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

Ray Truant

Showing results (41-50 of 62) with videos related to

Pageof 7
Sort By:
Journal of Lipid Research|November 3, 2006
Regulation of SR-BI-mediated selective lipid uptake in Chinese hamster ovary-derived cells by protein kinase signaling pathwaysYi Zhang, Ayesha M Ahmed, Nicole McFarlane, et al.
Journal of Huntington'S Disease|February 13, 2021
DNA Repair in Huntington's Disease and Spinocerebellar Ataxias: Somatic Instability and Alternative HypothesesTamara Maiuri, Claudia L K Hung, Celeste Suart, et al.
The Journal of Biological Chemistry|August 11, 2005
Inhibition of metabotropic glutamate receptor signaling by the huntingtin-binding protein optineurinPieter H Anborgh, Christina Godin, Macarena Pampillo, et al.
Molecular Membrane Biology|August 22, 2007
The inhibition of endocytosis affects HDL-lipid uptake mediated by the human scavenger receptor class B type IYi Zhang, Ayesha M Ahmed, Thu L Tran, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2012
Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease miceAlba Di Pardo, Vittorio Maglione, Melanie Alpaugh, et al.
Human Genome Variation|April 15, 2022
Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipelineSiddharth Nath, Nicholas S Caron, Linda May, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 11, 2018
N6-Furfuryladenine is protective in Huntington's disease models by signaling huntingtin phosphorylationLaura E Bowie, Tamara Maiuri, Melanie Alpaugh, et al.
Molecular Biology of the Cell|September 27, 2018
A patient-derived cellular model for Huntington's disease reveals phenotypes at clinically relevant CAG lengthsClaudia Lin-Kar Hung, Tamara Maiuri, Laura Erin Bowie, et al.
The Journal of Biological Chemistry|July 25, 2007
Proteolytic cleavage of ataxin-7 by caspase-7 modulates cellular toxicity and transcriptional dysregulationJessica E Young, Launce Gouw, Stephanie Propp, et al.
Research Square|March 22, 2023
PAM-Flexible Genome Editing with an Engineered Chimeric Cas9Sabrina Koseki, Lauren Hong, Vivian Yudistyra, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Journal of Lipid Research|November 3, 2006
Regulation of SR-BI-mediated selective lipid uptake in Chinese hamster ovary-derived cells by protein kinase signaling pathwaysYi Zhang, Ayesha M Ahmed, Nicole McFarlane, et al.
Journal of Huntington'S Disease|February 13, 2021
DNA Repair in Huntington's Disease and Spinocerebellar Ataxias: Somatic Instability and Alternative HypothesesTamara Maiuri, Claudia L K Hung, Celeste Suart, et al.
The Journal of Biological Chemistry|August 11, 2005
Inhibition of metabotropic glutamate receptor signaling by the huntingtin-binding protein optineurinPieter H Anborgh, Christina Godin, Macarena Pampillo, et al.
Molecular Membrane Biology|August 22, 2007
The inhibition of endocytosis affects HDL-lipid uptake mediated by the human scavenger receptor class B type IYi Zhang, Ayesha M Ahmed, Thu L Tran, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2012
Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease miceAlba Di Pardo, Vittorio Maglione, Melanie Alpaugh, et al.
Human Genome Variation|April 15, 2022
Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipelineSiddharth Nath, Nicholas S Caron, Linda May, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 11, 2018
N6-Furfuryladenine is protective in Huntington's disease models by signaling huntingtin phosphorylationLaura E Bowie, Tamara Maiuri, Melanie Alpaugh, et al.
Molecular Biology of the Cell|September 27, 2018
A patient-derived cellular model for Huntington's disease reveals phenotypes at clinically relevant CAG lengthsClaudia Lin-Kar Hung, Tamara Maiuri, Laura Erin Bowie, et al.
The Journal of Biological Chemistry|July 25, 2007
Proteolytic cleavage of ataxin-7 by caspase-7 modulates cellular toxicity and transcriptional dysregulationJessica E Young, Launce Gouw, Stephanie Propp, et al.
Research Square|March 22, 2023
PAM-Flexible Genome Editing with an Engineered Chimeric Cas9Sabrina Koseki, Lauren Hong, Vivian Yudistyra, et al.
Pageof 7