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The New England Journal of Medicine
|
January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129
Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
The EMBO Journal
|
November 29, 2002
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein
Emmanuel A Asante, Jacqueline M Linehan, Melanie Desbruslais, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2008
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice
Jonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Neuropathology and Applied Neurobiology
|
February 12, 2009
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L)
T Webb, S Mead, J Beck, et al.
The Journal of General Virology
|
July 9, 2010
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein
Malin K Sandberg, Huda Al-Doujaily, Christina J Sigurdson, et al.
The Journal of Pathology
|
February 5, 2011
Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study
Jonathan D F Wadsworth, Inmaculada Dalmau-Mena, Susan Joiner, et al.
Scientific Reports
|
May 8, 2015
A novel and rapid method for obtaining high titre intact prion strains from mammalian brain
Adam Wenborn, Cassandra Terry, Nathalie Gros, et al.
Science (New York, N.Y.)
|
November 13, 2004
Human prion protein with valine 129 prevents expression of variant CJD phenotype
Jonathan D F Wadsworth, Emmanuel A Asante, Melanie Desbruslais, et al.
The Journal of Biological Chemistry
|
September 20, 2002
Tamapin, a venom peptide from the Indian red scorpion (Mesobuthus tamulus) that targets small conductance Ca2+-activated K+ channels and afterhyperpolarization currents in central neurons
Paola Pedarzani, Dieter D'hoedt, Kevina B Doorty, et al.
Brain : a Journal of Neurology
|
August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity
Simon Mead, Mark Poulter, Jon Beck, et al.
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Showing results (101-110 of 137) with videos related to
Sort By:
Page
of 14
The New England Journal of Medicine
|
January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129
Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
The EMBO Journal
|
November 29, 2002
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein
Emmanuel A Asante, Jacqueline M Linehan, Melanie Desbruslais, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2008
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice
Jonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Neuropathology and Applied Neurobiology
|
February 12, 2009
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L)
T Webb, S Mead, J Beck, et al.
The Journal of General Virology
|
July 9, 2010
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein
Malin K Sandberg, Huda Al-Doujaily, Christina J Sigurdson, et al.
The Journal of Pathology
|
February 5, 2011
Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study
Jonathan D F Wadsworth, Inmaculada Dalmau-Mena, Susan Joiner, et al.
Scientific Reports
|
May 8, 2015
A novel and rapid method for obtaining high titre intact prion strains from mammalian brain
Adam Wenborn, Cassandra Terry, Nathalie Gros, et al.
Science (New York, N.Y.)
|
November 13, 2004
Human prion protein with valine 129 prevents expression of variant CJD phenotype
Jonathan D F Wadsworth, Emmanuel A Asante, Melanie Desbruslais, et al.
The Journal of Biological Chemistry
|
September 20, 2002
Tamapin, a venom peptide from the Indian red scorpion (Mesobuthus tamulus) that targets small conductance Ca2+-activated K+ channels and afterhyperpolarization currents in central neurons
Paola Pedarzani, Dieter D'hoedt, Kevina B Doorty, et al.
Brain : a Journal of Neurology
|
August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity
Simon Mead, Mark Poulter, Jon Beck, et al.
Page
of 14