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Marion MacFarlane

Researcher at University of Leicester

Publications -  111
Citations -  16072

Marion MacFarlane is an academic researcher from University of Leicester. The author has contributed to research in topics: Apoptosis & Programmed cell death. The author has an hindex of 50, co-authored 98 publications receiving 12811 citations. Previous affiliations of Marion MacFarlane include Thomas Jefferson University & University of Cambridge.

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

Lorenzo Galluzzi, +186 more
TL;DR: The Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives.
Journal Article

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

Lorenzo Galluzzi, +168 more
- 01 Jan 2018 - 
TL;DR: An updated classification of cell death subroutines focusing on mechanistic and essential aspects of the process is proposed, and the utility of neologisms that refer to highly specialized instances of these processes are discussed.
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Distinct Caspase Cascades Are Initiated in Receptor-mediated and Chemical-induced Apoptosis

TL;DR: It is demonstrated that both receptor-induced (CD95 and tumor necrosis factor) and chemical-induced apoptosis result in a similar time-dependent activation of caspases-3, -7, -8, and -9 in Jurkat T cells and human leukemic U937 cells.
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cIAPs Block Ripoptosome Formation, a RIP1/Caspase-8 Containing Intracellular Cell Death Complex Differentially Regulated by cFLIP Isoforms

TL;DR: It is shown that loss of cIAPs promotes the spontaneous formation of an intracellular platform that activates either apoptosis or necroptosis and is argued that the Ripoptosome critically influences the outcome of membrane-bound receptor triggering.
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The Ripoptosome, a Signaling Platform that Assembles in Response to Genotoxic Stress and Loss of IAPs

TL;DR: Ripoptosome as mentioned in this paper contains RIP1, FADD, and caspase-8, and assembles in response to genotoxic stress-induced depletion of XIAP, cIAP1, and CIAP2.