(Q82509941)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

main subject

myelodysplastic syndrome

1 reference

1 reference

Okamoto M

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Shichishima T

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Noji H

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Ikeda K

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Nakamura A

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Akutsu K

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Maruyama Y

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

1 April 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

627-634

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16467865%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.leu.2404135

16 January 2020

exact match

0 references

cites work

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

The spectrum of PIG-A gene mutations in aplastic anemia/paroxysmal nocturnal hemoglobinuria (AA/PNH): a high incidence of multiple mutations and evidence of a mutational hot spot

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

Treatment of aplastic anemia with antilymphocyte globulin and methylprednisolone with or without cyclosporine. The German Aplastic Anemia Study Group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

Proposals for the classification of the myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

The aplastic anaemia--paroxysmal nocturnal haemoglobinuria syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

PIG-A mutations in normal hematopoiesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

The dual pathogenesis of paroxysmal nocturnal hemoglobinuria.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404135

7 January 2021