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Ellen Sidransky

Showing results (41-50 of 166) with videos related to

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Biomolecules|April 30, 2021
The Role of Exosomes in Lysosomal Storage DisordersAdenrele M Gleason, Elizabeth G Woo, Cindy McKinney, et al.
International Journal of Molecular Sciences|July 2, 2021
Behavioral Phenotyping in a Murine Model of <i>GBA1</i>-Associated Parkinson DiseaseJenny Do, Gani Perez, Bahafta Berhe, et al.
Expert Review of Endocrinology & Metabolism|July 31, 2018
Recent advances in the diagnosis and management of Gaucher diseaseSam E Gary, Emory Ryan, Alta M Steward, et al.
American Journal of Medical Genetics. Part A|April 22, 2024
Phenotypic consequences of GBA1 pathological variant R463C (p.R502C)Emory Ryan, Samantha Nishimura, Grisel Lopez, et al.
Expert Review of Proteomics|April 22, 2016
Progress and potential of non-inhibitory small molecule chaperones for the treatment of Gaucher disease and its implications for Parkinson diseaseOlive Jung, Samarjit Patnaik, Juan Marugan, et al.
Molecular Genetics and Metabolism|December 26, 2012
Membrane-bound α-synuclein interacts with glucocerebrosidase and inhibits enzyme activityThai Leong Yap, Arash Velayati, Ellen Sidransky, et al.
International Journal of Molecular Sciences|May 28, 2022
Neuropathological Features of Gaucher Disease and Gaucher Disease with ParkinsonismMakaila L Furderer, Ellen Hertz, Grisel J Lopez, et al.
Acta Neuropathologica|September 15, 2010
Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disordersOzlem Goker-Alpan, Barbara K Stubblefield, Benoit I Giasson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2009
The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonismJohn DePaolo, Ozlem Goker-Alpan, Ted Samaddar, et al.
Blood Cells, Molecules & Diseases|September 18, 2010
Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseasesEbrahim Miri-Moghaddam, Arash Velayati, Majid Naderi, et al.
Pageof 17

Showing results (41-50 of 166) with videos related to

Sort By:
Pageof 17
Biomolecules|April 30, 2021
The Role of Exosomes in Lysosomal Storage DisordersAdenrele M Gleason, Elizabeth G Woo, Cindy McKinney, et al.
International Journal of Molecular Sciences|July 2, 2021
Behavioral Phenotyping in a Murine Model of <i>GBA1</i>-Associated Parkinson DiseaseJenny Do, Gani Perez, Bahafta Berhe, et al.
Expert Review of Endocrinology & Metabolism|July 31, 2018
Recent advances in the diagnosis and management of Gaucher diseaseSam E Gary, Emory Ryan, Alta M Steward, et al.
American Journal of Medical Genetics. Part A|April 22, 2024
Phenotypic consequences of GBA1 pathological variant R463C (p.R502C)Emory Ryan, Samantha Nishimura, Grisel Lopez, et al.
Expert Review of Proteomics|April 22, 2016
Progress and potential of non-inhibitory small molecule chaperones for the treatment of Gaucher disease and its implications for Parkinson diseaseOlive Jung, Samarjit Patnaik, Juan Marugan, et al.
Molecular Genetics and Metabolism|December 26, 2012
Membrane-bound α-synuclein interacts with glucocerebrosidase and inhibits enzyme activityThai Leong Yap, Arash Velayati, Ellen Sidransky, et al.
International Journal of Molecular Sciences|May 28, 2022
Neuropathological Features of Gaucher Disease and Gaucher Disease with ParkinsonismMakaila L Furderer, Ellen Hertz, Grisel J Lopez, et al.
Acta Neuropathologica|September 15, 2010
Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disordersOzlem Goker-Alpan, Barbara K Stubblefield, Benoit I Giasson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2009
The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonismJohn DePaolo, Ozlem Goker-Alpan, Ted Samaddar, et al.
Blood Cells, Molecules & Diseases|September 18, 2010
Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseasesEbrahim Miri-Moghaddam, Arash Velayati, Majid Naderi, et al.
Pageof 17