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Dive into the research topics where Richard James Lewis is active.

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Featured researches published by Richard James Lewis.


Venoms to Drugs: Venom as a Source for the Development of Human Therapeutics | 2015

CHAPTER 3:Venoms-Based Drug Discovery: Proteomic and Transcriptomic Approaches

Sébastien Dutertre; Eivind Ab Undheim; Sandy S. Pineda; Ai-Hua Jin; Vincent Lavergne; Bryan G. Fry; Richard James Lewis; Paul F. Alewood; Glenn F. King

Modern proteomic and transcriptomic approaches have revolutionised our understanding of the chemical diversity of animal venoms. Moreover, recent studies have highlighted the value of combining these approaches (for example, by combining mass spectrometry derived sequence tags with deep sequencing information). These approaches are allowing more rapid deconvolution of hit venoms, as well as identification of orthologues/paralogues of lead molecules with potentially useful variations in activity. The aim of this chapter is to demonstrate the impact of modern proteomic and transcriptomic approaches on venoms-based drug discovery and to discuss their likely impact in future years.


Archive | 2013

CHAPTER 7:Peptide Therapeutics from Venomous Creatures

Vincent Lavergne; Glenn F. King; Richard James Lewis; Paul F. Alewood

Venomous animals have evolved sophisticated strategies for prey capture, defence and competitor deterrence. Their venom is a complex chemical cocktail of salts, small molecules, peptide toxins and enzymes. The extraordinary richness and diversity of bioactive venom peptides, which have evolved primarily to act on the nervous systems of heterologous species from various taxa, makes them an attractive source of molecular probes for studying the pharmacology of ion channels and receptors as well as templates for the design of therapeutics for pain management. This chapter provides an overview of venom peptides that are already used as antinociceptive drugs or which are undergoing clinical trials and preclinical studies, with a particular emphasis on their structure, function and pharmacology.


Journal of Biological Chemistry | 2002

Solution structure of μ-conotoxin PIIIA, a preferential inhibitor of persistent tetrodotoxin-sensitive sodium channels

Katherine J. Nielsen; Michael Watson; David J. Adams; Anna K. Hammarström; Peter W. Gage; Justine M. Hill; David J. Craik; Linda Thomas; Denise Adams; Paul F. Alewood; Richard James Lewis


Archive | 2003

Novel x-conotoxin peptides (-ii)

Richard James Lewis; Paul F. Alewood; Dianne Alewood; Elka Palant


Archive | 2014

Dinoflagellate Toxins: An Overview

Michael J. Holmes; Andreas Brust; Richard James Lewis


Archive | 2003

Type II chi-conotoxin peptides (noradrenaline transporter inhibitors)

Richard James Lewis; Paul F. Alewood; Dianne Alewood; Elka Palant


Archive | 2003

NOVEL χ-CONOTOXIN PEPTIDES (-II)

Richard James Lewis; Paul F. Alewood; Dianne Alewood; Elka Palant


Archive | 2004

NOVEL mu-CONOTOXIN PEPTIDES

Richard James Lewis; Roger Drinkwater; Denise Adams; Katherine J. Nielsen; Jenny Ekberg


Archive | 2003

χ-conotoxin peptides (-1)

Richard James Lewis; Paul F. Alewood; Dianne Alewood; Elka Palant


Archive | 2017

PEPTIDES DE VENIN D'ARAIGNÉE ET PROCÉDÉS D'UTILISATION POUR MODULER LES CANAUX SODIQUES.

Paul F. Alewood; Zoltan Dekan; Jennifer R. Deuis; Richard James Lewis; Irina Vetter

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Andreas Brust

University of Queensland

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Denise Adams

Australian National University

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Glenn F. King

University of Queensland

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Iain A. Sharpe

University of Queensland

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Irina Vetter

University of Queensland

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Bryan G. Fry

Biotechnology Institute

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