Oliveira C - Search Results

1

A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function.

Melo SA, Ropero S, Moutinho C, Aaltonen LA, Yamamoto H, Calin GA, Rossi S, Fernandez AF, Carneiro F, Oliveira C, Ferreira B, Liu CG, Villanueva A, Capella G, Schwartz S Jr, Shiekhattar R, Esteller M. Melo SA, et al. Among authors: oliveira c. Nat Genet. 2009 Mar;41(3):365-70. doi: 10.1038/ng.317. Epub 2009 Feb 15. Nat Genet. 2009. PMID: 19219043 Free PMC article. Retracted.

2

Screening E-cadherin in gastric cancer families reveals germline mutations only in hereditary diffuse gastric cancer kindred.

Oliveira C, Bordin MC, Grehan N, Huntsman D, Suriano G, Machado JC, Kiviluoto T, Aaltonen L, Jackson CE, Seruca R, Caldas C. Oliveira C, et al. Hum Mutat. 2002 May;19(5):510-7. doi: 10.1002/humu.10068. Hum Mutat. 2002. PMID: 11968083

3

Identification of CDH1 germline missense mutations associated with functional inactivation of the E-cadherin protein in young gastric cancer probands.

Suriano G, Oliveira C, Ferreira P, Machado JC, Bordin MC, De Wever O, Bruyneel EA, Moguilevsky N, Grehan N, Porter TR, Richards FM, Hruban RH, Roviello F, Huntsman D, Mareel M, Carneiro F, Caldas C, Seruca R. Suriano G, et al. Among authors: oliveira c. Hum Mol Genet. 2003 Mar 1;12(5):575-82. doi: 10.1093/hmg/ddg048. Hum Mol Genet. 2003. PMID: 12588804

4

Intragenic deletion of CDH1 as the inactivating mechanism of the wild-type allele in an HDGC tumour.

Oliveira C, de Bruin J, Nabais S, Ligtenberg M, Moutinho C, Nagengast FM, Seruca R, van Krieken H, Carneiro F. Oliveira C, et al. Oncogene. 2004 Mar 18;23(12):2236-40. doi: 10.1038/sj.onc.1207335. Oncogene. 2004. PMID: 14661064

5

BRAF mutations characterize colon but not gastric cancer with mismatch repair deficiency.

Oliveira C, Pinto M, Duval A, Brennetot C, Domingo E, Espín E, Armengol M, Yamamoto H, Hamelin R, Seruca R, Schwartz S Jr. Oliveira C, et al. Oncogene. 2003 Dec 11;22(57):9192-6. doi: 10.1038/sj.onc.1207061. Oncogene. 2003. PMID: 14668801

6

Activated BRAF targets proximal colon tumors with mismatch repair deficiency and MLH1 inactivation.

Domingo E, Espín E, Armengol M, Oliveira C, Pinto M, Duval A, Brennetot C, Seruca R, Hamelin R, Yamamoto H, Schwartz S Jr. Domingo E, et al. Among authors: oliveira c. Genes Chromosomes Cancer. 2004 Feb;39(2):138-42. doi: 10.1002/gcc.10310. Genes Chromosomes Cancer. 2004. PMID: 14695993

7

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

Oliveira C, Westra JL, Arango D, Ollikainen M, Domingo E, Ferreira A, Velho S, Niessen R, Lagerstedt K, Alhopuro P, Laiho P, Veiga I, Teixeira MR, Ligtenberg M, Kleibeuker JH, Sijmons RH, Plukker JT, Imai K, Lage P, Hamelin R, Albuquerque C, Schwartz S Jr, Lindblom A, Peltomaki P, Yamamoto H, Aaltonen LA, Seruca R, Hofstra RM. Oliveira C, et al. Hum Mol Genet. 2004 Oct 1;13(19):2303-11. doi: 10.1093/hmg/ddh238. Epub 2004 Aug 4. Hum Mol Genet. 2004. PMID: 15294875

8

Role of pathology in the identification of hereditary diffuse gastric cancer: report of a Portuguese family.

Oliveira C, Moreira H, Seruca R, de Oliveira MC, Carneiro F. Oliveira C, et al. Virchows Arch. 2005 Feb;446(2):181-4. doi: 10.1007/s00428-004-1156-4. Epub 2004 Dec 11. Virchows Arch. 2005. PMID: 15735979

9

BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes.

Domingo E, Niessen RC, Oliveira C, Alhopuro P, Moutinho C, Espín E, Armengol M, Sijmons RH, Kleibeuker JH, Seruca R, Aaltonen LA, Imai K, Yamamoto H, Schwartz S Jr, Hofstra RM. Domingo E, et al. Among authors: oliveira c. Oncogene. 2005 Jun 2;24(24):3995-8. doi: 10.1038/sj.onc.1208569. Oncogene. 2005. PMID: 15782118

10

Concomitant RASSF1A hypermethylation and KRAS/BRAF mutations occur preferentially in MSI sporadic colorectal cancer.

Oliveira C, Velho S, Domingo E, Preto A, Hofstra RM, Hamelin R, Yamamoto H, Seruca R, Schwartz S Jr. Oliveira C, et al. Oncogene. 2005 Nov 17;24(51):7630-4. doi: 10.1038/sj.onc.1208906. Oncogene. 2005. PMID: 16007118

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