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Items: 1 to 20 of 93

1.

Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing Heritability.

Chen JS, Hu F, Kugathasan S, Jorde LB, Nix D, Rutherford A, Denson L, Watkins WS, Prahalad S, Huff C, Guthery SL.

G3 (Bethesda). 2018 Aug 30;8(9):2881-2888. doi: 10.1534/g3.118.200404.

2.

A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn's Disease.

Frade-Proud'Hon-Clerc S, Smol T, Frenois F, Sand O, Vaillant E, Dhennin V, Bonnefond A, Froguel P, Fumery M, Guillon-Dellac N, Gower-Rousseau C, Vasseur F.

Int J Mol Sci. 2019 Feb 15;20(4). pii: E835. doi: 10.3390/ijms20040835.

3.

Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients.

Hama I, Ratbi I, Reggoug S, Elkerch F, Kharrasse G, Errabih I, Ouazzani H, Sefiani A.

Gene. 2012 May 10;499(1):121-3. doi: 10.1016/j.gene.2011.12.045. Epub 2012 Jan 14.

PMID:
22266421
4.

NOD2 exonic variations in Iranian Crohn's disease patients.

Naderi N, Farnood A, Habibi M, Zojaji H, Balaii H, Firouzi F, Chiani M, Derakhshan F, Tahami A, Aghazadeh R, Daryani NE, Zali MR.

Int J Colorectal Dis. 2011 Jun;26(6):775-81. doi: 10.1007/s00384-011-1145-4. Epub 2011 Jan 28.

PMID:
21274544
5.

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. Epub 2010 Dec 12.

6.

Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience.

Strisciuglio C, Auricchio R, Martinelli M, Staiano A, Giugliano FP, Andreozzi M, De Rosa M, Giannetti E, Gianfrani C, Izzo P, Troncone R, Miele E.

Dig Liver Dis. 2014 Jun;46(6):512-7. doi: 10.1016/j.dld.2014.02.016. Epub 2014 Mar 19.

PMID:
24656308
7.

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
8.

Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.

Török HP, Glas J, Endres I, Tonenchi L, Teshome MY, Wetzke M, Klein W, Lohse P, Ochsenkühn T, Folwaczny M, Göke B, Folwaczny C, Müller-Myhsok B, Brand S.

Am J Gastroenterol. 2009 Jul;104(7):1723-33. doi: 10.1038/ajg.2009.184. Epub 2009 May 19.

PMID:
19455129
9.

CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins.

Halfvarson J, Bresso F, D'Amato M, Järnerot G, Pettersson S, Tysk C.

Dig Liver Dis. 2005 Oct;37(10):768-72.

PMID:
16002353
10.

[NOD2 gene mutation in Moroccan patients with Crohn's disease: prevalence, genotypic study and correlation of NOD2 gene mutation with the phenotype of Crohn's disease].

Tamzaourte M, Errabih I, Krami H, Maha F, Maria L, Benzzoubeir N, Ouazzani L, Sefiani A, Ouazzani H.

Pan Afr Med J. 2017 Jun 14;27:116. doi: 10.11604/pamj.2017.27.116.9187. eCollection 2017. French.

11.

Genetic studies of Crohn's disease: past, present and future.

Liu JZ, Anderson CA.

Best Pract Res Clin Gastroenterol. 2014 Jun;28(3):373-86. doi: 10.1016/j.bpg.2014.04.009. Epub 2014 May 6. Review.

12.

CARD15/NOD2, CD14 and toll-like 4 receptor gene polymorphisms in Saudi patients with Crohn's Disease.

Azzam N, Nounou H, Alharbi O, Aljebreen A, Shalaby M.

Int J Mol Sci. 2012;13(4):4268-80. doi: 10.3390/ijms13044268. Epub 2012 Apr 2.

13.

Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.

Bianchi V, Maconi G, Ardizzone S, Colombo E, Ferrara E, Russo A, Tenchini ML, Porro GB.

Eur J Gastroenterol Hepatol. 2007 Mar;19(3):217-23.

PMID:
17301648
14.

A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasis.

Young C, Allen MH, Cuthbert A, Ameen M, Veal C, Leman J, Burden AD, Kirby B, Griffiths CE, Trembath RC, Mathew CG, Barker JN.

Exp Dermatol. 2003 Aug;12(4):506-9.

PMID:
12930309
15.

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
16.

Gastroduodenal Crohn's disease is associated with NOD2/CARD15 gene polymorphisms, particularly L1007P homozygosity.

Mardini HE, Gregory KJ, Nasser M, Selby L, Arsenescu R, Winter TA, de Villiers WJ.

Dig Dis Sci. 2005 Dec;50(12):2316-22.

PMID:
16416181
17.

NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Lacher M, Helmbrecht J, Schroepf S, Koletzko S, Ballauff A, Classen M, Uhlig H, Hubertus J, Hartl D, Lohse P, von Schweinitz D, Kappler R.

J Pediatr Surg. 2010 Aug;45(8):1591-7. doi: 10.1016/j.jpedsurg.2009.10.046.

PMID:
20713205
18.

Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.

Christodoulou K, Wiskin AE, Gibson J, Tapper W, Willis C, Afzal NA, Upstill-Goddard R, Holloway JW, Simpson MA, Beattie RM, Collins A, Ennis S.

Gut. 2013 Jul;62(7):977-84. doi: 10.1136/gutjnl-2011-301833. Epub 2012 Apr 28.

19.

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.

Ellinghaus D, Zhang H, Zeissig S, Lipinski S, Till A, Jiang T, Stade B, Bromberg Y, Ellinghaus E, Keller A, Rivas MA, Skieceviciene J, Doncheva NT, Liu X, Liu Q, Jiang F, Forster M, Mayr G, Albrecht M, Häsler R, Boehm BO, Goodall J, Berzuini CR, Lee J, Andersen V, Vogel U, Kupcinskas L, Kayser M, Krawczak M, Nikolaus S, Weersma RK, Ponsioen CY, Sans M, Wijmenga C, Strachan DP, McArdle WL, Vermeire S, Rutgeerts P, Sanderson JD, Mathew CG, Vatn MH, Wang J, Nöthen MM, Duerr RH, Büning C, Brand S, Glas J, Winkelmann J, Illig T, Latiano A, Annese V, Halfvarson J, D'Amato M, Daly MJ, Nothnagel M, Karlsen TH, Subramani S, Rosenstiel P, Schreiber S, Parkes M, Franke A.

Gastroenterology. 2013 Aug;145(2):339-47. doi: 10.1053/j.gastro.2013.04.040. Epub 2013 Apr 25.

20.

Epistatic interaction between TLR4 and NOD2 in patients with Crohn's Disease: relation with risk and phenotype in a Spanish cohort.

Martinez-Chamorro A, Moreno A, Gómez-García M, Cabello MJ, Martin J, Lopez-Nevot MÁ.

Immunobiology. 2016 Sep;221(9):927-33. doi: 10.1016/j.imbio.2016.05.015. Epub 2016 May 28.

PMID:
27290609

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