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Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia.
de Figueiredo AF, Land MGP, Ferreira GM, Mencalha A, Binato R, Capela de Matos RR, Liehr T, Silva MLM, Abdelhay E. de Figueiredo AF, et al. Among authors: capela de matos rr. Br J Haematol. 2020 Jun;189(6):e245-e248. doi: 10.1111/bjh.16675. Epub 2020 Apr 21. Br J Haematol. 2020. PMID: 32314797 Free article. No abstract available.
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
Ney Garcia DR, de Souza MT, de Figueiredo AF, Othman MAK, Rittscher K, Abdelhay E, Capela de Matos RR, Meyer C, Marschalek R, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Ney Garcia DR, et al. Among authors: capela de matos rr. Hematol Oncol. 2017 Dec;35(4):760-768. doi: 10.1002/hon.2299. Epub 2016 Jun 10. Hematol Oncol. 2017. PMID: 27282883
An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia.
Monteso KCDA, Othman MAK, Capela de Matos RR, Ney Garcia DR, da Rocha MM, de Souza MT, Albagli LF, Liehr T, Land MGP, Silva MLM, Costa ES. Monteso KCDA, et al. Among authors: capela de matos rr. J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e371-e374. doi: 10.1097/MPH.0000000000001776. J Pediatr Hematol Oncol. 2021. PMID: 32134839
GAS6 Oncogene and Reverse MLLT3-KMT2A Duplications in an Infant with Acute Myeloid Leukemia and a Novel Complex Hyperdiploid Karyotype: Detailed High-Resolution Molecular Cytogenetic Studies.
Capela de Matos RR, Ney Garcia DR, Cifoni E, Othman MAK, Tavares de Souza M, Carboni EK, Ferreira GM, Liehr T, Ribeiro RC, M Silva ML. Capela de Matos RR, et al. Cytogenet Genome Res. 2017;152(1):33-37. doi: 10.1159/000477108. Epub 2017 Jun 9. Cytogenet Genome Res. 2017. PMID: 28595195
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.
Capela de Matos RR, Othman M, Ferreira GM, Monteso K, de Souza MT, Rouxinol M, Melo JB, Carreira IM, Abdelhay E, Liehr T, Ribeiro RC, Silva M. Capela de Matos RR, et al. Cancer Genet. 2022 Apr;262-263:16-22. doi: 10.1016/j.cancergen.2021.12.003. Epub 2021 Dec 22. Cancer Genet. 2022. PMID: 34974289
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
Capela de Matos RR, Ney Garcia DR, Othman MAK, Moura Ferreira G, Melo JB, Carreira IM, Meyer C, Marschalek R, Costa ES, Land MGP, Liehr T, Ribeiro RC, Silva MLM. Capela de Matos RR, et al. Cytogenet Genome Res. 2019;157(4):213-219. doi: 10.1159/000499640. Epub 2019 Apr 12. Cytogenet Genome Res. 2019. PMID: 30974445
Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia.
Borges ML, Capela de Matos RR, Amaral BD, Soares-Ventura EM, Leite EP, Silva MO, Cornélio MT, Silva ML, Liehr T, Marques-Salles TD. Borges ML, et al. Among authors: capela de matos rr. J Pediatr Hematol Oncol. 2017 Mar;39(2):e85-e91. doi: 10.1097/MPH.0000000000000720. J Pediatr Hematol Oncol. 2017. PMID: 28212262
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.
Lovatel VL, de Souza DC, Alvarenga TF, Capela de Matos RR, Diniz C, Schramm MT, Llerena Júnior JC, Silva MLM, Abdelhay E, de Souza Fernandez T. Lovatel VL, et al. Among authors: capela de matos rr. Mol Cytogenet. 2018 Jul 11;11:40. doi: 10.1186/s13039-018-0389-x. eCollection 2018. Mol Cytogenet. 2018. PMID: 30008805 Free PMC article.
11 results