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American Journal of Human Genetics
|
June 1, 1993
Phenotype/genotype correlations in Gaucher disease type I: clinical and therapeutic implications
A Sibille, C M Eng, S J Kim, et al.
The Journal of Biological Chemistry
|
July 19, 1996
Proteolytic processing patterns of prosaposin in insect and mammalian cells
T Leonova, X Qi, A Bencosme, et al.
Clinical Genetics
|
May 1, 1985
Glycosphingolipid studies of visceral tissues and brain from type 1 Gaucher disease variants
O Nilsson, G A Grabowski, M D Ludman, et al.
DNA (Mary Ann Liebert, Inc.)
|
October 1, 1988
Gaucher disease type 1: cloning and characterization of a cDNA encoding acid beta-glucosidase from an Ashkenazi Jewish patient
P N Graves, G A Grabowski, R Eisner, et al.
Human Molecular Genetics
|
August 7, 2001
Enzyme therapy for lysosomal acid lipase deficiency in the mouse
H Du, S Schiavi, M Levine, et al.
Biochimica Et Biophysica Acta
|
September 29, 1993
Synthesis and use of novel fluorescent glycosphingolipids for estimating beta-glucosidase activity in vitro in the absence of detergents and subtyping Gaucher disease variants following administration into intact cells
V Agmon, S Cherbu, A Dagan, et al.
Metabolism: Clinical and Experimental
|
March 1, 1988
Abnormalities in lipoprotein metabolism in Gaucher type 1 disease
N A Le, J C Gibson, A Rubinstein, et al.
The Journal of Biological Chemistry
|
January 21, 1994
Analysis of human acid beta-glucosidase by site-directed mutagenesis and heterologous expression
M E Grace, K M Newman, V Scheinker, et al.
Biochemistry
|
May 13, 1999
Conformational and amino acid residue requirements for the saposin C neuritogenic effect
X Qi, K Kondoh, D Krusling, et al.
Molecular Genetics and Metabolism
|
January 25, 2011
Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models
Y H Xu, Y Sun, H Ran, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 126) with videos related to
Sort By:
Page
of 13
American Journal of Human Genetics
|
June 1, 1993
Phenotype/genotype correlations in Gaucher disease type I: clinical and therapeutic implications
A Sibille, C M Eng, S J Kim, et al.
The Journal of Biological Chemistry
|
July 19, 1996
Proteolytic processing patterns of prosaposin in insect and mammalian cells
T Leonova, X Qi, A Bencosme, et al.
Clinical Genetics
|
May 1, 1985
Glycosphingolipid studies of visceral tissues and brain from type 1 Gaucher disease variants
O Nilsson, G A Grabowski, M D Ludman, et al.
DNA (Mary Ann Liebert, Inc.)
|
October 1, 1988
Gaucher disease type 1: cloning and characterization of a cDNA encoding acid beta-glucosidase from an Ashkenazi Jewish patient
P N Graves, G A Grabowski, R Eisner, et al.
Human Molecular Genetics
|
August 7, 2001
Enzyme therapy for lysosomal acid lipase deficiency in the mouse
H Du, S Schiavi, M Levine, et al.
Biochimica Et Biophysica Acta
|
September 29, 1993
Synthesis and use of novel fluorescent glycosphingolipids for estimating beta-glucosidase activity in vitro in the absence of detergents and subtyping Gaucher disease variants following administration into intact cells
V Agmon, S Cherbu, A Dagan, et al.
Metabolism: Clinical and Experimental
|
March 1, 1988
Abnormalities in lipoprotein metabolism in Gaucher type 1 disease
N A Le, J C Gibson, A Rubinstein, et al.
The Journal of Biological Chemistry
|
January 21, 1994
Analysis of human acid beta-glucosidase by site-directed mutagenesis and heterologous expression
M E Grace, K M Newman, V Scheinker, et al.
Biochemistry
|
May 13, 1999
Conformational and amino acid residue requirements for the saposin C neuritogenic effect
X Qi, K Kondoh, D Krusling, et al.
Molecular Genetics and Metabolism
|
January 25, 2011
Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models
Y H Xu, Y Sun, H Ran, et al.
Page
of 13