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A Grabowski

Showing results (161-170 of 259) with videos related to

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Human Molecular Genetics|August 3, 2019
Intravenous infusion of iPSC-derived neural precursor cells increases acid β-glucosidase function in the brain and lessens the neuronopathic phenotype in a mouse model of Gaucher diseaseYanyan Peng, Benjamin Liou, Venette Inskeep, et al.
Human Molecular Genetics|March 14, 2007
Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin traffickingYing Sun, David P Witte, Matt Zamzow, et al.
Blood|March 11, 2004
Gaucher disease: alendronate disodium improves bone mineral density in adults receiving enzyme therapyRichard J Wenstrup, Laurie Bailey, Gregory A Grabowski, et al.
American Journal of Nephrology|September 1, 1983
Silicon nephropathy mimicking Fabry's diseaseD E Banks, J Milutinovic, R J Desnick, et al.
The Journal of Biological Chemistry|June 25, 1986
Human acid beta-glucosidase. Use of conduritol B epoxide derivatives to investigate the catalytically active normal and Gaucher disease enzymesG A Grabowski, K Osiecki-Newman, T Dinur, et al.
The Journal of Cell Biology|May 26, 2010
The role of UDP-Glc:glycoprotein glucosyltransferase 1 in the maturation of an obligate substrate prosaposinBradley R Pearse, Taku Tamura, Johan C Sunryd, et al.
Journal of Lipid Research|April 6, 2001
Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life spanH Du, M Heur, M Duanmu, et al.
Enzyme|January 1, 1988
Human acid beta-glucosidase: inhibition studies using glucose analogues and pH variation to characterize the normal and Gaucher disease glycon binding sitesK Osiecki-Newman, G Legler, M Grace, et al.
Journal of Lipid Research|August 28, 2007
Apolipoprotein E-deficient lipoproteins induce foam cell formation by downregulation of lysosomal hydrolases in macrophagesDongFang Wu, Chakradhari Sharan, Hong Yang, et al.
The Journal of Pediatrics|January 24, 2007
Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapyT Andrew Burrow, Mitchell B Cohen, Ronald Bokulic, et al.
Pageof 26

Showing results (161-170 of 259) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|August 3, 2019
Intravenous infusion of iPSC-derived neural precursor cells increases acid β-glucosidase function in the brain and lessens the neuronopathic phenotype in a mouse model of Gaucher diseaseYanyan Peng, Benjamin Liou, Venette Inskeep, et al.
Human Molecular Genetics|March 14, 2007
Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin traffickingYing Sun, David P Witte, Matt Zamzow, et al.
Blood|March 11, 2004
Gaucher disease: alendronate disodium improves bone mineral density in adults receiving enzyme therapyRichard J Wenstrup, Laurie Bailey, Gregory A Grabowski, et al.
American Journal of Nephrology|September 1, 1983
Silicon nephropathy mimicking Fabry's diseaseD E Banks, J Milutinovic, R J Desnick, et al.
The Journal of Biological Chemistry|June 25, 1986
Human acid beta-glucosidase. Use of conduritol B epoxide derivatives to investigate the catalytically active normal and Gaucher disease enzymesG A Grabowski, K Osiecki-Newman, T Dinur, et al.
The Journal of Cell Biology|May 26, 2010
The role of UDP-Glc:glycoprotein glucosyltransferase 1 in the maturation of an obligate substrate prosaposinBradley R Pearse, Taku Tamura, Johan C Sunryd, et al.
Journal of Lipid Research|April 6, 2001
Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life spanH Du, M Heur, M Duanmu, et al.
Enzyme|January 1, 1988
Human acid beta-glucosidase: inhibition studies using glucose analogues and pH variation to characterize the normal and Gaucher disease glycon binding sitesK Osiecki-Newman, G Legler, M Grace, et al.
Journal of Lipid Research|August 28, 2007
Apolipoprotein E-deficient lipoproteins induce foam cell formation by downregulation of lysosomal hydrolases in macrophagesDongFang Wu, Chakradhari Sharan, Hong Yang, et al.
The Journal of Pediatrics|January 24, 2007
Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapyT Andrew Burrow, Mitchell B Cohen, Ronald Bokulic, et al.
Pageof 26