Do MYO9B genetic variants predispose to coeliac disease? An association study in a cohort of South Italian children

Digestive and Liver Disease

Volumn 39, Issue 3, 2007, Pages 228-231

  Cirillo, G ^a   Di Domenico, M R ^a   Corsi, I ^a   Gagliardo, T ^a   del Giudice, E M ^a   Perrone, L ^a   Tolone, C ^a  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

Association study; Children; Coeliac disease; MYO9B polymorphism

Indexed keywords

MYOSIN; MYOSIN 9B; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CELIAC DISEASE; CHILD; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; HUMAN; ITALY; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CASE-CONTROL STUDIES; CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; ITALY; MALE; MYOSINS; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33846650943     PISSN: 15908658     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dld.2006.12.009     Document Type: Article

References (17)

1. Alaedini A., and Green P.H. Narrative review: celiac disease: understanding a complex autoimmune disorder. Ann Intern Med 142 (2005) 289-298
2. Ascher H. Paediatric aspects of coeliac disease: old challenges and new ones .... Dig Liver Dis 34 (2002) 216-224
3. Walker-Smith J., Guandalini S., Schmitz J., Schmerling D., and Visakorpi J. Report of working group of European Society of Paediatric Gastroenterology and Nutrition: revised criteria for diagnosis of coeliac disease. Arch Dis Child 65 (1991) 909-911
4. Dieterich W., Ehnis T., Bauer M., Donner P., Volta U., Riecken E.O., et al. Identification of tissue transglutaminase as the autoantigen of celiac disese. Nat Med 3 (1997) 797-801
5. Greco L., Romino R., Coto I., Di Cosmo N., Percopo S., Maglio M., et al. The first large population based twin study of coeliac disease. Gut 50 (2002) 624-628
6. Boniotto M., Braida L., Ventura A., Percopo S., Amoroso A., and Crovella S. Promoter polymorphisms of the CD14 gene in Italian patients with coeliac disease. J Med Genet 40 (2003) e108
7. Martucci S., Biagi F., Di Sabatino A., and Corazza G.R. Coeliac disease. Dig Liver Dis 34 Suppl. 2 (2002) S150-S153
8. van Heel D.A., Hunt K., Greco L., and Wijmenga C. Genetics in coeliac disease. Best Pract Res Clin Gastroenterol 19 (2005) 323-339
9. Van Belzen M.J., Meijer J.W., Sandkuijl L.A., Bardoel A.F., Mulder C.J., Pearson P.L., et al. A major non-HLA locus in celiac disease maps to chromosome 19. Gastroenterology 125 (2003) 1032-1041
10. Babron M.C., Nilsson S., Adamovic S., Naluai A.T., Wahlstrom J., Ascher H., et al. European Genetics Cluster on Coeliac Disease. Meta and pooled analysis of European coeliac disease data. Eur J Hum Genet 11 (2003) 828-834
11. Monsuur A.J., de Bakker P.I., Alizadeh B.Z., Zhernakova A., Bevova M.R., Strengman E., et al. Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defects. Nat Genet 37 (2005) 1341-1344
12. Hunt K.A., Monsuur A.J., McArdle W.L., Kumar P.J., Travis S.P., Walters J.R., et al. Lack of association of MYO9B genetic variants with coeliac disease in a British cohort. Gut 55 (2006) 969-972
13. Amundsen S.S., Monsuur A.J., Wapenaar M.C., Lie B.A., Ek J., Gudjónsdóttir A.H., et al. Association analysis of MYO9B gene polymorphism with celiac disease in a Swedish/Norwegian cohort. Hum Immunol 67 (2006) 341-345
14. Post P.L., Tyska M.J., O'Connell C.B., Johung K., Hayward A., and Mooseker M.S. Myosin-IXb is a single-headed and processive motor. J Biol Chem 277 (2002) 11679-11683
15. Matter K., and Balda M.S. Signalling to and from tight junctions. Nat Rev Mol Cell Biol 4 (2003) 225-236
16. Giordano M., Marano C., Mellai M., Limongelli M.G., Bolognesi E., Clerget-Darpoux F., et al. A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population. Genes Immun 7 (2006) 606-608
17. Hebebrand J., Friedel S., Schäuble N., Geller F., and Hinney A. Perspectives: molecular genetic research in human obesity. Obesity 4 (2003) 139-146