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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 mice
Jonathan 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 studies
Andrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Neurobiology of Aging
|
March 2, 2015
Rare structural genetic variation in human prion diseases
Ana 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 disease
Luke 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 heterogeneity
Simon 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 diseases
Durrenajaf 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 years
Peter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Nature Communications
|
August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
Penny 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 GSS
Emmanuel 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 aphasia
Jonathan D Rohrer, Jonathan Beck, Vincent Plagnol, et al.
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of 24
Search research articles
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Showing results (111-120 of 231) with videos related to
Sort By:
Page
of 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 mice
Jonathan 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 studies
Andrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Neurobiology of Aging
|
March 2, 2015
Rare structural genetic variation in human prion diseases
Ana 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 disease
Luke 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 heterogeneity
Simon 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 diseases
Durrenajaf 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 years
Peter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Nature Communications
|
August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
Penny 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 GSS
Emmanuel 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 aphasia
Jonathan D Rohrer, Jonathan Beck, Vincent Plagnol, et al.
Page
of 24