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John Collinge

Showing results (241-250 of 295) with videos related to

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Acta Neuropathologica|September 12, 2015
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathologyEmma L Clayton, Sarah Mizielinska, James R Edgar, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Molecular Cell|May 1, 2007
Disease-associated prion protein oligomers inhibit the 26S proteasomeMark Kristiansen, Pelagia Deriziotis, Derek E Dimcheff, et al.
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Communications Biology|July 31, 2020
Structural effects of the highly protective V127 polymorphism on human prion proteinLaszlo L P Hosszu, Rebecca Conners, Daljit Sangar, et al.
Brain : a Journal of Neurology|February 28, 2012
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic miceShabnam Ghazi-Noori, Kristina E Froud, Sarah Mizielinska, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Pageof 30

Showing results (241-250 of 295) with videos related to

Sort By:
Pageof 30
Acta Neuropathologica|September 12, 2015
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathologyEmma L Clayton, Sarah Mizielinska, James R Edgar, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Molecular Cell|May 1, 2007
Disease-associated prion protein oligomers inhibit the 26S proteasomeMark Kristiansen, Pelagia Deriziotis, Derek E Dimcheff, et al.
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Communications Biology|July 31, 2020
Structural effects of the highly protective V127 polymorphism on human prion proteinLaszlo L P Hosszu, Rebecca Conners, Daljit Sangar, et al.
Brain : a Journal of Neurology|February 28, 2012
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic miceShabnam Ghazi-Noori, Kristina E Froud, Sarah Mizielinska, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Pageof 30