Výsledky vyhledávání - "Adriana I. Dore"

The association of ICAM-1 Exon 6 (E469K) but not of ICAM-1 Exon 4 (G241R) and PECAM-1 Exon 3 (L125V) polymorphisms with the development of differentiation syndrome in acute promyelocytic leukemia

Autor: Adriana I. Dore, Jorge Elias, Barbara A. Santana-Lemos, Eduardo Magalhães Rego, Leandro F. Dalmazzo, Roberto Passetto Falcão, Rafael H. Jacomo, Waldir Veiga Pereira, Virginia Maria Coser, Ana Silvia G. Lima, Flávia Leite Souza Santos

Publikováno v: Journal of Leukocyte Biology. 82:1340-1343

The use of all trans-retinoic acid (ATRA) is the basis of treatment of acute promyelocytic leukemia (APL) and represents the paradigm of differentiation therapy. In general, ATRA is well-tolerated but may be associated with a potentially lethal side-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e01130183560a0f6883f8b8e36d1430c
https://doi.org/10.1189/jlb.0207095

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Características hematológicas e perfil de expressão de antígenos mielóides de pacientes com leucemia promielocítica aguda: análise de fatores prognósticos para o desenvolvimento da síndrome do ácido retinóico Hematological features and expression profile of myeloid antigens of acute promyelocytic leukemia patients: analysis of prognostic factors for development of the retinoic acid syndrome

Autor: Flávia Leite Souza Santos, Adriana I. Dore, Ana Sílvia G. Lima, Aglair B. Garcia, Marco A. Zago, Edgar G. Rizzatti, Jorge Elias Jr, Roberto Passetto Falcão, Eduardo Magalhães Rego

Publikováno v: Revista da Associação Médica Brasileira, Vol 50, Iss 3, Pp 286-292 (2004)

OBJETIVO: A leucemia promielocítica aguda (LPA) apresenta uma boa resposta ao tratamento com o ácido all trans retinóico (ATRA). Entretanto, alguns pacientes desenvolvem uma complicação grave chamada síndrome do ácido retinóico (SAR). O objet

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::6a231a63e68c07e140438a392053b731
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302004000300036

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Nuclear SET Domain (NSD) Protein Lysine Methyltransferases (KMT) Family Members Expression in Acute Myeloid Leukemia

Autor: Luisa C A Koury, Luciana Yamamoto Almeida, Lorena Lôbo de Figueiredo Pontes, Antonio R. Lucena-Araujo, Virginia Mara De Deus Wagatsuma, Adriana I. Dore, Felipe Saldanha-Araujo, Fabiola Traina, Fabio Pittella-Silva, Eduardo Magalhães Rego, Silvia Elena Sánchez, Ana Silvia Gouvêa de Lima, Fernanda Borges da Silva

Publikováno v: Blood. 128:5097-5097

The Nuclear SET Domain (NSD) Protein Lysine Methyltransferases (KMT) family is composed of three members: NSD1/KMT3B, NSD2/WHSC1/MMSET and NSD3/WHSC1L1 which regulate gene expression through methylation of lysine 36 of histone H3 (H3K36). NSD2 overex

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ac849485729289b7092d588fa4e62af
https://doi.org/10.1182/blood.v128.22.5097.5097

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[Hematological features and expression profile of myeloid antigens of acute promyelocytic leukemia patients: analysis of prognostic factors for development of the retinoic acid syndrome]

Autor: Flávia Leite Souza, Santos, Adriana I, Dore, Ana Sílvia G, Lima, Aglair B, Garcia, Marco A, Zago, Edgar G, Rizzatti, Jorge, Elias, Roberto Passetto, Falcão, Eduardo Magalhães, Rego

Publikováno v: Revista da Associacao Medica Brasileira (1992). 50(3)

Acute Promyelocytic Leukemia (APL) is characterized by its good response to treatment with all trans retinoic acid (ATRA). However, some patients receiving ATRA develop a serious complication called retinoid syndrome (RS). The objective of this study

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::df36c4ec715ef683a2a55e622b775a6a
https://pubmed.ncbi.nlm.nih.gov/15499481

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Hematological features and expression profile of myeloid antigens of acute promyelocytic leukemia patients: analysis of prognostic factors for development of the retinoic acid syndrome

Autor: Flávia Leite Souza Santos, Eduardo Magalhães Rego, Adriana I. Dore, Marco Antonio Zago, Aglair Bergamo Garcia, Ana Silvia G. Lima, Edgar Gil Rizzatti, Jorge Elias, Roberto Passetto Falcão

Publikováno v: Revista da Associação Médica Brasileira v.50 n.3 2004
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
Revista da Associação Médica Brasileira, Volume: 50, Issue: 3, Pages: 286-292, Published: SEP 2004

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33f5ca55cdb4720fce400c4d895386ec
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302004000300036

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Distinct Profile of FLT3 Mutations in Brazil

Autor: Dirceu Silva, Adriana I. Dore, Guilherme A.A. Santos, Lidiane C. Melato, Wilson A. Silva, Danielle Leão C. F. Souza, Sebastião José Ismael, Ana Silvia G. Lima, Eduardo Magalhães Rego

Publikováno v: Blood. 106:4532-4532

Mutations in the tyrosine kinase receptor FLT3 are the most common molecular abnormality in acute myeloid leukemia (AML) being detected in about 30% of AML cases. According to the protein domain altered FLT3 mutations may be classified as juxtamembra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::08a0c9818690738605a5239cca0e0c81
https://doi.org/10.1182/blood.v106.11.4532.4532

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