The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts (Q73746065)

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6 November 2019

title

The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts (English)

1 reference

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paroxysmal nocturnal hemoglobinuria

6 November 2019

main subject

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H Noji

1

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6 November 2019

T Shichishima

2

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6 November 2019

Y Saitoh

3

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6 November 2019

T Kai

4

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6 November 2019

T Yamamoto

5

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6 November 2019

K Ogawa

6

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6 November 2019

M Okamoto

7

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6 November 2019

K Ikeda

8

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6 November 2019

Y Maruyama

9

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6 November 2019

publication date

1 April 2001

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6 November 2019

published in

Experimental Hematology

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6 November 2019

volume

29

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issue

4

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page(s)

391-400

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Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody

6 November 2019

cites work

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Variations in the Red Cells in Paroxysmal Nocturnal Haemoglobinuria

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7 January 2021

Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor

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7 January 2021

Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria

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7 January 2021

Amino-terminal amino acid sequence and chemical and functional properties of a membrane attack complex-inhibitory factor from human erythrocyte membranes

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7 January 2021

CD59, an LY-6-like protein expressed in human lymphoid cells, regulates the action of the complement membrane attack complex on homologous cells

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7 January 2021

Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria

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7 January 2021

Erythrocytes of patients with paroxysmal nocturnal haemoglobinuria acquire resistance to complement attack by purified 20-kD homologous restriction factor

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7 January 2021

Structural and functional roles of glycosyl-phosphatidylinositol in membranes

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7 January 2021

Distribution of decay-accelerating factor in the peripheral blood of normal individuals and patients with paroxysmal nocturnal hemoglobinuria

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7 January 2021

Heterogenous expression of decay accelerating factor and CD59/membrane attack complex inhibition factor on paroxysmal nocturnal haemoglobinuria (PNH) erythrocytes

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7 January 2021

The erythrocytes in paroxysmal nocturnal haemoglobinuria of intermediate sensitivity to complement lysis

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7 January 2021

Diagnosis of paroxysmal nocturnal haemoglobinuria by phenotypic analysis of erythrocytes using two-colour flow cytometry with monoclonal antibodies to DAF and CD59/MACIF

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7 January 2021

A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies

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7 January 2021

Mechanism of complement-mediated activation of human blood platelets in vitro: comparison of normal and paroxysmal nocturnal hemoglobinuria platelets

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7 January 2021

Paroxysmal Nocturnal Hemoglobinuria (PNH) as a Clonal Disorder

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7 January 2021

Estimation of PI-bound proteins on blood cells from PNH patients by quantitative flow cytometry

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7 January 2021

Diagnosis of paroxysmal nocturnal haemoglobinuria using immunophenotyping of peripheral blood cells

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7 January 2021

Decay-accelerating factor and CD59 expression in peripheral blood cells in aplastic anaemia and report of a case of paroxysmal nocturnal haemoglobinuria secondary to aplastic anaemia

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7 January 2021

Decay-accelerating factor is present on paroxysmal nocturnal hemoglobinuria erythroid progenitors and lost during erythropoiesis in vitro

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7 January 2021

Defective and normal haematopoietic stem cells in paroxysmal nocturnal haemoglobinuria

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7 January 2021

Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria

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7 January 2021

Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria

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7 January 2021

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

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7 January 2021

Leukemia arising out of paroxysmal nocturnal hemoglobinuria

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7 January 2021

STUDIES ON DESTRUCTION OF RED BLOOD CELLS. II. CHRONIC HEMOLYTIC ANEMIA WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA: CERTAIN IMMUNOLOGICAL ASPECTS OF THE HEMOLYTIC MECHANISM WITH SPECIAL REFERENCE TO SERUM COMPLEMENT.

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7 January 2021

In vivo effects of various therapies on complement-sensitive erythrocytes in paroxysmal nocturnal hemoglobinuria

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7 January 2021

Expression of Bcl-x in erythroid precursors from patients with polycythemia vera

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7 January 2021

Biological defense mechanisms. The effect of bacteria and serum on superoxide production by granulocytes

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7 January 2021

Complement sensitivity of erythroblasts and erythropoietic precursors in paroxysmal nocturnal haemoglobinuria (PNH).

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7 January 2021

Erythroid colony formation in cultures of mouse and human bone marrow: Analysis of the requirement for erythropoietin by gel filtration and affinity chromatography on agarose-concanavalin A

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7 January 2021

Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21

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7 January 2021

Epstein-Barr virus shuttle vector for stable episomal replication of cDNA expression libraries in human cells

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7 January 2021

In vivo transfer of GPI-linked complement restriction factors from erythrocytes to the endothelium

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7 January 2021

Molecular basis of paroxysmal nocturnal hemoglobinuria

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7 January 2021

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

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7 January 2021

Genotypic, immunophenotypic and clinical features of Thai patients with paroxysmal nocturnal haemoglobinuria

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7 January 2021

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

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7 January 2021

10.1016/S0301-472X(00)00684-6

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11301179%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference