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Nov 7, 2007 (publication date) through Apr 23, 2024
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World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
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Cantó E, Ricart E, Busquets D, Monfort D, García-Planella E, González D, Balanzó J, Rodríguez-Sánchez JL, Vidal S. Influence of a nucleotide oligomerization domain 1 |
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| URL: | https://www.wjgnet.com/1007-9327/full/v13/i41/5446.htm |
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C. Ozbayer, H. Kurt, M. N. Kebapci, H. V. Gunes, E. Colak, I. Degirmenci. Effects of genetic variations in the genes encoding NOD1 and NOD2 on type 2 diabetes mellitus and insulin resistance. Journal of Clinical Pharmacy and Therapeutics 2017; 42(1): 98 doi: 10.1111/jcpt.12482
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Javier Martín-de-Carpi, Alejandro Rodríguez, Esther Ramos, Santiago Jiménez, María José Martínez-Gómez, Enrique Medina. Increasing Incidence of Pediatric Inflammatory Bowel Disease in Spain (1996–2009). Inflammatory Bowel Diseases 2013; 19(1): 73 doi: 10.1002/ibd.22980
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Elisabet Cantó, Esther Moga, Elena Ricart, Orlando Garcia-Bosch, Esther Garcia-Planella, Candido Juarez, Silvia Vidal. MDP-Induced selective tolerance to TLR4 ligands: Impairment in NOD2 mutant Crohnʼs disease patients. Inflammatory Bowel Diseases 2009; 15(11): 1686 doi: 10.1002/ibd.21013
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Francis Vasseur, Boualem Sendid, Thierry Jouault, Annie Standaert-Vitse, Laurent Dubuquoy, Nadine Francois, Corinne Gower-Rousseau, Pierre Desreumaux, Franck Broly, Severine Vermeire, Jean-Fréderic Colombel, Daniel Poulain. Variants of NOD1 and NOD2 genes display opposite associations with familial risk of crohnʼs disease and anti-saccharomyces cerevisiae antibody levels. Inflammatory Bowel Diseases 2012; 18(3): 430 doi: 10.1002/ibd.21817
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Tomoyuki Oikawa, Naoki Asano, Akira Imatani, Motoki Ohyauchi, Jun Fushiya, Yutaka Kondo, Yasuhiko Abe, Tomoyuki Koike, Katsunori Iijima, Tooru Shimosegawa. Gene polymorphisms of NOD1 and interleukin-8 influence the susceptibility to erosive esophagitis in Helicobacter pylori infected Japanese population. Human Immunology 2012; 73(11): 1184 doi: 10.1016/j.humimm.2012.08.004
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Michael Mendall, Maria Christina Harpsøe, Devinder Kumar, Mikael Andersson, Tine Jess, Rasheed Ahmad. Relation of body mass index to risk of developing inflammatory bowel disease amongst women in the Danish National Birth Cohort. PLOS ONE 2018; 13(1): e0190600 doi: 10.1371/journal.pone.0190600
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Calen A. Steiner, Jeffrey A. Berinstein, Jeremy Louissaint, Peter D.R. Higgins, Jason R. Spence, Carol Shannon, Cathy Lu, Ryan W. Stidham, Joel G. Fletcher, David H. Bruining, Brian G. Feagan, Vipul Jairath, Mark E. Baker, Dominik Bettenworth, Florian Rieder. Biomarkers for the Prediction and Diagnosis of Fibrostenosing Crohn’s Disease: A Systematic Review. Clinical Gastroenterology and Hepatology 2022; 20(4): 817 doi: 10.1016/j.cgh.2021.05.054
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Nagi Elleisy, Sarah Rohde, Astrid Huth, Nicole Gittel, Änne Glass, Steffen Möller, Georg Lamprecht, Holger Schäffler, Robert Jaster. Genetic association analysis of <i>CLEC5A</i> and <i>CLEC7A</i> gene single-nucleotide polymorphisms and Crohn’s disease. World Journal of Gastroenterology 2020; 26(18): 2194-2202 doi: 10.3748/wjg.v26.i18.2194
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Jeremy Adler, Sujal C Rangwalla, Ben A Dwamena, Peter DR Higgins. The Prognostic Power of the NOD2 Genotype for Complicated Crohn's Disease: A Meta-Analysis. American Journal of Gastroenterology 2011; 106(4): 699 doi: 10.1038/ajg.2011.19
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Nahla Azzam, Howaida Nounou, Othman Alharbi, Abedulrahman Aljebreen, Manal Shalaby. CARD15/NOD2, CD14 and Toll-like 4 Receptor Gene Polymorphisms in Saudi Patients with Crohn’s Disease. International Journal of Molecular Sciences 2012; 13(4): 4268 doi: 10.3390/ijms13044268
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N.K. Kharwar, K.N. Prasad, V.K. Paliwal, D.R. Modi. Association of NOD1 and NOD2 polymorphisms with Guillain-Barré syndrome in Northern Indian population. Journal of the Neurological Sciences 2016; 363: 57 doi: 10.1016/j.jns.2016.02.028
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Holger Schäffler, David Geiss, Nicole Gittel, Sarah Rohde, Astrid Huth, Änne Glass, Gunnar Brandhorst, Robert Jaster, Georg Lamprecht. Mutations in the NOD2 gene are associated with a specific phenotype and lower anti‐tumor necrosis factor trough levels in Crohn's disease. Journal of Digestive Diseases 2018; 19(11): 678 doi: 10.1111/1751-2980.12677
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