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Simon Mead

Showing results (111-120 of 231) with videos related to

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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 miceJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Brain : a Journal of Neurology|April 4, 2013
The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studiesAndrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.
Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, et al.
Brain : a Journal of Neurology|August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneitySimon Mead, Mark Poulter, Jon Beck, et al.
Brain : a Journal of Neurology|October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseasesDurrenajaf Siddique, Harpreet Hyare, Stephen Wroe, et al.
Brain : a Journal of Neurology|August 14, 2015
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 yearsPeter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, et al.
Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2013
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasiaJonathan D Rohrer, Jonathan Beck, Vincent Plagnol, et al.
Pageof 24

Showing results (111-120 of 231) with videos related to

Sort By:
Pageof 24
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 miceJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Brain : a Journal of Neurology|April 4, 2013
The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studiesAndrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.
Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, et al.
Brain : a Journal of Neurology|August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneitySimon Mead, Mark Poulter, Jon Beck, et al.
Brain : a Journal of Neurology|October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseasesDurrenajaf Siddique, Harpreet Hyare, Stephen Wroe, et al.
Brain : a Journal of Neurology|August 14, 2015
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 yearsPeter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, et al.
Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2013
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasiaJonathan D Rohrer, Jonathan Beck, Vincent Plagnol, et al.
Pageof 24