Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin - Wikidata - thesis-toulmin - TriplyDB

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

http://www.wikidata.org/entity/Q34013865

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Paroxysmal nocturnal hemoglobinuria from bench to bedside How I treat paroxysmal nocturnal hemoglobinuria Diagnosis and management of paroxysmal nocturnal hemoglobinuria Human genetic disorders involving glycosylphosphatidylinositol (GPI) anchors and glycosphingolipids (GSL)Pesg PNH diagnosis, follow-up and treatment guidelines Clonal hematopoiesis in acquired aplastic anemia Clustering induces redistribution of syndecan-4 core protein into raft membrane domains GPI-anchor synthesis is indispensable for the germline development of the nematode Caenorhabditis elegans.Abnormalities in the expression of CD55 and CD59 surface molecules on peripheral blood cells are not specific to paroxysmal nocturnal hemoglobinuria.Predictors of hemoglobin response to eculizumab therapy in paroxysmal nocturnal hemoglobinuria.Flow cytometry screening for paroxysmal nocturnal hemoglobinuria: A single-center experience in Saudi Arabia.The challenging world of cytopenias: distinguishing myelodysplastic syndromes from other disorders of marrow failure Multiparameter flow cytometry for the diagnosis and monitoring of small GPI-deficient cellular populations Detection of paroxysmal nocturnal hemoglobinuria clones to exclude inherited bone marrow failure syndromes.PIG-A mutations in normal hematopoiesis Paroxysmal nocturnal hemoglobinuria Simple monitoring of gene targeting efficiency in human somatic cell lines using the PIGA gene.Paroxysmal nocturnal hemoglobinuria: a single Spanish center's experience over the last 40 yr Complement blockade with a C1 esterase inhibitor in paroxysmal nocturnal hemoglobinuria Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.Natural history of paroxysmal nocturnal hemoglobinuria clones in patients presenting as aplastic anemia Paroxysmal nocturnal hemoglobinuria (PNH): higher sensitivity and validity in diagnosis and serial monitoring by flow cytometric analysis of reticulocytes.Clinical management of aplastic anemia.Paroxysmal nocturnal hemoglobinuria clones in children with acquired aplastic anemia: a multicentre study.A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria.The management of paroxysmal nocturnal hemoglobinuria: recent advances in diagnosis and treatment and new hope for patients.The small population of PIG-A mutant cells in myelodysplastic syndromes do not arise from multipotent hematopoietic stem cells Transbilayer lipid interactions mediate nanoclustering of lipid-anchored proteins Leukemic blasts with the paroxysmal nocturnal hemoglobinuria phenotype in children with acute lymphoblastic leukemia.Paroxysmal nocturnal hemoglobinuria: a complement-mediated hemolytic anemia Advances in the diagnosis and therapy of paroxysmal nocturnal hemoglobinuria Apical sorting of lysoGPI-anchored proteins occurs independent of association with detergent-resistant membranes but dependent on their N-glycosylation.Detection of paroxysmal nocturnal hemoglobinuria clones in patients with myelodysplastic syndromes and related bone marrow diseases, with emphasis on diagnostic pitfalls and caveats.Glycosylphosphatidylinositol-anchored protein deficiency confers resistance to apoptosis in PNH.Generation of glycosylphosphatidylinositol anchor protein-deficient blood cells from human induced pluripotent stem cells Silencing of genes required for glycosylphosphatidylinositol anchor biosynthesis in Burkitt lymphoma.The pathophysiology of paroxysmal nocturnal hemoglobinuria and treatment with eculizumab.Diagnosis of acquired aplastic anemia.Paroxysmal nocturnal hemoglobinuria and the age of therapeutic complement inhibition.Requirement of N-glycan on GPI-anchored proteins for efficient binding of aerolysin but not Clostridium septicum alpha-toxin.

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P2860

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

http://www.wikidata.org/entity/Q34013865

description

2000 nî lūn-bûn

@nan

2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2000年の論文

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2000年論文

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2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

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2000年論文

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2000年论文

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name

Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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type

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Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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prefLabel

Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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Improved detection and charact ...... ia using fluorescent aerolysin

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P1433

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P1433

American Journal of Clinical Pathology

P1476

Improved detection and charact ...... ia using fluorescent aerolysin

@en

P2093

G L Mukhina

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J T Buckley

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K L Nelson

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M J Borowitz

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P L Chiurazzi

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R A Brodsky

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S Li

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P2860

Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene

Alternative membrane forms of Fc gamma RIII(CD16) on human natural killer cells and neutrophils. Cell type-specific expression of two genes that differ in single nucleotide substitutions

Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis

Aerolysin--the ins and outs of a model channel-forming toxin.

Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link.

Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay.

Resistance to apoptosis caused by PIG-A gene mutations in paroxysmal nocturnal hemoglobinuria

A knock-out model of paroxysmal nocturnal hemoglobinuria: Pig-a(-) hematopoiesis is reconstituted following intercellular transfer of GPI-anchored proteins.

P304

459-466

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scholarly article

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10.1093/AJCP/114.3.459

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3

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114

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2000-09-01T00:00:00Z

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10989647

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4124633

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