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James E. Haber

Researcher at Brandeis University

Publications -  373
Citations -  48101

James E. Haber is an academic researcher from Brandeis University. The author has contributed to research in topics: DNA repair & Homologous recombination. The author has an hindex of 105, co-authored 354 publications receiving 43655 citations. Previous affiliations of James E. Haber include Pasteur Institute & University of California, Berkeley.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae

Frédéric Pâques, +1 more
- 01 Jun 1999 - 
TL;DR: This review encompasses different aspects of DSB-induced recombination in Saccharomyces and attempts to relate genetic, molecular biological, and biochemical studies of the processes of DNA repair and recombination.
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Pan-cancer analysis of whole genomes

Peter J. Campbell, +1332 more
- 06 Feb 2020 - 
TL;DR: The flagship paper of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium describes the generation of the integrative analyses of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types, the structures for international data sharing and standardized analyses, and the main scientific findings from across the consortium studies.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
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Saccharomyces Ku70, Mre11/Rad50, and RPA Proteins Regulate Adaptation to G2/M Arrest after DNA Damage

Sang Eun Lee, +5 more
- 07 Aug 1998 - 
TL;DR: It is suggested that escape from the DNA damage-induced G2/M checkpoint depends on the extent of ssDNA created at broken chromosome ends and RPA appears to play a key intermediate step in this adaptation.