Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase (Q80260413)

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scientific article published on 01 December 2006

Language	Label	Description	Also known as
English	Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase	scientific article published on 01 December 2006

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scholarly article

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30 December 2019

Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase (English)

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30 December 2019

chronic granulomatous disease

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Mustafa Yavuz Koker

3

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30 December 2019

10

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30 December 2019

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Dirk Roos

1

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30 December 2019

Martin de Boer

2

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30 December 2019

Jan Dekker

4

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30 December 2019

Vinita Singh-Gupta

5

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30 December 2019

Anders Ahlin

6

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30 December 2019

Jan Palmblad

7

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30 December 2019

Ozden Sanal

8

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30 December 2019

Magdalena Kurenko-Deptuch

9

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30 December 2019

Baruch Wolach

11

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30 December 2019

publication date

1 December 2006

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30 December 2019

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30 December 2019

27

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30 December 2019

12

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30 December 2019

1218-1229

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30 December 2019

Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23

1 reference

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7 January 2021

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Successful renal transplantation in patients with chronic granulomatous disease

1 reference

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Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The cytosolic activating factors p47phox and p67phox have distinct roles in the regulation of electron flow in NADPH oxidase

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20413

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20413

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20413

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection

1 reference

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7 January 2021

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A Controlled Trial of Interferon Gamma to Prevent Infection in Chronic Granulomatous Disease

1 reference

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7 January 2021

based on heuristic

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Homologous dinucleotide (GT or TG) deletion in Japanese patients with chronic granulomatous disease with p47-phox deficiency

1 reference

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7 January 2021

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Trimethoprim-sulfamethoxazole prophylaxis in the management of chronic granulomatous disease

1 reference

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7 January 2021

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Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes

1 reference

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7 January 2021

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Purification and cryopreservation of phagocytes from human blood

1 reference

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7 January 2021

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Limitations on the use of dihydrorhodamine 123 for flow cytometric analysis of the neutrophil respiratory burst

1 reference

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7 January 2021

based on heuristic

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Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

1 reference

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In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease

1 reference

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Clinical differences in chronic granulomatous disease in patients with cytochrome b-negative or cytochrome b-positive neutrophils.

1 reference

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Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

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Identifiers

10.1002/HUMU.20413

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16972229%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16972229%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

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