Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Crohn Disease and NOD2[original query] |
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| CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. American journal of human genetics 2002 Apr 70 (4): 845-57. Lesage Suzanne, Zouali Habib, Cézard Jean-Pierre, Colombel Jean-Frédéric, Belaiche Jacques, Almer Sven, Tysk Curt, O'Morain Colm, Gassull Miquel, Binder Vibeke, Finkel Yigael, Modigliani Robert, Gower-Rousseau Corinne, Macry Jeanne, Merlin Françoise, Chamaillard Mathias, Jannot Anne-Sophie, Thomas Gilles, Hugot Jean-Pierre, , , |
| Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15). American journal of ophthalmology 2003 Nov 136 (5): 933-5. Martin Tammy M, Doyle Trudy M, Smith Justine R, Dinulescu Denis, Rust Kristal, Rosenbaum James |
| Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation. Blood 2004 Aug 104 (3): 889-94. Holler E, Rogler G, Herfarth H, Brenmoehl J, Wild PJ, Hahn J, Eissner G, Schölmerich J, Andreesen R |
| Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease. Scandinavian journal of gastroenterology 2003 Dec 38 (12): 1235-40. Mendoza J L, Murillo L S, Fernández L, Peña A S, Lana R, Urcelay E, Cruz-Santamaría D M, de la Concha E G, Díaz-Rubio M, García-Paredes |
| CARD15 mutations are rare in Swedish pediatric Crohn disease. Journal of pediatric gastroenterology and nutrition 2005 Apr 40 (4): 456-60. Ideström Maja, Rubio Carlos, Granath Fredrik, Finkel Yigael, Hugot J |
| Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15. Human mutation 2006 Jan 27 (1): 44-54. King Kathy, Sheikh Mohammed F, Cuthbert Andrew P, Fisher Sheila A, Onnie Clive M, Mirza Muddassar M, Pattni Reenal C, Sanderson Jeremy, Forbes Alastair, Mansfield John, Lewis Cathryn M, Roberts Roland G, Mathew Christopher |
| Ileal lymphonodular hyperplasia is not associated with NOD2/CARD15 mutations. Journal of pediatric gastroenterology and nutrition 2006 Jul 43 (1): 30-4. Shaoul Ron, Eliakim Rami, Tamir Ada, Karban Am |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
PloS one 2007 2 (8): e691. Franke Andre, Hampe Jochen, Rosenstiel Philip, Becker Christian, Wagner Florian, Häsler Robert, Little Randall D, Huse Klaus, Ruether Andreas, Balschun Tobias, Wittig Michael, Elsharawy Abdou, Mayr Gabriele, Albrecht Mario, Prescott Natalie J, Onnie Clive M, Fournier Hélène, Keith Tim, Radelof Uwe, Platzer Matthias, Mathew Christopher G, Stoll Monika, Krawczak Michael, Nürnberg Peter, Schreiber Stef |
| Frequency and clinical correlations of granulomas in children with Crohn disease. Journal of pediatric gastroenterology and nutrition 2008 Apr 46 (4): 392-8. De Matos Vera, Russo Pierre A, Cohen Aaron B, Mamula Petar, Baldassano Robert N, Piccoli David |
| Polymorphisms in the IBD5 locus are associated with Crohn disease in pediatric Ashkenazi Jewish patients. Journal of pediatric gastroenterology and nutrition 2009 May 48 (5): 531-7. Tomer Gitit, Wetzler Graciela, Keddache Mehdi, Denson Lee |
| NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease. Journal of pediatric surgery 2010 Aug 45 (8): 1591-7. Lacher Martin, Helmbrecht Johanna, Schroepf Sebastian, Koletzko Sibylle, Ballauff Antje, Classen Martin, Uhlig Holm, Hubertus Jochen, Hartl Dominik, Lohse Peter, von Schweinitz Dietrich, Kappler Rola |
