Search Results - "Silva, Maria Luiza M."

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 by Capela de Matos, Roberto R, Ney Garcia, Daniela R, Cifoni, Elaine, Othman, Moneeb A K, Tavares de Souza, Mariana, Carboni, Edna K, Ferreira, Gerson M, Liehr, Thomas, Ribeiro, Raul C, M Silva, Maria Luiza

“…Pediatric acute myeloid leukemia (AML) is a highly heterogeneous disease, presenting cytogenetic and molecular abnormalities which turned out to be critical…”
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Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia by de Figueiredo, Amanda F., Land, Marcelo G. P., Ferreira, Gerson M., Mencalha, Andre, Binato, Renata, Capela de Matos, Roberto R., Liehr, Thomas, Silva, Maria Luiza M., Abdelhay, Eliana

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An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype by Garcia, Daniela Rn, Bhatt, Samarth, Manvelyan, Marina, de Souza, Mariana T, Binato, Renata, Aguiar, Thais F, Abdelhay, Eliana, Silva, Maria Luiza M

“…Near-tetraploid (model #81-103) and near-triploid (model #67-81) karyotypes are found in around 1% of childhood acute lymphoblastic leukemia. Due to its…”
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KMT2A - MLLT1 and the Novel SEC16A - KMT2A in a Cryptic 3-Way Translocation t(9;11;19) Present in an Infant With Acute Lymphoblastic Leukemia by de Matos, Roberto R.C., Ferreira, Gerson M., Meyer, Claus, Marschalek, Rolf, Larghero, Patrizia, Ribeiro, Raul C., Liehr, Thomas, Othman, Moneeb, Bizarro, Mariana T. de S.M., Sobral da Costa, Elaine, Land, Marcelo G.P., Abdelhay, Eliana, Binato, Renata, Silva, Maria Luiza M.

“…About 25% of the patients with the translocation t(11;19)(q23;p13.3)/ KMT2A - MLLT1 present three-way or more complex fusions, associated with a worse…”
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An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia by Monteso, Kelly C.d.A., Othman, Moneeb A.K., Capela de Matos, Roberto R., Ney Garcia, Daniela R., da Rocha, Moisés M., de Souza, Mariana T., Albagli, Luiza F., Liehr, Thomas, Land, Marcelo G.P., Silva, Maria Luiza M., Costa, Elaine S.

“…KMT2A gene rearrangements represent the most frequent group of abnormalities in childhood leukemia (~70% of cases), with over 120 rearrangements described. The…”
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Altered neutrophil immunophenotypes in childhood B‑cell precursor acute lymphoblastic leukemia by Oliveira, Elen, Bacelar, Thiago S, Ciudad, Juana, Ribeiro, Maria Cecília M, Garcia, Daniela R N, Sedek, Lukasz, Maia, Simone F, Aranha, Daniel B, Machado, Indyara C, Ikeda, Arissa, Baglioli, Bianca F, Lopez-Duarte, Nathalia, Teixeira, Lisandra A C, Szczepanski, Tomasz, Silva, Maria Luiza M, Land, Marcelo G P, Orfao, Alberto, Costa, Elaine S

“…An increasing number of evidences suggest a genetic predisposition in acute lymphoblastic leukemia (ALL) that might favor the occurrence of the driver genetic…”
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Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm by Capela de Matos, Roberto R., Othman, Moneeb A.K., Ferreira, Gerson M., Costa, Elaine S., Melo, Joana B., Carreira, Isabel M., de Souza, Mariana T., Lopes, Bruno A., Emerenciano, Mariana, Land, Marcelo G.P., Liehr, Thomas, Ribeiro, Raul C., Silva, Maria Luiza M.

“…•The t(3;7)(q26;q21) juxtaposes MECOM and CDK6 genes. MECOM disruption affects cell differentiation and proliferation.•MECOM overexpression is associated with…”
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Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8 by De Souza, Mariana T, Vera-Lozada, Gabriela, Othman, Moneeb, Marques-Salles, Teresinha J, Pinto, Luciana W, da Rocha, Moisés M, Rouxinol, Soraia, Liehr, Thomas, Ribeiro, Raul C, Hassan, Rocio, Silva, Maria Luiza M

“…Dear Editor, Burkitt lymphoma/leukemia (BL/L) was the first neoplasia associated with rearrangement in MYC that is the molecular hallmark of this disease…”
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Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia by Ney-Garcia, Daniela R., Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana T., Capela de Matos, Roberto R., Binato, Renata, Jordy, Fernanda C., Abdelhay, Eliana, Ribeiro, Raul C., Silva, Maria Luiza M.

