(Q34443724)

English

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Crohn's disease

0 references

Christiane Wolf

3

object named as

Christiane Wolf

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Europe PubMed Central

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2 August 2017

author name string

Fabian Schnitzler

1

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Europe PubMed Central

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2 August 2017

Matthias Friedrich

2

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Europe PubMed Central

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2 August 2017

Marianne Angelberger

4

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Europe PubMed Central

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2 August 2017

Julia Diegelmann

5

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Europe PubMed Central

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2 August 2017

Torsten Olszak

6

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Europe PubMed Central

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2 August 2017

Florian Beigel

7

1 reference

Europe PubMed Central

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2 August 2017

Cornelia Tillack

8

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Europe PubMed Central

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2 August 2017

Johannes Stallhofer

9

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Europe PubMed Central

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2 August 2017

Burkhard Göke

10

1 reference

Europe PubMed Central

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2 August 2017

Jürgen Glas

11

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2 August 2017

Peter Lohse

12

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2 August 2017

Stephan Brand

13

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2 August 2017

language of work or name

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publication date

3 November 2014

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2 August 2017

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Europe PubMed Central

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2 August 2017

9

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Europe PubMed Central

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2 August 2017

11

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2 August 2017

e108503

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Europe PubMed Central

PubMed publication ID

2 August 2017

copyright license

Creative Commons Attribution 4.0 International

3 November 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Targeting TNF-α for the treatment of inflammatory bowel disease

1 reference

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6 July 2018

Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway

1 reference

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6 July 2018

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

1 reference

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6 July 2018

Gene expression profiling of CD8+ T cells predicts prognosis in patients with Crohn disease and ulcerative colitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

The prognostic power of the NOD2 genotype for complicated Crohn's disease: a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Foxo transcription factors control regulatory T cell development and function

1 reference

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6 July 2018

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Transcription factors Foxo3a and Foxo1 couple the E3 ligase Cbl-b to the induction of Foxp3 expression in induced regulatory T cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

A CD8+ T cell transcription signature predicts prognosis in autoimmune disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

The FoxO transcription factors and metabolic regulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: report of a Working Party of the 2005 Montreal World Congress of Gastroenterology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

FoxOs at the crossroads of cellular metabolism, differentiation, and transformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

FOXO proteins regulate tumor necrosis factor-related apoptosis inducing ligand expression. Implications for PTEN mutation in prostate cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Cell cycle and death control: long live Forkheads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Classification of inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4217717

6 July 2018

Moving the genetics of inflammatory bowel diseases from bench to bedside: first steps towards personalised medicine

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective study.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Foxo proteins cooperatively control the differentiation of Foxp3+ regulatory T cells.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108503

21 January 2018

Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25365249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TheATG16L1Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population

1 reference

https://pubmed.ncbi.nlm.nih.gov/25365249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/25365249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant disease-causing effect of NOD2 mutations in a family with all family members affected by Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25365249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for the NOD2 p.Leu1007fsX1008 variant is the main genetic predictor for fibrostenotic Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25365249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0108503

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

2014PLoSO...9j8503S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

0 references

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