Molecular basis of celiac disease.
By Ludvig M. Sollid. Annual Review of Immunology, 2000
678 citations recorded by the source corpus.
Subfields: Epidemiology, Gastroenterology, Immunology
View Paper: https://www.semanticscholar.org/paper/6149b14e190aa627c889fe9355ef3cce76de8010
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Citations in the corpus
- Wheat seed storage proteins: Advances in molecular genetics, diversity and breeding applications (2014, background): “Strikingly, most of the gluten peptides implicated in 689 CD require modification by the enzyme transglutaminase before they can bind to the 690 disease-predisposing HLA-DQ molecules and trigger T cell responses ( Koning 2003).”
- Proteins from land plants – Potential resources for human nutrition and food security (2013, background): “Plant proteins have also suffered from an unfavourable image with regard to the allergic reactions they cause in 1e2% of the population and the link with coeliac disease from consuming specific proteins from wheat, barley and rye (Mills, Jenkins, Alcocer, & Shewry, 2004; Sollid, 2000).”
- Coeliac disease: dissecting a complex inflammatory disorder (2002, result): “Although the immunogenetic data are less clear regarding the primary disease-susceptibility determinant of the DR4–DQ8 haplotype, most data favour DQ8 (Ref”
- Coordinated induction by IL15 of a TCR-independent NKG2D signaling pathway converts CTL into lymphokine-activated killer cells in celiac disease. (2004, background): “In addition, NKG2D mediated lysis of gluten-specific DQ2- or DQ8-restricted CD4 T cells is well established in the lamina propria (Koning, 2003; of C1R/MIC but not control cells in TCR CD8 CTL lines cultured with 100 U/ml IL2 or 20 ng/ml IL15 and Sollid, 2000), a key pathologic event is a massive ce”
- Celiac disease (2006, background): “Based on the high association between human leukocyte antigens (HLA) and celiac disease (over 95%) [96], it is thought that HLA-DQ2 positive antigen-presenting cells have gliadin peptides toxic to CD4+ T cells.”