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・ Cynthia Hopkins
・ Cynthia Horner
・ Cynthia Huntington
・ Cynthia II
・ Cynthia in the Wilderness
・ Cynthia Irwin-Williams
・ Cynthia J. Becker
・ Cynthia J. Popp
・ Cynthia Jele
・ Cynthia Jenkins
・ Cynthia Johnson
・ Cynthia Johnston Turner
・ Cynthia Kadohata
・ Cynthia Kauffman
・ Cynthia Kenny
Cynthia Kenyon
・ Cynthia Kereluk
・ Cynthia Khan
・ Cynthia Kirchner
・ Cynthia Klitbo
・ Cynthia Knott
・ Cynthia Koh
・ Cynthia Krupat
・ Cynthia L. Bauerly
・ Cynthia L. Mahoney
・ Cynthia L. Quarterman
・ Cynthia L. Stacey
・ Cynthia Lamontagne
・ Cynthia Lander
・ Cynthia Lawson


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Cynthia Kenyon : ウィキペディア英語版
Cynthia Kenyon

Cynthia Jane Kenyon (born c. 1955) is an American molecular biologist and biogerontologist known for her genetic dissection of aging in a widely used model organism, the roundworm ''Caenorhabditis elegans''.
==Career==
Cynthia Kenyon graduated valedictorian in chemistry and biochemistry from the University of Georgia in 1976. She received her PhD in 1981 from MIT where, in Graham Walker's laboratory, she was the first to look for genes on the basis of their activity profiles, discovering that DNA-damaging agents activate a battery of DNA repair genes in E. coli. She then did postdoctoral studies with Nobel laureate Sydney Brenner at the MRC Laboratory of Molecular Biology in Cambridge, England, studying the development of C. elegans.
Since 1986 she has been at the University of California, San Francisco (UCSF), where she was the Herbert Boyer Distinguished Professor of Biochemistry and Biophysics and is now an American Cancer Society Professor.
In April 2014, Kenyon was named Vice President of Aging Research at Calico, a new company focused on health and well-being. Prior to that, she served as a part-time advisor beginning in November 2013. Kenyon will remain affiliated with UCSF as an emeritus professor.
Her early work led to the discovery that Hox genes, which were known to pattern the body segments of the fruit fly Drosophila, also pattern the body of ''C. elegans''. These findings demonstrated that Hox genes were not simply involved in segmentation, as thought, but instead were part of a much more ancient and fundamental metazoan patterning system.
Michael Klass discovered that lifespan of ''C. elegans'' could be altered by mutations, but Klass believed that the effect was due to reduced food consumption (calorie restriction). Thomas Johnson later showed that the 65% life extension effect was due to the mutation itself rather than due to calorie restriction. In 1993, Dr. Kenyon's discovery that a single-gene mutation (Daf-2) could double the lifespan of ''C. elegans'' and that this could be reversed by a second mutation in daf-16m,〔 sparked an intensive study of the molecular biology of aging. Dr. Kenyon's findings have led to the discovery that an evolutionarily-conserved hormone signaling system influences aging in other organisms, perhaps also including mammals.
Kenyon has received many honors, including the King Faisal Prize for Medicine, the American Association of Medical Colleges Award for Distinguished Research, the Ilse & Helmut Wachter Award for Exceptional Scientific Achievement, and La Fondation IPSEN Prize, for her findings. She is a member of the U.S. National Academy of Sciences and the American Academy of Arts and Sciences. She is now the director of the Hillblom Center for the Biology of Aging at UCSF. She is also one of featured biologists in the 1995 science documentary Death by Design / The Life and Times of Life and Times.

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