(Q45207564)

10 December 2017

title

NCF1 (p47phox) and ncf1 pseudogenes are not associated with inflammatory bowel disease (English)

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inflammatory bowel diseases

10 December 2017

main subject

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4

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10 December 2017

Nirosha Suraweera

1

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10 December 2017

Evi Zampeli

2

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10 December 2017

Pauline Rogers

3

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10 December 2017

Alistair Forbes

5

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10 December 2017

Marcus Harbord

6

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10 December 2017

Andrew Silver

7

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10 December 2017

publication date

1 November 2004

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Inflammatory Bowel Diseases

10 December 2017

published in

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10 December 2017

volume

10

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10 December 2017

issue

6

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10 December 2017

page(s)

758-762

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Genetics of inflammatory bowel disease: progress and prospects

10 December 2017

cites work

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https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Association between p47phox pseudogenes and inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Chronic granulomatous disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Identification of genomic regions controlling experimental autoimmune uveoretinitis in rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Positional identification of Ncf1 as a gene that regulates arthritis severity in rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00054725-200411000-00010

10.1097/00054725-200411000-00010

21 January 2018

Identifiers

DOI

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10 December 2017

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