|School||UCSF School of Medicine|
|Department||Cellular & Molecular Pharmacology|
|Address||1700 4th Street|
San Francisco CA 94158
|University of Regina||2012||Distinguished Alumni Award|
|W. M. Keck Foundation||2009
||2014||Keck Distinguished Young Scholar|
|Sciencewatch.com||2008||Top 25 authors of high-impact papers in molecular biology and genetics from 2002 to 2006 |
|University of Toronto||2005||L. W. Macpherson Microbiology Award|
|University of Toronto||2004||Hannah Farkas-Himsley and Alexander Memorial Award|
|Canadian Institute of Health Research||2001
||2004||CIHR Doctoral Fellowship |
|Natural Sciences and Engineering Research Council ||1999
||2001||PGS-B Award |
|Society of Chemical Industry ||1997||Merit Award|
|Canadian Cancer Society ||1995
Dr. Krogan was born and raised in Regina, Saskatchewan, Canada and obtained his undergraduate degree from the University of Regina. As a graduate student at the University of Toronto, Dr. Krogan led a project that systematically identified protein complexes in the model organism, Saccharomyces cerevisiae, through an affinity tagging-purification/mass spectrometry strategy. This work led to the characterization of 547 complexes, comprising over 4000 proteins, and represents the most comprehensive protein-protein interaction map to date in any organism. To complement this physical interaction data, Dr. Krogan developed an approach, termed E-MAP (or epistatic miniarray profile), which allows for high-throughput generation and quantitative analysis of genetic interaction data. Dr. Krogan’s lab at UCSF focuses on applying these global proteomic and genomic approaches to formulate hypotheses about various biological processes, including transcriptional regulation, DNA repair/ replication and RNA processing. His lab at UCSF is now developing and applying methodologies to create genetic and physical interactions between pathogenic organisms, including HIV, Mtb, and Dengue, and their hosts, which is providing insight into the human pathways and complexes that are being hijacked during the course of infection.
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