Plasma concentrations of hemopexin, haptoglobin and heme in patients with various hemolytic diseases.
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Ibuprofen impairs allosterically peroxynitrite isomerization by ferric human serum heme-albuminHemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contendersHeme-based catalytic properties of human serum albuminHaptoglobin, hemopexin, and related defense pathways-basic science, clinical perspectives, and drug developmentA mechanistic investigation of thrombotic microangiopathy associated with IV abuse of Opana ER.Tissue factor-dependent coagulation activation by heme: A thromboelastometry study.Heme degradation and vascular injury.Immunoregulatory networks in sickle cell alloimmunization.Molecular controls of the oxygenation and redox reactions of hemoglobinA cryptic polyreactive antibody recognizes distinct clades of HIV-1 glycoprotein 120 by an identical binding mechanismGlobal gene expression profiling of endothelium exposed to heme reveals an organ-specific induction of cytoprotective enzymes in sickle cell disease.A systems biology consideration of the vasculopathy of sickle cell anemia: the need for multi-modality chemo-prophylaxsis.Placental heme receptor LRP1 correlates with the heme exporter FLVCR1 and neonatal iron statusHeme oxygenase-1 is a modulator of inflammation and vaso-occlusion in transgenic sickle mice.Alterations in bone and erythropoiesis in hemolytic anemia: comparative study in bled, phenylhydrazine-treated and Plasmodium-infected mice.Sites of formation of the serum proteins transferrin and hemopexin.Preconditioning with hemin decreases Plasmodium chabaudi adami parasitemia and inhibits erythropoiesis in BALB/c mice.Discovery and characterization of potential prognostic biomarkers for dengue hemorrhagic fever.Vasculotoxic and Proinflammatory Effects of Plasma Heme: Cell Signaling and Cytoprotective Responses.Increased striatal injury and behavioral deficits after intracerebral hemorrhage in hemopexin knockout mice.Control of intracellular heme levels: heme transporters and heme oxygenasesThe reaction of cell-free oxyhemoglobin with nitrite under physiologically relevant conditions: Implications for nitrite-based therapies.Heme interacts with c1q and inhibits the classical complement pathway.Iron, inflammation, and early death in adults with sickle cell disease.Haptoglobin attenuates hemoglobin-induced heme oxygenase-1 in renal proximal tubule cells and kidneys of a mouse model of sickle cell disease.Reversal of hemochromatosis by apotransferrin in non-transfused and transfused Hbbth3/+ (heterozygous B1/B2 globin gene deletion) mice.Disposal of plasma heme in normal man and patients with intravascular hemolysis.Identification of an iron-regulated outer membrane protein of Neisseria meningitidis involved in the utilization of hemoglobin complexed to haptoglobin.Hemopexin in severe inflammation and infection: mouse models and human diseasesBreakdown of albumin and haemalbumin by the cysteine protease interpain A, an albuminase of Prevotella intermedia.Red Blood Cells Preconditioned with Hemin Are Less Permissive to Plasmodium Invasion In Vivo and In VitroCirculating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease.Multifaceted Role of Heme during Severe Plasmodium falciparum Infections in IndiaGenetic variants and cell-free hemoglobin processing in sickle cell nephropathy.Synthesis of plasma haemopexin, albumin and fibrinogen by the regenerating rat liverIdentification of hemopexin as an anti-inflammatory factor that inhibits synergy of hemoglobin with HMGB1 in sterile and infectious inflammationInflammatory targets of therapy in sickle cell disease.Prolonged neutrophil dysfunction after Plasmodium falciparum malaria is related to hemolysis and heme oxygenase-1 inductionA novel hemoglobin-binding peptide reduces cell-free hemoglobin in murine hemolytic anemia.Endothelial-cell heme uptake from heme proteins: induction of sensitization and desensitization to oxidant damage.
P2860
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P2860
Plasma concentrations of hemopexin, haptoglobin and heme in patients with various hemolytic diseases.
description
1968 nî lūn-bûn
@nan
1968年の論文
@ja
1968年学术文章
@wuu
1968年学术文章
@zh
1968年学术文章
@zh-cn
1968年学术文章
@zh-hans
1968年学术文章
@zh-my
1968年学术文章
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1968年學術文章
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1968年學術文章
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name
Plasma concentrations of hemop ...... th various hemolytic diseases.
@en
Plasma concentrations of hemop ...... th various hemolytic diseases.
@nl
type
label
Plasma concentrations of hemop ...... th various hemolytic diseases.
@en
Plasma concentrations of hemop ...... th various hemolytic diseases.
@nl
prefLabel
Plasma concentrations of hemop ...... th various hemolytic diseases.
@en
Plasma concentrations of hemop ...... th various hemolytic diseases.
@nl
P2093
P1433
P1476
Plasma concentrations of hemop ...... th various hemolytic diseases.
@en
P2093
P304
P407
P577
1968-11-01T00:00:00Z