de Rooij FW - Search Results

1

A functional interleukin-10 mutation in Dutch patients with Crohn's disease.

van der Linde K, Boor PP, van Bodegraven AA, de Jong DJ, Crusius JB, Naber TH, Kuipers EJ, Wilson JH, de Rooij FW. van der Linde K, et al. Among authors: de rooij fw, de jong dj. Dig Liver Dis. 2005 May;37(5):330-5. doi: 10.1016/j.dld.2004.12.009. Dig Liver Dis. 2005. PMID: 15843082

2

[From gene to disease; 'frame shift'-mutation in the CARD15-gene and Crohn's disease].

van der Linde K, Kuipers EJ, de Rooij FW, Wilson JH. van der Linde K, et al. Among authors: de rooij fw. Ned Tijdschr Geneeskd. 2002 Dec 28;146(52):2539-42. Ned Tijdschr Geneeskd. 2002. PMID: 12532667 Dutch.

3

A Gly15Arg mutation in the interleukin-10 gene reduces secretion of interleukin-10 in Crohn disease.

van der Linde K, Boor PP, Sandkuijl LA, Meijssen MA, Savelkoul HF, Wilson JH, de Rooij FW. van der Linde K, et al. Among authors: de rooij fw. Scand J Gastroenterol. 2003 Jun;38(6):611-7. Scand J Gastroenterol. 2003. PMID: 12825869

4

Allele-sharing of cytokine genes in familial inflammatory bowel disease.

van der Linde K, Boor PP, Mejissen MA, Sandkuijl LA, Houwing-Duistermaat JJ, Kuipers EJ, Wilson JH, de Rooij FW. van der Linde K, et al. Among authors: de rooij fw. Hepatogastroenterology. 2007 Jul-Aug;54(77):1467-71. Hepatogastroenterology. 2007. PMID: 17708278

5

Card15 and Crohn's disease: healthy homozygous carriers of the 3020insC frameshift mutation.

Linde Kv, Boor PP, Houwing-Duistermaat JJ, Kuipers EJ, Wilson JH, de Rooij FW. Linde Kv, et al. Among authors: de rooij fw. Am J Gastroenterol. 2003 Mar;98(3):613-7. doi: 10.1111/j.1572-0241.2003.07287.x. Am J Gastroenterol. 2003. PMID: 12650796

6

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. van der Linde K, et al. Among authors: de rooij fw. Eur J Gastroenterol Hepatol. 2007 Jun;19(6):449-59. doi: 10.1097/01.meg.0000236887.44214.6a. Eur J Gastroenterol Hepatol. 2007. PMID: 17489054 Review.

7

Peutz-Jeghers syndrome: 78-year follow-up of the original family.

Westerman AM, Entius MM, de Baar E, Boor PP, Koole R, van Velthuysen ML, Offerhaus GJ, Lindhout D, de Rooij FW, Wilson JH. Westerman AM, et al. Among authors: de rooij fw, de baar e. Lancet. 1999 Apr 10;353(9160):1211-5. doi: 10.1016/s0140-6736(98)08018-0. Lancet. 1999. PMID: 10217080

8

Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.

Westerman AM, Entius MM, Boor PP, Koole R, de Baar E, Offerhaus GJ, Lubinski J, Lindhout D, Halley DJ, de Rooij FW, Wilson JH. Westerman AM, et al. Among authors: de rooij fw, de baar e. Hum Mutat. 1999;13(6):476-81. doi: 10.1002/(SICI)1098-1004(1999)13:6<476::AID-HUMU7>3.0.CO;2-2. Hum Mutat. 1999. PMID: 10408777

9

Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands.

de Rooij FW, Kavelaars FG, Koole-Lesuis H, Wilson JH. de Rooij FW, et al. Cell Mol Biol (Noisy-le-grand). 2009 Jul 1;55(2):64-9. Cell Mol Biol (Noisy-le-grand). 2009. PMID: 19656453

10

Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics.

Edixhoven-Bosdijk A, de Rooij FW, de Baar-Heesakkers E, Wilson JH. Edixhoven-Bosdijk A, et al. Among authors: de baar heesakkers e, de rooij fw. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):861-6. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699244

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