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CARD4/NOD1 is not involved in inflammatory bowel disease.
Zouali H, Lesage S, Merlin F, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Christensen S, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Chamaillard M, Thomas G, Hugot JP; EPWG group; EPIMAD group. Zouali H, et al. Among authors: lesage s. Gut. 2003 Jan;52(1):71-4. doi: 10.1136/gut.52.1.71. Gut. 2003. PMID: 12477763 Free PMC article.
Etiology of the inflammatory bowel diseases.
Hugot JP, Zouali H, Lesage S, Thomas G. Hugot JP, et al. Among authors: lesage s. Int J Colorectal Dis. 1999 Feb;14(1):2-9. doi: 10.1007/s003840050175. Int J Colorectal Dis. 1999. PMID: 10207723 Review.
Genetic analyses of chromosome 12 loci in Crohn's disease.
Lesage S, Zouali H, Colombel JF, Belaiche J, Cézard JP, Tysk C, Almer S, Gassull M, Binder V, Chamaillard M, Le Gall I, Thomas G, Hugot JP. Lesage S, et al. Gut. 2000 Dec;47(6):787-91. doi: 10.1136/gut.47.6.787. Gut. 2000. PMID: 11076876 Free PMC article.
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G. Hugot JP, et al. Among authors: lesage s. Nature. 2001 May 31;411(6837):599-603. doi: 10.1038/35079107. Nature. 2001. PMID: 11385576
Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease.
Zouali H, Chamaillard M, Lesage S, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Macry J, Selinger-Leneman H, Thomas G, Hugot JP; GETAID. Zouali H, et al. Among authors: lesage s. Eur J Hum Genet. 2001 Oct;9(10):731-42. doi: 10.1038/sj.ejhg.5200710. Eur J Hum Genet. 2001. PMID: 11781683
Lessons to be learned from the NOD2 gene in Crohn's disease.
Hugot JP, Zouali H, Lesage S. Hugot JP, et al. Among authors: lesage s. Eur J Gastroenterol Hepatol. 2003 Jun;15(6):593-7. doi: 10.1097/00042737-200306000-00003. Eur J Gastroenterol Hepatol. 2003. PMID: 12840668 Review.
CARD15 mutations in Blau syndrome.
Miceli-Richard C, Lesage S, Rybojad M, Prieur AM, Manouvrier-Hanu S, Häfner R, Chamaillard M, Zouali H, Thomas G, Hugot JP. Miceli-Richard C, et al. Among authors: lesage s. Nat Genet. 2001 Sep;29(1):19-20. doi: 10.1038/ng720. Nat Genet. 2001. PMID: 11528384
414 results