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Craig Blackstone

Showing results (61-70 of 125) with videos related to

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Brain : a Journal of Neurology|January 13, 2022
Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neuronsZhenyu Chen, Eric Chai, Yongchao Mou, et al.
Molecular Neurobiology|April 2, 2025
A depression-associated protein FKBP5 functions in autophagy initiation through scaffolding the VPS34 complexHyungsun Park, Jisoo Park, Taewan Kim, et al.
Stem Cells (Dayton, Ohio)|October 15, 2013
Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegiaKyle R Denton, Ling Lei, Jeremy Grenier, et al.
Human Molecular Genetics|June 9, 2014
Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3APeng-Peng Zhu, Kyle R Denton, Tyler Mark Pierson, et al.
Science Signaling|January 9, 2020
Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesionSeongju Lee, Hyungsun Park, Peng-Peng Zhu, et al.
Nature Structural & Molecular Biology|November 11, 2008
Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1BDong Yang, Neggy Rismanchi, Benoît Renvoisé, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 18, 2017
Roles for the VCP co-factors Npl4 and Ufd1 in neuronal function in Drosophila melanogasterDwayne J Byrne, Mark J Harmon, Jeremy C Simpson, et al.
The Journal of Biological Chemistry|June 23, 2004
Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1Peng-Peng Zhu, Andrew Patterson, Julia Stadler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 26, 2007
A progressive, fatal dystonia-Parkinsonism syndrome in a patient with primary immunodeficiency receiving chronic IVIG therapySpiridon Papapetropoulos, Jennifer Friedman, Craig Blackstone, et al.
Human Molecular Genetics|August 4, 2022
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype-phenotype correlationsJulian E Alecu, Afshin Saffari, Catherine Jordan, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
Brain : a Journal of Neurology|January 13, 2022
Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neuronsZhenyu Chen, Eric Chai, Yongchao Mou, et al.
Molecular Neurobiology|April 2, 2025
A depression-associated protein FKBP5 functions in autophagy initiation through scaffolding the VPS34 complexHyungsun Park, Jisoo Park, Taewan Kim, et al.
Stem Cells (Dayton, Ohio)|October 15, 2013
Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegiaKyle R Denton, Ling Lei, Jeremy Grenier, et al.
Human Molecular Genetics|June 9, 2014
Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3APeng-Peng Zhu, Kyle R Denton, Tyler Mark Pierson, et al.
Science Signaling|January 9, 2020
Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesionSeongju Lee, Hyungsun Park, Peng-Peng Zhu, et al.
Nature Structural & Molecular Biology|November 11, 2008
Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1BDong Yang, Neggy Rismanchi, Benoît Renvoisé, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 18, 2017
Roles for the VCP co-factors Npl4 and Ufd1 in neuronal function in Drosophila melanogasterDwayne J Byrne, Mark J Harmon, Jeremy C Simpson, et al.
The Journal of Biological Chemistry|June 23, 2004
Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1Peng-Peng Zhu, Andrew Patterson, Julia Stadler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 26, 2007
A progressive, fatal dystonia-Parkinsonism syndrome in a patient with primary immunodeficiency receiving chronic IVIG therapySpiridon Papapetropoulos, Jennifer Friedman, Craig Blackstone, et al.
Human Molecular Genetics|August 4, 2022
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype-phenotype correlationsJulian E Alecu, Afshin Saffari, Catherine Jordan, et al.
Pageof 13