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

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Sexually dimorphic characteristics of the small intestine and colon of prepubescent C57BL/6 mice Genetic polymorphisms and susceptibility to lung disease NCF1 gene and pseudogene pattern: association with parasitic infection and autoimmunity.

P2860

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

Item

http://www.wikidata.org/entity/Q45207564

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2004 nî lūn-bûn

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2004年の論文

@ja

2004年学术文章

@wuu

2004年学术文章

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2004年学术文章

@zh-cn

2004年学术文章

@zh-hans

2004年学术文章

@zh-my

2004年学术文章

@zh-sg

2004年學術文章

@yue

2004年學術文章

@zh-hant

name

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

@en

NCF1

@nl

type

Item

label

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

@en

NCF1

@nl

prefLabel

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

@en

NCF1

@nl

P1476

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

@en

P2093

Alistair Forbes

http://www.w3.org/2001/XMLSchema#string

Andrew Silver

http://www.w3.org/2001/XMLSchema#string

Evi Zampeli

http://www.w3.org/2001/XMLSchema#string

Marcus Harbord

http://www.w3.org/2001/XMLSchema#string

Nirosha Suraweera

http://www.w3.org/2001/XMLSchema#string

Pauline Rogers

http://www.w3.org/2001/XMLSchema#string

P2860

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

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

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

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

Chronic granulomatous disease.

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

Genetics of inflammatory bowel disease: progress and prospects.

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

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

Association between p47phox pseudogenes and inflammatory bowel disease.

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758-762

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scholarly article

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10.1097/00054725-200411000-00010

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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Wendy S Atkin

P577

2004-11-01T00:00:00Z

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P5875

8103865

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P698

15626894

http://www.w3.org/2001/XMLSchema#string

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

about

P2860

P2860

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

description

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698