PubMed (OMIM) for id: 1684759

Year	Number of Results
1982	1
1985	2
1990	2
1993	1
1996	2
1997	1
1998	1
2000	1
2001	5
2002	8
2003	8
2004	6
2005	5
2006	1
2023	0

1

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

King K, Sheikh MF, Cuthbert AP, Fisher SA, Onnie CM, Mirza MM, Pattni RC, Sanderson J, Forbes A, Mansfield J, Lewis CM, Roberts RG, Mathew CG. King K, et al. Hum Mutat. 2006 Jan;27(1):44-54. doi: 10.1002/humu.20264. Hum Mutat. 2006. PMID: 16278823

2

Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.

van Heel DA, Ghosh S, Butler M, Hunt KA, Lundberg AM, Ahmad T, McGovern DP, Onnie C, Negoro K, Goldthorpe S, Foxwell BM, Mathew CG, Forbes A, Jewell DP, Playford RJ. van Heel DA, et al. Lancet. 2005 May 21-27;365(9473):1794-6. doi: 10.1016/S0140-6736(05)66582-8. Lancet. 2005. PMID: 15910952

3

A new CARD15 mutation in Blau syndrome.

van Duist MM, Albrecht M, Podswiadek M, Giachino D, Lengauer T, Punzi L, De Marchi M. van Duist MM, et al. Eur J Hum Genet. 2005 Jun;13(6):742-7. doi: 10.1038/sj.ejhg.5201404. Eur J Hum Genet. 2005. PMID: 15812565

4

Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing.

Maeda S, Hsu LC, Liu H, Bankston LA, Iimura M, Kagnoff MF, Eckmann L, Karin M. Maeda S, et al. Science. 2005 Feb 4;307(5710):734-8. doi: 10.1126/science.1103685. Science. 2005. PMID: 15692052

5

Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract.

Kobayashi KS, Chamaillard M, Ogura Y, Henegariu O, Inohara N, Nuñez G, Flavell RA. Kobayashi KS, et al. Science. 2005 Feb 4;307(5710):731-4. doi: 10.1126/science.1104911. Science. 2005. PMID: 15692051

6

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome.

Kanazawa N, Okafuji I, Kambe N, Nishikomori R, Nakata-Hizume M, Nagai S, Fuji A, Yuasa T, Manki A, Sakurai Y, Nakajima M, Kobayashi H, Fujiwara I, Tsutsumi H, Utani A, Nishigori C, Heike T, Nakahata T, Miyachi Y. Kanazawa N, et al. Blood. 2005 Feb 1;105(3):1195-7. doi: 10.1182/blood-2004-07-2972. Epub 2004 Sep 30. Blood. 2005. PMID: 15459013 Free article.

7

NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses.

Watanabe T, Kitani A, Murray PJ, Strober W. Watanabe T, et al. Nat Immunol. 2004 Aug;5(8):800-8. doi: 10.1038/ni1092. Epub 2004 Jun 27. Nat Immunol. 2004. PMID: 15220916 Free article.

8

Genetic variation in DLG5 is associated with inflammatory bowel disease.

Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S. Stoll M, et al. Nat Genet. 2004 May;36(5):476-80. doi: 10.1038/ng1345. Epub 2004 Apr 11. Nat Genet. 2004. PMID: 15107852

9

Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation.

Kanazawa N, Matsushima S, Kambe N, Tachibana T, Nagai S, Miyachi Y. Kanazawa N, et al. J Invest Dermatol. 2004 Mar;122(3):851-2. doi: 10.1111/j.0022-202X.2004.22341.x. J Invest Dermatol. 2004. PMID: 15086578 Free article. No abstract available.

10

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. Tukel T, et al. Am J Hum Genet. 2004 Apr;74(4):623-36. doi: 10.1086/382226. Epub 2004 Mar 5. Am J Hum Genet. 2004. PMID: 15024686 Free PMC article.

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