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pubmed-article:21320717pubmed:abstractTextAllergy, the most common disease of immune dysregulation, has a substantial genetic component that is poorly understood. Although complete disruption of T-cell receptor (TCR) signaling causes profound immunodeficiency, little is known about the consequences of inherited genetic variants that cause partial quantitative decreases in particular TCR-signaling pathways, despite their potential to dysregulate immune responses and cause immunopathology.lld:pubmed
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pubmed-article:21320717pubmed:copyrightInfoCopyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.lld:pubmed
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pubmed-article:21320717pubmed:dateRevised2011-10-10lld:pubmed
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pubmed-article:21320717pubmed:articleTitleDecreased T-cell receptor signaling through CARD11 differentially compromises forkhead box protein 3-positive regulatory versus T(H)2 effector cells to cause allergy.lld:pubmed
pubmed-article:21320717pubmed:affiliationDepartment of Immunology, John Curtin School of Medical Research, Australian National University, Canberra, Australia.lld:pubmed
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