Role of oxidative stress in the pathogenesis of sickle cell disease. - Wikidata - wikimedia - TriplyDB

Role of oxidative stress in the pathogenesis of sickle cell disease.

Role of oxidative stress in the pathogenesis of sickle cell disease.

http://www.wikidata.org/entity/Q37963311

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Precipitating factors and targeted therapies in combating the perils of sickle cell disease--- A special nutritional consideration Antioxidants of Edible Mushrooms Reactive nitrogen species in cellular signaling Heme-induced neutrophil extracellular traps contribute to the pathogenesis of sickle cell disease.2D DIGE based proteomics study of erythrocyte cytosol in sickle cell disease: altered proteostasis and oxidative stress.Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.Respiratory Burst Enzymes, Pro-Oxidants and Antioxidants Status in Bangladeshi Population with β-Thalassemia Major.Association of DNA Damage Repair Gene Polymorphisms hOGG1, XRCC1and p53 with Sickle Cell Disease Patients in India.Hematopoietic stem cell function in a murine model of sickle cell disease Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study In vitro organo-protective effect of bark extracts from Syzygium guineense var macrocarpum against ferric-nitrilotriacetate-induced stress in wistar rats homogenates.Albuminuria, serum antioxidant enzyme levels and markers of hemolysis and inflammation in steady state children with sickle cell anemia.Gum Arabic as novel anti-oxidant agent in sickle cell anemia, phase II trial.Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease.Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity.Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.Emerging drugs for sickle cell anemia.New concepts to fight oxidative stress: nanosized three-dimensional supramolecular antioxidant assemblies.Role of Exercise-Induced Oxidative Stress in Sickle Cell Trait and Disease.Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa.Oxidative pathways in the sickle cell and beyond.Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease.Oxidative stress in sickle cell disease.Efficient Quantitative Analysis of Carboxyalkylpyrrole Ethanolamine Phospholipids: Elevated Levels in Sickle Cell Disease Blood.Quercetin reduces hydroxyurea induced cytotoxicity in immortalized mouse aortic endothelial cells.Brain neurochemical and hemodynamic findings in the NY1DD mouse model of mild sickle cell disease.Association of erythrocytes antioxidant enzymes and their cofactors with markers of oxidative stress in patients with sickle cell anemia.Monodora myristica (African nutmeg) modulates redox homeostasis and alters functional chemistry in sickled erythrocytes.Scavenging reactive oxygen species production normalizes ferroportin expression and ameliorates cellular and systemic iron disbalances in hemolytic mouse model.Increased oxidative stress alters nucleosides metabolite levels in sickle cell anemia.Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities.Specificity of Hydrolysable Tannins from Rhus typhina L. to Oxidants in Cell and Cell-Free Models.Effect of α-thalassaemia on exercise-induced oxidative stress in sickle cell trait.Oxidative stress is decreased in physically active sickle cell SAD mice.Targeting βCys93 in hemoglobin S with an antisickling agent possessing dual allosteric and antioxidant effects.Rheumatoid Arthritis in Sickle-Cell Population: Pathophysiologic Insights, Clinical Evaluation and Management.Haemolysis and abnormal haemorheology in sickle cell anaemia.Leucocyte telomere length in patients with sickle cell disease.The effect of xanthine oxidase and hypoxanthine on the permeability of red cells from patients with sickle cell anemia.Perioperative Management of Sickle Cell Disease.

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Role of oxidative stress in the pathogenesis of sickle cell disease.

http://www.wikidata.org/entity/Q37963311

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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2011年學術文章

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name

Role of oxidative stress in the pathogenesis of sickle cell disease.

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Role of oxidative stress in the pathogenesis of sickle cell disease.

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type

label

Role of oxidative stress in the pathogenesis of sickle cell disease.

@en

Role of oxidative stress in the pathogenesis of sickle cell disease.

@nl

prefLabel

Role of oxidative stress in the pathogenesis of sickle cell disease.

@en

Role of oxidative stress in the pathogenesis of sickle cell disease.

@nl

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Role of oxidative stress in the pathogenesis of sickle cell disease.

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Erica N Chirico

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Vincent Pialoux

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P2860

Role of free radicals in the pathogenesis of acute chest syndrome in sickle cell disease

Sickle-cell disease

Xanthine oxidase mediates cytokine-induced, but not hormone-induced bone resorption

Heme degradation and vascular injury.

Tetrahydrobiopterin, superoxide, and vascular dysfunction.

Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.

Vascular cell adhesion molecule-1 (VCAM-1) gene transcription and expression are regulated through an antioxidant-sensitive mechanism in human vascular endothelial cells.

Arginase levels and their association with Th17-related cytokines, soluble adhesion molecules (sICAM-1 and sVCAM-1) and hemolysis markers among steady-state sickle cell anemia patients.

Free heme and the polymerization of sickle cell hemoglobin

Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease

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72-80

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10.1002/IUB.584

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1

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64

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22131167

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sickle-cell disease