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

Gillian P Bates

Showing results (61-70 of 142) with videos related to

Pageof 15
Sort By:
Scientific Reports|October 4, 2017
HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse modelsAndreas Neueder, Theresa A Gipson, Sophie Batterton, et al.
Molecular Medicine (Cambridge, Mass.)|March 8, 2024
Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissuesFranziska Hoschek, Julia Natan, Maximilian Wagner, et al.
Iscience|May 24, 2024
Mitochondrial clearance and increased HSF-1 activity are coupled to promote longevity in fasted <i>Caenorhabditis elegans</i>Nikolaos Tataridas-Pallas, Yahyah Aman, Rhianna Williams, et al.
Brain Communications|June 16, 2021
Use of high-content imaging to quantify transduction of AAV-PHP viruses in the brain following systemic deliveryEdward J Smith, Pamela P Farshim, Rachel Flomen, et al.
Scientific Reports|September 21, 2017
Disruption to schizophrenia-associated gene Fez1 in the hippocampus of HDAC11 knockout miceDale T Bryant, Christian Landles, Aikaterini S Papadopoulou, et al.
Human Molecular Genetics|October 15, 2009
Identical oligomeric and fibrillar structures captured from the brains of R6/2 and knock-in mouse models of Huntington's diseaseKirupa Sathasivam, Amin Lane, Justin Legleiter, et al.
Annals of Neurology|February 9, 2002
Environmental enrichment slows disease progression in R6/2 Huntington's disease miceEmma Hockly, Patricia M Cordery, Benjamin Woodman, et al.
Human Molecular Genetics|April 30, 2004
Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approachDavid G Hay, Kirupa Sathasivam, Sönke Tobaben, et al.
International Journal of Molecular Sciences|August 27, 2021
Transglutaminase 6 Is Colocalized and Interacts with Mutant Huntingtin in Huntington Disease Rodent Animal ModelsAnja Schulze-Krebs, Fabio Canneva, Judith Stemick, et al.
Nature Cell Biology|February 21, 2002
Arfaptin 2 regulates the aggregation of mutant huntingtin proteinPeter J Peters, Ke Ning, Felipe Palacios, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
Scientific Reports|October 4, 2017
HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse modelsAndreas Neueder, Theresa A Gipson, Sophie Batterton, et al.
Molecular Medicine (Cambridge, Mass.)|March 8, 2024
Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissuesFranziska Hoschek, Julia Natan, Maximilian Wagner, et al.
Iscience|May 24, 2024
Mitochondrial clearance and increased HSF-1 activity are coupled to promote longevity in fasted <i>Caenorhabditis elegans</i>Nikolaos Tataridas-Pallas, Yahyah Aman, Rhianna Williams, et al.
Brain Communications|June 16, 2021
Use of high-content imaging to quantify transduction of AAV-PHP viruses in the brain following systemic deliveryEdward J Smith, Pamela P Farshim, Rachel Flomen, et al.
Scientific Reports|September 21, 2017
Disruption to schizophrenia-associated gene Fez1 in the hippocampus of HDAC11 knockout miceDale T Bryant, Christian Landles, Aikaterini S Papadopoulou, et al.
Human Molecular Genetics|October 15, 2009
Identical oligomeric and fibrillar structures captured from the brains of R6/2 and knock-in mouse models of Huntington's diseaseKirupa Sathasivam, Amin Lane, Justin Legleiter, et al.
Annals of Neurology|February 9, 2002
Environmental enrichment slows disease progression in R6/2 Huntington's disease miceEmma Hockly, Patricia M Cordery, Benjamin Woodman, et al.
Human Molecular Genetics|April 30, 2004
Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approachDavid G Hay, Kirupa Sathasivam, Sönke Tobaben, et al.
International Journal of Molecular Sciences|August 27, 2021
Transglutaminase 6 Is Colocalized and Interacts with Mutant Huntingtin in Huntington Disease Rodent Animal ModelsAnja Schulze-Krebs, Fabio Canneva, Judith Stemick, et al.
Nature Cell Biology|February 21, 2002
Arfaptin 2 regulates the aggregation of mutant huntingtin proteinPeter J Peters, Ke Ning, Felipe Palacios, et al.
Pageof 15