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Michael A Calderwood, Ph.D.

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Research
The research activities and funding listed below are automatically derived from NIH ExPORTER and other sources, which might result in incorrect or missing items. Faculty can login to make corrections and additions.
  1. R21AI153738 (CALDERWOOD, MICHAEL A) Feb 22, 2021 - Jan 31, 2023
    NIH
    Exploring alternate targets for inhibition of virus infection by PPI disruption
    Role: Principal Investigator
  2. R21HG010934 (CALDERWOOD, MICHAEL A) Sep 1, 2020 - Aug 31, 2022
    NIH
    Development of an OPTogenetic InteractoMics Assay (OPTIMA)
    Role: Principal Investigator
  3. R01GM133185 (VIDAL, MARC) Sep 10, 2019 - Aug 31, 2023
    NIH
    Incomplete Penetrance via Edgetic Suppression
    Role: Co-Principal Investigator
  4. R01GM109199 (CALDERWOOD, MICHAEL A) Aug 1, 2014 - Jul 31, 2019
    NIH
    Functional Profiling of Human Disease Targets
    Role: Principal Investigator
  5. R01HG006061 (VIDAL, MARC) Feb 17, 2011 - Nov 30, 2015
    NIH
    A S. cerevisiae high-coverage high-quality protein-protein binary interactome map
    Role: Principal Investigator

Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Lee S, Sakakibara S, Maruo S, Zhao B, Calderwood MA, Holthaus AM, Lai CY, Takada K, Kieff E, Johannsen E. Epstein-Barr virus nuclear protein 3C domains necessary for lymphoblastoid cell growth: interaction with RBP-Jkappa regulates TCL1. J Virol. 2009 Dec; 83(23):12368-77. PMID: 19776126.
    Citations: 22     Fields:    Translation:HumansCells
  2. Calderwood MA, Holthaus AM, Johannsen E. The Epstein-Barr virus LF2 protein inhibits viral replication. J Virol. 2008 Sep; 82(17):8509-19. PMID: 18562535.
    Citations: 24     Fields:    Translation:HumansCells
  3. Calderwood MA, Venkatesan K, Xing L, Chase MR, Vazquez A, Holthaus AM, Ewence AE, Li N, Hirozane-Kishikawa T, Hill DE, Vidal M, Kieff E, Johannsen E. Epstein-Barr virus and virus human protein interaction maps. Proc Natl Acad Sci U S A. 2007 May 01; 104(18):7606-11. PMID: 17446270.
    Citations: 163     Fields:    Translation:HumansCells
  4. Calderwood M, White RE, Griffiths RA, Whitehouse A. Open reading frame 73 is required for herpesvirus saimiri A11-S4 episomal persistence. J Gen Virol. 2005 Oct; 86(Pt 10):2703-2708. PMID: 16186223.
    Citations: 12     Fields:    Translation:Cells
  5. Calderwood MA, White RE, Whitehouse A. Development of herpesvirus-based episomally maintained gene delivery vectors. Expert Opin Biol Ther. 2004 Apr; 4(4):493-505. PMID: 15102599.
    Citations: 1     Fields:    Translation:HumansCells
  6. Calderwood MA, Hall KT, Matthews DA, Whitehouse A. The herpesvirus saimiri ORF73 gene product interacts with host-cell mitotic chromosomes and self-associates via its C terminus. J Gen Virol. 2004 Jan; 85(Pt 1):147-153. PMID: 14718629.
    Citations: 15     Fields:    Translation:AnimalsCells
  7. White RE, Calderwood MA, Whitehouse A. Generation and precise modification of a herpesvirus saimiri bacterial artificial chromosome demonstrates that the terminal repeats are required for both virus production and episomal persistence. J Gen Virol. 2003 Dec; 84(Pt 12):3393-3403. PMID: 14645920.
    Citations: 25     Fields:    Translation:HumansAnimalsCells
  8. Hall KT, Giles MS, Calderwood MA, Goodwin DJ, Matthews DA, Whitehouse A. The Herpesvirus Saimiri open reading frame 73 gene product interacts with the cellular protein p32. J Virol. 2002 Nov; 76(22):11612-22. PMID: 12388722.
    Citations: 21     Fields:    Translation:AnimalsCells
  9. Hall KT, Giles MS, Goodwin DJ, Calderwood MA, Markham AF, Whitehouse A. Characterization of the herpesvirus saimiri ORF73 gene product. J Gen Virol. 2000 Nov; 81(Pt 11):2653-2658. PMID: 11038376.
    Citations: 14     Fields:    Translation:HumansCells
  10. Goodwin DJ, Hall KT, Giles MS, Calderwood MA, Markham AF, Whitehouse A. The carboxy terminus of the herpesvirus saimiri ORF 57 gene contains domains that are required for transactivation and transrepression. J Gen Virol. 2000 Sep; 81(Pt 9):2253-2265. PMID: 10950983.
    Citations: 17     Fields:    Translation:AnimalsCells
  11. Stevenson AJ, Giles MS, Hall KT, Goodwin DJ, Calderwood MA, Markham AF, Whitehouse A. Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells. Br J Cancer. 2000 Aug; 83(3):329-32. PMID: 10917547.
    Citations: 3     Fields:    Translation:HumansCells
  12. Hall KT, Giles MS, Goodwin DJ, Calderwood MA, Carr IM, Stevenson AJ, Markham AF, Whitehouse A. Analysis of gene expression in a human cell line stably transduced with herpesvirus saimiri. J Virol. 2000 Aug; 74(16):7331-7. PMID: 10906186.
    Citations: 11     Fields:    Translation:HumansAnimalsCells
  13. Calderwood MA. Gastrin Releasing Peptide-Receptor and its Role in Gastrointestinal Tumorigenesis. 1999.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.