| Penetrance of NOD2/CARD15 genetic variants in the general population. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2010 Apr 182 (7): 661-5. Yazdanyar Shiva, Kamstrup Pia R, Tybjaerg-Hansen Anne, Nordestgaard Børge |
| Nucleotide-binding oligomerization domain containing 2 (NOD2) variants are genetic risk factors for death and spontaneous bacterial peritonitis in liver cirrhosis. Hepatology (Baltimore, Md.) 2010 Apr 51 (4): 1327-33. Appenrodt Beate, Grünhage Frank, Gentemann Martin G, Thyssen Lydia, Sauerbruch Tilman, Lammert Fra |
| Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease. American journal of human genetics 2011 Dec 89 (6): 798-805. Elding Heather, Lau Winston, Swallow Dallas M, Maniatis Nikol |
| Immunologic and genetic markers in patients with idiopathic ocular inflammation and a family history of inflammatory bowel disease. American journal of ophthalmology 2012 Jul 154 (1): 72-7. Abbasian Javaneh, Martin Tammy M, Patel Sarju, Tessler Howard H, Goldstein Debra |
| Low mannose-binding lectin (MBL) is associated with paediatric inflammatory bowel diseases and ileal involvement in patients with Crohn disease. Journal of Crohn's & colitis 2013 Mar 7 (2): 134-41. Kovacs Marta, Papp Maria, Lakatos Peter Laszlo, Jacobsen Silvia, Nemes Eva, Polgar Marianne, Solyom Eniko, Bodi Piroska, Horvath Agnes, Molnar Kriszta, Szabo Doloresz, Cseh Aron, Muller Katalin Eszter, Dezsofi Antal, Arato Andras, Veres Gab |
| Genetic association and functional role of Crohn disease risk alleles involved in microbial sensing, autophagy, and endoplasmic reticulum (ER) stress. Autophagy 2013 Dec 9 (12): 2046-55. Hoefkens Eveline, Nys Kris, John Jestinah M, Van Steen Kristel, Arijs Ingrid, Van der Goten Jan, Van Assche Gert, Agostinis Patrizia, Rutgeerts Paul, Vermeire Séverine, Cleynen Isabel |
| Role of HLA typing on Crohn's disease pathogenesis. Annals of medicine and surgery (2012) 2015 Sep 4 (3): 248-53. Mahdi Batool Mut |
| Genetic Polymorphisms in Autophagy-Associated Genes in Korean Children With Early-Onset Crohn Disease. Journal of pediatric gastroenterology and nutrition 2015 Sep 61 (3): 285-91. Na So Young, Park Sung Sup, Seo Jeong K |
| Crohn's Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes. Journal of clinical medicine 2021 9 10 (17): . Kaczmarek-Ry? Marta, Hryhorowicz Szymon Tytus, Lis Emilia, Banasiewicz Tomasz, Paszkowski Jacek, Borejsza-Wysocki Maciej, Walkowiak Jaros?aw, Cichy Wojciech, Krokowicz Piotr, Czkwianianc El?bieta, Hnatyszyn Andrzej, Krela-Ka?mierczak Iwona, Dobrowolska Agnieszka, S?omski Ryszard, P?awski Andrz |
| NOD2 polymorphisms may direct a Crohn's disease phenotype in patients with Very EarlyOnset Inflammatory Bowel Disease. Journal of pediatric gastroenterology and nutrition 2023 5 . Ashleigh Watson, Lisa Forbes Satter, Ashley Reiland Sauceda, Richard Kellermayer, Lina B Kar |
| Impaired reprogramming of the autophagy flux in maturing dendritic cells from crohn disease patients with core autophagy gene-related polymorphisms. Autophagy 2024 4 1-17. Gaëlle Quiniou, Leslie Andromaque, Rémi Duclaux-Loras, Océane Dinet, Ornella Cervantes, Mallorie Verdet, Camille Meunier, Gilles Boschetti, Christophe Viret, Stéphane Nancey, Mathias Faure, Aurore Rozièr |
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