149 related articles for article (PubMed ID: 24386489)
1. Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis.
Nijmeijer RM; van Santvoort HC; Zhernakova A; Teller S; Scheiber JA; de Kovel CG; Besselink MG; Visser JT; Lutgendorff F; Bollen TL; Boermeester MA; Rijkers GT; Weiss FU; Mayerle J; Lerch MM; Gooszen HG; Akkermans LM; Wijmenga C;
PLoS One; 2013; 8(12):e85870. PubMed ID: 24386489
[TBL] [Abstract][Full Text] [Related]
2. Replication of genetic variation in the MYO9B gene in Crohn's disease.
Wolters VM; Xu W; Zhao X; Walters TD; Griffiths AM; Silverberg MS; Muise AM
Hum Immunol; 2011 Jul; 72(7):592-7. PubMed ID: 21515326
[TBL] [Abstract][Full Text] [Related]
3. Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.
Wapenaar MC; Monsuur AJ; van Bodegraven AA; Weersma RK; Bevova MR; Linskens RK; Howdle P; Holmes G; Mulder CJ; Dijkstra G; van Heel DA; Wijmenga C
Gut; 2008 Apr; 57(4):463-7. PubMed ID: 17989107
[TBL] [Abstract][Full Text] [Related]
4. Myosin IXb variants and their pivotal role in maintaining the intestinal barrier: a study in Crohn's disease.
Prager M; Durmus T; Büttner J; Molnar T; de Jong DJ; Drenth JP; Baumgart DC; Sturm A; Farkas K; Witt H; Büning C
Scand J Gastroenterol; 2014 Oct; 49(10):1191-200. PubMed ID: 25098938
[TBL] [Abstract][Full Text] [Related]
5. Genetic variation in myosin IXB is associated with ulcerative colitis.
van Bodegraven AA; Curley CR; Hunt KA; Monsuur AJ; Linskens RK; Onnie CM; Crusius JB; Annese V; Latiano A; Silverberg MS; Bitton A; Fisher SA; Steinhart AH; Forbes A; Sanderson J; Prescott NJ; Strachan DP; Playford RJ; Mathew CG; Wijmenga C; Daly MJ; Rioux JD; van Heel DA
Gastroenterology; 2006 Dec; 131(6):1768-74. PubMed ID: 17087940
[TBL] [Abstract][Full Text] [Related]
6. Association between genetic variants in myosin IXB and Crohn's disease.
Cooney R; Cummings JR; Pathan S; Beckly J; Geremia A; Hancock L; Guo C; Morris A; Jewell DP
Inflamm Bowel Dis; 2009 Jul; 15(7):1014-21. PubMed ID: 19235913
[TBL] [Abstract][Full Text] [Related]
7. Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability.
Wolters VM; Alizadeh BZ; Weijerman ME; Zhernakova A; van Hoogstraten IM; Mearin ML; Wapenaar MC; Wijmenga C; Schreurs MW
Hum Immunol; 2010 Apr; 71(4):392-6. PubMed ID: 20096742
[TBL] [Abstract][Full Text] [Related]
8. 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; 27(3):241-8. PubMed ID: 17944996
[TBL] [Abstract][Full Text] [Related]
9. Association analysis of myosin IXB and type 1 diabetes.
Persengiev S; Koeleman BP; Downes K; Valdigem G; van der Slik AR; Eerligh P; Monsuur A; Bruining GJ; Wijmenga C; Todd JA; Roep BO; Alizadeh BZ
Hum Immunol; 2010 Jun; 71(6):598-601. PubMed ID: 20303373
[TBL] [Abstract][Full Text] [Related]
10. Association of MYO9B gene polymorphisms with inflammatory bowel disease in Chinese Han population.
Hu J; Mei Q; Huang J; Hu NZ; Liu XC; Xu JM
World J Gastroenterol; 2014 Jun; 20(23):7466-72. PubMed ID: 24966617
[TBL] [Abstract][Full Text] [Related]
11. Lack of association of MYO9B genetic variants with coeliac disease in a British cohort.
Hunt KA; Monsuur AJ; McArdle WL; Kumar PJ; Travis SP; Walters JR; Jewell DP; Strachan DP; Playford RJ; Wijmenga C; van Heel DA
Gut; 2006 Jul; 55(7):969-72. PubMed ID: 16423886
[TBL] [Abstract][Full Text] [Related]
12. Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort.
Amundsen SS; Vatn M; ; Wijmenga C; Sollid LM; Lie BA
Tissue Antigens; 2006 Sep; 68(3):249-52. PubMed ID: 16948647
[TBL] [Abstract][Full Text] [Related]
13. Myo9B is associated with an increased risk of Barrett's esophagus and esophageal adenocarcinoma.
Menke V; Van Zoest KP; Moons LM; Pot RG; Siersema PD; Kuipers EJ; Kusters JG
Scand J Gastroenterol; 2012 Dec; 47(12):1422-8. PubMed ID: 22954106
[TBL] [Abstract][Full Text] [Related]
14. Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort.
Amundsen SS; Monsuur AJ; Wapenaar MC; Lie BA; Ek J; Gudjónsdóttir AH; Ascher H; Wijmenga C; Sollid LM
Hum Immunol; 2006; 67(4-5):341-5. PubMed ID: 16720215
[TBL] [Abstract][Full Text] [Related]
15. MYO9B gene polymorphisms are associated with the risk of inflammatory bowel diseases.
Wang MJ; Xu XL; Yao GL; Yu Q; Zhu CF; Kong ZJ; Zhao H; Tang LM; Qin XH
Oncotarget; 2016 Sep; 7(37):58862-58875. PubMed ID: 27556856
[TBL] [Abstract][Full Text] [Related]
16. Do MYO9B genetic variants predispose to coeliac disease? An association study in a cohort of South Italian children.
Cirillo G; Di Domenico MR; Corsi I; Gagliardo T; Del Giudice EM; Perrone L; Tolone C
Dig Liver Dis; 2007 Mar; 39(3):228-31. PubMed ID: 17267307
[TBL] [Abstract][Full Text] [Related]
17. A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.
Giordano M; Marano C; Mellai M; Limongelli MG; Bolognesi E; Clerget-Darpoux F; Momigliano-Richiardi P; Greco L
Genes Immun; 2006 Oct; 7(7):606-8. PubMed ID: 16943798
[TBL] [Abstract][Full Text] [Related]
18. Genetic variation and expression levels of tight junction genes identifies association between MAGI3 and inflammatory bowel disease.
Norén E; Almer S; Söderman J
BMC Gastroenterol; 2017 May; 17(1):68. PubMed ID: 28545409
[TBL] [Abstract][Full Text] [Related]
19. A role for myosin IXb, a motor-RhoGAP chimera, in epithelial wound healing and tight junction regulation.
Chandhoke SK; Mooseker MS
Mol Biol Cell; 2012 Jul; 23(13):2468-80. PubMed ID: 22573889
[TBL] [Abstract][Full Text] [Related]
20. Association of MYO9B haplotype with type 1 diabetes.
Santiago JL; Martínez A; Núñez C; de la Calle H; Fernández-Arquero M; de la Concha EG; Urcelay E
Hum Immunol; 2008 Feb; 69(2):112-5. PubMed ID: 18361936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]