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Birth Defects Original Article Series
|
January 1, 1980
Status of enzyme replacement therapy for Gaucher disease
R O Brady, J A Barranger, A E Gal, 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.
Biochemical and Biophysical Research Communications
|
August 14, 1978
Studies of lysosomal function: I. Metabolism of some complex lipids by isolated hepatocytes and Kupffer cells
J A Barranger, P G Pentchev, F S Furbish, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 16, 1977
A practical chromogenic procedure for the diagnosis of Krabbe's disease
A E Gal, R O Brady, P G Pentchev, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1978
Factors that influence the uptake and turnover of glucocerebrosidase and alpha-galactosidase in mammalian liver
P G Pentchev, J W Kusiak, J A Barranger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1981
Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrier
E A Neuwelt, J A Barranger, R O Brady, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1982
Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease
E I Ginns, R O Brady, S Pirruccello, et al.
The Journal of Biological Chemistry
|
March 10, 1982
Enhanced macrophage uptake of synthetically glycosylated human placental beta-glucocerebrosidase
T W Doebber, M S Wu, R L Bugianesi, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Birth Defects Original Article Series
|
January 1, 1980
Status of enzyme replacement therapy for Gaucher disease
R O Brady, J A Barranger, A E Gal, 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.
Biochemical and Biophysical Research Communications
|
August 14, 1978
Studies of lysosomal function: I. Metabolism of some complex lipids by isolated hepatocytes and Kupffer cells
J A Barranger, P G Pentchev, F S Furbish, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 16, 1977
A practical chromogenic procedure for the diagnosis of Krabbe's disease
A E Gal, R O Brady, P G Pentchev, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1978
Factors that influence the uptake and turnover of glucocerebrosidase and alpha-galactosidase in mammalian liver
P G Pentchev, J W Kusiak, J A Barranger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1981
Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrier
E A Neuwelt, J A Barranger, R O Brady, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1982
Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease
E I Ginns, R O Brady, S Pirruccello, et al.
The Journal of Biological Chemistry
|
March 10, 1982
Enhanced macrophage uptake of synthetically glycosylated human placental beta-glucocerebrosidase
T W Doebber, M S Wu, R L Bugianesi, et al.
Page
of 2