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Enzyme
|
January 1, 1980
Comparative physical, kinetic and immunologic properties of the acidic and neutral alpha-D-mannosidase isozymes from human liver
G A Grabowski, J U Ikonne, R J Desnick
Archives of Neurology
|
November 1, 1993
The role of neurogenetics in Gaucher disease
R O Brady, N W Barton, G A Grabowski
Human Molecular Genetics
|
August 13, 1998
Targeted disruption of the mouse lysosomal acid lipase gene: long-term survival with massive cholesteryl ester and triglyceride storage
H Du, M Duanmu, D Witte, et al.
Human Mutation
|
January 1, 1992
Gaucher disease: four rare alleles encoding F213I, P289L, T323I, and R463C in type 1 variants
G S He, M E Grace, G A Grabowski
Archives of Biochemistry and Biophysics
|
May 15, 1984
Human lysosomal beta-glucosidase: kinetic characterization of the catalytic, aglycon, and hydrophobic binding sites
G A Grabowski, S Gatt, J Kruse, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1982
Gaucher type I (Ashkenazi) disease: a new method for heterozygote detection using a novel fluorescent natural substrate
G A Grabowski, T Dinur, S Gatt, et al.
The Biochemical Journal
|
November 22, 2000
Prosaposin: promoter analysis and central-nervous-system-preferential elements for expression in vivo
Y Sun, P Jin, D P Witte, 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.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher type I (Ashkenazi) disease: considerations for heterozygote detection and prenatal diagnosis
G A Grabowski, T Dinur, S Gatt, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 126) with videos related to
Sort By:
Page
of 13
Enzyme
|
January 1, 1980
Comparative physical, kinetic and immunologic properties of the acidic and neutral alpha-D-mannosidase isozymes from human liver
G A Grabowski, J U Ikonne, R J Desnick
Archives of Neurology
|
November 1, 1993
The role of neurogenetics in Gaucher disease
R O Brady, N W Barton, G A Grabowski
Human Molecular Genetics
|
August 13, 1998
Targeted disruption of the mouse lysosomal acid lipase gene: long-term survival with massive cholesteryl ester and triglyceride storage
H Du, M Duanmu, D Witte, et al.
Human Mutation
|
January 1, 1992
Gaucher disease: four rare alleles encoding F213I, P289L, T323I, and R463C in type 1 variants
G S He, M E Grace, G A Grabowski
Archives of Biochemistry and Biophysics
|
May 15, 1984
Human lysosomal beta-glucosidase: kinetic characterization of the catalytic, aglycon, and hydrophobic binding sites
G A Grabowski, S Gatt, J Kruse, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1982
Gaucher type I (Ashkenazi) disease: a new method for heterozygote detection using a novel fluorescent natural substrate
G A Grabowski, T Dinur, S Gatt, et al.
The Biochemical Journal
|
November 22, 2000
Prosaposin: promoter analysis and central-nervous-system-preferential elements for expression in vivo
Y Sun, P Jin, D P Witte, 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.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher type I (Ashkenazi) disease: considerations for heterozygote detection and prenatal diagnosis
G A Grabowski, T Dinur, S Gatt, et al.
Page
of 13