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Abstract
Rights: UNKNOWN · cc-by-nc-nd · Source: journal-auto-sync:external:CROSSREF_ISSN
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Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development
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Apaf1 is required for mitochondrial pathways of apoptosis and brain development
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Apoptosis induction by caspase-8 is amplified through the mitochondrial release of cytochrome c
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Membrane oligomerization and cleavage activates the caspase-8 (FLICE/MACHalpha1) death signal
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Caspase cleaved BID targets mitochondria and is required for cytochrome c release, Bcl-XL prevents this release but not tumor necrosis factor R1/Fas Death
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Bid, a Bcl2 interacting protein, mediates cytochrome c release from mitochondria in response to activation of cell surface death receptors
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Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis
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The C. elegans protein EGL-1 is required for programmed cell death and interacts with the Bcl-2-like protein CED-9
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An induced proximity model for caspase-8 activation
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