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The Journal of Biological Chemistry
|
October 25, 1981
The mannose 6-phosphate receptor of Chinese Hamster ovary cells. Isolation of mutants with altered receptors
A R Robbins, R Myerowitz, R J Youle, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease
N W Barton, F S Furbish, G J Murray, et al.
Human Gene Therapy
|
July 1, 1995
Retroviral coexpression of a multidrug resistance gene (MDR1) and human alpha-galactosidase A for gene therapy of Fabry disease
Y Sugimoto, I Aksentijevich, G J Murray, et al.
Journal of Immunological Methods
|
March 1, 1991
Gaucher's disease: lack of antibody response in 12 patients following repeated intravenous infusions of mannose terminal glucocerebrosidase
G J Murray, K D Howard, S M Richards, et al.
Biochemical Medicine
|
February 1, 1985
Lectin-specific targeting of beta-glucocerebrosidase to different liver cells via glycosylated liposomes
P K Das, G J Murray, G C Zirzow, et al.
Neurochemical Research
|
February 11, 1999
Delivery, distribution, and neuronal uptake of exogenous mannose-terminal glucocerebrosidase in the intact rat brain
G C Zirzow, O A Sanchez, G J Murray, et al.
Analytical Biochemistry
|
June 1, 1985
Purification of beta-glucocerebrosidase by preparative-scale high-performance liquid chromatography: the use of ethylene glycol-containing buffers for chromatography of hydrophobic glycoprotein enzymes
G J Murray, R J Youle, S E Gandy, et al.
The Journal of Biological Chemistry
|
August 25, 1984
Structure of the N-asparagine-linked oligosaccharide units of human placental beta-glucocerebrosidase
S Takasaki, G J Murray, F S Furbish, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vector
J A Medin, M Tudor, R Simovitch, et al.
Analytical Biochemistry
|
May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies
J M Aerts, W E Donker-Koopman, G J Murray, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
The Journal of Biological Chemistry
|
October 25, 1981
The mannose 6-phosphate receptor of Chinese Hamster ovary cells. Isolation of mutants with altered receptors
A R Robbins, R Myerowitz, R J Youle, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease
N W Barton, F S Furbish, G J Murray, et al.
Human Gene Therapy
|
July 1, 1995
Retroviral coexpression of a multidrug resistance gene (MDR1) and human alpha-galactosidase A for gene therapy of Fabry disease
Y Sugimoto, I Aksentijevich, G J Murray, et al.
Journal of Immunological Methods
|
March 1, 1991
Gaucher's disease: lack of antibody response in 12 patients following repeated intravenous infusions of mannose terminal glucocerebrosidase
G J Murray, K D Howard, S M Richards, et al.
Biochemical Medicine
|
February 1, 1985
Lectin-specific targeting of beta-glucocerebrosidase to different liver cells via glycosylated liposomes
P K Das, G J Murray, G C Zirzow, et al.
Neurochemical Research
|
February 11, 1999
Delivery, distribution, and neuronal uptake of exogenous mannose-terminal glucocerebrosidase in the intact rat brain
G C Zirzow, O A Sanchez, G J Murray, et al.
Analytical Biochemistry
|
June 1, 1985
Purification of beta-glucocerebrosidase by preparative-scale high-performance liquid chromatography: the use of ethylene glycol-containing buffers for chromatography of hydrophobic glycoprotein enzymes
G J Murray, R J Youle, S E Gandy, et al.
The Journal of Biological Chemistry
|
August 25, 1984
Structure of the N-asparagine-linked oligosaccharide units of human placental beta-glucocerebrosidase
S Takasaki, G J Murray, F S Furbish, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vector
J A Medin, M Tudor, R Simovitch, et al.
Analytical Biochemistry
|
May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies
J M Aerts, W E Donker-Koopman, G J Murray, et al.
Page
of 6