(Q42836089)

English

Lack of association of the pregnane X receptor (PXR/NR1I2) gene with inflammatory bowel disease: parallel allelic association study and gene wide haplotype analysis.

scientific article published on November 2006

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scholarly article

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20 December 2019

Lack of association of the pregnane X receptor (PXR/NR1I2) gene with inflammatory bowel disease: parallel allelic association study and gene wide haplotype analysis (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17047126%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

inflammatory bowel diseases

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2

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20 December 2019

1

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20 December 2019

author name string

S K Tate

3

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20 December 2019

H Drummond

4

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20 December 2019

E R Nimmo

5

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20 December 2019

A Tenesa

6

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20 December 2019

I D Arnott

7

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20 December 2019

J Satsangi

8

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20 December 2019

language of work or name

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publication date

1 November 2006

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20 December 2019

1 reference

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20 December 2019

55

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20 December 2019

11

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20 December 2019

1676-1677

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20 December 2019

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

27 May 2018

The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

27 May 2018

PXR, CAR and drug metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

27 May 2018

The pregnane X receptor locus is associated with susceptibility to inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

16 August 2018

Loss of detoxification in inflammatory bowel disease: dysregulation of pregnane X receptor target genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

16 August 2018

NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

16 August 2018

ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

1 December 2018

A single-nucleotide polymorphism tagging set for human drug metabolism and transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

1 December 2018

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1860087

1 December 2018

Identifiers

10.1136/GUT.2006.105106

1 reference

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20 December 2019

1 reference

Europe PubMed Central

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20 December 2019

1 reference

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20 December 2019

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