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Archives of Biochemistry and Biophysics
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April 1, 1985
Sucrose gradient analysis of phospholipid-activated beta-glucosidase in type 1 and type 2 Gaucher's disease
K O Garrett, E M Prence, R H Glew
The Biochemical Journal
|
August 1, 1986
A kinetic study of the effects of galactocerebroside 3-sulphate on human spleen glucocerebrosidase. Evidence for two activator-binding sites
E M Prence, K O Garrett, R H Glew
The Journal of Cell Biology
|
February 1, 1990
Modulation of the transport of a lysosomal enzyme by PDGF
E M Prence, J M Dong, G G Sahagian
The Journal of Biological Chemistry
|
May 5, 1989
Mechanism for selective secretion of a lysosomal protease by transformed mouse fibroblasts
J M Dong, E M Prence, G G Sahagian
Clinical Pediatrics
|
April 1, 1995
Marked heterogeneity in Niemann-Pick disease, type C. Clinical and ultrastructural findings
M R Natowicz, J M Stoler, E M Prence, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 1, 1985
Lysosomal storage diseases
R H Glew, A Basu, E M Prence, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1988
Mammalian glucocerebrosidase: implications for Gaucher's disease
R H Glew, A Basu, K L LaMarco, et al.
Clinical Chemistry
|
February 1, 1996
Urine sulfatides and the diagnosis of metachromatic leukodystrophy
M R Natowicz, E M Prence, P Chaturvedi, et al.
Journal of Medical Screening
|
January 1, 1997
Heterozygosity for Tay-Sachs and Sandhoff diseases among Massachusetts residents with French Canadian background
E M Prence, C A Jerome, B L Triggs-Raine, et al.
American Journal of Human Genetics
|
April 1, 1995
Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New England
B Triggs-Raine, M Richard, N Wasel, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Archives of Biochemistry and Biophysics
|
April 1, 1985
Sucrose gradient analysis of phospholipid-activated beta-glucosidase in type 1 and type 2 Gaucher's disease
K O Garrett, E M Prence, R H Glew
The Biochemical Journal
|
August 1, 1986
A kinetic study of the effects of galactocerebroside 3-sulphate on human spleen glucocerebrosidase. Evidence for two activator-binding sites
E M Prence, K O Garrett, R H Glew
The Journal of Cell Biology
|
February 1, 1990
Modulation of the transport of a lysosomal enzyme by PDGF
E M Prence, J M Dong, G G Sahagian
The Journal of Biological Chemistry
|
May 5, 1989
Mechanism for selective secretion of a lysosomal protease by transformed mouse fibroblasts
J M Dong, E M Prence, G G Sahagian
Clinical Pediatrics
|
April 1, 1995
Marked heterogeneity in Niemann-Pick disease, type C. Clinical and ultrastructural findings
M R Natowicz, J M Stoler, E M Prence, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 1, 1985
Lysosomal storage diseases
R H Glew, A Basu, E M Prence, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1988
Mammalian glucocerebrosidase: implications for Gaucher's disease
R H Glew, A Basu, K L LaMarco, et al.
Clinical Chemistry
|
February 1, 1996
Urine sulfatides and the diagnosis of metachromatic leukodystrophy
M R Natowicz, E M Prence, P Chaturvedi, et al.
Journal of Medical Screening
|
January 1, 1997
Heterozygosity for Tay-Sachs and Sandhoff diseases among Massachusetts residents with French Canadian background
E M Prence, C A Jerome, B L Triggs-Raine, et al.
American Journal of Human Genetics
|
April 1, 1995
Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New England
B Triggs-Raine, M Richard, N Wasel, et al.
Page
of 3