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2. ER stress and distinct outputs of the IRE1α RNase control proliferation and senescence in response to oncogenic Ras. Blazanin N, Son J, Craig-Lucas AB, John CL, Breech KJ, Podolsky MA, Glick AB. Proc Natl Acad Sci U S A; 2017 Sep 12; 114(37):9900-9905. PubMed ID: 28847931 [Abstract] [Full Text] [Related]
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6. A Molecular Mechanism for Turning Off IRE1α Signaling during Endoplasmic Reticulum Stress. Li X, Sun S, Appathurai S, Sundaram A, Plumb R, Mariappan M. Cell Rep; 2020 Dec 29; 33(13):108563. PubMed ID: 33378667 [Abstract] [Full Text] [Related]
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9. PARP16 is a tail-anchored endoplasmic reticulum protein required for the PERK- and IRE1α-mediated unfolded protein response. Jwa M, Chang P. Nat Cell Biol; 2012 Nov 23; 14(11):1223-30. PubMed ID: 23103912 [Abstract] [Full Text] [Related]
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14. Peptides derived from the bifunctional kinase/RNase enzyme IRE1α modulate IRE1α activity and protect cells from endoplasmic reticulum stress. Bouchecareilh M, Higa A, Fribourg S, Moenner M, Chevet E. FASEB J; 2011 Sep 01; 25(9):3115-29. PubMed ID: 21680894 [Abstract] [Full Text] [Related]
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