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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
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
Importance of genetic cancer risk assessment as a strategy to stratify risk and provide precision prevention in high-risk patients and families.
Ashton-Prolla P, Achatz MIW, Moreira MAM, Palmero EI, Soares DCQ, Ferraz VEF, Caires IQS, Guindalini RSC, Gifoni ACLVC. Ashton-Prolla P, et al. Among authors: achatz miw. Rev Assoc Med Bras (1992). 2024 Jun 7;70(suppl 1):e2024S117. doi: 10.1590/1806-9282.2024S117. eCollection 2024. Rev Assoc Med Bras (1992). 2024. PMID: 38865537 Free PMC article. No abstract available.
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.
113 results