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Results: 1 to 20 of 108

1.

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, Mascheretti S, Sanderson J, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG.

Gastroenterology. 2002 Apr;122(4):867-74.

PMID:
11910337
[PubMed - indexed for MEDLINE]
2.

Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.

Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J.

Am J Gastroenterol. 2002 Dec;97(12):3095-101.

PMID:
12492195
[PubMed - indexed for MEDLINE]
3.

[NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study].

Lakatos L, Lakatos PL, Willheim-Polli C, Reinisch W, Ferenci P, Tulassay Z, Molnár T, Kovács A, Papp J, Szalay F; Hungarian IBD Study Group.

Orv Hetil. 2004 Jul 4;145(27):1403-11. Hungarian.

PMID:
15320482
[PubMed - indexed for MEDLINE]
4.

CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.

van der Linde K, Boor PP, Houwing-Duistermaat JJ, Crusius BJ, Wilson PJ, Kuipers EJ, de Rooij FW.

Eur J Gastroenterol Hepatol. 2007 Jun;19(6):449-59. Review.

PMID:
17489054
[PubMed - indexed for MEDLINE]
5.

Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan.

Bonen DK, Ogura Y, Nicolae DL, Inohara N, Saab L, Tanabe T, Chen FF, Foster SJ, Duerr RH, Brant SR, Cho JH, Nuñez G.

Gastroenterology. 2003 Jan;124(1):140-6.

PMID:
12512038
[PubMed - indexed for MEDLINE]
6.

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.

Heliö T, Halme L, Lappalainen M, Fodstad H, Paavola-Sakki P, Turunen U, Färkkilä M, Krusius T, Kontula K.

Gut. 2003 Apr;52(4):558-62.

PMID:
12631669
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.

Heresbach D, Gicquel-Douabin V, Birebent B, D'halluin PN, Heresbach-Le Berre N, Dreano S, Siproudhis L, Dabadie A, Gosselin M, Mosser J, Semana G, Bretagne JF, Yaouanq J.

Eur J Gastroenterol Hepatol. 2004 Jan;16(1):55-62.

PMID:
15095853
[PubMed - indexed for MEDLINE]
8.

Association of NOD2/CARD15 variants with Crohn's disease in a Greek population.

Gazouli M, Zacharatos P, Mantzaris GJ, Barbatis C, Ikonomopoulos I, Archimandritis AJ, Lukas JC, Papalambros E, Gorgoulis V.

Eur J Gastroenterol Hepatol. 2004 Nov;16(11):1177-82.

PMID:
15489579
[PubMed - indexed for MEDLINE]
9.

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.

Lesage S, Zouali H, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, Chamaillard M, Jannot AS, Thomas G, Hugot JP; EPWG-IBD Group; EPIMAD Group; GETAID Group.

Am J Hum Genet. 2002 Apr;70(4):845-57. Epub 2002 Mar 1.

PMID:
11875755
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease.

Mendoza JL, Murillo LS, Fernández L, Peña AS, Lana R, Urcelay E, Cruz-Santamaría DM, de la Concha EG, Díaz-Rubio M, García-Paredes J.

Scand J Gastroenterol. 2003 Dec;38(12):1235-40.

PMID:
14750643
[PubMed - indexed for MEDLINE]
11.

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]
12.

Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.

Annese V, Palmieri O, Latiano A, Ardizzone S, Castiglione F, Cottone M, D'Incà R, Gionchetti P, Papi C, Riegler G, Vecchi M, Andriulli A; Italian Group for Inflammatory Bowel Disease.

Dig Liver Dis. 2004 Feb;36(2):121-4.

PMID:
15002819
[PubMed - indexed for MEDLINE]
13.

Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease.

Rigoli L, Romano C, Caruso RA, Lo Presti MA, Di Bella C, Procopio V, Lo Giudice G, Amorini M, Costantino G, Sergi MD, Cuppari C, Calabro GE, Gallizzi R, Salpietro CD, Fries W.

World J Gastroenterol. 2008 Jul 28;14(28):4454-61.

PMID:
18680223
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families.

Tukel T, Shalata A, Present D, Rachmilewitz D, Mayer L, Grant D, Risch N, Desnick RJ.

Am J Hum Genet. 2004 Apr;74(4):623-36. Epub 2004 Mar 5.

PMID:
15024686
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.

Tomer G, Ceballos C, Concepcion E, Benkov KJ.

Am J Gastroenterol. 2003 Nov;98(11):2479-84.

PMID:
14638352
[PubMed - indexed for MEDLINE]
16.

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.

Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG.

Lancet. 2001 Jun 16;357(9272):1925-8. Erratum in: Lancet 2002 Sep 7;360(9335):806.

PMID:
11425413
[PubMed - indexed for MEDLINE]
17.

Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations.

Lakatos PL, Lakatos L, Szalay F, Willheim-Polli C, Osterreicher C, Tulassay Z, Molnar T, Reinisch W, Papp J, Mozsik G, Ferenci P; Hungarian IBD Study Group.

World J Gastroenterol. 2005 Mar 14;11(10):1489-95.

PMID:
15770725
[PubMed - indexed for MEDLINE]
Free Article
18.

NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.

Karban A, Waterman M, Panhuysen CI, Pollak RD, Nesher S, Datta L, Weiss B, Suissa A, Shamir R, Brant SR, Eliakim R.

Am J Gastroenterol. 2004 Jun;99(6):1134-40.

PMID:
15180737
[PubMed - indexed for MEDLINE]
19.

Association of NOD2 with Crohn's disease in a homogenous Irish population.

Bairead E, Harmon DL, Curtis AM, Kelly Y, O'Leary C, Gardner M, Leahy DT, Vaughan P, Keegan D, O'Morain C, O'Donoghue D, Shanahan F, Parfrey NA, Quane KA.

Eur J Hum Genet. 2003 Mar;11(3):237-44.

PMID:
12673278
[PubMed - indexed for MEDLINE]
Free Article
20.

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease.

Abreu MT, Taylor KD, Lin YC, Hang T, Gaiennie J, Landers CJ, Vasiliauskas EA, Kam LY, Rojany M, Papadakis KA, Rotter JI, Targan SR, Yang H.

Gastroenterology. 2002 Sep;123(3):679-88.

PMID:
12198692
[PubMed - indexed for MEDLINE]

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