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

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

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

http://www.wikidata.org/entity/Q37216685

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A proposed classification of the immunological diseases Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort Inflammatory bowel disease Defects in mucosal immunity leading to Crohn's disease Recent Insights Into the Genetics of Inflammatory Bowel Disease The molecular chaperone HSP70 binds to and stabilizes NOD2, an important protein involved in Crohn disease Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)The SPINK gene family and celiac disease susceptibility Anti-Saccharomyces cerevisiae antibodies (ASCA) in Crohn's disease are associated with disease severity but not NOD2/CARD15 mutations Association of the T allele of an intronic single nucleotide polymorphism in the colony stimulating factor 1 receptor with Crohn's disease: a case-control study Novel biomarkers of fibrosis in Crohn's disease Genetic Influences on the Development of Fibrosis in Crohn's Disease Mechanisms of Microbe-Host Interaction in Crohn's Disease: Dysbiosis vs. Pathobiont Selection Host-microbiome interaction in Crohn's disease: A familiar or familial issue?Role of Nucleotide-binding and Oligomerization Domain 2 Protein (NOD2) in the Development of Atherosclerosis Roles of NOD1 (NLRC1) and NOD2 (NLRC2) in innate immunity and inflammatory diseases Correlations between psoriasis and inflammatory bowel diseases The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing Genetically determined epithelial dysfunction and its consequences for microflora-host interactions Inflammatory Bowel Disease Drugs: A Focus on Autophagy Nod2: A Critical Regulator of Ileal Microbiota and Crohn's Disease International Union of Basic and Clinical Pharmacology. XCVI. Pattern recognition receptors in health and disease NOD2: ethnic and geographic differences CARD15/NOD2 mutations in Crohn's disease Associations between NOD2/CARD15 genotype and phenotype in Crohn's disease--Are we there yet?Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease Organic dust augments nucleotide-binding oligomerization domain expression via an NF-{kappa}B pathway to negatively regulate inflammatory responses A new arthritis therapy with oxidative burst inducers Modeling-Enabled Characterization of Novel NLRX1 Ligands Role of nod2 in the response of macrophages to toll-like receptor agonists Critical role of NOD2 in regulating the immune response to Staphylococcus aureus Inflammatory bowel disease Inflammatory bowel disease Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility Negligible impact of rare autoimmune-locus coding-region variants on missing heritability Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease Genotypes and phenotypes in Crohn's disease: do they help in clinical management?The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants CARD15/NOD2 is required for Peyer's patches homeostasis in mice.Positional cloning of Ncf1--a piece in the puzzle of arthritis genetics.

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

http://www.wikidata.org/entity/Q37216685

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on March 2002

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

CARD15/NOD2 mutational analysi ...... ith inflammatory bowel disease

@en

CARD15/NOD2 mutational analysi ...... th inflammatory bowel disease.

@nl

type

label

CARD15/NOD2 mutational analysi ...... ith inflammatory bowel disease

@en

CARD15/NOD2 mutational analysi ...... th inflammatory bowel disease.

@nl

prefLabel

CARD15/NOD2 mutational analysi ...... ith inflammatory bowel disease

@en

CARD15/NOD2 mutational analysi ...... th inflammatory bowel disease.

@nl

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American Journal of Human Genetics

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CARD15/NOD2 mutational analysi ...... ith inflammatory bowel disease

@en

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Colm O'Morain

http://www.w3.org/2001/XMLSchema#string

Corinne Gower-Rousseau

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Curt Tysk

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EPIMAD Group

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EPWG-IBD Group

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Françoise Merlin

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GETAID Group

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Gilles Thomas

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Habib Zouali

http://www.w3.org/2001/XMLSchema#string

Jacques Belaiche

http://www.w3.org/2001/XMLSchema#string

P2860

Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB

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

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

Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome c-dependent activation of caspase-3

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

Human CARD4 protein is a novel CED-4/Apaf-1 cell death family member that activates NF-kappaB

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

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

Etiology of the inflammatory bowel diseases.

Human Nod1 confers responsiveness to bacterial lipopolysaccharides.

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845-857

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scholarly article

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10.1086/339432

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P433

4

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70

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Jean-Frédéric Colombel

Corinne Gower-Rousseau

Jean-Pierre Hugot

Anne-Sophie Jannot

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2002-03-01T00:00:00Z

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11486453

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11875755

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inflammatory bowel diseases

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379113

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