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

W Cleveland

Showing results (381-390 of 499) with videos related to

Pageof 50
Sort By:
Nature Communications|January 13, 2019
Phosphorylation of CENP-A on serine 7 does not control centromere functionViviana Barra, Glennis A Logsdon, Andrea Scelfo, et al.
Cell|May 5, 2009
Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURPDaniel R Foltz, Lars E T Jansen, Aaron O Bailey, et al.
Nature Neuroscience|March 4, 2014
Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factorsAndrea Crotti, Christopher Benner, Bilal E Kerman, et al.
Science (New York, N.Y.)|September 22, 1998
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1L I Bruijn, M K Houseweart, S Kato, et al.
Acta Neuropathologica Communications|December 5, 2024
CK1δ/ε-mediated TDP-43 phosphorylation contributes to early motor neuron disease toxicity in amyotrophic lateral sclerosisVivian I Ko, Kailee Ong, Deborah Y Kwon, et al.
Acta Neuropathologica|October 25, 2000
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutationS Kato, S Horiuchi, J Liu, et al.
The Journal of Biological Chemistry|October 16, 2004
Human Zwint-1 specifies localization of Zeste White 10 to kinetochores and is essential for mitotic checkpoint signalingHongmei Wang, Xiaoyu Hu, Xia Ding, et al.
Nature Neuroscience|March 13, 2002
Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loadingJamuna R Subramaniam, W Ernest Lyons, Jian Liu, et al.
Nature Neuroscience|March 18, 2008
ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degenerationZhihui Zhong, Rashid Deane, Zarina Ali, et al.
The Journal of Cell Biology|June 1, 1996
Subunit composition of neurofilaments specifies axonal diameterZ Xu, J R Marszalek, M K Lee, et al.
Pageof 50

Showing results (381-390 of 499) with videos related to

Sort By:
Pageof 50
Nature Communications|January 13, 2019
Phosphorylation of CENP-A on serine 7 does not control centromere functionViviana Barra, Glennis A Logsdon, Andrea Scelfo, et al.
Cell|May 5, 2009
Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURPDaniel R Foltz, Lars E T Jansen, Aaron O Bailey, et al.
Nature Neuroscience|March 4, 2014
Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factorsAndrea Crotti, Christopher Benner, Bilal E Kerman, et al.
Science (New York, N.Y.)|September 22, 1998
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1L I Bruijn, M K Houseweart, S Kato, et al.
Acta Neuropathologica Communications|December 5, 2024
CK1δ/ε-mediated TDP-43 phosphorylation contributes to early motor neuron disease toxicity in amyotrophic lateral sclerosisVivian I Ko, Kailee Ong, Deborah Y Kwon, et al.
Acta Neuropathologica|October 25, 2000
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutationS Kato, S Horiuchi, J Liu, et al.
The Journal of Biological Chemistry|October 16, 2004
Human Zwint-1 specifies localization of Zeste White 10 to kinetochores and is essential for mitotic checkpoint signalingHongmei Wang, Xiaoyu Hu, Xia Ding, et al.
Nature Neuroscience|March 13, 2002
Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loadingJamuna R Subramaniam, W Ernest Lyons, Jian Liu, et al.
Nature Neuroscience|March 18, 2008
ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degenerationZhihui Zhong, Rashid Deane, Zarina Ali, et al.
The Journal of Cell Biology|June 1, 1996
Subunit composition of neurofilaments specifies axonal diameterZ Xu, J R Marszalek, M K Lee, et al.
Pageof 50