Literature DB >> 21783421

From genome-wide association studies to etiology: probing autoimmunity genes by RNAi.

Stephan Kissler1.   

Abstract

Autoimmunity cannot yet be prevented or cured, in large part due to our poor understanding of disease etiology. Remarkable advances in genomic technology have recently enabled the discovery of a large number of disease-associated gene variations by genome-wide association studies. The next step towards understanding autoimmune disorders entails the functional study of susceptibility genes within experimental disease models. RNA interference (RNAi) is a promising tool for such investigations. Several features of RNAi, including its specificity, versatility and reversible nature, allow experimental systems to be tailored to relevant gene variations. This review discusses how the experimental use of RNAi is invaluable in bridging the gap between the identification of susceptibility genes and the elucidation of their functional contribution to autoimmune disease.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21783421     DOI: 10.1016/j.molmed.2011.06.006

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  2 in total

Review 1.  Everything is autoimmune until proven otherwise.

Authors:  Yehuda Shoenfeld
Journal:  Clin Rev Allergy Immunol       Date:  2013-10       Impact factor: 8.667

2.  The autoimmunity-associated gene RGS1 affects the frequency of T follicular helper cells.

Authors:  C Caballero-Franco; S Kissler
Journal:  Genes Immun       Date:  2016-03-31       Impact factor: 2.676

  2 in total

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