X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1461) 1461
Publication (167) 167
Book Chapter (19) 19
Book Review (17) 17
Book / eBook (9) 9
Conference Proceeding (3) 3
Dissertation (3) 3
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (861) 861
neurosciences (843) 843
index medicus (688) 688
animals (613) 613
male (473) 473
clinical neurology (456) 456
female (408) 408
pathology (407) 407
multiple system atrophy (375) 375
glial cytoplasmic inclusions (372) 372
alpha-synuclein (332) 332
immunohistochemistry (286) 286
neurons (284) 284
middle aged (281) 281
aged (267) 267
brain (266) 266
mice (252) 252
parkinsons-disease (252) 252
glial fibrillary acidic protein - metabolism (239) 239
alzheimers-disease (236) 236
neurodegeneration (229) 229
neurodegenerative diseases (227) 227
proteins (225) 225
nervous system (222) 222
neurology (200) 200
brain - pathology (195) 195
astrocytes (191) 191
parkinson's disease (187) 187
neuronal-glial interactions (184) 184
rats (182) 182
nervous system diseases (180) 180
neurons - metabolism (172) 172
cell biology (165) 165
glial cells (160) 160
α-synuclein (157) 157
brain - metabolism (156) 156
mutation (148) 148
adult (146) 146
progressive supranuclear palsy (145) 145
biochemistry & molecular biology (144) 144
analysis (142) 142
lewy bodies (141) 141
atrophy (139) 139
article (135) 135
multiple system atrophy - pathology (135) 135
astrocytes - metabolism (134) 134
aged, 80 and over (133) 133
neurons - pathology (133) 133
nerve tissue proteins - metabolism (131) 131
amyotrophic-lateral-sclerosis (129) 129
central-nervous-system (129) 129
alpha-synuclein - metabolism (127) 127
disease models, animal (125) 125
dementia (124) 124
glial fibrillary acidic protein (122) 122
medicine (122) 122
expression (118) 118
disease (117) 117
amyotrophic lateral sclerosis (116) 116
research article (115) 115
glial-cells (114) 114
olivopontocerebellar atrophy (114) 114
synucleins (114) 114
cells, cultured (113) 113
research (113) 113
inclusion bodies - pathology (110) 110
rodents (108) 108
degeneration (107) 107
synuclein (107) 107
oxidative stress (103) 103
inclusion bodies - metabolism (101) 101
multidisciplinary sciences (100) 100
neuroscience (99) 99
apoptosis (98) 98
gene expression (98) 98
medicine & public health (98) 98
alzheimer's disease (97) 97
science (96) 96
transgenic mice (96) 96
inflammation (94) 94
oligodendrocytes (91) 91
mice, transgenic (88) 88
multiple system atrophy - metabolism (88) 88
fibrillary acidic protein (87) 87
microglia (87) 87
neuroglia - metabolism (86) 86
neuroglia - pathology (85) 85
phosphorylation (85) 85
central nervous system (83) 83
genetic aspects (82) 82
movement disorders (82) 82
physiological aspects (81) 81
diagnosis (80) 80
pathogenesis (79) 79
astrocytes - pathology (77) 77
glial fibrillary acidic protein - genetics (77) 77
microscopy, electron (76) 76
tau proteins - metabolism (75) 75
glial cytoplasmic inclusion (74) 74
oligodendroglia - metabolism (74) 74
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1472) 1472
French (5) 5
Spanish (5) 5
Japanese (3) 3
Chinese (1) 1
German (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Neuropathology and Applied Neurobiology, ISSN 0305-1846, 10/2012, Volume 38, Issue 6, pp. 559 - 571
Y. Chiba, S. Takei, N. Kawamura, Y. Kawaguchi, K. Sasaki, S. Hasegawa‐Ishii, A. Furukawa, M. Hosokawa and A. Shimada (2012) Neuropathology and Applied... 
