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Sam W. Lee

Researcher at Harvard University

Publications -  148
Citations -  22846

Sam W. Lee is an academic researcher from Harvard University. The author has contributed to research in topics: Cancer & DNA damage. The author has an hindex of 65, co-authored 148 publications receiving 19066 citations. Previous affiliations of Sam W. Lee include University of Michigan & Broad Institute.

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Cellular senescence and organismal ageing in the absence of p21CIP1/WAF1 in ku80−/− mice

TL;DR: The results show that the increased lifespan of ku80−/− MEFs owing to the loss of p21 is not associated with an improvement of the premature ageing phenotypes of kU80/− mice observed at the organismal level.
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The human orthologue of Drosophila ecdysoneless protein interacts with p53 and regulates its function.

TL;DR: The human orthologue of Drosophila melanogaster ecdysoneless (hEcd) is identified as a novel p53-interacting protein that represents a novel regulator of p53 stability and function and the possibility that altered hEcd levels and/or function may contribute to oncogenesis.
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Corrigendum: Selective killing of cancer cells by a small molecule targeting the stress response to ROS.

TL;DR: This corrects the article to show that the method used to derive the H2O2 “spatially aggregating force” is a two-step process, rather than a single step, like in the previous version of this paper.
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Clonal Selection in Malignant Transformation of Human Fibroblasts Transduced with Defined Cellular Oncogenes

TL;DR: The findings indicate that the minimum number of events required for malignant transformation of human fibroblasts is greater than has been enumerated by such oncogene addition strategies and support a stochastic cancer progression model initiated by four defined cellular alterations.
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GAMT joins the p53 network: branching into metabolism.

TL;DR: A role of p53 in coordinating stress response with changes in cellular metabolism would help to bring a better understanding of how cancer cells acquire unique metabolic features to maintain their own survival and proliferation, and might provide interesting clues toward the development of novel therapies.