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Journal of Inherited Metabolic Disease
|
January 1, 1994
Modifying exogenous glucocerebrosidase for effective replacement therapy in Gaucher disease
R O Brady, G J Murray, N W Barton
The Biochemical Journal
|
November 1, 1979
Lectin-binding proteins in central-nervous-system myelin. Detection of glycoproteins of purified myelin on polyacrylamide gels by [3h]concanavalin A binding
L J McIntyre, R H Quarles, R O Brady
Life Sciences
|
October 1, 1974
Evolution of enzyme replacement therapy for lipid storage diseases
R O Brady, A E Gal, P G Pentchev
Journal of Neurochemistry
|
August 1, 1973
Evidence that the major protein in rat sciatic nerve myelin is a glycoprotein
J L Everly, R O Brady, R H Quarles
Birth Defects Original Article Series
|
January 1, 1980
Access of enzymes to brain following osmotic alteration of the blood-brain barrier
J A Barranger, S I Rapoport, R O Brady
Federation Proceedings
|
April 1, 1975
Investigations in enzyme replacement therapy in lipid storage diseases
R O Brady, P G Pentchev, A G Gal
Biochemistry
|
January 13, 1976
A comparison of membrane glycoconjugates from mouse cells transformed by murine and primate RNA sarcoma viruses
P H Fishman, R O Brady, S T Aaronson
The New England Journal of Medicine
|
May 27, 1993
Treatment of Gaucher's disease
N W Barton, R O Brady, J M Dambrosia
Progress in Liver Diseases
|
January 1, 1982
The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features
R O Brady, S P James, J A Barranger
Biochemical and Biophysical Research Communications
|
May 14, 1980
Factors that influence the uptake of beta-hexosaminidase A by rat peritoneal macrophages
J W Kusiak, J M Quirk, R O Brady
Page
of 36
Search research articles
Search
Showing results (81-90 of 352) with videos related to
Sort By:
Page
of 36
Journal of Inherited Metabolic Disease
|
January 1, 1994
Modifying exogenous glucocerebrosidase for effective replacement therapy in Gaucher disease
R O Brady, G J Murray, N W Barton
The Biochemical Journal
|
November 1, 1979
Lectin-binding proteins in central-nervous-system myelin. Detection of glycoproteins of purified myelin on polyacrylamide gels by [3h]concanavalin A binding
L J McIntyre, R H Quarles, R O Brady
Life Sciences
|
October 1, 1974
Evolution of enzyme replacement therapy for lipid storage diseases
R O Brady, A E Gal, P G Pentchev
Journal of Neurochemistry
|
August 1, 1973
Evidence that the major protein in rat sciatic nerve myelin is a glycoprotein
J L Everly, R O Brady, R H Quarles
Birth Defects Original Article Series
|
January 1, 1980
Access of enzymes to brain following osmotic alteration of the blood-brain barrier
J A Barranger, S I Rapoport, R O Brady
Federation Proceedings
|
April 1, 1975
Investigations in enzyme replacement therapy in lipid storage diseases
R O Brady, P G Pentchev, A G Gal
Biochemistry
|
January 13, 1976
A comparison of membrane glycoconjugates from mouse cells transformed by murine and primate RNA sarcoma viruses
P H Fishman, R O Brady, S T Aaronson
The New England Journal of Medicine
|
May 27, 1993
Treatment of Gaucher's disease
N W Barton, R O Brady, J M Dambrosia
Progress in Liver Diseases
|
January 1, 1982
The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features
R O Brady, S P James, J A Barranger
Biochemical and Biophysical Research Communications
|
May 14, 1980
Factors that influence the uptake of beta-hexosaminidase A by rat peritoneal macrophages
J W Kusiak, J M Quirk, R O Brady
Page
of 36