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Ellen Sidransky

Showing results (11-20 of 166) with videos related to

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Molecular Genetics and Metabolism|September 18, 2017
The role of epigenetics in lysosomal storage disorders: Uncharted territoryShahzeb Hassan, Ellen Sidransky, Nahid Tayebi
Biomolecules|May 28, 2022
Lyso-IP: Uncovering Pathogenic Mechanisms of Lysosomal DysfunctionChase Chen, Ellen Sidransky, Yu Chen
Neuron|February 24, 2017
The Complicated Relationship between Gaucher Disease and Parkinsonism: Insights from a Rare DiseaseElma Aflaki, Wendy Westbroek, Ellen Sidransky
Molecular Genetics and Metabolism|January 23, 2021
Diagnosing neuronopathic Gaucher disease: New considerations and challenges in assigning Gaucher phenotypesEmily C Daykin, Emory Ryan, Ellen Sidransky
Macrophage|June 20, 2015
New macrophage models of Gaucher disease offer new tools for drug developmentDaniel K Borger, Ellen Sidransky, Elma Aflaki
Current Neurology and Neuroscience Reports|April 29, 2010
The role of glucocerebrosidase mutations in Parkinson disease and Lewy body disordersArash Velayati, W Haung Yu, Ellen Sidransky
Trends in Molecular Medicine|July 5, 2011
Exploring the link between glucocerebrosidase mutations and parkinsonismWendy Westbroek, Ann Marie Gustafson, Ellen Sidransky
Frontiers in Cell and Developmental Biology|June 9, 2020
Small Molecule Chaperones for the Treatment of Gaucher Disease and <i>GBA1</i>-Associated Parkinson DiseaseTae-Un Han, Richard Sam, Ellen Sidransky
Molecular Neurodegeneration|August 30, 2019
Glucocerebrosidase and its relevance to Parkinson diseaseJenny Do, Cindy McKinney, Pankaj Sharma, et al.
Molecular Genetics and Metabolism Reports|December 23, 2015
Bilateral Femoral Osteolytic Lesions in a Patient with Type 3 Gaucher DiseaseEnock Teefe, Jenny Kim, Grisel Lopez, et al.
Pageof 17

Showing results (11-20 of 166) with videos related to

Sort By:
Pageof 17
Molecular Genetics and Metabolism|September 18, 2017
The role of epigenetics in lysosomal storage disorders: Uncharted territoryShahzeb Hassan, Ellen Sidransky, Nahid Tayebi
Biomolecules|May 28, 2022
Lyso-IP: Uncovering Pathogenic Mechanisms of Lysosomal DysfunctionChase Chen, Ellen Sidransky, Yu Chen
Neuron|February 24, 2017
The Complicated Relationship between Gaucher Disease and Parkinsonism: Insights from a Rare DiseaseElma Aflaki, Wendy Westbroek, Ellen Sidransky
Molecular Genetics and Metabolism|January 23, 2021
Diagnosing neuronopathic Gaucher disease: New considerations and challenges in assigning Gaucher phenotypesEmily C Daykin, Emory Ryan, Ellen Sidransky
Macrophage|June 20, 2015
New macrophage models of Gaucher disease offer new tools for drug developmentDaniel K Borger, Ellen Sidransky, Elma Aflaki
Current Neurology and Neuroscience Reports|April 29, 2010
The role of glucocerebrosidase mutations in Parkinson disease and Lewy body disordersArash Velayati, W Haung Yu, Ellen Sidransky
Trends in Molecular Medicine|July 5, 2011
Exploring the link between glucocerebrosidase mutations and parkinsonismWendy Westbroek, Ann Marie Gustafson, Ellen Sidransky
Frontiers in Cell and Developmental Biology|June 9, 2020
Small Molecule Chaperones for the Treatment of Gaucher Disease and <i>GBA1</i>-Associated Parkinson DiseaseTae-Un Han, Richard Sam, Ellen Sidransky
Molecular Neurodegeneration|August 30, 2019
Glucocerebrosidase and its relevance to Parkinson diseaseJenny Do, Cindy McKinney, Pankaj Sharma, et al.
Molecular Genetics and Metabolism Reports|December 23, 2015
Bilateral Femoral Osteolytic Lesions in a Patient with Type 3 Gaucher DiseaseEnock Teefe, Jenny Kim, Grisel Lopez, et al.
Pageof 17