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Molecular Biology

D-Index
94
Citations
40475
World Ranking
646
National Ranking
15

Overview

John Silke is affiliated with the Walter and Eliza Hall Institute of Medical Research in Australia. Their work spans multiple fields, primarily focusing on biochemistry, genetics, and molecular biology, with a significant contribution to medicine. Their subfields of study include molecular biology, immunology, oncology, cancer research, and epidemiology.

The main topics in John Silke's research concentrate on cell death mechanisms and regulation, interferon and immune responses, ubiquitin and proteasome pathways, the inflammasome and immune disorders, NF-κB signaling pathways, PARP inhibition in cancer therapy, and immunotherapy and immune responses.

Noteworthy recent publications include:

  • MLKL trafficking and accumulation at the plasma membrane control the kinetics and threshold for necroptosis (2020, Nature Communications)
  • Immunogenic cell death in cancer: targeting necroptosis to induce antitumour immunity (2024, Nature reviews. Cancer)
  • Cell death in chronic inflammation: breaking the cycle to treat rheumatic disease (2020, Nature Reviews Rheumatology)
  • Future Therapeutic Directions for Smac-Mimetics (2020, Cells)
  • An overview of mammalian p38 mitogen-activated protein kinases, central regulators of cell stress and receptor signaling (2020, F1000Research)

John Silke frequently collaborates with several researchers, including:

  • James M. Murphy
  • Holly Anderton
  • Natasha Silke
  • Joanne M. Hildebrand
  • Lorraine A. O'Reilly

Their research is regularly published in venues such as Faculty Opinions - Post-Publication Peer Review of the Biomedical Literature, bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Cell Death and Differentiation, and Cell Death and Disease.

Best Publications

  • Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018

    Lorenzo Galluzzi;Ilio Vitale;Stuart A. Aaronson;John M. Abrams

  • Identification of DIABLO, a Mammalian Protein that Promotes Apoptosis by Binding to and Antagonizing IAP Proteins

    Anne M Verhagen;Paul G Ekert;Paul G Ekert;Miha Pakusch;John Silke

  • IAP Antagonists Target cIAP1 to Induce TNFα-Dependent Apoptosis

    James E. Vince;W. Wei-Lynn Wong;Nufail Khan;Rebecca Feltham

  • Identification and validation of oncogenes in liver cancer using an integrative oncogenomic approach

    Lars. Zender;Mona S. Spector;Wen. Xue;Peer. Flemming

  • The Pseudokinase MLKL Mediates Necroptosis via a Molecular Switch Mechanism

    James M. Murphy;Peter E. Czabotar;Peter E. Czabotar;Joanne M. Hildebrand;Joanne M. Hildebrand;Isabelle S. Lucet

  • Linear ubiquitination prevents inflammation and regulates immune signalling

    Bjã¶rn Gerlach;Stefanie M. Cordier;Anna C. Schmukle;Christoph H. Emmerich;Christoph H. Emmerich

  • Recruitment of the Linear Ubiquitin Chain Assembly Complex Stabilizes the TNF-R1 Signaling Complex and Is Required for TNF-Mediated Gene Induction

    Tobias L. Haas;Christoph H. Emmerich;Christoph H. Emmerich;Bjã¶rn Gerlach;Bjã¶rn Gerlach;Anna C. Schmukle

  • HtrA2 promotes cell death through its serine protease activity and its ability to antagonize inhibitor of apoptosis proteins.

    Anne M Verhagen;John Silke;Paul G Ekert;Paul G Ekert;Miha Pakusch

  • IAPs, RINGs and ubiquitylation

    David L. Vaux;John Silke

  • Apoptosis initiated by Bcl-2-regulated caspase activation independently of the cytochrome c/Apaf-1/caspase-9 apoptosome

    Vanessa S. Marsden;Liam O'Connor;Liam O'Connor;Lorraine A. O'Reilly;John Silke

  • RIPK3 promotes cell death and NLRP3 inflammasome activation in the absence of MLKL

    Kate E. Lawlor;Nufail Khan;Alison Mildenhall;Motti Gerlic

  • RIPK1 regulates RIPK3-MLKL-driven systemic inflammation and emergency hematopoiesis.

    James A Rickard;James A Rickard;Joanne A O'Donnell;Joanne A O'Donnell;Joseph M Evans;Joseph M Evans;Najoua Lalaoui;Najoua Lalaoui

  • Inhibitor of apoptosis proteins limit RIP3 kinase-dependent interleukin-1 activation.

    James E. Vince;W. Wei Lynn Wong;W. Wei Lynn Wong;Ian Gentle;Kate E. Lawlor;Kate E. Lawlor

  • XIAP discriminates between type I and type II FAS-induced apoptosis

    Philipp. Jost;Stephanie. Grabow;Stephanie. Grabow;Daniel. Gray;Mark D. McKenzie;Mark D. McKenzie

  • Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death

    Joanne M. Hildebrand;Maria C. Tanzer;Isabelle S. Lucet;Isabelle S. Lucet;Samuel N. Young

  • AIM2 and NLRP3 inflammasomes activate both apoptotic and pyroptotic death pathways via ASC

    V Sagulenko;S J Thygesen;D P Sester;A Idris

  • The diverse role of RIP kinases in necroptosis and inflammation

    John Silke;James A Rickard;Motti Gerlic

  • The Drosophila caspase DRONC is regulated by DIAP1.

    Pascal Meier;John Silke;Sally J. Leevers;Gerard I. Evan;Gerard I. Evan;Gerard I. Evan

  • The Ubiquitin Ligase XIAP Recruits LUBAC for NOD2 Signaling in Inflammation and Innate Immunity

    Rune Busk Damgaard;Ueli Nachbur;Ueli Nachbur;Ueli Nachbur;Monica Yabal;Wendy Wei-Lynn Wong;Wendy Wei-Lynn Wong

  • The diverse role of RIP kinases in necroptosis and inflammation (vol 16, pg 930, 2016)

    John Silke;James A Rickard;Motti Gerlic

Frequent Co-Authors

David L. Vaux
David L. Vaux Walter and Eliza Hall Institute of Medical Research
James M. Murphy
James M. Murphy Walter and Eliza Hall Institute of Medical Research
Paul G Ekert
Paul G Ekert University of New South Wales
James E. Vince
James E. Vince Walter and Eliza Hall Institute of Medical Research
Andreas Strasser
Andreas Strasser Walter and Eliza Hall Institute of Medical Research
Warren S. Alexander
Warren S. Alexander Walter and Eliza Hall Institute of Medical Research
Andrew I. Webb
Andrew I. Webb Walter and Eliza Hall Institute of Medical Research
Peter E. Czabotar
Peter E. Czabotar Walter and Eliza Hall Institute of Medical Research
Kate E. Lawlor
Kate E. Lawlor Hudson Institute of Medical Research
Marc Pellegrini
Marc Pellegrini Walter and Eliza Hall Institute of Medical Research

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