Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Kyle R Denton

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|December 19, 2014
Modeling Axonal Phenotypes with Human Pluripotent Stem CellsKyle R Denton, Chong-Chong Xu, Xue-Jun Li
Frontiers in Biology|December 14, 2016
Modeling Axonal Defects in Hereditary Spastic Paraplegia with Human Pluripotent Stem CellsKyle R Denton, Chongchong Xu, Harsh Shah, et al.
Frontiers in Cellular Neuroscience|May 4, 2023
Reduced C9orf72 expression exacerbates polyGR toxicity in patient iPSC-derived motor neurons and a Type I protein arginine methyltransferase inhibitor reduces that toxicityTherese L Dane, Anna L Gill, Fernando G Vieira, et al.
Disease Models & Mechanisms|November 21, 2015
Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophyChong-Chong Xu, Kyle R Denton, Zhi-Bo Wang, 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.
Acta Neuropathologica Communications|December 8, 2020
Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegiaYongchao Mou, Yi Dong, Zhenyu Chen, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|December 19, 2014
Modeling Axonal Phenotypes with Human Pluripotent Stem CellsKyle R Denton, Chong-Chong Xu, Xue-Jun Li
Frontiers in Biology|December 14, 2016
Modeling Axonal Defects in Hereditary Spastic Paraplegia with Human Pluripotent Stem CellsKyle R Denton, Chongchong Xu, Harsh Shah, et al.
Frontiers in Cellular Neuroscience|May 4, 2023
Reduced C9orf72 expression exacerbates polyGR toxicity in patient iPSC-derived motor neurons and a Type I protein arginine methyltransferase inhibitor reduces that toxicityTherese L Dane, Anna L Gill, Fernando G Vieira, et al.
Disease Models & Mechanisms|November 21, 2015
Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophyChong-Chong Xu, Kyle R Denton, Zhi-Bo Wang, 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.
Acta Neuropathologica Communications|December 8, 2020
Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegiaYongchao Mou, Yi Dong, Zhenyu Chen, et al.
Pageof 1