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注意：仅列出部分参考文献，下载原文获取全部文献信息。Search and Insights into Novel Genetic Alterations Leading to Classical and Atypical Werner Syndrome
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Model of human aging: Recent findings on Werner's and Hutchinson-Gilford progeria syndromes
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Increased chromosome instability and accumulation of DNA double-strand breaks in Werner syndrome cells
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Alterations in mitosis and cell cycle progression caused by a mutant lamin A known to accelerate human aging
Thomas Dechat et al.
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Human laminopathies: nuclei gone genetically awry
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Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci
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Werner protein protects nonproliferating cells from oxidative DNA damage
AM Szekely et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome
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EXPERIMENTAL CELL RESEARCH (2004)
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