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Results: 1 to 20 of 173

1.

Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn disease.

Leshinsky-Silver E, Karban A, Dalal I, Eliakim R, Shirin H, Tzofi T, Boaz M, Levine A.

J Pediatr Gastroenterol Nutr. 2007 Oct;45(4):405-8.

PMID:
18030204
[PubMed - indexed for MEDLINE]
2.

Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.

Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.

Am J Gastroenterol. 2008 Mar;103(3):615-20. Epub 2007 Nov 28.

PMID:
18047539
[PubMed - indexed for MEDLINE]
3.

Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in Northern Europe.

Van Limbergen J, Russell RK, Nimmo ER, Drummond HE, Smith L, Anderson NH, Davies G, Gillett PM, McGrogan P, Weaver LT, Bisset WM, Mahdi G, Arnott ID, Wilson DC, Satsangi J.

Inflamm Bowel Dis. 2008 Mar;14(3):338-46.

PMID:
18088053
[PubMed - indexed for MEDLINE]
4.

Replication of interleukin 23 receptor and autophagy-related 16-like 1 association in adult- and pediatric-onset inflammatory bowel disease in Italy.

Latiano A, Palmieri O, Valvano MR, D'Incà R, Cucchiara S, Riegler G, Staiano AM, Ardizzone S, Accomando S, de Angelis GL, Corritore G, Bossa F, Annese V.

World J Gastroenterol. 2008 Aug 7;14(29):4643-51.

PMID:
18698678
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.

Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.

Tissue Antigens. 2008 Jun;71(6):538-47. doi: 10.1111/j.1399-0039.2008.01047.x.

PMID:
18489434
[PubMed - indexed for MEDLINE]
6.

CARD15 gene mutations and risk for early surgery in pediatric-onset Crohn's disease.

Kugathasan S, Collins N, Maresso K, Hoffmann RG, Stephens M, Werlin SL, Rudolph C, Broeckel U.

Clin Gastroenterol Hepatol. 2004 Nov;2(11):1003-9.

PMID:
15551253
[PubMed - indexed for MEDLINE]
7.

Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.

de Ridder L, Weersma RK, Dijkstra G, van der Steege G, Benninga MA, Nolte IM, Taminiau JA, Hommes DW, Stokkers PC.

Inflamm Bowel Dis. 2007 Sep;13(9):1083-92.

PMID:
17476680
[PubMed - indexed for MEDLINE]
8.

CARD15 mutations are rare in Swedish pediatric Crohn disease.

Ideström M, Rubio C, Granath F, Finkel Y, Hugot JP.

J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):456-60.

PMID:
15795594
[PubMed - indexed for MEDLINE]
9.

DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's disease.

Biank V, Friedrichs F, Babusukumar U, Wang T, Stoll M, Broeckel U, Kugathasan S.

Am J Gastroenterol. 2007 Feb;102(2):391-8. Epub 2006 Dec 11.

PMID:
17156146
[PubMed - indexed for MEDLINE]
10.

IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease.

Dubinsky MC, Wang D, Picornell Y, Wrobel I, Katzir L, Quiros A, Dutridge D, Wahbeh G, Silber G, Bahar R, Mengesha E, Targan SR, Taylor KD, Rotter JI; Western Regional Research Alliance for Pediatric IBD.

Inflamm Bowel Dis. 2007 May;13(5):511-5.

PMID:
17309073
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility.

Levine A, Kugathasan S, Annese V, Biank V, Leshinsky-Silver E, Davidovich O, Kimmel G, Shamir R, Palmieri O, Karban A, Broeckel U, Cucchiara S.

Inflamm Bowel Dis. 2007 Dec;13(12):1509-15. Erratum in: Inflamm Bowel Dis. 2008 Dec;14(12):1760. Orazio, Palmieri [corrected to Palmieri, Orazio].

PMID:
17763471
[PubMed - indexed for MEDLINE]
12.

