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Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.
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- American Journal of Hematology, 2008, v. 83, n. 2, p. 103, doi. 10.1002/ajh.21041
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- Article
Up-regulation of NADPH oxidase components and increased production of interferon-gamma by leukocytes from sickle cell disease patients.
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- American Journal of Hematology, 2008, v. 83, n. 1, p. 41, doi. 10.1002/ajh.20991
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- Article
Genetic variability of platelet glycoprotein Ibα gene.
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- American Journal of Hematology, 2004, v. 77, n. 2, p. 107, doi. 10.1002/ajh.20148
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- Article
Follow?up of sickle cell disease patients with priapism treated by hydroxyurea.
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- American Journal of Hematology, 2004, v. 77, n. 1, p. 45, doi. 10.1002/ajh.20142
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- Article
Increased levels of soluble ICAM‐1 in the plasma of sickle cell patients are reversed by hydroxyurea.
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- American Journal of Hematology, 2004, v. 76, n. 4, p. 343, doi. 10.1002/ajh.20129
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- Article
Sickle Cell Health Awareness, Perspectives, and Experiences (SHAPE) survey: Perspectives of adolescent and adult patients, caregivers, and healthcare professionals on the burden of sickle cell disease.
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- European Journal of Haematology, 2024, v. 113, n. 2, p. 172, doi. 10.1111/ejh.14211
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- Article
Global analysis of erythroid cells redox status reveals the involvement of Prdx1 and Prdx2 in the severity of beta thalassemia.
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- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208316
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- Article
Identification of protein-coding and non-coding RNA expression profiles in CD34+ and in stromal cells in refractory anemia with ringed sideroblasts.
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- BMC Medical Genomics, 2010, v. 3, p. 30, doi. 10.1186/1755-8794-3-30
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- Article
Association of genetic variants rs641153 (CFB), rs2230199 (C3), and rs1410996 (CFH) with age-related macular degeneration in a Brazilian population.
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- Experimental Biology & Medicine, 2021, v. 246, n. 21, p. 2290, doi. 10.1177/15353702211024543
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- Article
Evaluation of APOE polymorphisms and the risk for age-related macular degeneration in a Southeastern Brazilian population.
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- Experimental Biology & Medicine, 2021, v. 246, n. 10, p. 1148, doi. 10.1177/1535370220985466
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- Article
Highlight Article: Different morphological and gene expression profile in placentas of the same sickle cell anemia patient in pregnancies of opposite outcomes.
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- Experimental Biology & Medicine, 2019, v. 244, n. 5, p. 395, doi. 10.1177/1535370219834305
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- Article
Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
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- Experimental Biology & Medicine, 2017, v. 242, n. 3, p. 267, doi. 10.1177/1535370216668052
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- Article
Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency in Brazil.
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- Human Heredity, 1997, v. 47, n. 1, p. 17, doi. 10.1159/000154383
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- Article
Hydroxyurea reduces leukocyte interactions with the vessel wall in a haemolytic mouse model via a possible NO/cGMP-mediated effect.
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- 2013
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- Abstract
Brain perfusion impairment in neurologically asymptomatic adult patients with sickle-cell disease shown by voxel-based analysis of SPECT images.
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- Frontiers in Neurology, 2013, v. 4, p. 1, doi. 10.3389/fneur.2013.00207
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- Article
Effect of Cytokines and Chemokines on Sickle Neutrophil Adhesion to Fibronectin.
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- Acta Haematologica, 2005, v. 113, n. 2, p. 130, doi. 10.1159/000083451
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- Article
Possible Association between Cytomegalovirus Infection and Gastrointestinal Bleeding in Hemophiliac Patients.
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- Acta Haematologica, 2000, v. 103, n. 2, p. 73, doi. 10.1159/000041023
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- Article
Expression of Spectrin αI/50 Hereditary Elliptocytosis and Its Association with the α[sup LELY] Allele.
