(Q80903968)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15503241%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

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

1 reference

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4 January 2020

author name string

Keiko Yamazaki

1

1 reference

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4 January 2020

Masakazu Takazoe

2

1 reference

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4 January 2020

Torao Tanaka

3

1 reference

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4 January 2020

Toshiki Ichimori

4

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4 January 2020

Susumu Saito

5

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4 January 2020

Aritoshi Iida

6

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4 January 2020

Yoshihiro Onouchi

7

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4 January 2020

Akira Hata

8

1 reference

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4 January 2020

Yusuke Nakamura

9

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4 January 2020

publication date

19 October 2004

1 reference

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Journal of Human Genetics

4 January 2020

published in

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4 January 2020

volume

49

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4 January 2020

page(s)

664-668

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4 January 2020

issue

12

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https://scigraph.springernature.com/pub.10.1007/s10038-004-0204-x

4 January 2020

exact match

0 references

cites work

HLA-linked susceptibility and resistance genes in Crohn's disease

1 reference

12 December 2020

Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci

1 reference

12 December 2020

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

1 reference

12 December 2020

Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease

1 reference

12 December 2020

A high-throughput SNP typing system for genome-wide association studies

1 reference

12 December 2020

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

1 reference

12 December 2020

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

1 reference

12 December 2020

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

1 reference

12 December 2020

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

1 reference

12 December 2020

Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibilit

1 reference

12 December 2020

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12

1 reference

12 December 2020

Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis

1 reference

12 December 2020

Genetic variation in DLG5 is associated with inflammatory bowel disease

1 reference

12 December 2020

JSNP: a database of common gene variations in the Japanese population

1 reference

12 December 2020

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

1 reference

12 December 2020

The molecular classification of the clinical manifestations of Crohn's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

1 reference

12 December 2020

High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population

1 reference

12 December 2020

Classification of inflammatory bowel disease

1 reference

12 December 2020

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

1 reference

12 December 2020

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

1 reference

12 December 2020

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation

1 reference

12 December 2020

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

1 reference

12 December 2020

Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.

1 reference

12 December 2020

10.1007/S10038-004-0204-X

Identifiers

DOI

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4 January 2020

1 reference