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Science,
2002]
The nematode worm known as Caenorhabditis elegans is not much to look at. Just a millimeter long and transparent to boot, it is almost invisible to the naked eye. But in biological research the tiny worm looms large, providing a model system for studying everything from embryonic development to aging. Now, three researchers who pioneered the use of C. elegans as a model organism have won the Nobel Prize in Physiology or Medicine.
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[
Discover,
1991]
Undulating under the microscope, its muscle and nerve cells visible within its transparent body, the tiny roundworm Caenorhabditis elegans is normally a creature of surprising grace. But one mutant strain is not elegans at all. It thrashes about in such an uncoordinated fashion that researchers have dubbed the mutant worm "unc"...
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Nature,
1992]
Dissecting the sex life of the nematode worm Caenorhabditis elegans has already provided surprises for biologists interested in life-history theory. In a report on page 456 of this issue, Van Voorhies throws another spanner in the works by demonstrating that the costs of producing sperm are not as negligible as we might have thought.
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[
Nature,
1996]
During the development of many, if not all, complex organisms, specific cells are marked out for elimination in a process known as programmed cell death, or apoptosis, a form of cell suicide. For example, during the development of the hermaphrodite nematode worm Caenorhabditis elegans, 131 of the 1,090 cells produced are genetically destined to die. Drosophila embryos without the necessary genes to execute this death programme do not survive. In vertebrates, failure to delete malformed or potentially autoreactive immune cells during development can eventually lead to autoimmunity or leukaemia. So too much or too little cell death threatens the whole organism.
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Nature,
2003]
The genome of the microscopic worm Caenorhabditis briggsae has been sequenced, and show some remarkable differences from the genome of the better known - and physically similar - C. elegans.
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[
Science,
1990]
Can a lowly worm help neurobiologists untangle the pathology of Alzheimer's, Huntington's, Parkinson's, and other human brain diseases? That surprising question kept cropping up at a recent Dahlem conference on degenerative brain disorders. Although progress has been made toward understanding those disorders, conference participants had to conclude that they don't yet know nearly enough about how brain cells die. And that's where the lowly worm may
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Science,
1997]
A gene that helps control the life-span of the nematode C. elegans encodes the worm version of the insulin receptor, thereby providing a possible link between aging and glucose metabolism.
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Nature,
1997]
Who scapes the lurking sepent's mortal sting? Not he that sets his foot upon her back. Even the smallest of worms will turn, when trodden on.
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Nat Neurosci,
2001]
A characterization of C. elegans lacking the gene for Rim suggests that this protein may be involved in pruning synaptic vesicles for fusion, not in docking or organizing active zones.
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[
Science,
1991]
The millimeter-long roundworm Caenorhabditis elegans is amassing a sizable research following. As more and more people have joined teh confederation of research efforts loosely called the worm project (see Science, 15 June 1990, p. 1310), the community's biennial meeting has outgrown the traditional watering hole at Cold Spring Harbor. This year, the researchers moved inland for the Eighth International C. elegans Meeting, held June 1-5 on Lake Mendota at the University of Wisconsin, Madison. More than 500 "worm people" turned out to absorb progress reports on the sequencing of the C. elegans genome, the study of its developmental pathways-and some newer topics as well.