Robert E. W. Hancock

Hancock in 2016 Robert Ernest William Hancock (born March 23, 1949) is a Canadian microbiologist and University of British Columbia Killam Professor of Microbiology and Immunology, an Associate Faculty Member of the Wellcome Trust Sanger Institute, and a Canada Research Chair in Health and Genomics.

Over his career he has published more than 800 papers and reviews, has 72 patents awarded, and is an ISI highly cited author in Microbiology with more than 113,000 citations and an h-index of 168. He has won several awards and is an Officer of the Order of Canada. He is a co-founder of Migenix, Inimex Pharmaceuticals, ABT Innovations, Sepset Biotherapeutics, and the Centre for Drug Research and Development. He serves as a member of the Scientific Advisory Board for Qu Biologics. Provided by Wikipedia
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  1. 1
    Rethinking the Antibiotic Discovery Paradigm
    by Robert E.W. Hancock
    Published 2015-07-01
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  2. 2
    NtrBC Regulates Invasiveness and Virulence of Pseudomonas aeruginosa During High-Density Infection
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  3. 3
    Synergy between conventional antibiotics and anti-biofilm peptides in a murine, sub-cutaneous abscess model caused by recalcitrant ESKAPE pathogens.
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  4. 4
    Synthetic host defense peptide IDR-1002 reduces inflammation in Pseudomonas aeruginosa lung infection.
    by Kelli C Wuerth, Reza Falsafi, Robert E W Hancock
    Published 2017-01-01
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  5. 5
    Synthetic Peptides to Target Stringent Response-Controlled Virulence in a Pseudomonas aeruginosa Murine Cutaneous Infection Model
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  6. 6
    Reassessing the Host Defense Peptide Landscape
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  7. 7
    Genome-wide identification of genes conferring energy related resistance to a synthetic antimicrobial peptide (Bac8c).
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  8. 8
    Expression of an engineered heterologous antimicrobial peptide in potato alters plant development and mitigates normal abiotic and biotic responses.
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  9. 9
    An Overview of Biological and Computational Methods for Designing Mechanism-Informed Anti-biofilm Agents
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  10. 10
    Exploring the pathophysiology of post-sepsis syndrome to identify therapeutic opportunities
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    Article
  11. 11
    In vivo Anti-inflammatory Activity of Lipidated Peptidomimetics Pam-(Lys-βNspe)6-NH2 and Lau-(Lys-βNspe)6-NH2 Against PMA-Induced Acute Inflammation
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  12. 12
    Critical Assessment of Methods to Quantify Biofilm Growth and Evaluate Antibiofilm Activity of Host Defence Peptides
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  13. 13
    NtrBC Selectively Regulates Host-Pathogen Interactions, Virulence, and Ciprofloxacin Susceptibility of Pseudomonas aeruginosa
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  14. 14
    Treatment of Oral Multispecies Biofilms by an Anti-Biofilm Peptide.
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  15. 15
    Treatment of Oral Biofilms by a D-Enantiomeric Peptide.
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  16. 16
    New Mouse Model for Chronic Infections by Gram-Negative Bacteria Enabling the Study of Anti-Infective Efficacy and Host-Microbe Interactions
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  17. 17
    Overexpression of the Small RNA PA0805.1 in Pseudomonas aeruginosa Modulates the Expression of a Large Set of Genes and Proteins, Resulting in Altered Motility, Cytotoxicity, and Tobramycin Resistance
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  18. 18
    The Pseudomonas aeruginosa autoinducer 3O-C12 homoserine lactone provokes hyperinflammatory responses from cystic fibrosis airway epithelial cells.
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  19. 19
    A novel small RNA is important for biofilm formation and pathogenicity in Pseudomonas aeruginosa.
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  20. 20
    Broad-spectrum anti-biofilm peptide that targets a cellular stress response.
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