Achatz MI - Search Results

1

Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.

Torrezan GT, da Silva FC, Santos EM, Krepischi AC, Achatz MI, Aguiar S Jr, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: achatz mi. Orphanet J Rare Dis. 2013 Apr 5;8:54. doi: 10.1186/1750-1172-8-54. Orphanet J Rare Dis. 2013. PMID: 23561487 Free PMC article.

2

The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.

Achatz MI, Olivier M, Le Calvez F, Martel-Planche G, Lopes A, Rossi BM, Ashton-Prolla P, Giugliani R, Palmero EI, Vargas FR, Da Rocha JC, Vettore AL, Hainaut P. Achatz MI, et al. Cancer Lett. 2007 Jan 8;245(1-2):96-102. doi: 10.1016/j.canlet.2005.12.039. Epub 2006 Feb 21. Cancer Lett. 2007. PMID: 16494995

3

Integration of genomics in cancer care.

Santos EM, Edwards QT, Floria-Santos M, Rogatto SR, Achatz MI, MacDonald DJ. Santos EM, et al. Among authors: achatz mi. J Nurs Scholarsh. 2013 Mar;45(1):43-51. doi: 10.1111/j.1547-5069.2012.01465.x. Epub 2013 Jan 7. J Nurs Scholarsh. 2013. PMID: 23294839 Review.

4

Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.

de Ávila AL, Krepischi AC, Moredo LF, Aguiar TF, da Silva FC, de Sá BC, de Nóbrega AF, Achatz MI, Duprat JP, Landman G, Carraro DM. de Ávila AL, et al. Among authors: achatz mi. Fam Cancer. 2014 Dec;13(4):645-9. doi: 10.1007/s10689-014-9736-1. Fam Cancer. 2014. PMID: 25023876

5

Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations.

de Araújo É, Marchi FA, Rodrigues TC, Vieira HC, Kuasne H, Achatz MI, Moredo LF, de Sá BC, Duprat JP, Brentani HP, Rosenberg C, Carraro DM, Krepischi AC. de Araújo É, et al. Among authors: achatz mi. Exp Mol Pathol. 2014 Dec;97(3):425-32. doi: 10.1016/j.yexmp.2014.09.009. Epub 2014 Sep 16. Exp Mol Pathol. 2014. PMID: 25236571 Free article.

6

Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

Vieira IA, Pezzi EH, Bandeira IC, Reis LB, de Araújo Rocha YM, Fernandes BV, Siebert M, Miyamoto KN, Siqueira MB, Achatz MI, Galvão HCR, Garcia FAO, Campacci N, Carraro DM, Formiga MN, Vianna FSL, Palmero EI, Macedo GS, Ashton-Prolla P. Vieira IA, et al. Among authors: achatz mi. Gene. 2024 Mar 10;898:148069. doi: 10.1016/j.gene.2023.148069. Epub 2023 Dec 7. Gene. 2024. PMID: 38070788

7

Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil.

Palmero EI, Schüler-Faccini L, Caleffi M, Achatz MI, Olivier M, Martel-Planche G, Marcel V, Aguiar E, Giacomazzi J, Ewald IP, Giugliani R, Hainaut P, Ashton-Prolla P. Palmero EI, et al. Among authors: achatz mi. Cancer Lett. 2008 Mar 8;261(1):21-5. doi: 10.1016/j.canlet.2007.10.044. Epub 2008 Jan 11. Cancer Lett. 2008. PMID: 18248785

8

Highly prevalent TP53 mutation predisposing to many cancers in the Brazilian population: a case for newborn screening?

Achatz MI, Hainaut P, Ashton-Prolla P. Achatz MI, et al. Lancet Oncol. 2009 Sep;10(9):920-5. doi: 10.1016/S1470-2045(09)70089-0. Lancet Oncol. 2009. PMID: 19717094

9

(18)F-FDG PET-CT for Surveillance of Brazilian Patients with Li-Fraumeni Syndrome.

Nogueira ST, Lima EN, Nóbrega AF, Torres Ido C, Cavicchioli M, Hainaut P, Achatz MI. Nogueira ST, et al. Among authors: achatz mi. Front Oncol. 2015 Feb 19;5:38. doi: 10.3389/fonc.2015.00038. eCollection 2015. Front Oncol. 2015. PMID: 25745605 Free PMC article.

10

Oral and maxillofacial considerations in Gardner's syndrome: a report of two cases.

Pereira DL, Carvalho PA, Achatz MI, Rocha A, TardinTorrezan G, Alves FA. Pereira DL, et al. Among authors: achatz mi. Ecancermedicalscience. 2016 Feb 24;10:623. doi: 10.3332/ecancer.2016.623. eCollection 2016. Ecancermedicalscience. 2016. PMID: 26981152 Free PMC article.

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