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 (Q79354248)

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scientific article published on 01 December 2006

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English	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	scientific article published on 01 December 2006

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scholarly article

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21 December 2019

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 (English)

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21 December 2019

Crohn's disease

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based on heuristic

inferred from title

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based on heuristic

inferred from title

surgical intervention

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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Julia Seiderer

1

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21 December 2019

Fabian Schnitzler

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21 December 2019

Stephan Brand

3

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21 December 2019

Tanja Staudinger

4

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21 December 2019

Simone Pfennig

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21 December 2019

Karin Herrmann

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21 December 2019

Katrin Hofbauer

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21 December 2019

Julia Dambacher

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21 December 2019

Cornelia Tillack

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21 December 2019

Michael Sackmann

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21 December 2019

Burkhard Göke

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21 December 2019

Peter Lohse

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21 December 2019

Thomas Ochsenkühn

13

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21 December 2019

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1 December 2006

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21 December 2019

Scandinavian Journal of Gastroenterology

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21 December 2019

41

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21 December 2019

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21 December 2019

1421-1432

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21 December 2019

Inflammatory bowel disease: etiology and pathogenesis

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Inflammatory Bowel Disease

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

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https://api.crossref.org/works/10.1080%2F00365520600703900

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

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

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Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB

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

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Human Nod1 confers responsiveness to bacterial lipopolysaccharides

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

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Induction of Nod2 in Myelomonocytic and Intestinal Epithelial Cells via Nuclear Factor-κB Activation

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Card15 gene overexpression in mononuclear and epithelial cells of the inflamed Crohn's disease colon

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TNF-alpha and IFN-gamma regulate the expression of the NOD2 (CARD15) gene in human intestinal epithelial cells.

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CARD15/NOD2 functions as an antibacterial factor in human intestinal epithelial cells

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NODs: intracellular proteins involved in inflammation and apoptosis

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

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21 January 2018

NOD2 and Crohn's disease: loss or gain of function?

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21 January 2018

NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses

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21 January 2018

Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing

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Getting to the guts of NOD2.

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

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The genetics of inflammatory bowel disease

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

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21 January 2018

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

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

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21 January 2018

Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.

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21 January 2018

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

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21 January 2018

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

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21 January 2018

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

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21 January 2018

Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations

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21 January 2018

Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.

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21 January 2018

CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease

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21 January 2018

Variants of CARD15 are Associated with an Aggressive Clinical Course of Crohn's Disease-An IG-IBD Study

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21 January 2018

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

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

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21 January 2018

Postoperative maintenance of Crohn's disease remission with 6-mercaptopurine, mesalamine, or placebo: a 2-year trial

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Crohn's disease: step up or top down therapy

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21 January 2018

Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease

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21 January 2018

NOD2 mediates anti-inflammatory signals induced by TLR2 ligands: implications for Crohn's disease

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NOD2 (CARD15) mutations in Crohn's disease are associated with diminished mucosal alpha-defensin expression

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Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract

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

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21 December 2019

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Europe PubMed Central

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21 December 2019

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