Associated Papers
Common inherited loss-of-function mutations in the innate sensor NOD2 contribute to exceptional immune response to cancer immunotherapy.
Barnet MB et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
Goblet Cell Loss Linked to NOD2 and Secondary Resection in Crohn's Disease Is Induced by Dysbiosis and Epithelial MyD88.
Wong SY et al.
Cellular and Molecular Gastroenterology and Hepatology, 2025
NOD2-mediated dual negative regulation of inflammatory responses triggered by TLRs in the gastrointestinal tract.
Masaki S et al.
Frontiers in Immunology, 2024
Germline variants in UNC13D and AP3B1 are enriched in COVID-19 patients experiencing severe cytokine storms.
Luo H et al.
European Journal of Human Genetics : Ejhg, 2021
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
Genetic deficiency of NOD2 confers resistance to invasive aspergillosis.
Gresnigt MS et al.
Nature Communications, 2018
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Henmyr V et al.
Bmc Medical Genetics, 2017
Epistatic interaction between TLR4 and NOD2 in patients with Crohn's Disease: relation with risk and phenotype in a Spanish cohort.
Martinez-Chamorro A et al.
Immunobiology, 2016
Role of Nucleotide-binding and Oligomerization Domain 2 Protein (NOD2) in the Development of Atherosclerosis.
Kim HJ
The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology, 2015
NOD2/CARD15 single nucleotide polymorphism 13 (3020insC) is associated with risk of sepsis and single nucleotide polymorphism 8 (2104C>T) with herpes viruses reactivation in patients after allogeneic hematopoietic stem cell transplantation.
Jaskula E et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation, 2014
A two-marker haplotype in the IRF5 gene is associated with inflammatory bowel disease in a North American cohort.
Gathungu G et al.
Genes and Immunity, 2012
Toll-like receptor 9, NOD2 and IL23R gene polymorphisms influenced outcome in AML patients transplanted from HLA-identical sibling donors.
Elmaagacli AH et al.
Bone Marrow Transplantation, 2011
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.
Glas J et al.
Plos One, 2010
Toll-like receptor 9 gene mutations and polymorphisms in Japanese ulcerative colitis patients.
Fuse K et al.
World Journal of Gastroenterology, 2010
Pyrosequencing of toll-like receptor polymorphisms of functional relevance.
Ahmad-Nejad P
Methods in Molecular Biology (clifton, N.j.), 2009
Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
Cummings JR et al.
Inflammatory Bowel Diseases, 2007
CARD15/NOD2 mutations in Crohn's disease.
Hugot JP
Annals of the New York Academy of Sciences, 2006