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Human Immunology|January 26, 2010
Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeabilityVictorien M Wolters, Behrooz Z Alizadeh, Michel E Weijerman, et al.Epilepsia|May 12, 2006
A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 yearsGerrit-Jan de Haan, Dalila Pinto, Dietbrandt Carton, et al.Journal of Pediatric Gastroenterology and Nutrition|January 6, 2011
Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion diseaseAgata M Szperl, Magdalena R Golachowska, Marcel Bruinenberg, et al.Nature Genetics|November 12, 2005
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defectAlienke J Monsuur, Paul I W de Bakker, Behrooz Z Alizadeh, et al.Nature Genetics|June 15, 2007
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21David A van Heel, Lude Franke, Karen A Hunt, et al.Nature Genetics|March 4, 2008
Newly identified genetic risk variants for celiac disease related to the immune responseKaren A Hunt, Alexandra Zhernakova, Graham Turner, et al.Pageof 2