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- Acta Haematologica, 1998, v. 100, n. 1, p. 32, doi. 10.1159/000040860
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- Article
Cytomegalovirus Infection as Cause of Severe Thrombocytopenia in a Nonimmunosuppressed Patient.
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- Acta Haematologica, 1997, v. 98, n. 4, p. 228, doi. 10.1159/000203630
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- Article
Economic burden of sickle cell disease in Brazil.
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- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269703
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- Article
Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition.
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- PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263424
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- Article
Role of Macrophages in Sickle Cell Disease Erythrophagocytosis and Erythropoiesis.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6333, doi. 10.3390/ijms24076333
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- Article
An ESR study of pathologic red blood cell membranes (RBCM).
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- Magnetic Resonance in Medicine, 1990, v. 16, n. 1, p. 132, doi. 10.1002/mrm.1910160112
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- Article
Polymorphisms in methylenetetrahydrofolate reductase gene ( MTHFR) and the age of onset of sporadic colorectal adenocarcinoma.
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- International Journal of Colorectal Disease, 2007, v. 22, n. 7, p. 757, doi. 10.1007/s00384-006-0237-z
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- Article
p53, Mdm2, and c-Myc overexpression is associated with a poor prognosis in aggressive non-Hodgkin's lymphomas.
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- American Journal of Hematology, 2001, v. 67, n. 2, p. 84, doi. 10.1002/ajh.1084
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- Article
β-thalassemia trait might increase the severity of hemochromatosis in subjects with the C282Y mutation in the HFE gene.
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- American Journal of Hematology, 2000, v. 63, n. 4, p. 230, doi. 10.1002/(SICI)1096-8652(200004)63:4<230::AID-AJH12>3.0.CO;2-5
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- Article
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahidrofolate reductase among patients with sickle cell disease in Brazil.
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- American Journal of Hematology, 1998, v. 59, n. 1, p. 46, doi. 10.1002/(SICI)1096-8652(199809)59:1<46::AID-AJH9>3.0.CO;2-#
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- Article
Haplotype analysis and <sup>A</sup>γ gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin.
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- American Journal of Hematology, 1998, v. 58, n. 1, p. 49, doi. 10.1002/(SICI)1096-8652(199805)58:1<49::AID-AJH9>3.0.CO;2-0
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- Article
Presence of allele α<sup>LELY</sup> in an Amazonian Indian population.
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- American Journal of Hematology, 1998, v. 57, n. 3, p. 212, doi. 10.1002/(SICI)1096-8652(199803)57:3<212::AID-AJH5>3.0.CO;2-Y
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- Article
Factor V Leiden (FVQ 506) is common in a Brazilian population.
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- American Journal of Hematology, 1995, v. 49, n. 3, p. 242, doi. 10.1002/ajh.2830490312
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- Article
Diagnostic Accuracy of HemotypeSC as a Point-of-Care Testing Device for Sickle Cell Disease: Findings from a Southwestern State in Nigeria and Implications for Patient Care in Resource-Poor Settings of sub-Saharan Africa.
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- Global Pediatric Health, 2021, p. 1, doi. 10.1177/2333794X211016789
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- Publication type:
- Article
Diagnostic Accuracy of HemotypeSC as a Point-of-Care Testing Device for Sickle Cell Disease: Findings from a Southwestern State in Nigeria and Implications for Patient Care in Resource-Poor Settings of sub-Saharan Africa.
- Published in:
- Global Pediatric Health, 2021, p. 1, doi. 10.1177/2333794X211016789
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- Publication type:
- Article
Viability of umbilical cord blood mononuclear cell subsets until 96 hours after collection.
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- Transfusion, 2013, v. 53, n. 9, p. 2034, doi. 10.1111/trf.12078
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- Article
A prospective study on the prevalence and risk factors for neonatal thrombocytopenia and platelet alloimmunization among 9332 unselected Brazilian newborns.
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- Transfusion, 2007, v. 47, n. 1, p. 59, doi. 10.1111/j.1537-2995.2007.01064.x
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- Article
An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis.
