Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. (Q35597793)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15955786%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

title

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease (English)

1 reference

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12 January 2020

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14

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author name string

H-P Török

1

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12 January 2020

J Glas

2

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12 January 2020

L Tonenchi

3

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12 January 2020

P Lohse

4

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12 January 2020

B Müller-Myhsok

5

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12 January 2020

O Limbersky

6

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C Neugebauer

7

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F Schnitzler

8

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12 January 2020

J Seiderer

9

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12 January 2020

C Tillack

10

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12 January 2020

S Brand

11

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12 January 2020

G Brünnler

12

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P Jagiello

13

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12 January 2020

T Griga

15

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12 January 2020

W Klein

16

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12 January 2020

U Schiemann

17

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12 January 2020

M Folwaczny

18

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T Ochsenkühn

19

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12 January 2020

C Folwaczny

20

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language of work or name

English

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publication date

14 June 2005

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12 January 2020

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12 January 2020

volume

54

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12 January 2020

issue

10

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12 January 2020

page(s)

1421-1427

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Genetic variation in DLG5 is associated with inflammatory bowel disease

12 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Functional variants of OCTN cation transporter genes are associated with Crohn disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patients

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

A comparison of bayesian methods for haplotype reconstruction from population genotype data

27 July 2018

1 reference

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IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Lack of common NOD2 variants in Japanese patients with Crohn's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

27 July 2018

1 reference

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

A New Statistical Method for Haplotype Reconstruction from Population Data

27 July 2018

1 reference

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A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

27 July 2018

1 reference

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Preliminary report on the Mount Sinai Hospital Inflammatory Bowel Disease Genetics Project

27 July 2018

1 reference

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A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis

26 September 2018

1 reference

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Interaction of polymorphisms in the CARD15 and CD14 genes in patients with Crohn disease.

26 September 2018

1 reference

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Pedigree disequilibrium tests for multilocus haplotypes.

26 September 2018

1 reference

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774699

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

7 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15955786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15955786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15955786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/GUT.2005.066340

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15955786%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15955786%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

PubMed publication ID

15955786

1 reference