13, Num 7, pp 2038-2045, issn 1078-0432, 8 p.Article

Association of rare MSH6 variants with familial breast cancerWASIELEWSKI, Marijke; RIAZ, Muhammad; SCHUTTE, Mieke et al.Breast cancer research and treatment. 2010, Vol 123, Num 2, pp 315-320, issn 0167-6806, 6 p.Article

Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancerRENKONEN, Elise; YANGE ZHANG; PELTOMÄKI, Päivi et al.Journal of clinical oncology. 2003, Vol 21, Num 19, pp 3629-3637, issn 0732-183X, 9 p.Article

MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancerCHARBONNIER, Francoise; OLSCHWANG, Sylviane; QING WANG et al.Cancer research (Baltimore). 2002, Vol 62, Num 3, pp 848-853, issn 0008-5472Article

Frameshift mutations of the hMSH6 gene in human leukemia cell linesHOSOYA, N; HANGAISHI, A; OGAWA, S et al.Japanese journal of cancer research. 1998, Vol 89, Num 1, pp 33-39, issn 0910-5050Article

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeBONADONA, Valérie; BONAITI, Bernard; COLAS, Chrystelle et al.JAMA, the journal of the American Medical Association. 2011, Vol 305, Num 22, pp 2304-2310, issn 0098-7484, 7 p.Article

Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeatsYOU, J.-F; BUHARD, O; COLLURA, A et al.British journal of cancer. 2010, Vol 103, Num 12, pp 1840-1845, issn 0007-0920, 6 p.Article

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population-based study in northern swedenCEDERQUIST, Kristina; EMANUELSSON, Monica; GÖRANSSON, Ingela et al.International journal of cancer. 2004, Vol 109, Num 3, pp 370-376, issn 0020-7136, 7 p.Article

Functional analysis of the mismatch repair system in bladder cancerTHYKJAER, T; CHRISTENSEN, M; CLARK, A. B et al.British journal of cancer. 2001, Vol 85, Num 4, pp 568-575, issn 0007-0920Article

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