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Page 1
A TP53 founder mutation, p.R337H, is associated with phyllodes breast tumors in Brazil.
Giacomazzi J, Koehler-Santos P, Palmero EI, Graudenz MS, Rivero LF, Lima E, Pütten AC, Hainaut P, Camey SA, Michelli RD, Neto CS, Fitarelli-Kiehl M, Geyer G, Meurer L, Geiger A, Azevedo MB, da Silva VD, Ashton-Prolla P. Giacomazzi J, et al. Among authors: hainaut p. Virchows Arch. 2013 Jul;463(1):17-22. doi: 10.1007/s00428-013-1439-8. Epub 2013 Jun 21. Virchows Arch. 2013. PMID: 23794094
Increased oxidative damage in carriers of the germline TP53 p.R337H mutation.
Macedo GS, Lisbôa da Motta L, Giacomazzi J, Netto CB, Manfredini V, Vanzin CS, Vargas CR, Hainaut P, Klamt F, Ashton-Prolla P. Macedo GS, et al. Among authors: hainaut p. PLoS One. 2012;7(10):e47010. doi: 10.1371/journal.pone.0047010. Epub 2012 Oct 9. PLoS One. 2012. PMID: 23056559 Free PMC article.
The TP53 fertility network.
Paskulin Dd, Paixão-Côrtes VR, Hainaut P, Bortolini MC, Ashton-Prolla P. Paskulin Dd, et al. Among authors: hainaut p. Genet Mol Biol. 2012 Dec;35(4 (suppl)):939-46. doi: 10.1590/s1415-47572012000600008. Epub 2012 Dec 18. Genet Mol Biol. 2012. PMID: 23412905 Free PMC article.
Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil.
Giacomazzi J, Selistre SG, Rossi C, Alemar B, Santos-Silva P, Pereira FS, Netto CB, Cossio SL, Roth DE, Brunetto AL, Zagonel-Oliveira M, Martel-Planche G, Goldim JR, Hainaut P, Camey SA, Ashton-Prolla P. Giacomazzi J, et al. Among authors: hainaut p. Cancer. 2013 Dec 15;119(24):4341-9. doi: 10.1002/cncr.28346. Epub 2013 Oct 7. Cancer. 2013. PMID: 24122735 Free article.
Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil.
Giacomazzi J, Graudenz MS, Osorio CA, Koehler-Santos P, Palmero EI, Zagonel-Oliveira M, Michelli RA, Scapulatempo Neto C, Fernandes GC, Achatz MI, Martel-Planche G, Soares FA, Caleffi M, Goldim JR, Hainaut P, Camey SA, Ashton-Prolla P. Giacomazzi J, et al. Among authors: hainaut p. PLoS One. 2014 Jun 17;9(6):e99893. doi: 10.1371/journal.pone.0099893. eCollection 2014. PLoS One. 2014. PMID: 24936644 Free PMC article.
Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome.
Macedo GS, Araujo Vieira I, Brandalize AP, Giacomazzi J, Inez Palmero E, Volc S, Rodrigues Paixão-Côrtes V, Caleffi M, Silva Alves M, Achatz MI, Hainaut P, Ashton-Prolla P. Macedo GS, et al. Among authors: hainaut p. Cancer Genet. 2016 Mar;209(3):97-106. doi: 10.1016/j.cancergen.2015.12.012. Epub 2016 Jan 7. Cancer Genet. 2016. PMID: 26823150
Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil.
Palmero EI, Alemar B, Schüler-Faccini L, Hainaut P, Moreira-Filho CA, Ewald IP, Santos PK, Ribeiro PL, Oliveira CB, Calvez-Kelm FL, Tavtigian S, Cossio SL, Giugliani R, Caleffi M, Ashton-Prolla P. Palmero EI, et al. Among authors: hainaut p. Genet Mol Biol. 2016 May 24;39(2):210-22. doi: 10.1590/1678-4685-GMB-2014-0363. Genet Mol Biol. 2016. PMID: 27223485 Free PMC article.
476 results