CARD15 gene polymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis.

Protic MB, Pavlovic ST, Bojic DZ, Krstic MN, Radojicic ZA, Tarabar DK, Stevanovic AZ, Karan Djurasevic TZ, Godjevac MV, Svorcan PV, Dapcevic BD, Jojic NZ.

Eur J Gastroenterol Hepatol. 2008 Oct;20(10):978-84. doi: 10.1097/MEG.0b013e328302f45e.

PMID:
18787464
[PubMed - indexed for MEDLINE]
13.

NOD2/CARD15 mutations and presence of granulomas in pediatric and adult Crohn's disease.

Shaoul R, Karban A, Weiss B, Reif S, Wasserman D, Pacht A, Eliakim R, Wardi J, Shirin H, Wine E, Leshinsky-Silver E, Levine A.

Inflamm Bowel Dis. 2004 Nov;10(6):709-14.

PMID:
15626887
[PubMed - indexed for MEDLINE]
14.

ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients.

Lakatos PL, Szamosi T, Szilvasi A, Molnar E, Lakatos L, Kovacs A, Molnar T, Altorjay I, Papp M, Tulassay Z, Miheller P, Papp J, Tordai A, Andrikovics H; Hungarian IBD Study Group.

Dig Liver Dis. 2008 Nov;40(11):867-73. doi: 10.1016/j.dld.2008.03.022. Epub 2008 May 22.

PMID:
18499543
[PubMed - indexed for MEDLINE]
15.

Disease behavior in children with Crohn's disease: the effect of disease duration, ethnicity, genotype, and phenotype.

Shaoul R, Karban A, Reif S, Weiss B, Shamir R, Tamir A, Davidovich O, Halevi J, Silver EL, Levine A.

Dig Dis Sci. 2009 Jan;54(1):142-50. doi: 10.1007/s10620-008-0326-7. Epub 2008 Jul 2.

PMID:
18594982
[PubMed - indexed for MEDLINE]
16.

Genetic variants in IL-23R and ATG16L1 independently predispose to increased susceptibility to Crohn's disease in a Canadian population.

Newman WG, Zhang Q, Liu X, Amos CI, Siminovitch KA.

J Clin Gastroenterol. 2009 May-Jun;43(5):444-7. doi: 10.1097/MCG.0b013e318168bdf0.

PMID:
19276991
[PubMed - indexed for MEDLINE]
17.

IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.

Roberts RL, Gearry RB, Hollis-Moffatt JE, Miller AL, Reid J, Abkevich V, Timms KM, Gutin A, Lanchbury JS, Merriman TR, Barclay ML, Kennedy MA.

Am J Gastroenterol. 2007 Dec;102(12):2754-61. Epub 2007 Sep 25.

PMID:
17894849
[PubMed - indexed for MEDLINE]
18.

Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease.

Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG.

Aliment Pharmacol Ther. 2009 May 1;29(9):1025-31. doi: 10.1111/j.1365-2036.2009.03953.x. Epub 2009 Feb 7. Erratum in: Aliment Pharmacol Ther. 2009 Aug 15;30(4):422.

PMID:
19210299
[PubMed - indexed for MEDLINE]
19.

Contribution of OCTN variants within the IBD5 locus to pediatric onset Crohn's disease.

Babusukumar U, Wang T, McGuire E, Broeckel U, Kugathasan S.

Am J Gastroenterol. 2006 Jun;101(6):1354-61.

PMID:
16771961
[PubMed - indexed for MEDLINE]
20.

Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.

Seiderer J, Elben I, Diegelmann J, Glas J, Stallhofer J, Tillack C, Pfennig S, Jürgens M, Schmechel S, Konrad A, Göke B, Ochsenkühn T, Müller-Myhsok B, Lohse P, Brand S.

Inflamm Bowel Dis. 2008 Apr;14(4):437-45.

PMID:
18088064
[PubMed - indexed for MEDLINE]

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