Search Results - "Barbosa de Melo, M"

GSTT1, GSTM1, and GSTP1 polymorphisms as a prognostic factor in women with breast cancer by Oliveira, A L, Oliveira Rodrigues, F F, Dos Santos, R E, Rozenowicz, R L, Barbosa de Melo, M

“…The glutathione S-transferase (GST) family comprises phase-II cellular detoxification enzymes that catalyze the conjugation of chemotherapy drugs to…”
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Myocardial Delayed Enhancement by Magnetic Resonance Imaging in Patients With Muscular Dystrophy by Silva, Marly Conceição, MD, Meira, Zilda Maria Alves, MD, PhD, Gurgel Giannetti, Juliana, MD, PhD, da Silva, Marcelo Moreira, Oliveira Campos, Alysson Félix, RT, de Melo Barbosa, Márcia, MD, PhD, Filho, Geraldo Moll Starling, MD, de Aguiar Ferreira, Rogério, MD, Zatz, Mayana, PhD, Rochitte, Carlos Eduardo, MD, PhD

“…Myocardial Delayed Enhancement by MRI in Patients With Muscular Dystrophy Marly Conceição Silva, Zilda Maria Alves Meira, Juliana Gurgel Giannetti, Marcelo…”
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Penetrance and Phenotype of the Cys433Arg Myocilin Mutation in a Family Pedigree with Primary Open-Angle Glaucoma by de Vasconcellos, José Paulo Cabral, de Melo, Mônica Barbosa, Schimiti, Rui, Costa, Fernando Ferreira, Costa, Vital Paulino

“…PURPOSETo evaluate the penetrance and the clinical characteristics of the Cys433Arg myocilin mutation in a family pedigree with primary open-angle glaucoma…”
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A possible hot spot in exon 21 of the retinoblastoma gene predisposing to a low penetrant retinoblastoma phenotype? by Ahmad, N. Nina, Barbosa de Melo, Mônica, Singh, Arun D., Donoso, Larry A., Shields, Jerry A.

“…Purpose: To identify the mutation in the RB1 gene in a Syrian family showing incomplete penetrance of retinoblastoma (RB). Methods: Genomic DNA was used as a…”
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Molecular analysis of the retinoblastoma ( RB1) gene in acute myeloid leukemia patients by Barbosa de Melo, Mônica, Costa, Fernando Ferreira, Saad, Sara Teresinha Olalla, Lorand-Metze, Irene, Bordin, Silvana, Ahmad, Nilofer Nina

“…The pathogenesis of acute leukemia is still poorly understood. In the past few years several groups have reported deletion of the RB1 gene or altered pRB…”
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