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

J Collinge

Showing results (111-120 of 171) with videos related to

Pageof 18
Sort By:
Lancet (London, England)|July 31, 2001
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assayJ D Wadsworth, S Joiner, A F Hill, et al.
Brain Research. Molecular Brain Research|April 1, 1990
An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob diseaseF Owen, M Poulter, T Shah, et al.
Lancet (London, England)|July 1, 1989
Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysisJ Collinge, A E Harding, F Owen, et al.
Neuroscience|February 1, 2011
Threshold for epileptiform activity is elevated in prion knockout miceS Ratté, M Vreugdenhil, J K R Boult, et al.
Neurology|November 10, 2004
A presenilin 1 R278I mutation presenting with language impairmentA K Godbolt, J A Beck, J Collinge, et al.
Neurology|October 9, 2002
Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalitiesS O'Riordan, P McMonagle, J C Janssen, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Journal of Medical Genetics|September 23, 2008
Association of a null allele of SPRN with variant Creutzfeldt-Jakob diseaseJ A Beck, T A Campbell, G Adamson, et al.
Biochimica Et Biophysica Acta|April 21, 1999
Multiple folding pathways for heterologously expressed human prion proteinG S Jackson, A F Hill, C Joseph, et al.
FEBS Letters|April 1, 1997
Conformational properties of the prion octa-repeat and hydrophobic sequencesC J Smith, A F Drake, B A Banfield, et al.
Pageof 18

Showing results (111-120 of 171) with videos related to

Sort By:
Pageof 18
Lancet (London, England)|July 31, 2001
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assayJ D Wadsworth, S Joiner, A F Hill, et al.
Brain Research. Molecular Brain Research|April 1, 1990
An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob diseaseF Owen, M Poulter, T Shah, et al.
Lancet (London, England)|July 1, 1989
Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysisJ Collinge, A E Harding, F Owen, et al.
Neuroscience|February 1, 2011
Threshold for epileptiform activity is elevated in prion knockout miceS Ratté, M Vreugdenhil, J K R Boult, et al.
Neurology|November 10, 2004
A presenilin 1 R278I mutation presenting with language impairmentA K Godbolt, J A Beck, J Collinge, et al.
Neurology|October 9, 2002
Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalitiesS O'Riordan, P McMonagle, J C Janssen, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Journal of Medical Genetics|September 23, 2008
Association of a null allele of SPRN with variant Creutzfeldt-Jakob diseaseJ A Beck, T A Campbell, G Adamson, et al.
Biochimica Et Biophysica Acta|April 21, 1999
Multiple folding pathways for heterologously expressed human prion proteinG S Jackson, A F Hill, C Joseph, et al.
FEBS Letters|April 1, 1997
Conformational properties of the prion octa-repeat and hydrophobic sequencesC J Smith, A F Drake, B A Banfield, et al.
Pageof 18