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Manuela Neumann

Showing results (91-100 of 175) with videos related to

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Acta Neuropathologica|July 31, 2012
Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutationsManuela Neumann, Chiara F Valori, Olaf Ansorge, et al.
Alzheimer Disease and Associated Disorders|December 14, 2004
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer diseaseHans H Klünemann, Ekaterina Rogaeva, Manuela Neumann, et al.
Acta Neuropathologica|January 7, 2009
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathiesManuela Neumann, Linda K Kwong, Edward B Lee, et al.
Cell Host & Microbe|July 13, 2018
Arabidopsis thaliana and Pseudomonas Pathogens Exhibit Stable Associations over Evolutionary TimescalesTalia L Karasov, Juliana Almario, Claudia Friedemann, et al.
Archives of Neurology|October 10, 2007
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusionsMurray Grossman, Elisabeth M Wood, Peachie Moore, et al.
Acta Neuropathologica|June 7, 2011
A harmonized classification system for FTLD-TDP pathologyIan R A Mackenzie, Manuela Neumann, Atik Baborie, et al.
Brain : a Journal of Neurology|May 11, 2023
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment responseCarlo Wilke, David Pellerin, David Mengel, et al.
Archives of Neurology|August 19, 2007
Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutationsVivianna M Van Deerlin, Elisabeth McCarty Wood, Peachie Moore, et al.
EMBO Reports|May 30, 2002
Hyperphosphorylation and insolubility of alpha-synuclein in transgenic mouse oligodendrocytesPhilipp J Kahle, Manuela Neumann, Laurence Ozmen, et al.
Journal of Neuropathology and Experimental Neurology|June 4, 2008
Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathiesKunihiro Uryu, Hanae Nakashima-Yasuda, Mark S Forman, et al.
Pageof 18

Showing results (91-100 of 175) with videos related to

Sort By:
Pageof 18
Acta Neuropathologica|July 31, 2012
Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutationsManuela Neumann, Chiara F Valori, Olaf Ansorge, et al.
Alzheimer Disease and Associated Disorders|December 14, 2004
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer diseaseHans H Klünemann, Ekaterina Rogaeva, Manuela Neumann, et al.
Acta Neuropathologica|January 7, 2009
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathiesManuela Neumann, Linda K Kwong, Edward B Lee, et al.
Cell Host & Microbe|July 13, 2018
Arabidopsis thaliana and Pseudomonas Pathogens Exhibit Stable Associations over Evolutionary TimescalesTalia L Karasov, Juliana Almario, Claudia Friedemann, et al.
Archives of Neurology|October 10, 2007
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusionsMurray Grossman, Elisabeth M Wood, Peachie Moore, et al.
Acta Neuropathologica|June 7, 2011
A harmonized classification system for FTLD-TDP pathologyIan R A Mackenzie, Manuela Neumann, Atik Baborie, et al.
Brain : a Journal of Neurology|May 11, 2023
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment responseCarlo Wilke, David Pellerin, David Mengel, et al.
Archives of Neurology|August 19, 2007
Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutationsVivianna M Van Deerlin, Elisabeth McCarty Wood, Peachie Moore, et al.
EMBO Reports|May 30, 2002
Hyperphosphorylation and insolubility of alpha-synuclein in transgenic mouse oligodendrocytesPhilipp J Kahle, Manuela Neumann, Laurence Ozmen, et al.
Journal of Neuropathology and Experimental Neurology|June 4, 2008
Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathiesKunihiro Uryu, Hanae Nakashima-Yasuda, Mark S Forman, et al.
Pageof 18