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Spontaneous mutation of the Dock2 gene in Irf5(−/−) mice complicates interpretation of type I interferon production and antibody responses

Genome-wide studies have identified associations between polymorphisms in the IFN regulatory factor-5 (Irf5) gene and a variety of human autoimmune diseases. Its functional role in disease pathogenesis, however, remains unclear, as studies in Irf5(−/−) mice have reached disparate conclusions regardi...

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Main Authors: Purtha, Whitney E., Swiecki, Melissa, Colonna, Marco, Diamond, Michael S., Bhattacharya, Deepta
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 2012
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3326475/
https://ncbi.nlm.nih.gov/pubmed/22431588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1118155109
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