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Manuela Neumann

Showing results (101-110 of 175) with videos related to

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Journal of Neuropathology and Experimental Neurology|March 16, 2007
TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusionsManuela Neumann, Linda K Kwong, Adam C Truax, et al.
Nature Communications|October 20, 2021
Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactionsShu Liu, André Hossinger, Stefanie-Elisabeth Heumüller, et al.
The Journal of Clinical Investigation|November 20, 2002
Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathiesManuela Neumann, Philipp J Kahle, Benoit I Giasson, et al.
Plos One|February 2, 2013
FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophyChristine L Kragh, Gwenaëlle Fillon, Amanda Gysbers, et al.
Acta Neuropathologica|February 6, 2013
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutationsKohji Mori, Sven Lammich, Ian R A Mackenzie, et al.
Acta Neuropathologica Communications|August 5, 2018
Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriersPetra Frick, Chantal Sellier, Ian R A Mackenzie, et al.
Annals of Neurology|August 2, 2003
Beta-amyloid peptides in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseJens Wiltfang, Hermann Esselmann, Alexander Smirnov, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 4, 2010
TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97Gillian P Ritson, Sara K Custer, Brian D Freibaum, et al.
The American Journal of Pathology|June 7, 2008
Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosisLionel M Igaz, Linda K Kwong, Yan Xu, et al.
Acta Neuropathologica|June 21, 2020
Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALSKatherine D LaClair, Qihui Zhou, Meike Michaelsen, et al.
Pageof 18

Showing results (101-110 of 175) with videos related to

Sort By:
Pageof 18
Journal of Neuropathology and Experimental Neurology|March 16, 2007
TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusionsManuela Neumann, Linda K Kwong, Adam C Truax, et al.
Nature Communications|October 20, 2021
Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactionsShu Liu, André Hossinger, Stefanie-Elisabeth Heumüller, et al.
The Journal of Clinical Investigation|November 20, 2002
Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathiesManuela Neumann, Philipp J Kahle, Benoit I Giasson, et al.
Plos One|February 2, 2013
FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophyChristine L Kragh, Gwenaëlle Fillon, Amanda Gysbers, et al.
Acta Neuropathologica|February 6, 2013
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutationsKohji Mori, Sven Lammich, Ian R A Mackenzie, et al.
Acta Neuropathologica Communications|August 5, 2018
Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriersPetra Frick, Chantal Sellier, Ian R A Mackenzie, et al.
Annals of Neurology|August 2, 2003
Beta-amyloid peptides in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseJens Wiltfang, Hermann Esselmann, Alexander Smirnov, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 4, 2010
TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97Gillian P Ritson, Sara K Custer, Brian D Freibaum, et al.
The American Journal of Pathology|June 7, 2008
Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosisLionel M Igaz, Linda K Kwong, Yan Xu, et al.
Acta Neuropathologica|June 21, 2020
Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALSKatherine D LaClair, Qihui Zhou, Meike Michaelsen, et al.
Pageof 18