Wilson JH - 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: wilson jh. 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: wilson jh. 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: wilson jh. 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: wilson jh. Hepatogastroenterology. 2007 Jul-Aug;54(77):1467-71. Hepatogastroenterology. 2007. PMID: 17708278

5

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: wilson jh. Lancet. 1999 Apr 10;353(9160):1211-5. doi: 10.1016/s0140-6736(98)08018-0. Lancet. 1999. PMID: 10217080

6

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: wilson jh. 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

7

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. Among authors: wilson jh. Cell Mol Biol (Noisy-le-grand). 2009 Jul 1;55(2):64-9. Cell Mol Biol (Noisy-le-grand). 2009. PMID: 19656453

8

Vitamin D deficiency in patients with erythropoietic protoporphyria.

Spelt JM, de Rooij FW, Wilson JH, Zandbergen AA. Spelt JM, et al. Among authors: wilson jh. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S1-4. doi: 10.1007/s10545-008-1037-0. J Inherit Metab Dis. 2010. PMID: 24137761

9

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: wilson jh. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):861-6. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699244

10

Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures.

Hinnen P, Siersema PD, Edixhoven A, Wilson JH, de Rooij FW. Hinnen P, et al. Among authors: wilson jh. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):903-9. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699249

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