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Mia Horowitz

Showing results (1-10 of 46) with videos related to

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Human Molecular Genetics|July 8, 2005
ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneityIdit Ron, Mia Horowitz
Molecular Genetics and Metabolism|December 28, 2007
Intracellular cholesterol modifies the ERAD of glucocerebrosidase in Gaucher disease patientsIdit Ron, Mia Horowitz
Human Mutation|May 25, 2012
Gaucher disease paradigm: from ERAD to comorbidityInna Bendikov-Bar, Mia Horowitz
Human Molecular Genetics|December 21, 2012
ITCH regulates degradation of mutant glucocerebrosidase: implications to Gaucher diseaseGali Maor, Mirella Filocamo, Mia Horowitz
Human Molecular Genetics|January 8, 2019
The effect of mutant GBA1 on accumulation and aggregation of α-synucleinGali Maor, Debora Rapaport, Mia Horowitz
Plos One|July 31, 2015
SUMOylation of EHD3 Modulates Tubulation of the Endocytic Recycling CompartmentOr Cabasso, Olga Pekar, Mia Horowitz
Cells|October 15, 2024
Functional Analysis of Human <i>GBA1</i> Missense Mutations in <i>Drosophila</i>: Insights into Gaucher Disease Pathogenesis and Phenotypic ConsequencesAparna Kuppuramalingam, Or Cabasso, Mia Horowitz
Human Molecular Genetics|July 21, 2010
Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher diseaseIdit Ron, Debora Rapaport, Mia Horowitz
Plos One|March 23, 2010
Loss of SNAP29 impairs endocytic recycling and cell motilityDebora Rapaport, Yevgenia Lugassy, Eli Sprecher, et al.
Plos One|March 21, 2017
Correction: Past1 Modulates Drosophila Eye DevelopmentOrly Dorot, Hermann Steller, Daniel Segal, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|July 8, 2005
ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneityIdit Ron, Mia Horowitz
Molecular Genetics and Metabolism|December 28, 2007
Intracellular cholesterol modifies the ERAD of glucocerebrosidase in Gaucher disease patientsIdit Ron, Mia Horowitz
Human Mutation|May 25, 2012
Gaucher disease paradigm: from ERAD to comorbidityInna Bendikov-Bar, Mia Horowitz
Human Molecular Genetics|December 21, 2012
ITCH regulates degradation of mutant glucocerebrosidase: implications to Gaucher diseaseGali Maor, Mirella Filocamo, Mia Horowitz
Human Molecular Genetics|January 8, 2019
The effect of mutant GBA1 on accumulation and aggregation of α-synucleinGali Maor, Debora Rapaport, Mia Horowitz
Plos One|July 31, 2015
SUMOylation of EHD3 Modulates Tubulation of the Endocytic Recycling CompartmentOr Cabasso, Olga Pekar, Mia Horowitz
Cells|October 15, 2024
Functional Analysis of Human <i>GBA1</i> Missense Mutations in <i>Drosophila</i>: Insights into Gaucher Disease Pathogenesis and Phenotypic ConsequencesAparna Kuppuramalingam, Or Cabasso, Mia Horowitz
Human Molecular Genetics|July 21, 2010
Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher diseaseIdit Ron, Debora Rapaport, Mia Horowitz
Plos One|March 23, 2010
Loss of SNAP29 impairs endocytic recycling and cell motilityDebora Rapaport, Yevgenia Lugassy, Eli Sprecher, et al.
Plos One|March 21, 2017
Correction: Past1 Modulates Drosophila Eye DevelopmentOrly Dorot, Hermann Steller, Daniel Segal, et al.
Pageof 5