Search Results - "Olalla Saad, Sara Terezinha"

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    Inflammatory Dendritic Cells Contribute to Regulate the Immune Response in Sickle Cell Disease by Sesti-Costa, Renata, Borges, Marina Dorigatti, Lanaro, Carolina, de Albuquerque, Dulcinéia Martins, Saad, Sara Terezinha Olalla, Costa, Fernando Ferreira

    Published in Frontiers in immunology (04-02-2021)
    “…Sickle cell disease (SCD), one of the most common hemoglobinopathies worldwide, is characterized by a chronic inflammatory component, with systemic release of…”
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    Journal Article
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    ARHGAP21 modulates FAK activity and impairs glioblastoma cell migration by Bigarella, Carolina Louzão, Borges, Luciene, Costa, Fernando Ferreira, Saad, Sara Terezinha Olalla

    Published in Biochimica et biophysica acta (01-05-2009)
    “…Glioblastoma multiforme is highly aggressive and is the most common glial tumor type. Although there have been advances in treatment, the average survival…”
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    Acute myocardial infarction in sickle cell disease: a possible complication of hydroxyurea treatment by Fattori, André, de Souza, Robenílson Almeida, Saad, Sara Terezinha Olalla, Costa, Fernando Ferreira

    “…We describe a 28-year-old man treated with hydroxyurea for sickle cell anemia, who was admitted to the University Hospital with an acute myocardial infarction…”
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    Expression of Sara2 human gene in erythroid progenitors by Jardim, Denis Leonardo Fontes, da Cunha, Anderson Ferreira, Duarte, Adriana da Silva Santos, dos Santos, Camila Oresco, Saad, Sara Terezinha Olalla, Costa, Fernando Ferreira

    “…A human homologue of Sar1, named Sara2, was shown to be preferentially expressed during erythropoiesis in a culture stimulated by EPO. Previous studies, in…”
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    Hydroxycarbamide reduces eosinophil adhesion and degranulation in sickle cell anaemia patients by Pallis, Flavia Rubia, Conran, Nicola, Fertrin, Kleber Yotsumoto, Olalla Saad, Sara Terezinha, Costa, Fernando Ferreira, Franco‐Penteado, Carla Fernanda

    Published in British journal of haematology (01-01-2014)
    “…Summary Inflammation, leucocyte and red cell adhesion to the endothelium contribute to the pathogenesis of sickle cell anaemia. Neutrophils appear to be…”
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    Increased Inflammatory Markers and Their Correlations To Clinical Complications In Hemoglobin SC Disease by Colella, Marina Pereira, Vinicius de Paula, Erich, Conran, Nicola, Machado-Neto, Joao, Quaino, Susan K.P., Annichino-Bizzacchi, Joyce M., Costa, Fernando Ferreira, Olalla-Saad, Sara Terezinha, Traina, Fabiola

    Published in Blood (15-11-2013)
    “…Hemoglobin SC (HbSC) disease is the second most prevalent hemoglobinopathy after sickle cell anemia (SCA – homozygous HbSS). Despite its high prevalence, most…”
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    Hydroxyurea Therapy Reduces The Hypercoagulability State In a Sickle Cell Mouse Model by Colella, Marina Pereira, Almeida, Camila Bononi, Conran, Nicola, Pallis, Flavia Rubia, Franco-Penteado, Carla Fernanda, Annichino-Bizzacchi, Joyce Maria, Costa, Fernando Ferreira, Vinicius de Paula, Erich, Olalla-Saad, Sara Terezinha, Traina, Fabiola

    Published in Blood (15-11-2013)
    “…Several lines of evidence show that sickle cell anemia (SCA) is characterized by a hypercoagulable state. SCA patients present an elevated rate of thrombotic…”
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    IFN-β, IFN-γ, and TNF-α decrease erythrophagocytosis by human monocytes independent of SIRP-α or SHP-1 expression by de Almeida, Ana Carolina, Barbosa, Soraya Massaro, de Lourdes Rios Barjas-Castro, Maria, Olalla-Saad, Sara Terezinha, Condino-Neto, Antonio

    Published in Immunopharmacology and immunotoxicology (01-12-2012)
    “…Background: Many cases of autoimmune hemolytic anemia have been reported after viral infection. Phagocyte activation and accompanying erythrophagocytosis are…”
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    Discrepancies in p21ras, p53, and Mdm2 Protein Expression Predict Worse Prognosis in Acute Myeloid Leukemia by Schulz, Elizabeth, Lorand-Metze, Irene, Koch, Rainer, Costa, Solange Campelo, Costa, Fernando Ferreira, Saad, Sara Terezinha Olalla

    Published in Blood (16-11-2005)
    “…Tumor progress is a multistep process in which clones of cells become abnormal by accumulating growth alterations until they are transformed and/or…”
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