proteasome | gamma‐tubulin | multiple system atrophy | histone deacetylase 6 | glial cytoplasmic inclusion | aggresome | Aggresome | Glial cytoplasmic inclusion | Multiple system atrophy | Gamma-tubulin | Histone deacetylase 6 | Proteasome | NEURODEGENERATIVE DISEASE | ALPHA-SYNUCLEIN INCLUSIONS | PATHOLOGY | PONTINE NUCLEI | NEUROSCIENCES | CLINICAL NEUROLOGY | gamma-tubulin | OLIVOPONTOCEREBELLAR ATROPHY | MOUSE MODEL | BODY FORMATION | LEWY BODIES | PARKINSONS-DISEASE | TRANSGENIC MICE | Neurons - pathology | Histone Deacetylase 6 | Multiple System Atrophy - pathology | Neuroglia - pathology | Humans | Middle Aged | Histone Deacetylases - metabolism | Male | Brain - metabolism | Tubulin - metabolism | Multiple System Atrophy - metabolism | Aged, 80 and over | Brain - pathology | Inclusion Bodies - pathology | Female | Neuroglia - metabolism | Aged | Neurons - metabolism | Lewy Bodies - metabolism | Proteasome Endopeptidase Complex - metabolism | Inclusion Bodies - metabolism | Lewy Bodies - pathology | Atrophy | Immunohistochemistry | Viral antibodies | Embryonic development | Nervous system diseases | Parkinson's disease | Analysis | Antibodies | Heat shock proteins | Biosynthesis | Tubulins | Dementia | Histone deacetylase | Hsp90 protein | Neurodegenerative diseases | Neuropathology | Fibrils | Hsp70 protein | Neuronal-glial interactions | Lewy bodies | Neurological diseases | Tubulin | aggresomes | Inclusion bodies | Oligodendrocytes | Dementia disorders | Immunoelectron microscopy | Immunofluorescence | Movement disorders
Journal Article
Journal Article
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 11/2011, Volume 45, Issue 3, pp. 409 - 421
Fused in sarcoma (FUS)-immunoreactive neuronal and glial inclusions define a novel molecular pathology called FUS proteinopathy. FUS has been shown to be a... 
Neurochemistry | Neurology | Neurosciences | Neurofilament | Biomedicine | FUS | α-Internexin | Proteomics | Frontotemporal lobar degeneration | Immunoelectron microscopy | Neuronal intermediate filament inclusion disease | Cell Biology | alpha-Internexin | PRO-ONCOPROTEIN TLS/FUS | BODY DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | AMYOTROPHIC-LATERAL-SCLEROSIS | PARASPECKLES | NEUROSCIENCES | NUCLEAR FACTOR TDP-43 | IN-VIVO | TARDBP MUTATIONS | INTRANUCLEAR INCLUSIONS | BINDING | Immunohistochemistry | Frontotemporal Lobar Degeneration - pathology | Neurons - pathology | Intermediate Filaments - pathology | Microscopy, Electron, Transmission - methods | Humans | Middle Aged | Male | RNA-Binding Protein FUS - metabolism | Intermediate Filaments - metabolism | Frontotemporal Lobar Degeneration - metabolism | Brain - pathology | Inclusion Bodies - pathology | Adult | Female | Aged | Microscopy, Immunoelectron - methods | Neurofilament Proteins - metabolism | Immunopathology | Usage | Care and treatment | Sarcoma | Transmission electron microscopes | Diagnosis | Research | RNA | Intermediate filaments | FUS gene | Amyotrophic lateral sclerosis | Nervous system | Neuronal-glial interactions | Cytomegalic inclusion disease | FUS protein | Inclusion bodies | Euchromatin | Neurofilament protein | Immunoreactivity | Mutation | Frontotemporal dementia | Cytoplasm | Esclerosi lateral amiotròfica | Neurodegenerative diseases | Malalties neurodegeneratives | immunoelectron microscopy | neurofilament | frontotemporal lobar degeneration | α-internexin
Journal Article