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G A Grabowski

Showing results (41-50 of 126) with videos related to

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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 liverG A Grabowski, J U Ikonne, R J Desnick
Archives of Neurology|November 1, 1993
The role of neurogenetics in Gaucher diseaseR 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 storageH 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 variantsG 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 sitesG A Grabowski, S Gatt, J Kruse, et al.
American Journal of Human Genetics|August 1, 1989
Gaucher disease: molecular heterogeneity and phenotype-genotype correlationsB 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 substrateG 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 vivoY Sun, P Jin, D P Witte, et al.
Molecular Genetics and Metabolism|December 26, 2001
Temporal and spatial expression of murine acid beta-glucosidase mRNAE 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 diagnosisG A Grabowski, T Dinur, S Gatt, et al.
Pageof 13

Showing results (41-50 of 126) with videos related to

Sort By:
Pageof 13
Enzyme|January 1, 1980
Comparative physical, kinetic and immunologic properties of the acidic and neutral alpha-D-mannosidase isozymes from human liverG A Grabowski, J U Ikonne, R J Desnick
Archives of Neurology|November 1, 1993
The role of neurogenetics in Gaucher diseaseR 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 storageH 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 variantsG 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 sitesG A Grabowski, S Gatt, J Kruse, et al.
American Journal of Human Genetics|August 1, 1989
Gaucher disease: molecular heterogeneity and phenotype-genotype correlationsB 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 substrateG 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 vivoY Sun, P Jin, D P Witte, et al.
Molecular Genetics and Metabolism|December 26, 2001
Temporal and spatial expression of murine acid beta-glucosidase mRNAE 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 diagnosisG A Grabowski, T Dinur, S Gatt, et al.
Pageof 13