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KMT2A-MLLT1 and the Novel SEC16A-KMT2A in a Cryptic 3-Way Translocation t(9;11;19) Present in an Infant With Acute Lymphoblastic Leukemia by de Matos, Roberto R.C., Ferreira, Gerson M., Meyer, Claus, Marschalek, Rolf, Larghero, Patrizia, Ribeiro, Raul C., Liehr, Thomas, Othman, Moneeb, Bizarro, Mariana T. de S.M., Sobral da Costa, Elaine, Land, Marcelo G.P., Abdelhay, Eliana, Binato, Renata, Silva, Maria Luiza M.

“…About 25% of the patients with the translocation t(11;19)(q23;p13.3)/KMT2A-MLLT1 present three-way or more complex fusions, associated with a worse prognosis,…”
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A new case of t(5;15)(p15;q11∼q13) in infant acute lymphoblastic leukemia by Silva, Maria Luiza M., de Brito, Gilena Dantas, Simões, Felippe, Otero, Luize, Land, Marcelo Gerardin Poirot, Guerra, Maria Celia, Salles, Terezinha J.M., Pombo-de-Oliveira, Maria S.

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Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8 by De Souza, Mariana T, Vera-Lozada, Gabriela, Othman, Moneeb, Marques-Salles, Teresinha J, Pinto, Luciana W, da Rocha, Moisés M, Rouxinol, Soraia, Liehr, Thomas, Ribeiro, Raul C, Hassan, Rocio, Silva, Maria Luiza M

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90 Bone marrow culture studies in myelodysplastic syndromes by de Souza Femandez, Teresa, Diamond, Hilda R., de Vasconcelos, Zilton F.M., Silva, Maria Luiza M., Tabak, Daniel, dos Santos, Luis Antoˆnio Olímpio, Abdelhay, Eliana

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Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia by Ney-Garcia, Daniela R, Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana T, de Matos, Roberto R Capela, Binato, Renata, Jordy, Fernanda C, Abdelhay, Eliana, Ribeiro, Raul C, Silva, Maria Luiza M

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Natural killer cell activity in a patient with Chédiak-Higashi syndrome submitted to bone marrow transplantation by Diamond, H R, Souza, M H, Silva, M L, Tabak, D G, Ferman, S, M-Silva, V M, de La Rocque, L, Rumjanek, V M

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142 5q- Syndrome: Breakpoint investigation by Abdelhay, Eliana, de Souza Fernandez, Teresa, de Souza, Jamison M., Silva, Maria Luíza M.

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Cytogenetic study of 50 Brazilian patients with primary myelodysplastic syndrome by Fernandez, Teresa de Souza, Silva, Maria Luiza M., Souza, Jamison M. de, Tabak, Daniel, Abdelhay, Eliana

“…In this work we analyzed cytogenetically 50 patients with primary myelodysplastic syndrome from several hospitals of Rio de Janeiro, Brazil. The frequency of…”
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117 Cytogenetic and molecular study in primary myelodysplastic syndrome by de Souza Fernandez, Teresa, Silva, Maria Luíza M., de Souza, Jamison M., Soares, Rose Mary P., Tabak, Daniel, Abdelhay, Eliana

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Immunophenotypic study of acute lymphoblastic leukemia (a prospective study in Brazilian children) by de Souza, Maria Helena Ornellas, Diamond, Hilda Rachel, Santos, Marcia P.E., Silva, Maria Luiza M., de Azevedo, Alice Maria B., Wajnberg, Henrique, da Silva, Tamara Mitchel R., Schmidt, Leila de H., Deterling, Louise C.S., Campos, Mercia Mendes, Harab, Ramza Cabral, Básica, Pesquisa

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Isochromosome 14q in T cell childhood acute lymphoblastic leukemia by Silva, Maria Luiza M., Zalcberg, Ilana Q., De Souza, M.Helena O., Simões, Felippe V., Carriço, Kadma C., Tabak, Daniel G., Ribeiro, Paul C., Abdelhay, Eliana

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