Jeffrey C. Dyason - Concepedia

Author

Jeffrey C. Dyason

Griffith University

Also Known As

J C Dyason, J. C. DYASON, J. C. Dyason, J.C. Dyason, Jeffrey C Dyason, Jeffrey C. Dyason, Jeffrey Dyason

Publications

Citations

H-Index

Concepts

All Affiliations

Griffith University Monash University The University of Melbourne University of St Andrews Czech Academy of Sciences, Institute of Biotechnology

About

Jeffrey C. Dyason is an author at Griffith University specializing in medicine, virology, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	2.9K
2	Biochemistry	10	10	686
3	Natural Sciences	9	9	506
4	Engineering	4	4	268
5	Health Sciences	1	1	22

Jeffrey C. Dyason

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Rational design of potent sialidase-based inhibitors of influenza virus replication Mark von Itzstein, Wen‐Yang Wu, Gaik B. Kok, Nature Rational DesignMedicineAntiviral TherapySynthetic BiologyVirology	1993	1.8K
α-Tocopheryl succinate induces apoptosis by targeting ubiquinone-binding sites in mitochondrial respiratory complex II Lan‐Feng Dong, Philip S. Low, Jeffrey C. Dyason, Oncogene Mitochondrial FunctionBiochemistryMedicineMitochondrial DynamicApoptosis	2008	294
Mitochondrial Targeting of Vitamin E Succinate Enhances Its Pro-apoptotic and Anti-cancer Activity via Mitochondrial Complex II Lan‐Feng Dong, Victoria J.A. Jameson, David Tilly, Journal of Biological Chemistry	2010	200
Sialic acid dependence in rotavirus host cell invasion Thomas Haselhorst, Fiona E. Fleming, Jeffrey C. Dyason, Nature Chemical Biology Molecular VirologyPathogenesisViral PathogenesisVirologyMicrobiology	2008	171
A Study of the Active Site of Influenza Virus Sialidase: An Approach to the Rational Design of Novel Anti-influenza Drugs Mark von Itzstein, Jeffrey C. Dyason, Stuart W. Oliver, Journal of Medicinal Chemistry Bioorganic ChemistryAntiviral DrugChemical BiologyPharmaceutical ChemistryInfluenza Virus Sialidase	1996	116
Lewis-base adducts of Group 11 metal(I) compounds. Part 27. Solid-state phosphorus-31 cross-polarization magic-angle spinning nuclear magnetic resonance, far-infrared, and structural studies on the mononuclear 2 : 1 adducts of triphenylphosphine with copper(I) and gold(I) halides Graham A. Bowmaker, Jeffrey C. Dyason, Peter C. Healy, Journal of the Chemical Society Dalton Transactions Materials ScienceInorganic ChemistryInorganic SynthesisEngineeringPhysics	1987	112
Novel sialic acid derivatives lock open the 150-loop of an influenza A virus group-1 sialidase Santosh Rudrawar, Jeffrey C. Dyason, Marie‐Anne Rameix‐Welti, Nature Communications	2010	108
Lewis-base adducts of Group 1B metal(<scp>I</scp>) compounds. Part 16. Synthesis, structure, and solid-state phosphorus-31 nuclear magnetic resonance spectra of some novel [Cu<sub>4</sub>X<sub>4</sub>L<sub>4</sub>](X = halogen, L = N, P base)‘cubane’ clusters Jeffrey C. Dyason, Peter C. Healy, Lutz M. Engelhardt, Journal of the Chemical Society Dalton Transactions	1985	106
Lewis-base adducts of Group 11 metal(I) compounds. Part 28. Solid-state phosphorus-31 cross-polarization magic-angle spinning nuclear magnetic resonance and structural studies on the mononuclear 3: 1 adducts of triphenylphosphine with copper(I) halides Peter F. Barron, Jeffrey C. Dyason, Peter C. Healy, Journal of the Chemical Society Dalton Transactions Inorganic ChemistryEngineeringBiochemistryPhysicsGroup 11	1987	77
Complexity in Influenza Virus Targeted Drug Design: Interaction with Human Sialidases Leonard M. G. Chavas, Ryuichi Kato, Nobuhiro Suzuki, Journal of Medicinal Chemistry Global SpreadStrain SelectionAntiviral DrugViral Structural ProteinInfluenza Virus Sialidase	2010	68

Page 1