Modeling Werner Syndrome in Drosophila melanogaster: hyper-recombination in flies lacking WRN-like exonuclease.

Human progeroid Werner syndrome provides the current best model for analysis of human aging, recapitulating many aspects of normal aging as a result of mutation of the WRN gene. This gene encodes a RecQ-type helicase with additional exonuclease activity. While biochemical studies in vitro have prove...

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書目詳細資料
Main Authors: Cox, L, Clancy, D, Boubriak, I, Saunders, R
格式: Journal article
語言:English
出版: 2007