Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management. - Wikidata - wikimedia - TriplyDB

Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management.

Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management.

http://www.wikidata.org/entity/Q37872265

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Intracerebral Hemorrhage, Oxidative Stress, and Antioxidant Therapy Sickle Cells Abolish Melanoma Tumorigenesis in Hemoglobin SS Knockin Mice and Augment the Tumoricidal Effect of Oncolytic Virus In Vivo Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia.Heme-induced neutrophil extracellular traps contribute to the pathogenesis of sickle cell disease.Clinical biomarkers in sickle cell disease.2D DIGE based proteomics study of erythrocyte cytosol in sickle cell disease: altered proteostasis and oxidative stress.Respiratory Burst Enzymes, Pro-Oxidants and Antioxidants Status in Bangladeshi Population with β-Thalassemia Major.Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease Hematopoietic stem cell function in a murine model of sickle cell disease Albuminuria, serum antioxidant enzyme levels and markers of hemolysis and inflammation in steady state children with sickle cell anemia.Sympathetic Hyperactivity, Increased Tyrosine Hydroxylase and Exaggerated Corpus Cavernosum Relaxations Associated with Oxidative Stress Plays a Major Role in the Penis Dysfunction in Townes Sickle Cell Mouse Osteoarticular involvement in sickle cell disease.Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease.Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease.Band 3 Erythrocyte Membrane Protein Acts as Redox Stress Sensor Leading to Its Phosphorylation by p (72) Syk Protective effect of flavonoids against reactive oxygen species production in sickle cell anemia patients treated with hydroxyurea.Kidney dysfunction and beta S-haplotypes in patients with sickle cell disease Nucleosomes and neutrophil activation in sickle cell disease painful crisis.New insights on pathophysiology, clinical manifestations, diagnosis, and treatment of sickle cell nephropathy.Biomarkers in sickle cell disease.Role of oxidative stress in the pathogenesis of sickle cell disease.Emerging drugs for sickle cell anemia.Triterpenoid inducers of Nrf2 signaling as potential therapeutic agents in sickle cell disease: a review.Spectrin's chimeric E2/E3 enzymatic activity.Role of Exercise-Induced Oxidative Stress in Sickle Cell Trait and Disease.Endothelin receptor antagonists in sickle cell disease: A promising new therapeutic approach.Targeting Mac-1-mediated leukocyte-RBC interactions uncouples the benefits for acute vaso-occlusion and chronic organ damage.Red cell DAMPs and inflammation.Proteasome inhibition induces both antioxidant and hb f responses in sickle cell disease via the nrf2 pathway.Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study.Oxidative stress in sickle cell disease.Efficient Quantitative Analysis of Carboxyalkylpyrrole Ethanolamine Phospholipids: Elevated Levels in Sickle Cell Disease Blood.Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use.Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease Brain neurochemical and hemodynamic findings in the NY1DD mouse model of mild sickle cell disease.Nitric oxide status in sickle cell anemia.Air pollution and children's health: sickle cell disease.Beneficial Effect of the Nitric Oxide Donor Compound 3-(1,3-Dioxoisoindolin-2-yl)Benzyl Nitrate on Dysregulated Phosphodiesterase 5, NADPH Oxidase, and Nitrosative Stress in the Sickle Cell Mouse Penis: Implication for Priapism Treatment.Association of erythrocytes antioxidant enzymes and their cofactors with markers of oxidative stress in patients with sickle cell anemia.The effect of hemolysis on plasma oxidation and nitration in patients with sickle cell disease.

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Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management.

http://www.wikidata.org/entity/Q37872265

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 04 May 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Oxidative stress in sickle cel ...... ations for disease management.

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Oxidative stress in sickle cel ...... ations for disease management.

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Oxidative stress in sickle cel ...... ations for disease management.

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Oxidative stress in sickle cel ...... ations for disease management.

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Oxidative stress in sickle cel ...... ations for disease management.

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Oxidative stress in sickle cel ...... ations for disease management.

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American Journal of Hematology

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Oxidative stress in sickle cel ...... ations for disease management.

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Bart J Biemond

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CURAMA Study Group

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Dees P Brandjes

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Erfan Nur

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Hans-Martin Otten

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John-John B Schnog

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P2860

Calcium-dependent phospholipid scrambling by TMEM16F

Oxidative protein folding in eukaryotes: mechanisms and consequences

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

Free radicals in the physiological control of cell function

Red blood cells induce hypoxic lung inflammation

A receptor for phosphatidylserine-specific clearance of apoptotic cells

Sickle Cell Anemia and Severe Infections Due to Encapsulated Bacteria

Andrographolide attenuates inflammation by inhibition of NF-kappa B activation through covalent modification of reduced cysteine 62 of p50.

Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation.

Antisickling property of fetal hemoglobin enhances nitric oxide bioavailability and ameliorates organ oxidative stress in transgenic-knockout sickle mice.

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484-489

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scholarly article

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10.1002/AJH.22012

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6

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86

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2011-05-04T00:00:00Z

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51100499

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21544855

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pathophysiology

sickle-cell disease