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American Journal of Human Genetics
|
August 1, 1989
Gaucher disease: molecular heterogeneity and phenotype-genotype correlations
B Theophilus, T Latham, G A Grabowski, et al.
American Journal of Medical Genetics
|
July 11, 1997
Gaucher disease: enzyme therapy in the acute neuronopathic variant
C A Prows, N Sanchez, C Daugherty, et al.
The Biochemical Journal
|
December 7, 2002
Analyses of temporal regulatory elements of the prosaposin gene in transgenic mice
Ying Sun, David P Witte, Peng Jin, et al.
Clinical Genetics
|
February 21, 2007
The effect of enzyme replacement therapy on bone crisis and bone pain in patients with type 1 Gaucher disease
J Charrow, B Dulisse, G A Grabowski, et al.
Journal of Lipid Research
|
August 3, 2005
Gaucher disease mouse models: point mutations at the acid beta-glucosidase locus combined with low-level prosaposin expression lead to disease variants
Ying Sun, Brian Quinn, David P Witte, et al.
Journal of Lipid Research
|
March 10, 2010
Multi-system disorders of glycosphingolipid and ganglioside metabolism
You-Hai Xu, Sonya Barnes, Ying Sun, et al.
Molecular Genetics and Metabolism
|
December 26, 2001
Temporal and spatial expression of murine acid beta-glucosidase mRNA
E Ponce, D P Witte, A Hung, et al.
Biophysical Journal
|
March 1, 2003
Phospholipid membrane interactions of saposin C: in situ atomic force microscopic study
Hong Xing You, Xiaoyang Qi, Gregory A Grabowski, et al.
Analytical Biochemistry
|
January 1, 1984
Synthesis of a fluorescent derivative of glucosyl ceramide for the sensitive determination of glucocerebrosidase activity
T Dinur, G A Grabowski, R J Desnick, et al.
Gene
|
September 30, 1998
Isolation and characterization of the human prosaposin promoter
Y Sun, P Jin, D P Witte, et al.
Page
of 26
Search research articles
Search
Showing results (81-90 of 259) with videos related to
Sort By:
Page
of 26
American Journal of Human Genetics
|
August 1, 1989
Gaucher disease: molecular heterogeneity and phenotype-genotype correlations
B Theophilus, T Latham, G A Grabowski, et al.
American Journal of Medical Genetics
|
July 11, 1997
Gaucher disease: enzyme therapy in the acute neuronopathic variant
C A Prows, N Sanchez, C Daugherty, et al.
The Biochemical Journal
|
December 7, 2002
Analyses of temporal regulatory elements of the prosaposin gene in transgenic mice
Ying Sun, David P Witte, Peng Jin, et al.
Clinical Genetics
|
February 21, 2007
The effect of enzyme replacement therapy on bone crisis and bone pain in patients with type 1 Gaucher disease
J Charrow, B Dulisse, G A Grabowski, et al.
Journal of Lipid Research
|
August 3, 2005
Gaucher disease mouse models: point mutations at the acid beta-glucosidase locus combined with low-level prosaposin expression lead to disease variants
Ying Sun, Brian Quinn, David P Witte, et al.
Journal of Lipid Research
|
March 10, 2010
Multi-system disorders of glycosphingolipid and ganglioside metabolism
You-Hai Xu, Sonya Barnes, Ying Sun, et al.
Molecular Genetics and Metabolism
|
December 26, 2001
Temporal and spatial expression of murine acid beta-glucosidase mRNA
E Ponce, D P Witte, A Hung, et al.
Biophysical Journal
|
March 1, 2003
Phospholipid membrane interactions of saposin C: in situ atomic force microscopic study
Hong Xing You, Xiaoyang Qi, Gregory A Grabowski, et al.
Analytical Biochemistry
|
January 1, 1984
Synthesis of a fluorescent derivative of glucosyl ceramide for the sensitive determination of glucocerebrosidase activity
T Dinur, G A Grabowski, R J Desnick, et al.
Gene
|
September 30, 1998
Isolation and characterization of the human prosaposin promoter
Y Sun, P Jin, D P Witte, et al.
Page
of 26