Contribution of the Unfolded Protein Response (UPR) to the Pathogenesis of Proteasome-Associated Autoinflammatory Syndromes (PRAAS)

Type I interferonopathies cover a phenotypically heterogeneous group of rare genetic diseases including the recently described proteasome-associated autoinflammatory syndromes (PRAAS). By definition, PRAAS are caused by inherited and/or de novo loss-of-function mutations in genes encoding proteasome...

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Detaylı Bibliyografya
Yayımlandı:Front Immunol
Asıl Yazarlar: Ebstein, Frédéric, Poli Harlowe, María Cecilia, Studencka-Turski, Maja, Krüger, Elke
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2019
Konular:
Immunology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6890838/
https://ncbi.nlm.nih.gov/pubmed/31827472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.02756
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