2010 - Member of the National Academy of Sciences
2009 - Fellow of the American Academy of Arts and Sciences
2005 - Fellow of the American Association for the Advancement of Science (AAAS)
1999 - Fellow of John Simon Guggenheim Memorial Foundation
The scientist’s investigation covers issues in Genetics, DNA repair, Molecular biology, Saccharomyces cerevisiae and Homologous recombination. His Genetics and DNA, DNA replication, Telomere, FLP-FRT recombination and Plasmid investigations all form part of his Genetics research activities. His DNA repair research is multidisciplinary, incorporating perspectives in Replication protein A, Gene conversion and Cell biology.
His research in Cell biology intersects with topics in G2-M DNA damage checkpoint, Chromatin, Histone and Histone code. His research integrates issues of DNA damage, Nucleotide excision repair, Double Strand Break Repair, Strand invasion and Rad50 in his study of Molecular biology. His study in Saccharomyces cerevisiae is interdisciplinary in nature, drawing from both Non-homologous end joining, Recombination and RAD52.
Genetics, Saccharomyces cerevisiae, Molecular biology, DNA repair and Homologous recombination are his primary areas of study. Genetics is represented through his Gene conversion, Gene, DNA, Locus and Chromosome research. His work deals with themes such as Recombination, Mutant and Mating type, which intersect with Saccharomyces cerevisiae.
James E. Haber works mostly in the field of Molecular biology, limiting it down to topics relating to DNA mismatch repair and, in certain cases, Heteroduplex, as a part of the same area of interest. His DNA repair research integrates issues from Replication protein A, DNA damage and Cell biology. His study looks at the intersection of Homologous recombination and topics like Meiosis with Ploidy.
James E. Haber spends much of his time researching Cell biology, Homologous recombination, DNA repair, Genetics and Saccharomyces cerevisiae. His Cell biology study combines topics from a wide range of disciplines, such as DNA damage, DNA, Chromatin, Nucleosome and Histone. He works mostly in the field of DNA, limiting it down to topics relating to Gene and, in certain cases, Cancer and Evolutionary biology.
The Homologous recombination study combines topics in areas such as Genome editing, Gene conversion, Computational biology and Homologous chromosome. His research investigates the connection with DNA repair and areas like Checkpoint Kinase 2 which intersect with concerns in Signal transduction, BAG3, Histone acetyltransferase and Histone H3. His work on Budding yeast as part of general Saccharomyces cerevisiae research is frequently linked to Cruciform, thereby connecting diverse disciplines of science.
James E. Haber focuses on Computational biology, Homologous recombination, Genetics, Saccharomyces cerevisiae and DNA repair. His biological study spans a wide range of topics, including Chaperone-mediated autophagy, Genome and Autolysosome. His is involved in several facets of Genetics study, as is seen by his studies on Double Strand Break Repair, Genome editing, Homology directed repair and Non-homologous end joining.
As part of one scientific family, James E. Haber deals mainly with the area of Saccharomyces cerevisiae, narrowing it down to issues related to the Cell biology, and often BAG3. Many of his studies on DNA repair apply to Gene conversion as well. His work in Gene conversion addresses issues such as Sgs1, which are connected to fields such as RecQ helicase, Homologous Recombination Pathway, Molecular biology and DNA.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif.
Autophagy (2021)
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae
Frédéric Pâques;James E. Haber.
Microbiology and Molecular Biology Reviews (1999)
Pan-cancer analysis of whole genomes
Peter J. Campbell;Gad Getz;Jan O. Korbel;Joshua M. Stuart.
(2020)
Saccharomyces Ku70, Mre11/Rad50, and RPA Proteins Regulate Adaptation to G2/M Arrest after DNA Damage
Sang Eun Lee;J.Kent Moore;Allyson Holmes;Keiko Umezu.
Cell (1998)
Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae.
J K Moore;J E Haber.
Molecular and Cellular Biology (1996)
DNA end resection, homologous recombination and DNA damage checkpoint activation require CDK1
Grzegorz Ira;Achille Pellicioli;Alitukiriza Balijja;Xuan Wang;Xuan Wang.
Nature (2004)
Partners and pathwaysrepairing a double-strand break.
James E Haber.
Trends in Genetics (2000)
Sources of DNA Double-Strand Breaks and Models of Recombinational DNA Repair
Anuja Mehta;James E. Haber.
Cold Spring Harbor Perspectives in Biology (2014)
INO80 and γ-H2AX Interaction Links ATP-Dependent Chromatin Remodeling to DNA Damage Repair
Ashby J. Morrison;Jessica Highland;Nevan J. Krogan;Ayelet Arbel-Eden.
Cell (2004)
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