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PreviewIssue DateTitleAuthor(s)
2017DR5 and caspase-8 are dispensable in ER stress-induced apoptosisGlab, J.; Doerflinger, M.; Nedeva, C.; Jose, I.; Mbogo, G.; Paton, J.; Paton, A.; Kueh, A.; Herold, M.; Huang, D.; Segal, D.; Brumatti, G.; Puthalakath, H.
2016The variable region of pneumococcal pathogenicity island 1 is responsible for unusually high virulence of a serotype 1 isolateHarvey, R.; Trappetti, C.; Mahdi, L.; Wang, H.; McAllister, L.; Scalvini, A.; Paton, A.; Paton, J.; Pirofski, L.
2015Identification of markers that functionally define a quiescent multiple myeloma cell sub-population surviving bortezomib treatmentAdomako, A.; Calvo, V.; Biran, N.; Osman, K.; Chari, A.; Paton, J.; Paton, A.; Moore, K.; Schewe, D.; Aguirre-Ghiso, J.
2012Escherichia coli 83972 expressing a P fimbriae oligosaccharide receptor mimic impairs adhesion of uropathogenic E. coliWatts, R.; Tan, C.; Ulett, G.; Carey, A.; Totsika, M.; Idris, A.; Paton, A.; Morona, R.; Paton, J.; Schembri, M.
2012The Escherichia coli subtilase cytotoxin A subunit specifically cleaves cell-surface GRP78 protein and abolishes COOH-terminal-dependent signalingRay, R.; de Ridder, G.; Eu, J.; Paton, A.; Paton, J.; Pizzo, S.
2012Limitation of individual folding resources in the ER leads to outcomes distinct from the unfolded protein responseEletto, D.; Maganty, A.; Eletto, D.; Dersh, D.; Makarewich, C.; Biswas, C.; Paton, J.; Paton, A.; Doroudgar, S.; Glembotski, C.; Argon, Y.
2014Opposing unfolded-protein-response signals converge on death receptor 5 to control apoptosisLu, M.; Lawrence, D.; Marsters, S.; Acosta-Alvear, D.; Kimmig, P.; Mendez, A.; Paton, A.; Paton, J.; Walter, P.; Ashkenazi, A.
2010Tissue factor-dependent procoagulant activity of subtilase cytotoxin, a potent AB5 toxin produced by shiga toxigenic Escherichia coliWang, H.; Paton, J.; Thorpe, C.; Bonder, C.; Sun, W.; Paton, A.

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