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Items: 1 to 20 of 83

1.

Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease.

Somasundaram R, Deuring JJ, van der Woude CJ, Peppelenbosch MP, Fuhler GM.

Gut. 2012 Jul;61(7):1097; author reply 1097-8. doi: 10.1136/gutjnl-2011-301344. No abstract available.

PMID:
22027479
2.

NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2.

Muise AM, Xu W, Guo CH, Walters TD, Wolters VM, Fattouh R, Lam GY, Hu P, Murchie R, Sherlock M, Gana JC; NEOPICS., Russell RK, Glogauer M, Duerr RH, Cho JH, Lees CW, Satsangi J, Wilson DC, Paterson AD, Griffiths AM, Silverberg MS, Brumell JH.

Gut. 2012 Jul;61(7):1028-35. doi: 10.1136/gutjnl-2011-300078. Erratum in: Gut. 2013 Oct;62(10):1432.

3.

Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort.

Roberts RL, Hollis-Moffatt JE, Gearry RB, Kennedy MA, Barclay ML, Merriman TR.

Genes Immun. 2008 Sep;9(6):561-5. doi: 10.1038/gene.2008.49.

PMID:
18580884
4.

rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.

Glas J, Seiderer J, Pasciuto G, Tillack C, Diegelmann J, Pfennig S, Konrad A, Schmechel S, Wetzke M, Török HP, Stallhofer J, Jürgens M, Griga T, Klein W, Epplen JT, Schiemann U, Mussack T, Lohse P, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Brand S.

Am J Gastroenterol. 2009 Mar;104(3):665-72. doi: 10.1038/ajg.2008.65.

PMID:
19262523
5.

Chronic granulomatous disease.

Heyworth PG, Cross AR, Curnutte JT.

Curr Opin Immunol. 2003 Oct;15(5):578-84. Review.

PMID:
14499268
6.

Novel human pathological mutations. Gene symbol: NCF2. Disease: Chronic granulomatous disease.

Köker MY.

Hum Genet. 2010 Jan;127(1):113. No abstract available.

PMID:
20108388
7.

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
8.

NELL1, NCF4, and FAM92B genes are not major susceptibility genes for Crohn's disease in Canadian children and young adults.

Amre DK, Mack DR, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Levy E.

Inflamm Bowel Dis. 2012 Mar;18(3):529-35. doi: 10.1002/ibd.21708.

PMID:
21472827
9.

Clinical and genetic risk factors for perianal Crohn's disease in a population-based cohort.

Eglinton TW, Roberts R, Pearson J, Barclay M, Merriman TR, Frizelle FA, Gearry RB.

Am J Gastroenterol. 2012 Apr;107(4):589-96. doi: 10.1038/ajg.2011.437.

PMID:
22158027
10.

Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W.

van Steensel MA, Badeloe S, Winnepenninckx V, Vreeburg M, Steijlen PM, van Geel M.

Exp Dermatol. 2008 Dec;17(12):1057-8. doi: 10.1111/j.1600-0625.2008.00753.x.

PMID:
18616576
11.

The association of MYO9B gene in Italian patients with inflammatory bowel diseases.

Latiano A, Palmieri O, Valvano MR, D'Incà R, Caprilli R, Cucchiara S, Sturniolo GC, Bossa F, Andriulli A, Annese V.

Aliment Pharmacol Ther. 2008 Feb 1;27(3):241-8.

12.

[The genetic basis of inflammatory bowel disease unravelled by genetic association studies].

Visschedijk MC, Festen EA, Wijmenga C, Weersma RK.

Ned Tijdschr Geneeskd. 2009;153:A402. Review. Dutch.

PMID:
19900309
13.

Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase.

Noack D, Rae J, Cross AR, Muñoz J, Salmen S, Mendoza JA, Rossi N, Curnutte JT, Heyworth PG.

Hum Genet. 1999 Nov;105(5):460-7.

PMID:
10598813
14.

X-linked chronic granulomatous disease: first report of mutations in patients of Argentina.

Barese C, Copelli S, Zandomeni R, Oleastro M, Zelazko M, Rivas EM.

J Pediatr Hematol Oncol. 2004 Oct;26(10):656-60.

PMID:
15454837
15.

[Haptoglobin polymorphism in patients with inflammatory bowel diseases].

Papp M, Lakatos PL; Hungarian IBD Study Group., Palatka K, Földi I, Udvardy M, Hársfalvi J, Tornai I, Vitális Z, Dinya T, Kovács A, Molnár T, Demeter P, Papp J, Lakatos L, Altorjay I.

Orv Hetil. 2006 Sep 10;147(36):1745-50. Hungarian.

PMID:
17087019
16.

NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.

Molnar T, Hofner P, Nagy F, Lakatos PL, Fischer S, Lakatos L, Kovacs A, Altorjay I, Papp M, Palatka K, Demeter P, Tulassay Z, Nyari T, Miheller P, Papp J, Mandi Y, Lonovics J; Hungarian IBD Study Group..

Dig Liver Dis. 2007 Dec;39(12):1064-70.

PMID:
17964870
17.
18.

Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease.

Freudenberg F, Wintergerst U, Roesen-Wolff A, Albert MH, Prell C, Strahm B, Koletzko S, Ehl S, Roos D, Tommasini A, Ventura A, Belohradsky BH, Seger R, Roesler J, Güngör T.

J Allergy Clin Immunol. 2010 Apr;125(4):943-946.e1. doi: 10.1016/j.jaci.2010.01.035. No abstract available.

PMID:
20371400
19.

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease.

Momozawa Y, Mni M, Nakamura K, Coppieters W, Almer S, Amininejad L, Cleynen I, Colombel JF, de Rijk P, Dewit O, Finkel Y, Gassull MA, Goossens D, Laukens D, Lémann M, Libioulle C, O'Morain C, Reenaers C, Rutgeerts P, Tysk C, Zelenika D, Lathrop M, Del-Favero J, Hugot JP, de Vos M, Franchimont D, Vermeire S, Louis E, Georges M.

Nat Genet. 2011 Jan;43(1):43-7. doi: 10.1038/ng.733.

PMID:
21151126
20.

Chronic granulomatous disease caused by a deficiency in p47(phox) mimicking Crohn's disease.

Huang JS, Noack D, Rae J, Ellis BA, Newbury R, Pong AL, Lavine JE, Curnutte JT, Bastian J.

Clin Gastroenterol Hepatol. 2004 Aug;2(8):690-5.

PMID:
15290662
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