HuGE Literature Finder
|
||
Records 1-16
|
Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2014 Jun 46 (6): 512-7. Strisciuglio Caterina, Auricchio Renata, Martinelli Massimo, Staiano Annamaria, Giugliano Francesca Paola, Andreozzi Marialuisa, De Rosa Marina, Giannetti Eleonora, Gianfrani Carmela, Izzo Paola, Troncone Riccardo, Miele Eras |
|
The NOD2insC polymorphism is associated with worse outcome following ileal pouch-anal anastomosis for ulcerative colitis.
Gut 2013 Oct 62 (10): 1433-9. Tyler Andrea D, Milgrom Raquel, Stempak Joanne M, Xu Wei, Brumell John Hunter, Muise Aleixo M, Sehgal Rishabh, Cohen Zane, Koltun Walter, Shen Bo, Silverberg Mark |
|
Impact of NOD2 polymorphisms on infectious complications following chemotherapy in patients with acute myeloid leukaemia.
Annals of hematology 2013 Aug 92 (8): 1071-7. Yomade Olaposi, Spies-Weisshart Bärbel, Glaser Anita, Schnetzke Ulf, Hochhaus Andreas, Scholl Sebasti |
|
Isolated active ileitis: is it a mild subtype of Crohn's disease?
Inflammatory bowel diseases 2013 Aug 19 (9): 1815-22. O'Donnell Sarah, Crotty Paul L, O'Sullivan Maria, Breslin Niall, O'Connor Humphrey J, O'Morain Colm A, Ryan Barbara |
|
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project.
Gut 2012 Dec . Cleynen I, González JR, Figueroa C, Franke A, McGovern D, Bortlík M, Crusius BJ, Vecchi M, Artieda M, Szczypiorska M, Bethge J, Arteta D, Ayala E, Danese S, van Hogezand RA, Panés J, Peña SA, Lukas M, Jewell DP, Schreiber S, Vermeire S, Sans M |
|
Pathway analysis of a genome-wide association study of ileal Crohn's disease.
DNA and cell biology 2012 Oct 31 (10): 1549-54. Lee Young Ho, Song Gwan G |
|
Genetic risk profiling and gene signature modeling to predict risk of complications after IPAA.
Diseases of the colon and rectum 2012 Mar 55 (3): 239-48. Sehgal Rishabh, Berg Arthur, Polinski Joseph I, Hegarty John P, Lin Zhenwu, McKenna Kevin J, Stewart David B, Poritz Lisa S, Koltun Walter |
|
Innate dysfunction promotes linear growth failure in pediatric Crohn's disease and growth hormone resistance in murine ileitis.
Inflammatory bowel diseases 2012 Feb 18 (2): 236-45. D'Mello Sharon, Trauernicht Anna, Ryan Anne, Bonkowski Erin, Willson Tara, Trapnell Bruce C, Frank Stuart J, Kugasathan Subra, Denson Lee |
|
NOD2/CARD15 mutations correlate with severe pouchitis after ileal pouch-anal anastomosis.
Diseases of the colon and rectum 2010 Nov 53 (11): 1487-94. Sehgal Rishabh, Berg Arthur, Hegarty John P, Kelly Ashley A, Lin Zhenwu, Poritz Lisa S, Koltun Walter |
|
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
The American journal of gastroenterology 2008 Mar 103 (3): 682-91. Glas Jürgen, Konrad Astrid, Schmechel Silke, Dambacher Julia, Seiderer Julia, Schroff Frieder, Wetzke Martin, Roeske Darina, Török Helga-Paula, Tonenchi Laurian, Pfennig Simone, Haller Dirk, Griga Thomas, Klein Wolfram, Epplen Jörg T, Folwaczny Christian, Lohse Peter, Göke Burkhard, Ochsenkühn Thomas, Mussack Thomas, Folwaczny Matthias, Müller-Myhsok Bertram, Brand Steph |
|
Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.
European journal of gastroenterology & hepatology 2008 Jan 20 (1): 37-45. Onnie Clive M, Fisher Sheila A, Prescott Natalie J, Mirza Muddassar M, Green Peter, Sanderson Jeremy, Forbes Alastair, Lewis Cathryn M, Mathew Christopher |
|
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
Gastroenterology 2007 May 132 (5): 1665-71. Prescott Natalie J, Fisher Sheila A, Franke Andre, Hampe Jochen, Onnie Clive M, Soars Dianne, Bagnall Richard, Mirza Muddassar M, Sanderson Jeremy, Forbes Alastair, Mansfield John C, Lewis Cathryn M, Schreiber Stefan, Mathew Christopher |
|
Combined carriership of TLR9-1237C and CD14-260T alleles enhances the risk of developing chronic relapsing pouchitis.
World journal of gastroenterology : WJG 2005 Dec 11 (46): 7323-9. Lammers K M, Ouburg S, Morré S A, Crusius J B A, Gionchett P, Rizzello F, Morselli C, Caramelli E, Conte R, Poggioli G, Campieri M, Peña A |
|
Innate immune receptor genetic polymorphisms in pouchitis: is CARD15 a susceptibility factor?
Inflammatory bowel diseases 2005 Nov 11 (11): 965-71. Meier Carmen B, Hegazi Refaat A, Aisenberg James, Legnani Peter E, Nilubol Naris, Cobrin Gena M, Duerr Richard H, Gorfine Stephen R, Bauer Joel J, Sachar David B, Plevy Scott |
|
Tumor necrosis factor receptor gene polymorphisms in Crohn's disease: association with clinical phenotypes.
The American journal of gastroenterology 2005 May 100 (5): 1126-33. Waschke Kevin A, Villani Alexandra-Chloe, Vermeire Severine, Dufresne Line, Chen Tsao-Chun, Bitton Alain, Cohen Albert, Thomson Alan B R, Wild Gary |
|
Association of NOD2/CARD15 variants with Crohn's disease in a Greek population.
European journal of gastroenterology & hepatology 2004 Nov 16 (11): 1177-82. Gazouli Maria, Zacharatos Panayotis, Mantzaris Gerassimos J, Barbatis Calypso, Ikonomopoulos Ioannis, Archimandritis Athanassios J, Lukas John C, Papalambros Efstathios, Gorgoulis Vassil |
- Page last reviewed:Jul 30, 2019
- Page last updated:Aug 22, 2019
- Content source: