NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease. - Wikidata - wikimedia - TriplyDB

NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

http://www.wikidata.org/entity/Q33782065

about

Role of genetics in the diagnosis and prognosis of Crohn's disease ATG16L1: A multifunctional susceptibility factor in Crohn disease Autophagy and lysosomal dysfunction as emerging mechanisms of nanomaterial toxicity Role of genetics in the diagnosis and prognosis of Crohn's disease Role of ATG16L, NOD2 and IL23R in Crohn's disease pathogenesis Association of Interleukin-23 receptor gene polymorphisms with susceptibility to Crohn's disease: A meta-analysis Pharmacologic modulation of RORγt translates to efficacy in preclinical and translational models of psoriasis and inflammatory arthritis Genetics of inflammatory bowel disease in Asia: systematic review and meta-analysis.The role of autophagy in Crohn's disease.Cellular and Molecular Mediators of Intestinal Fibrosis.Mechanisms of initiation and progression of intestinal fibrosis in IBD.ATG16L1 and IL23R variants and genetic susceptibility to crohn's disease: mode of inheritance based on meta-analysis of genetic association studies.Overcoming difficulty in diagnosis and differential diagnosis of Crohn's disease: the potential role of serological and genetic tests.Protective role of R381Q (rs11209026) polymorphism in IL-23R gene in immune-mediated diseases: A comprehensive review.Cellular and molecular mechanisms of intestinal fibrosis.Association between ATG16L1 gene polymorphism and the risk of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

http://www.wikidata.org/entity/Q33782065

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

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WJG.V16.I14.1753

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World Journal of Gastroenterology

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NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.

@en

P2093

Eleftheria Roma-Giannikou

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George Chrousos

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Gerassimos Mantzaris

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Ioanna Pachoula

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Ioanna Panayotou

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Maria Gazouli

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Nicholas P Anagnou

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P2860

A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5

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

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

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10.3748/WJG.V16.I14.1753

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Crohn's disease

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2852824

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