(Q53974880)

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Inflammatory bowel disease is associated with a novel promoter polymorphism of natural resistance-associated macrophage protein 1 (NRAMP1) gene.

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scholarly article

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Inflammatory bowel disease is associated with a novel promoter polymorphism of natural resistance-associated macrophage protein 1 (NRAMP1) gene. (English)

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

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inflammatory bowel diseases

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author name string

Kojima Y

1

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Kinouchi Y

2

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Takahashi S

3

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Negoro K

4

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Hiwatashi N

5

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Shimosegawa T

6

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

publication date

1 December 2001

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Tissue Antigens

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Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

58

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

379-384

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

6

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

Crohn's disease is associated with novel polymorphisms in the 5'-flanking region of the tumor necrosis factor gene

1 reference

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Respiratory burst of intestinal macrophages in inflammatory bowel disease is mainly caused by CD14+L1+ monocyte derived cells

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7 January 2021

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Cytokine profiles differ in newly recruited and resident subsets of mucosal macrophages from inflammatory bowel disease

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7 January 2021

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Randomised controlled trial of CDP571 antibody to tumour necrosis factor-alpha in Crohn's disease

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7 January 2021

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Tumour-necrosis-factor antibody treatment in Crohn's disease

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7 January 2021

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Understanding the multiple functions of Nramp1.

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Inflammatory bowel disease and the genes for the natural resistance-associated macrophage protein-1 and the interferon-gamma receptor 1

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7 January 2021

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NRAMP1 gene polymorphisms in patients with rheumatoid arthritis

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7 January 2021

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Polymorphism at NRAMP1 and D2S1471 loci associated with juvenile rheumatoid arthritis

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Genetic analysis of chromosome 2 in type 1 diabetes: analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster. IMDIAB Group

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The natural resistance-associated macrophage protein and susceptibility to intracellular pathogens

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Susceptibility to leprosy is linked to the human NRAMP1 gene.

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Identification of novel alleles at a polymorphic microsatellite repeat region in the human NRAMP1 gene promoter: analysis of allele frequencies in primary biliary cirrhosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2001.580606.X

7 January 2021

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The natural resistance-associated macrophage protein gene is associated with Crohn's disease

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7 January 2021

based on heuristic

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Intensive intravenous regimen for severe attacks of ulcerative colitis.

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The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis

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Polymorphic haplotypes of the interleukin-10 5' flanking region determine variable interleukin-10 transcription and are associated with particular phenotypes of juvenile rheumatoid arthritis.

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https://api.crossref.org/works/10.1034%2FJ.1399-0039.2001.580606.X

7 January 2021

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Polymorphism of the 5'-flanking region of the human tumor necrosis factor (TNF)-alpha gene in Japanese.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2001.580606.X

7 January 2021

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inferred from DOI database lookup

Identifiers

10.1034/J.1399-0039.2001.580606.X

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

1 reference

Europe PubMed Central

23 May 2018

http://europepmc.org/abstract/MED/11929588

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