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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. Among authors: lage p. 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
Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene.
Lage PA, Albuquerque C, Sousa RG, Cravo ML, Salazar M, Francisco I, Maia L, Claro I, Suspiro A, Rodrigues P, Raposo H, Fidalgo PA, Nobre-Leitão C. Lage PA, et al. Cancer. 2004 Jul 1;101(1):172-7. doi: 10.1002/cncr.20320. Cancer. 2004. PMID: 15222003 Free article.
The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families.
Pinheiro M, Francisco I, Pinto C, Peixoto A, Veiga I, Filipe B, Santos C, Maia S, Silva J, Pinto P, Santos R, Claro I, Lage P, Lopes P, Ferreira S, Rosa I, Fonseca R, Rodrigues P, Henrique R, Chaves P, Pereira AD, Brandão C, Albuquerque C, Teixeira MR. Pinheiro M, et al. Among authors: lage p. Genes Chromosomes Cancer. 2019 Sep;58(9):657-664. doi: 10.1002/gcc.22759. Epub 2019 Apr 26. Genes Chromosomes Cancer. 2019. PMID: 30968502
Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability.
Albuquerque C, Baltazar C, Filipe B, Penha F, Pereira T, Smits R, Cravo M, Lage P, Fidalgo P, Claro I, Rodrigues P, Veiga I, Ramos JS, Fonseca I, Leitão CN, Fodde R. Albuquerque C, et al. Among authors: lage p. Genes Chromosomes Cancer. 2010 Aug;49(8):746-59. doi: 10.1002/gcc.20786. Genes Chromosomes Cancer. 2010. PMID: 20544848
Pediatric Colorectal Cancer: A Heterogenous Entity.
Cortez-Pinto J, Claro I, Francisco I, Lage P, Filipe B, Rodrigues P, Chaves P, Albuquerque C, Dias Pereira A. Cortez-Pinto J, et al. Among authors: lage p. J Pediatr Hematol Oncol. 2020 Mar;42(2):131-135. doi: 10.1097/MPH.0000000000001526. J Pediatr Hematol Oncol. 2020. PMID: 31205225
Familial colorectal cancer type X syndrome: two distinct molecular entities?
Francisco I, Albuquerque C, Lage P, Belo H, Vitoriano I, Filipe B, Claro I, Ferreira S, Rodrigues P, Chaves P, Leitão CN, Pereira AD. Francisco I, et al. Among authors: lage p. Fam Cancer. 2011 Dec;10(4):623-31. doi: 10.1007/s10689-011-9473-7. Fam Cancer. 2011. PMID: 21837511
Serrated polyposis associated with a family history of colorectal cancer and/or polyps: The preferential location of polyps in the colon and rectum defines two molecular entities.
Silva P, Albuquerque C, Lage P, Fontes V, Fonseca R, Vitoriano I, Filipe B, Rodrigues P, Moita S, Ferreira S, Sousa R, Claro I, Nobre Leitão C, Chaves P, Dias Pereira A. Silva P, et al. Among authors: lage p. Int J Mol Med. 2016 Sep;38(3):687-702. doi: 10.3892/ijmm.2016.2666. Epub 2016 Jul 5. Int J Mol Med. 2016. PMID: 27430658 Free PMC article.
104 results