Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin (Q34013865)

30 July 2017

title

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin (English)

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paroxysmal nocturnal hemoglobinuria

30 July 2017

main subject

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R A Brodsky

1

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30 July 2017

G L Mukhina

2

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30 July 2017

S Li

3

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30 July 2017

K L Nelson

4

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30 July 2017

P L Chiurazzi

5

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30 July 2017

J T Buckley

6

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30 July 2017

M J Borowitz

7

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American Journal of Clinical Pathology

30 July 2017

language of work or name

English

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inferred from

publication date

1 September 2000

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American Journal of Clinical Pathology

30 July 2017

published in

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30 July 2017

volume

114

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30 July 2017

issue

3

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30 July 2017

page(s)

459-466

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Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Glycosylphosphatidylinositol Anchors of Membrane Glycoproteins Are Binding Determinants for the Channel-forming Toxin Aerolysin

28 July 2018

1 reference

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Resistance to apoptosis caused byPIG-Agene mutations in paroxysmal nocturnal hemoglobinuria

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Paroxysmal nocturnal hemoglobinuria as a molecular disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

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Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria

28 July 2018

1 reference

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

28 July 2018

1 reference

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The Cloning of PIG-A, a Component in the Early Step of GPI-Anchor Biosynthesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Anchoring mechanisms for LFA-3 cell adhesion glycoprotein at membrane surface.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotype

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Movement of a Loop in Domain 3 of Aerolysin Is Required for Channel Formation†

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4124633

Analysis of receptor binding by the channel-forming toxin aerolysin using surface plasmon resonance

10 December 2018

1 reference

12 December 2020

Correction of the PNH defect by GPI-anchored protein transfer

1 reference

12 December 2020

Riddle: what do aplastic anemia, paroxysmal nocturnal hemoglobinuria (PNH) and "hypoplastic" leukemia have in common?

1 reference

12 December 2020

Diagnosis of paroxysmal nocturnal haemoglobinuria using immunophenotyping of peripheral blood cells

1 reference

12 December 2020

Paroxysmal nocturnal haemoglobinuria

1 reference

12 December 2020

Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia

1 reference

12 December 2020

The Pore-forming Toxin Proaerolysin Is Activated by Furin

1 reference

12 December 2020

Complement sensitivity of erythrocytes in a patient with inherited complete deficiency of CD59 or with the Inab phenotype

1 reference

12 December 2020

The molecular basis of paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins

1 reference

12 December 2020

The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

Identifiers

DOI

10.1093/AJCP/114.3.459

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30 July 2017

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30 July 2017

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