(Q35670980)

9 August 2017

1 reference

title

A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria (English)

1 reference

9 August 2017

Tsutomu Shichishima

1

1 reference

9 August 2017

Hideyoshi Noji

series ordinal

2

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9 August 2017

publication date

1 August 2002

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9 August 2017

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9 August 2017

volume

7

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9 August 2017

issue

4

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9 August 2017

page(s)

211-227

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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

9 August 2017

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

21 January 2018

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Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria

21 January 2018

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Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Paroxysmal nocturnal haemoglobinuria with coexisting deficiency of the ninth component of complement: lack of massive haemolytic attack

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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The first step of glycosylphosphatidylinositol biosynthesis is mediated by a complex of PIG-A, PIG-H, PIG-C and GPI1.

21 January 2018

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Initial enzyme for glycosylphosphatidylinositol biosynthesis requires PIG-P and is regulated by DPM2

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients

21 January 2018

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PIG-A gene mutations in four Taiwanese patients with paroxysmal nocturnal haemoglobinuria following aplastic anaemia

21 January 2018

1 reference

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The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal hemoglobinuria: analysis of the effects of mutant PIG-A on gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The PNH phenotype cells that emerge in most patients after CAMPATH-1H therapy are present prior to treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Imbalance in X-chromosome expression: evidence for a human X-linked gene affecting growth of hemopoietic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Interactions of the platelets in paroxysmal nocturnal hemoglobinuria with complement. Relationship to defects in the regulation of complement and to platelet survival in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased sensitivity to complement of megakaryocyte progenitors in paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Natural history of paroxysmal nocturnal hemoglobinuria

21 January 2018

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https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors. French Society of Haematology

21 January 2018

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https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anaemia patients: the high prevalence at diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria. Evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone

21 January 2018

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https://api.crossref.org/works/10.1080%2F1024533021000024094

Primary treatment of acquired aplastic anemia: outcomes with bone marrow transplantation and immunosuppressive therapy. Seattle Bone Marrow Transplant Team.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Late clonal diseases of treated aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Leukemia arising out of paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

LEUKOKINETIC STUDIES. II. A METHOD FOR LABELING GRANULOCYTES IN VITRO WITH RADIOACTIVE DIISOPROPYLFLUOROPHOSPHATE (DFP)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Granulocytes from patients with paroxysmal nocturnal hemoglobinuria and normal individuals have the same sensitivity to spontaneous apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Impaired growth and elevated fas receptor expression in PIGA(+) stem cells in primary paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Genetic and environmental effects in paroxysmal nocturnal hemoglobinuria: this little PIG-A goes "Why? Why? Why?"

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased cytotoxic T cells with effector phenotype in aplastic anemia and myelodysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Limited heterogeneity of T cell receptor BV usage in aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

HLA class II haplotype and quantitation of WT1 RNA in Japanese patients with paroxysmal nocturnal hemoglobinuria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

MHC class II tetramers identify peptide-specific human CD4(+) T cells proliferating in response to influenza A antigen

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Cytotoxicity against lymphoblastoid cells mediated by a T-cell clone from an aplastic anaemia patient: role of CD59 on target cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Direct isolation, phenotyping and cloning of low-frequency antigen-specific cytotoxic T lymphocytes from peripheral blood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Quantitative analysis of hepatitis C virus-specific CD8(+) T cells in peripheral blood and liver using peptide-MHC tetramers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Physical and functional interaction between WT1 and p53 proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

A novel repressor, par-4, modulates transcription and growth suppression functions of the Wilms' tumor suppressor WT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Ciao 1 is a novel WD40 protein that interacts with the tumor suppressor protein WT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Phenotypes and phosphatidylinositol glycan-class A gene abnormalities during cell differentiation and maturation from precursor cells to mature granulocytes in patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Telomere length changes in patients with aplastic anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmale Haemoglobinurie

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Chronic Hemolytic Anemia with Paroxysmal Nocturnal Hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Liberation of material with platelet-like coagulant properties from intact red cells and particularly from reticulocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Studies on the sensitivity to complement-mediated lysis of erythrocytes (Inab phenotype) with a deficiency of DAF (decay accelerating factor)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

A family showing inheritance of the Inab phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

PIG-A, DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogenous leukaemia blasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Analysis of PIG-A gene in a patient who developed reciprocal translocation of chromosome 12 and paroxysmal nocturnal hemoglobinuria during follow-up of aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Recurrent PIG-A mutation (IVS5+1G-->A) in a paediatric case of paroxysmal nocturnal haemoglobinuria: detection by the protein truncation test

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal haemoglobinuria due to an 88 bp direct tandem repeat insertion in the PIG-A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Detection of GPI-anchored protein-deficient cells in patients with aplastic anaemia and evidence for clonal expansion during the clinical course

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Acute myelogenous leukemia with PIG-A gene mutation evolved from aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Defective and normal haematopoietic stem cells in paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Deficiency of glycosyl-phosphatidylinositol anchored proteins on paroxysmal nocturnal haemoglobinuria (PNH) neutrophils and monocytes: heterogeneous deficiency of decay-accelerating factor (DAF) and CD16 on PNH neutrophils

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Varying populations of CD59-negative, partly positive, and normally positive blood cells in different cell lineages in peripheral blood of paroxysmal nocturnal hemoglobinuria patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Flow cytometric measurement of glycosylphosphatidyl-inositol-linked surface proteins on blood cells of patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased sensitivity to complement of erythroid and myeloid progenitors in paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The aplastic anaemia--paroxysmal nocturnal haemoglobinuria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Late haematological complications in severe aplastic anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Deficiency of glycosylphosphatidyl inositol-anchored proteins in patients with aplastic anaemia does not affect response to immunosuppressive therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Coexistence of normal and clonal haemopoiesis in aplastic anaemia patients treated with immunosuppressive therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Glycosylphosphatidyl-inositol (GPI)-linked protein deficiency on the platelets of patients with aplastic anaemia and paroxysmal nocturnal haemoglobinuria: two distinct patterns correlating with expression on neutrophils

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Detection of CD55 and/or CD59 deficient red cell populations in patients with aplastic anaemia, myelodysplastic syndromes and myeloproliferative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Malignant tumors occurring after treatment of aplastic anemia. European Bone Marrow Transplantation-Severe Aplastic Anaemia Working Party

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Myelodysplasia following aplastic anaemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: evidence for the emergence of a separate clone

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The dual pathogenesis of paroxysmal nocturnal hemoglobinuria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Does HLA-DR predict response to specific immunosuppressive therapy in aplastic anaemia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

HLA-DR2 predicts a favorable response to cyclosporine therapy in patients with bone marrow failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased frequency of DR2 in patients with aplastic anaemia and increased DR sharing in their parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased frequency of HLA-DR2 in patients with paroxysmal nocturnal hemoglobinuria and the PNH/aplastic anemia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

HSP70 stimulates cytokine production through a CD14-dependant pathway, demonstrating its dual role as a chaperone and cytokine

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The cellular pathogenesis of paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Detection by monoclonal antibodies of the Wilms' tumor (WT1) nuclear protein in patients with acute leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

The Wilms' tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Human cytotoxic T-lymphocyte responses specific for peptides of the wild-type Wilms' tumor gene (WT1 ) product

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Increased frequency of somatic mutations at glycophorin A loci in patients with aplastic anaemia, myelodysplastic syndrome and paroxysmal nocturnal haemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Long-term support of hematopoiesis by a single stem cell clone in patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

Telomere length in leukocyte subpopulations of patients with aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000024094

10.1080/1024533021000024094

21 January 2018

Identifiers

DOI

1 reference

9 August 2017

1 reference