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Benjamin Haley
Researcher at Genentech
Publications - 81
Citations - 10702
Benjamin Haley is an academic researcher from Genentech. The author has contributed to research in topics: RNA interference & Biology. The author has an hindex of 33, co-authored 69 publications receiving 8718 citations. Previous affiliations of Benjamin Haley include University of California, Berkeley & University of Massachusetts Medical School.
Papers
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Journal ArticleDOI
Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
Nobuhiko Kayagaki,Irma B. Stowe,Bettina L. Lee,Karen O'Rourke,Keith R. Anderson,Søren Warming,Trinna L. Cuellar,Benjamin Haley,Merone Roose-Girma,Qui T. Phung,Peter Liu,Jennie R. Lill,Hong Li,Jiansheng Wu,Sarah K. Kummerfeld,Juan Zhang,Wyne P. Lee,Scott J. Snipas,Guy S. Salvesen,Lucy X. Morris,Linda Fitzgerald,Yafei Zhang,Edward M. Bertram,Christopher C. Goodnow,Christopher C. Goodnow,Christopher C. Goodnow,Vishva M. Dixit +26 more
TL;DR: It is shown that gasdermin D is essential for caspase-11-dependent pyroptosis and interleukin-1β maturation and a key mediator of the host response against Gram-negative bacteria.
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Ribo-gnome: the big world of small RNAs
Phillip D. Zamore,Benjamin Haley +1 more
TL;DR: Fifteen years after the discovery of RNA silencing, the authors are only just beginning to understand the depth and complexity of how these RNAs regulate gene expression and to consider their role in shaping the evolutionary history of higher eukaryotes.
Journal ArticleDOI
ATP requirements and small interfering RNA structure in the RNA interference pathway.
TL;DR: It is suggested that the RNAi reaction comprises at least four sequential steps: ATP-dependent processing of double-stranded RNA into small interfering RNAs (siRNAs), incorporation of siRNAs into an inactive approximately 360 kDa protein/RNA complex, ATP- dependent unwinding of the siRNA duplex to generate an active complex, and ATP-independent recognition and cleavage of the RNA target.
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A protein sensor for siRNA asymmetry.
TL;DR: In Drosophila, R2D2 is both a protein sensor for siRNA thermodynamic asymmetry and a licensing factor for entry of authentic siRNAs into the RNAi pathway.
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Evidence that siRNAs function as guides, not primers, in the Drosophila and human RNAi pathways
TL;DR: The in vitro data suggest that in both flies and mammals, each siRNA guides endonucleolytic cleavage of the target RNA at a single site, and that RNA-dependent RNA polymerases are not required for RNAi in these organisms.