Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease (Q43437819)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

title

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

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

main subject

inflammatory bowel diseases

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inflammation

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author name string

Fabian Schnitzler

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1

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Stephan Brand

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2

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Tanja Staudinger

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3

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Simone Pfennig

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4

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Katrin Hofbauer

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5

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Julia Seiderer

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6

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Cornelia Tillack

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7

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Burkhard Göke

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8

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Thomas Ochsenkühn

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9

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

Peter Lohse

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10

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PubMed publication ID

16485124

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23 November 2017

language of work or name

English

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publication date

17 February 2006

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PubMed publication ID

16485124

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23 November 2017

published in

Immunogenetics

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

volume

58

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

issue

2-3

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

page(s)

99-106

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Europe PubMed Central

PubMed publication ID

16485124

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23 November 2017

cites work

A simple classification of Crohn's disease: report of the Working Party for the World Congresses of Gastroenterology, Vienna 1998.

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00251-005-0073-2

retrieved

21 January 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of the Arabidopsis nucleotide binding site-leucine-rich repeat resistance gene RPS2.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant role of genetics in IBD: the NOD2 gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nods, Nalps and Naip: intracellular regulators of bacterial-induced inflammation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term evolution of disease behavior of Crohn's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NOD2/CARD15 does not influence response to infliximab in Crohn's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behaviour of Crohn's disease according to the Vienna classification: changing pattern over the course of the disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nods: a family of cytosolic proteins that regulate the host response to pathogens

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16485124

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00251-005-0073-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16485124

retrieved

23 November 2017

PubMed publication ID

16485124

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16485124

retrieved

23 November 2017

 

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