These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 19142207)

  • 1. MYO9B polymorphisms in multiple sclerosis.
    Kemppinen A; Suvela M; Tienari PJ; Elovaara I; Koivisto K; Pirttilä T; Reunanen M; Rautakorpi I; Hillert J; Lundmark F; Oturai A; Ryder L; Harbo HF; Celius EG; Palotie A; Daly M; Peltonen L; Saarela J
    Eur J Hum Genet; 2009 Jun; 17(6):840-3. PubMed ID: 19142207
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. No evidence of association of the MYO9B polymorphisms with celiac disease in the Spanish population.
    Núñez C; Márquez A; Varadé J; Martínez A; Polanco I; Maluenda C; Fernández-Arquero M; de la Concha EG; Urcelay E
    Tissue Antigens; 2006 Dec; 68(6):489-92. PubMed ID: 17176439
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Lack of Association between MYO9B Gene Polymorphisms and Susceptibility to Coeliac Disease in Caucasians: Evidence from a Meta-Analysis.
    Chen YQ; Zhang L; Lv XY; Wang HZ
    Immunol Invest; 2016 Jul; 45(5):396-405. PubMed ID: 27219348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Polymorphisms in genes encoding leptin, ghrelin and their receptors in German multiple sclerosis patients.
    Rey LK; Wieczorek S; Akkad DA; Linker RA; Chan A; Hoffjan S
    Mol Cell Probes; 2011; 25(5-6):255-9. PubMed ID: 21664965
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations.
    Kristjansdottir G; Sandling JK; Bonetti A; Roos IM; Milani L; Wang C; Gustafsdottir SM; Sigurdsson S; Lundmark A; Tienari PJ; Koivisto K; Elovaara I; Pirttilä T; Reunanen M; Peltonen L; Saarela J; Hillert J; Olsson T; Landegren U; Alcina A; Fernández O; Leyva L; Guerrero M; Lucas M; Izquierdo G; Matesanz F; Syvänen AC
    J Med Genet; 2008 Jun; 45(6):362-9. PubMed ID: 18285424
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.