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- Nature Genetics, 2006, v. 38, n. 7, p. 807, doi. 10.1038/ng1825
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- Article
Heme induces significant neutrophil adhesion in vitro via an NFκB and reactive oxygen species-dependent pathway.
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- Molecular & Cellular Biochemistry, 2021, v. 476, n. 11, p. 3963, doi. 10.1007/s11010-021-04210-5
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- Article
Expanding the Knowledge on Lignocellulolytic and Redox Enzymes of Worker and Soldier Castes from the Lower Termite Coptotermes gestroi.
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- Frontiers in Microbiology, 2016, v. 7, p. 1, doi. 10.3389/fmicb.2016.01518
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- Publication type:
- Article
Relationship Between the Type of BCR-ABL Rearrangement and Bone Marrow Histopathological Features in Chronic Myeloid Leukemia.
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- Acta Oncologica, 1997, v. 36, n. 3, p. 313, doi. 10.3109/02841869709001269
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- Publication type:
- Article
Elevated plasma levels and platelet-associated expression of the pro-thrombotic and pro-inflammatory protein, TNFSF14 (LIGHT), in sickle cell disease.
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- British Journal of Haematology, 2012, v. 158, n. 6, p. 788, doi. 10.1111/j.1365-2141.2012.09218.x
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- Article
Increased adhesive properties of platelets in sickle cell disease: roles for α<sub>IIb</sub>β<sub>3</sub>-mediated ligand binding, diminished cAMP signalling and increased phosphodiesterase 3A activity.
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- British Journal of Haematology, 2010, v. 149, n. 2, p. 280, doi. 10.1111/j.1365-2141.2010.08087.x
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- Article
High expression of the cGMP-specific phosphodiesterase, PDE9A, in sickle cell disease (SCD) and the effects of its inhibition in erythroid cells and SCD neutrophils.
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- British Journal of Haematology, 2008, v. 142, n. 5, p. 836, doi. 10.1111/j.1365-2141.2008.07264.x
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- Article
Inhibition of caspase-dependent spontaneous apoptosis via a cAMP-protein kinase A dependent pathway in neutrophils from sickle cell disease patients.
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- British Journal of Haematology, 2007, v. 139, n. 1, p. 148, doi. 10.1111/j.1365-2141.2007.06748.x
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- Publication type:
- Article
Expression of the γ-globin gene is sustained by the cAMP-dependent pathway in β-thalassaemia.
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- British Journal of Haematology, 2007, v. 138, n. 3, p. 382, doi. 10.1111/j.1365-2141.2007.06673.x
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- Article
research paper Increased soluble guanylate cyclase activity in the red blood cells of sickle cell patients.
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- British Journal of Haematology, 2004, v. 124, n. 4, p. 547, doi. 10.1111/j.1365-2141.2004.04810.x
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- Article
Beta-Spectrin S[supta] Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism.
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- British Journal of Haematology, 2001, v. 115, n. 2, p. 347, doi. 10.1046/j.1365-2141.2001.03103.x
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- Article
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis.
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- British Journal of Haematology, 2000, v. 111, n. 4, p. 1190, doi. 10.1046/j.1365-2141.2000.02441.x
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- Article
Hereditary Hemoglobin Disorders in a Brazilian Population.
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- Human Heredity, 1983, v. 33, n. 2, p. 125, doi. 10.1159/000153362
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- Article
Deferasirox associated with liver failure and death in a sickle cell anemia patient homozygous for the −1774delG polymorphism in the Abcc2 gene.
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- Clinical Case Reports, 2017, v. 5, n. 8, p. 1218, doi. 10.1002/ccr3.1040
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- Article
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47313-2
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- Article
Thalassemia major phenotypes secondary to the association of β 5′ UTR +20( C→ T) allele with β 39( C→ T).
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- European Journal of Haematology, 2012, v. 89, n. 3, p. 273, doi. 10.1111/j.1600-0609.2012.01813.x
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- Article