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

Isabelle Laffont-Proust

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
The Journal of Comparative Neurology|August 28, 2007
Developmental changes in cellular prion protein in primate visual cortexIsabelle Laffont-Proust, Caroline Fonta, Luc Renaud, et al.
Biological Chemistry|March 18, 2006
Truncated PrP(c) in mammalian brain: interspecies variation and location in membrane raftsIsabelle Laffont-Proust, Raymonde Hässig, Stéphane Haïk, et al.
FEBS Letters|November 3, 2005
The N-terminal cleavage of cellular prion protein in the human brainIsabelle Laffont-Proust, Baptiste A Faucheux, Raymonde Hässig, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|December 18, 2007
Human prion diseases: from antibody screening to a standardized fast immunodiagnosis using automationNicolas Privat, Isabelle Laffont-Proust, Baptiste A Faucheux, et al.
Neuroscience Letters|October 13, 2006
V180I mutation of the prion protein gene associated with atypical PrPSc glycosylationStéphanie Chasseigneaux, Stéphane Haïk, Isabelle Laffont-Proust, et al.
Plos One|July 31, 2008
Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strainsEtienne Levavasseur, Isabelle Laffont-Proust, Emilie Morain, et al.
Human Molecular Genetics|September 12, 2012
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disordersKatell Peoc'h, Etienne Levavasseur, Emilien Delmont, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Journal of Comparative Neurology|August 28, 2007
Developmental changes in cellular prion protein in primate visual cortexIsabelle Laffont-Proust, Caroline Fonta, Luc Renaud, et al.
Biological Chemistry|March 18, 2006
Truncated PrP(c) in mammalian brain: interspecies variation and location in membrane raftsIsabelle Laffont-Proust, Raymonde Hässig, Stéphane Haïk, et al.
FEBS Letters|November 3, 2005
The N-terminal cleavage of cellular prion protein in the human brainIsabelle Laffont-Proust, Baptiste A Faucheux, Raymonde Hässig, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|December 18, 2007
Human prion diseases: from antibody screening to a standardized fast immunodiagnosis using automationNicolas Privat, Isabelle Laffont-Proust, Baptiste A Faucheux, et al.
Neuroscience Letters|October 13, 2006
V180I mutation of the prion protein gene associated with atypical PrPSc glycosylationStéphanie Chasseigneaux, Stéphane Haïk, Isabelle Laffont-Proust, et al.
Plos One|July 31, 2008
Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strainsEtienne Levavasseur, Isabelle Laffont-Proust, Emilie Morain, et al.
Human Molecular Genetics|September 12, 2012
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disordersKatell Peoc'h, Etienne Levavasseur, Emilien Delmont, et al.
Pageof 1