Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Daniela Ribeiro Ney Garcia"'
1
Akademický článek
Intrachromosomal amplification of chromosome 21 (iAMP21) detected by ETV6/RUNX1 FISH screening in childhood acute lymphoblastic leukemia: a case report
Autor: Daniela Ribeiro Ney Garcia, Alejandro Mauricio Arancibia, Raul C. Ribeiro, Marcelo Gerardin Poirot Land, Maria Luiza Macedo Silva
Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 35, Iss 5, Pp 369-371 (2013)
Chromosome abnormalities that usually define high-risk acute lymphoblastic leukemia are the t(9;22)/ breakpoint cluster region protein-Abelson murine leukemia viral oncogene homolog 1, hypodiploid with < 44 chromosomes and 11q23/ myeloid/lymphoid leu
Externí odkaz: https://doaj.org/article/72fd49650dac4601a26f6daaea3db422
Zobrazit plný text záznamu
2
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes
Autor: Mariana Tavares de Souza, Thomas Liehr, Roberto R. Capela de Matos, Claus Meyer, Daniela Ribeiro Ney Garcia, Maria Luiza Macedo Silva, Rolf Marschalek, Eliana Abdelhay, Moneeb A.K. Othman, Raul C. Ribeiro, Katharina Rittscher, Marcelo Gerardin Poirot Land, Amanda Faria de Figueiredo
Publikováno v: Hematological Oncology. 35:760-768
In pediatric acute leukemias, reciprocal chromosomal translocations frequently cause gene fusions involving the lysine (K)-specific methyltransferase 2A gene (KMT2A, also known as MLL). Specific KMT2A fusion partners are associated with the disease p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9cba59c729fecef0bacb66e001f620d3
https://doi.org/10.1002/hon.2299
Zobrazit plný text záznamu
3
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis
Autor: Elaine Sobral da Costa, Alice Maria Boulhosa de Azevedo, Maria Luiza Macedo Silva, Mariana Tavares de Souza, Eliana Abdelhay, Hasmik Mkrtchyan, Rocio Hassan, Thomas Liehr, Daniela Ribeiro Ney-Garcia, Amanda Faria de Figueiredo
Publikováno v: International Journal of Hematology. 93:232-236
Classical Burkitt lymphoma/leukemia (BL/L) presenting L3 morphology is found in 1% of childhood ALL. Recently, it has been described that secondary abnormalities could influence the prognosis of these patients. However, little information is availabl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f2a26425497ae702aeee1b8eeccd338
https://doi.org/10.1007/s12185-010-0757-8
Zobrazit plný text záznamu
4
Altered neutrophil immunophenotypes in childhood B‑cell precursor acute lymphoblastic leukemia
Autor: Daniel B. Aranha, Arissa Ikeda, Simone F. Maia, Bianca F. Baglioli, Daniela Ribeiro Ney Garcia, Marcelo Gerardin Poirot Land, Elen Oliveira, Maria Luiza Macedo Silva, Elaine Sobral da Costa, Alberto Orfao, Nathalia Lopez‑Duarte, Tomasz Szczepański, Lukasz Sedek, Juana Ciudad, Thiago S. Bacelar, Maria Cecília Menks Ribeiro, Indyara C. Machado, Lisandra A. C. Teixeira
Publikováno v: Oncotarget
Digital.CSIC. Repositorio Institucional del CSIC
instname
An increasing number of evidences suggest a genetic predisposition in acute lymphoblastic leukemia (ALL) that might favor the occurrence of the driver genetic alterations. Such genetic background might also translate into phenotypic alterations of re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84bbdf275b93299854f5c8ea5b1ab6c9
https://pubmed.ncbi.nlm.nih.gov/27028865
Zobrazit plný text záznamu
6
Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11
Autor: Thomas Liehr, R. R. Capela de Matos, Raul C. Ribeiro, Samarth Bhatt, Maria Luiza Macedo Silva, W. Pulcheri, M. T. de Souza, Daniela Ribeiro Ney-Garcia, Eliana Abdelhay, G. Pimenta
Publikováno v: International Journal of Hematology. 95:112-114
The ETV6/RUNX1 (TEL/AML1) gene fusion is the most common gene rearrangement in childhood B-cell progenitor acute lymphoblastic leukemia (BCP-ALL) that occurs in 19–27% of cases [1]. This gene fusion is caused by the t(12;21)(p13;q22) mutation, whic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8fbd9d478931db415a3b9fe392e7441a
https://doi.org/10.1007/s12185-011-0981-x
Zobrazit plný text záznamu
8
Molecular studies reveal a MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype
Autor: Rolf Marschalek, Claus Meyer, Maria S. Pombo-de-Oliveira, Maria Luiza Macedo Silva, Mariana Emerenciano, Daniela Ribeiro Ney Garcia, Raul C. Ribeiro, Thomas Liehr, Marcelo Gerardin Poirot Land
Publikováno v: Cancer genetics. 208(4)
Rearrangement of the mixed lineage-leukemia gene (MLL-r) is common in hematological diseases and is generally associated with poor prognosis. The mixed-lineage leukemia gene translocated to, 3 (MLLT3) gene (9p22) is a frequent MLL-r partner (∼18% o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::314bdcc9359629e3ff2dc1a82d041d97
https://pubmed.ncbi.nlm.nih.gov/25843568
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje