Gary J. Murray

Medicine · Health Sciences

41h-index6.1kcitations81works0.02yr avg
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Research Topics

Lysosomal Storage Disorders Research(55), Carbohydrate Chemistry and Synthesis(28), Glycosylation and Glycoproteins Research(20), Cellular transport and secretion(17), Trypanosoma species research and implications(13)

Publications81 total

A Treaty Needs a House: Emplacing First Peoples’ A Priori Rights in Wurundjeri Country, Metropolitan Melbourne
2018
Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues
Molecular Genetics and Metabolism·2016· 2 cited
Physiological processes underlying organ injury in alcohol abuse
American Journal of Physiology-Endocrinology and Metabolism·2016· 30 citedOpen Access
Host homeostatic responses to alcohol-induced cellular stress in animal models of alcoholic liver disease
Expert Review of Gastroenterology & Hepatology·2015
Introduction
Advances in experimental medicine and biology·2014
Alcohol Metabolism and Its Implications for Cancer
2011
Use of lissamine rhodamine ceramide trihexoside as a functional assay for alpha-galactosidase A in intact cells
Journal of Lipid Research·2010· 6 citedOpen Access
Lysosomal Disease Network’s “WORLD Symposium 2009”
Molecular Genetics and Metabolism·2008
Skin-impedance in Fabry Disease: A prospective, controlled, non-randomized clinical study
BMC Neurology·2008· 13 citedOpen Access
Prediction of response of mutated alpha-galactosidase A to a pharmacological chaperone
Pharmacogenetics and Genomics·2008· 43 citedOpen Access
Isofagomine increases lysosomal delivery of exogenous glucocerebrosidase
Biochemical and Biophysical Research Communications·2008· 59 citedOpen Access
113. Identification of Fabry disease-causing mutations that are responsive to the pharmacological chaperone AT1001
Molecular Genetics and Metabolism·2008· 1 cited
Screening for pharmacological chaperones in Fabry disease
Biochemical and Biophysical Research Communications·2007· 52 citedOpen Access
Cellular and tissue distribution of intravenously administered agalsidase alfa
Molecular Genetics and Metabolism·2006· 41 citedOpen Access
Image-guided, direct convective delivery of glucocerebrosidase for neuronopathic Gaucher disease
Neurology·2006· 101 cited
Efficient correction of Fabry mice and patient cells mediated by lentiviral transduction of hematopoietic stem/progenitor cells
Gene Therapy·2006· 55 cited
Reexamination of the cysteine residues in glucocerebrosidase
FEBS Letters·2006· 8 citedOpen Access
Long-Term and Sustained Correction of the α-Galactosidase A Deficiency in Fabry Mice and Patient Cells Receiving Lentivirally Transduced Hematopoietic Stem/Progenitor Cells.
Blood·2005· 3 cited
Improved intracellular delivery of glucocerebrosidase mediated by the HIV-1 TAT protein transduction domain
Biochemical and Biophysical Research Communications·2005· 42 cited
Convection perfusion of glucocerebrosidase for neuronopathic Gaucher's disease
Annals of Neurology·2005· 58 cited
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Frequent Co-authors

Roscoe O. Brady(24), Jane M. Quirk(12), Raphael Schiffmann(9), John A. Barranger(8), Edward I. Ginns(7), Johannes M. F. G. Aerts(7), Norman W. Barton(6), J. M. Tager(6), Gregory C. Zirzow(5), Roscoe O. Brady(5), Toshio Ohshima(4), Ashok B. Kulkarni(4), Jeffrey A. Medin(4), Richard J. Youle(4), David M. Neville(4), Wilma E. Donker‐Koopman(4), F S Furbish(3), Pankaj Qasba(3), J. A. Barranger(3), Susan H. Sorrell(3)