Impact of molecular mutations on treatment response to DNMT inhibitors in myelodysplasia and related neoplasms von Traina, F, Visconte, V, Elson, P, Tabarroki, A, Jankowska, A M, Hasrouni, E, Sugimoto, Y, Szpurka, H, Makishima, H, O'Keefe, C L, Sekeres, M A, Advani, A S, Kalaycio, M, Copelan, E A, Saunthararajah, Y, Olalla Saad, S T, Maciejewski, J P, Tiu, R V

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Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil von Svidnicki, M. C. C. M., Zanetta, G. K., Congrains-Castillo, A., Costa, F. F., Saad, S. T. O.

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A simple score derived from bone marrow immunophenotyping is important for prognostic evaluation in myelodysplastic syndromes von Vido-Marques, J. R., Reis-Alves, S. C., Saad, S. T. O., Metze, K., Lorand-Metze, I.

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Cognitive effects of the GSK-3 inhibitor “lithium” in LPS/chronic mild stress rat model of depression: Hippocampal and cortical neuroinflammation and tauopathy von Ebeid, Mai A., Habib, Mohamed Z., Mohamed, Ahmed M., Faramawy, Yasser el, Saad, Sherin S.T., El-Kharashi, Omnyah A., El Magdoub, Hekmat M., Abd-Alkhalek, Hadwa A., Aboul-Fotouh, Sawsan, Abdel-Tawab, Ahmed M.

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Constitutive JunB expression, associated with the JAK2 V617F mutation, stimulates proliferation of the erythroid lineage von da Costa Reis Monte-Mór, B, Plo, I, da Cunha, A F, Costa, G G L, de Albuquerque, D M, Jedidi, A, Villeval, J-L, Badaoui, S, Lorand-Metze, I, Pagnano, K B B, Saad, S T O, Vainchenker, W, Costa, F F

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Hydroxyurea is associated with reductions in hypercoagulability markers in sickle cell anemia von COLELLA, M. P., De PAULA, E. V., CONRAN, N., MACHADO‐NETO, J. A., ANNICCHINO‐BIZZACCHI, J. M., COSTA, F. F., SAAD, S. T. O., TRAINA, F.

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Evaluation of reticulated platelets in patients with sickle cell diseases von Noronha, J.F.A, Costa, F.F, Saad, S.T.O, Lorand-Metze, I.G.H, Grotto, H.Z.W

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Effects of lithium on cytokine neuro-inflammatory mediators, Wnt/β-catenin signaling and microglial activation in the hippocampus of chronic mild stress-exposed rats von Habib, Mohamed Z., Ebeid, Mai A., el Faramawy, Yasser, Saad, Sherin S.T., El Magdoub, Hekmat M., Attia, Azza A., Aboul-Fotouh, Sawsan, Abdel-Tawab, Ahmed M.

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Elastic properties of irradiated RBCs measured by optical tweezers von Barjas-Castro, M.L., Brandão, M.M., Fontes, Adriana, Costa, F.F., Cesar, C.L., Saad, S.T.O.

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Elastic properties of stored red blood cells from sickle trait donor units von Brandão, M. M., Saad, S. T. O., Cezar, C. L., Fontes, A., Costa, F. F., Barjas-Castro, M. L.

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Umbilical cord blood CD34+ stem cells and other mononuclear cell subtypes processed up to 96 h from collection and stored at room temperature maintain a satisfactory functionality... von Pereira-Cunha, F. G., Duarte, A. S. S., Reis-Alves, S. C., Olalla Saad, S. T., Metze, K., Lorand-Metze, I., Luzo, Â. C. M.

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A novel DIA allele without the band 3-Memphis mutation in Amazonian Indians von Baleotti Jr, W., Rios, M., Reid, M. E., Fabron Jr, A., Pellegrino Jr, J., Saad, S. T. O., Castilho, L.

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High frequency of vitamin B12 deficiency in a Brazilian population von Xavier, JM, Costa, FF, Annichino-Bizzacchi, JM, Saad, STO

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Variant RH alleles and Rh immunisation in patients with sickle cell disease von Sippert, Emilia, Fujita, Claudia R, Machado, Debora, Guelsin, Glaucia, Gaspardi, Ane C, Pellegrino, Jr, Jordão, Gilli, Simone, Saad, Sara S T O, Castilho, Lilian

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Autonomous proliferation and bcl-2 expression involving haematopoietic cells in patients with myelodysplastic syndrome von BINCOLETTO, C, SAAD, S. T. O, SOARES DA SILVA, E, QUEIROZ, M. L. S

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Death switch for gene therapy: application to erythropoietin transgene expression von Souza, D S, Spencer, D M, Salles, T S I, Salomão, M A, Payen, E, Beuzard, Y, Carvalho, H F, Costa, F F, Saad, S T Olalla

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A novel FY allele in Brazilians von Castilho, L., Rios, M., Pellegrino Jr, J., Saad, S. T. O., Costa, F. F., Reid, M. E.

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IDENTIFICATION OF DIFFERENTIALLY EXPRESSED GENES INDUCED BY HYDROXYUREA IN RETICULOCYTES FROM SICKLE CELL ANAEMIA PATIENTS von Moreira, LS, De Andrade, TG, Albuquerque, DM, Cunha, AF, Fattori, A, Saad, STO, Costa, FF

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UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia von Fertrin, K. Y., Melo, M. B., Assis, Â. M., Saad, S. T. O., Costa, F. F.

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The association of cytokine gene polymorphisms with febrile non-hemolytic transfusion reaction in multitransfused patients von Addas-Carvalho, M., Salles, T. S. I., Saad, S. T. O.

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