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Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 7, p. 2374, doi. 10.3390/ijms21072374
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- Article
Phenotypes of STAT3 gain-of-function variant related to disruptive regulation of CXCL8/STAT3, KIT/STAT3, and IL-2/CD25/Treg axes.
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- Immunologic Research, 2021, v. 69, n. 5, p. 445, doi. 10.1007/s12026-021-09225-0
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- Article
Comparative transcriptomic analysis of circulating endothelial cells in sickle cell stroke.
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- Annals of Hematology, 2024, v. 103, n. 4, p. 1167, doi. 10.1007/s00277-024-05655-6
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- Article
Inflammatory Dendritic Cells Contribute to Regulate the Immune Response in Sickle Cell Disease.
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- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.617962
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The molecular mechanism responsible for HbSC retinopathy may depend on the action of the angiogenesis-related genes ROBO1 and SLC38A5.
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- Experimental Biology & Medicine, 2024, p. 1, doi. 10.3389/ebm.2024.10070
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- Article
Comparative transcriptome analysis of endothelial progenitor cells of HbSS patients with and without proliferative retinopathy.
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- Experimental Biology & Medicine, 2023, v. 248, n. 8, p. 677, doi. 10.1177/15353702231157927
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Gene expression profiles of erythroid precursors characterise several mechanisms of the action of hydroxycarbamide in sickle cell anaemia.
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- British Journal of Haematology, 2007, v. 136, n. 2, p. 333, doi. 10.1111/j.1365-2141.2006.06424.x
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- Article