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Vol. 15, No. 22, pp. 2922-2933, November 15, 2001
Howard Hughes Medical Institute and Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9050, USA
| The first 100 words of the full text of this article appear below. |
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Introduction |
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The initial insight into the genetic basis of
apoptosis, or programmed cell death, was gained from ingenious studies
of the roundworm Caenorhabditis elegans (for review, see
Horvitz 1999
). These studies revealed a linear pathway whereby the
products of two genes, designated Ced-3 and Ced-4,
were necessary and sufficient to trigger the perfectly timed and
orchestrated death of 131 preordained cells during development. The
relevance of this pathway to higher animals was established by the
discovery of apparent mammalian orthologs of these genes and the
demonstration that the mammalian Ced-3-related genes encode
proteases (designated caspases) whose activities are responsible
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