(Q80260413)

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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Europe PubMed Central

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

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)

1 reference

Europe PubMed Central

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

30 December 2019

chronic granulomatous disease

1 reference

based on heuristic

inferred from title

Mustafa Yavuz Koker

3

1 reference

Europe PubMed Central

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

30 December 2019

10

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Europe PubMed Central

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30 December 2019

author name string

Dirk Roos

1

1 reference

Europe PubMed Central

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30 December 2019

Martin de Boer

2

1 reference

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

30 December 2019

Jan Dekker

4

1 reference

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30 December 2019

Vinita Singh-Gupta

5

1 reference

Europe PubMed Central

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

30 December 2019

Anders Ahlin

6

1 reference

Europe PubMed Central

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

30 December 2019

Jan Palmblad

7

1 reference

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

30 December 2019

Ozden Sanal

8

1 reference

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30 December 2019

Magdalena Kurenko-Deptuch

9

1 reference

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30 December 2019

Baruch Wolach

11

1 reference

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30 December 2019

publication date

1 December 2006

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Europe PubMed Central

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30 December 2019

1 reference

Europe PubMed Central

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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

1 reference

Europe PubMed Central

PubMed publication ID

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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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Successful renal transplantation in patients with 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

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

1 reference

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

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

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

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

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

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

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

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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

A Controlled Trial of Interferon Gamma to Prevent Infection in 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

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Trimethoprim-sulfamethoxazole prophylaxis in the management of 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

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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Purification and cryopreservation of phagocytes from human blood

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from 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

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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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