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Craig Blackstone

Showing results (41-50 of 124) with videos related to

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Annals of Clinical and Translational Neurology|November 22, 2017
Multigeneration family with dominant SPG30 hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig Blackstone
Annals of Clinical and Translational Neurology|May 12, 2017
De novo <i>REEP2</i> missense mutation in pure hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig Blackstone
Biochemical and Biophysical Research Communications|July 23, 2005
The Troyer syndrome (SPG20) protein spartin interacts with Eps15Joanna C Bakowska, Russell Jenkins, James Pendleton, et al.
Frontiers in Neuroscience|July 9, 2021
Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical OptionsAndrea Martinuzzi, Craig Blackstone, Cahir J O'Kane, et al.
Molecular Neurodegeneration|August 22, 2021
Vesicle trafficking and pathways to neurodegenerationCraig Blackstone, Fiona Elwood, Helene Plun-Favreau, et al.
Biochemical and Biophysical Research Communications|May 15, 2003
Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1Craig Blackstone, Roland G Roberts, Daniel P Seeburg, et al.
Molecular Biology of the Cell|March 3, 2007
Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor traffickingJoanna C Bakowska, Henri Jupille, Parvin Fatheddin, et al.
Human Molecular Genetics|May 24, 2012
Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signalingBenoît Renvoisé, Julia Stadler, Rajat Singh, et al.
Brain Sciences|September 22, 2020
Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a <i>Drosophila</i> Model of Hereditary Spastic ParaplegiaPhilippa C Fowler, Dwayne J Byrne, Craig Blackstone, et al.
Human Molecular Genetics|February 14, 2008
Atlastin GTPases are required for Golgi apparatus and ER morphogenesisNeggy Rismanchi, Cynthia Soderblom, Julia Stadler, et al.
Pageof 13

Showing results (41-50 of 124) with videos related to

Sort By:
Pageof 13
Annals of Clinical and Translational Neurology|November 22, 2017
Multigeneration family with dominant SPG30 hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig Blackstone
Annals of Clinical and Translational Neurology|May 12, 2017
De novo <i>REEP2</i> missense mutation in pure hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig Blackstone
Biochemical and Biophysical Research Communications|July 23, 2005
The Troyer syndrome (SPG20) protein spartin interacts with Eps15Joanna C Bakowska, Russell Jenkins, James Pendleton, et al.
Frontiers in Neuroscience|July 9, 2021
Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical OptionsAndrea Martinuzzi, Craig Blackstone, Cahir J O'Kane, et al.
Molecular Neurodegeneration|August 22, 2021
Vesicle trafficking and pathways to neurodegenerationCraig Blackstone, Fiona Elwood, Helene Plun-Favreau, et al.
Biochemical and Biophysical Research Communications|May 15, 2003
Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1Craig Blackstone, Roland G Roberts, Daniel P Seeburg, et al.
Molecular Biology of the Cell|March 3, 2007
Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor traffickingJoanna C Bakowska, Henri Jupille, Parvin Fatheddin, et al.
Human Molecular Genetics|May 24, 2012
Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signalingBenoît Renvoisé, Julia Stadler, Rajat Singh, et al.
Brain Sciences|September 22, 2020
Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a <i>Drosophila</i> Model of Hereditary Spastic ParaplegiaPhilippa C Fowler, Dwayne J Byrne, Craig Blackstone, et al.
Human Molecular Genetics|February 14, 2008
Atlastin GTPases are required for Golgi apparatus and ER morphogenesisNeggy Rismanchi, Cynthia Soderblom, Julia Stadler, et al.
Pageof 13