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pro vyhledávání: '"C. Truax"'
Akademický článek
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Akademický článek
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Autor:
Leo McCluskey, John Q. Trojanowski, Bruce L. Miller, Linda K. Kwong, Virginia M.-Y. Lee, Murray Grossman, Manuela Neumann, Christopher M. Clark, Kunihiro Uryu, Lauren Elman, Lionel M. Igaz, Yan Xu, Adam C. Truax
Publikováno v:
The American Journal of Pathology. 173:182-194
TAR DNA-binding protein (TDP-43) has been recently described as a major pathological protein in both frontotemporal dementia with ubiquitin-positive inclusions (FTLD-U) and amyotrophic lateral sclerosis. However, little is known about the relative ab
Autor:
Adam C. Truax, Linda K. Kwong, John Q. Trojanowski, Hans A. Kretzschmar, Virginia M.-Y. Lee, Bruce L. Miller, Murray Grossman, Manuela Neumann, Ben Vanmassenhove, Chrisopher M. Clark, Vivianna M. Van Deerlin
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 66:177-183
TDP-43 was recently identified as the major disease protein in neuronal inclusions in frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U). TDP-43 is not only linked to disease mechanisms in FTLD-U, but it is also the most ro
Autor:
Thomas T. Chou, Adam C. Truax, Ian R. A. Mackenzie, Christopher M. Clark, Murray Grossman, Virginia M.-Y. Lee, Wolfgang Feiden, Deepak M. Sampathu, Matthew Micsenyi, Theresa Schuck, Bruce L. Miller, Manuela Neumann, Eliezer Masliah, John Q. Trojanowski, Howard Feldman, Jennifer Bruce, Hans A. Kretzschmar, Linda K. Kwong, Leo McCluskey
Publikováno v:
Science. 314:130-133
Ubiquitin-positive, tau- and α-synuclein–negative inclusions are hallmarks of frontotemporal lobar degeneration with ubiquitin-positive inclusions and amyotrophic lateral sclerosis. Although the identity of the ubiquitinated protein specific to ei
Autor:
Tsao-Wei Liang, Matthew B. Stern, Paul T. Kotzbauer, Adam C. Truax, Virginia M.-Y. Lee, John Q. Trojanowski
Publikováno v:
Movement Disorders. 21:718-722
We describe an atypical case of pantothenate kinase-associated neurodegeneration (PKAN) in which slowly progressive arm tremor was the predominant symptom beginning at the age of 25, with late-onset dystonia and dysarthria developing at the age of 50
Autor:
Craig H. Selzman, L. Cotiguala, K. Peterson-Short, Barbara C. Cahill, T. Maughan, Theodore G. Liou, Adrian Carlson, C. Truax, Sanjeev M. Raman, B. Sirandas, W. Doidge, Stephen H. McKellar
Publikováno v:
The Journal of Heart and Lung Transplantation. 36:S403
Publikováno v:
Journal of Contaminant Hydrology. 29:205-224
Few proven technologies exist that may be used to treat dense non-aqueous phase liquid (DNAPL) contaminants. In-situ chemical flushing is a proposed technology which consists of flushing DNAPL source zones with a reactive solution to degrade the cont
Autor:
Thomas T. Chou, Murray Grossman, Jennifer Bruce, Virginia M.-Y. Lee, Manuela Neumann, Deepak M. Sampathu, Adam C. Truax, Matthew Micsenyi, John Q. Trojanowski, Linda K. Kwong
Frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) is a common neuropathological subtype of frontotemporal dementia. Although this subtype of frontotemporal dementia is defined by the presence of ubiquitin-positive but tau-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::535f1c6f18d360d5ac4fd9dbca8f4317
https://europepmc.org/articles/PMC1780184/
https://europepmc.org/articles/PMC1780184/
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 25(3)
Mutations in the pantothenate kinase 2 (PANK2) gene have been identified in patients with neurodegeneration with brain iron accumulation (NBIA; formerly Hallervorden-Spatz disease). However, the mechanisms by which these mutations cause neurodegenera