Addison V. Wright
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Addison V. Wright has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Jennifer A. Doudna
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA
2 shared publications - Eva Nogales
Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA
1 shared publication - Gavin John Knott
Monash University
1 shared publication - Jun-Jie Gogo Liu
Beijing Frontier Research Center for Biological Structure Beijing Advanced Innovation Center for Structural Biology Center for Life Sciences School of Life Sciences State Key Laboratory of Membrane Biology Tsinghua-Peking Tsinghua University 100084 Beijing China
1 shared publication - Kevin W. Doxzen
Biophysics Graduate Group, University of California, Berkeley, Berkeley, CA 94720, USA
1 shared publication - Luciano A. Marraffini
Laboratory of Bacteriology, The Rockefeller University, New York, NY, USA
1 shared publication
Latest Publications
- 1 February 2019
- Published by Elsevier in Cell Host & Microbe
- Vol. 25 (2) , 242-249.e3
Spacer Acquisition Rates Determine the Immunological Diversity of the Type II CRISPR-Cas Immune Response
- 1 February 2019
- Published by Elsevier in Cell Host & Microbe
- Vol. 25 (2) , 242-249.e3
Spacer Acquisition Rates Determine the Immunological Diversity of the Type II CRISPR-Cas Immune Response
- 15 September 2017
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 357 (6356) , 1113-1118
Structures of the CRISPR genome integration complex
The CRISPR integration complex relies on structural features of DNA to achieve site-selective CRISPR array expansion.
- 15 September 2017
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 357 (6356) , 1113-1118
Structures of the CRISPR genome integration complex
The CRISPR integration complex relies on structural features of DNA to achieve site-selective CRISPR array expansion.