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

Graham S Jackson

Showing results (11-20 of 54) with videos related to

Pageof 6
Sort By:
Biochemistry|January 3, 2007
Inhibition of proteinase K activity by copper(II) ionsLisa A Stone, Graham S Jackson, John Collinge, et al.
Transfusion|June 22, 2010
A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase KM Howard Tattum, Samantha Jones, Suvankar Pal, et al.
Scientific Reports|October 13, 2022
Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathyGraham S Jackson, Jacqueline Linehan, Sebastian Brandner, et al.
Plos One|May 26, 2010
Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosisRuth Chia, M Howard Tattum, Samantha Jones, et al.
Immunology|May 9, 2008
The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cellsJeremy D Isaacs, Oliver A Garden, Gurman Kaur, et al.
The Journal of General Virology|August 16, 2005
PrP glycoforms are associated in a strain-specific ratio in native PrPScAzadeh Khalili-Shirazi, Linda Summers, Jacqueline Linehan, et al.
Scientific Reports|March 5, 2021
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseasesTze How Mok, Akin Nihat, Connie Luk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 2018
Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progressionAndrew Geoffrey Bourne Thompson, Connie Luk, Amanda J Heslegrave, et al.
The Biochemical Journal|August 8, 2008
Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysinSabrina Cronier, Nathalie Gros, M Howard Tattum, et al.
Biochimica Et Biophysica Acta|September 29, 2009
The R1441C mutation alters the folding properties of the ROC domain of LRRK2Yongchao Li, Laura Dunn, Elisa Greggio, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Biochemistry|January 3, 2007
Inhibition of proteinase K activity by copper(II) ionsLisa A Stone, Graham S Jackson, John Collinge, et al.
Transfusion|June 22, 2010
A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase KM Howard Tattum, Samantha Jones, Suvankar Pal, et al.
Scientific Reports|October 13, 2022
Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathyGraham S Jackson, Jacqueline Linehan, Sebastian Brandner, et al.
Plos One|May 26, 2010
Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosisRuth Chia, M Howard Tattum, Samantha Jones, et al.
Immunology|May 9, 2008
The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cellsJeremy D Isaacs, Oliver A Garden, Gurman Kaur, et al.
The Journal of General Virology|August 16, 2005
PrP glycoforms are associated in a strain-specific ratio in native PrPScAzadeh Khalili-Shirazi, Linda Summers, Jacqueline Linehan, et al.
Scientific Reports|March 5, 2021
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseasesTze How Mok, Akin Nihat, Connie Luk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 2018
Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progressionAndrew Geoffrey Bourne Thompson, Connie Luk, Amanda J Heslegrave, et al.
The Biochemical Journal|August 8, 2008
Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysinSabrina Cronier, Nathalie Gros, M Howard Tattum, et al.
Biochimica Et Biophysica Acta|September 29, 2009
The R1441C mutation alters the folding properties of the ROC domain of LRRK2Yongchao Li, Laura Dunn, Elisa Greggio, et al.
Pageof 6