Search research articles
Contact Us
Filters
Showing results (41-50 of 166) with videos related to
Page
of 17
Sort By:
Biomolecules
|
April 30, 2021
The Role of Exosomes in Lysosomal Storage Disorders
Adenrele 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 Disease
Jenny Do, Gani Perez, Bahafta Berhe, et al.
Expert Review of Endocrinology & Metabolism
|
July 31, 2018
Recent advances in the diagnosis and management of Gaucher disease
Sam 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 disease
Olive Jung, Samarjit Patnaik, Juan Marugan, et al.
Molecular Genetics and Metabolism
|
December 26, 2012
Membrane-bound α-synuclein interacts with glucocerebrosidase and inhibits enzyme activity
Thai 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 Parkinsonism
Makaila L Furderer, Ellen Hertz, Grisel J Lopez, et al.
Acta Neuropathologica
|
September 15, 2010
Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders
Ozlem 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 parkinsonism
John 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 diseases
Ebrahim Miri-Moghaddam, Arash Velayati, Majid Naderi, et al.
Page
of 17
Search research articles
Search
Showing results (41-50 of 166) with videos related to
Sort By:
Page
of 17
Biomolecules
|
April 30, 2021
The Role of Exosomes in Lysosomal Storage Disorders
Adenrele 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 Disease
Jenny Do, Gani Perez, Bahafta Berhe, et al.
Expert Review of Endocrinology & Metabolism
|
July 31, 2018
Recent advances in the diagnosis and management of Gaucher disease
Sam 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 disease
Olive Jung, Samarjit Patnaik, Juan Marugan, et al.
Molecular Genetics and Metabolism
|
December 26, 2012
Membrane-bound α-synuclein interacts with glucocerebrosidase and inhibits enzyme activity
Thai 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 Parkinsonism
Makaila L Furderer, Ellen Hertz, Grisel J Lopez, et al.
Acta Neuropathologica
|
September 15, 2010
Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders
Ozlem 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 parkinsonism
John 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 diseases
Ebrahim Miri-Moghaddam, Arash Velayati, Majid Naderi, et al.
Page
of 17