X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2770) 2770
Book Review (509) 509
Publication (252) 252
Newsletter (251) 251
Newspaper Article (71) 71
Book Chapter (46) 46
Conference Proceeding (28) 28
Book / eBook (18) 18
Dissertation (11) 11
Magazine Article (6) 6
Government Document (5) 5
Web Resource (5) 5
Reference (4) 4
Transcript (4) 4
Streaming Video (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2222) 2222
humans (1741) 1741
neuronal ceroid-lipofuscinosis (1404) 1404
animals (1040) 1040
neuronal ceroid-lipofuscinoses - genetics (729) 729
male (706) 706
female (693) 693
neuronal ceroid lipofuscinosis (624) 624
neuronal ceroid-lipofuscinoses - pathology (575) 575
neurosciences (541) 541
child (505) 505
genetics & heredity (493) 493
clinical neurology (464) 464
biochemistry & molecular biology (462) 462
mice (452) 452
mutation (418) 418
neuronal ceroid-lipofuscinoses - metabolism (354) 354
child, preschool (352) 352
adult (339) 339
batten disease (337) 337
disease models, animal (333) 333
neurons (328) 328
batten-disease (324) 324
neurodegeneration (306) 306
adolescent (300) 300
neuronal ceroid-lipofuscinoses - diagnosis (297) 297
disease (273) 273
brain - pathology (272) 272
genetic aspects (266) 266
brain (258) 258
mutations (255) 255
research (244) 244
medical research (241) 241
mouse model (240) 240
analysis (239) 239
infant (237) 237
neuronal ceroid-lipofuscinoses - physiopathology (236) 236
proteins (223) 223
medicine, experimental (219) 219
cell biology (217) 217
pediatrics (214) 214
membrane proteins - genetics (210) 210
gene (208) 208
nervous system diseases (207) 207
article (196) 196
protein (195) 195
pathology (193) 193
neurology (191) 191
medicine, research & experimental (188) 188
phenotype (187) 187
dogs (183) 183
mice, knockout (169) 169
enzymes (167) 167
cln3 (166) 166
mitochondrial atp synthase (163) 163
lysosomal storage disease (162) 162
brain - metabolism (156) 156
mice, inbred c57bl (156) 156
neuronal ceroid-lipofuscinoses - enzymology (151) 151
molecular sequence data (149) 149
microscopy, electron (147) 147
genes (145) 145
genetics (144) 144
epilepsy (142) 142
lysosomes - metabolism (141) 141
central-nervous-system (138) 138
diagnosis (136) 136
membrane glycoproteins - genetics (135) 135
storage (134) 134
children (131) 131
magnetic resonance imaging (129) 129
molecular chaperones - genetics (129) 129
neuronal ceroid-lipofuscinoses (128) 128
cells, cultured (126) 126
neuronal ceroid-lipofuscinoses - veterinary (124) 124
subunit-c (122) 122
ncl (121) 121
seizures (121) 121
expression (118) 118
pedigree (117) 117
neuronal ceroid-lipofuscinoses - complications (116) 116
neurons - pathology (115) 115
amino acid sequence (113) 113
gene therapy (113) 113
neurons - metabolism (112) 112
dipeptidyl-peptidases and tripeptidyl-peptidases (111) 111
sheep (111) 111
aminopeptidases (110) 110
serine proteases (109) 109
gene expression (107) 107
middle aged (106) 106
palmitoyl-protein thioesterase (103) 103
lysosomes (102) 102
medicine (102) 102
immunohistochemistry (101) 101
neurodegenerative diseases (100) 100
stem cells (100) 100
neuronal ceroid lipofuscinoses (99) 99
research article (99) 99
physiological aspects (98) 98
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (16) 16
Online Resources - Online (6) 6
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
Gerstein Science - Reference (1) 1
Scarborough Hospital - General (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Mississauga - Missing (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3006) 3006
German (40) 40
French (38) 38
Spanish (31) 31
Japanese (24) 24
Portuguese (10) 10
Czech (7) 7
Chinese (6) 6
Polish (6) 6
Turkish (4) 4
Dutch (3) 3
Italian (3) 3
Russian (3) 3
Finnish (2) 2
Danish (1) 1
Norwegian (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 01/2019, Volume 14, Issue 1, pp. 19 - 19
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 151 - 12
Neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative lysosomal storage disorders. CLN5 deficiency causes a subtype of NCL, referred... 
STORAGE | WILD-TYPE | A-BETA COMPONENT | MESSENGER-RNA | MONITORING AUTOPHAGY | PRESYNAPTIC PROTEIN | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | BATTEN-DISEASE | EXPRESSION | PARKINSONS-DISEASE | Pathogenicity | Proteins | Fibroblasts | Lysosomes | Lysosomal storage diseases | Neuronal ceroid lipofuscinosis | Synuclein | Lysosomal protein | Autophagy | Phagocytosis
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 10/2019, Volume 1861, Issue 10, pp. 182993 - 182993
Mutations in the gene (PARK9, CLN12, OMIM ) were initially associated with a form of Parkinson's Disease (PD) known as Kufor Rakeb Syndrome (KRS). However, the... 
P type ATPase | Parkinson's disease | Neuronal ceroid lipofuscinosis | Lipid homeostasis | P5B–ATP13A2 | Phospholipidosis | Index Medicus
Journal Article
Glia, ISSN 0894-1491, 10/2019, Volume 67, Issue 10, pp. 1933 - 1957
α‐Synucleinopathies are neurodegenerative diseases that are characterized pathologically by α‐synuclein inclusions in neurons and glia. The pathologic... 
Parkinson's disease | multiple system atrophy | glia | Drosophila | α‐Synuclein | Phenotypes | Dopamine | Transcription | Neurodegenerative diseases | Neurons | Inclusions | Synuclein | Neuronal-glial interactions | Neurological diseases | Atrophy | Insects | Autonomic nervous system | Neurodegeneration | Inclusion bodies | In vivo methods and tests | Dopamine receptors | Index Medicus
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 09/2019, Volume 42, Issue 5, pp. 944 - 954
Mutations in at least 13 different genes (called CLN s) underlie various forms of neuronal ceroid lipofuscinoses (NCLs), a group of the most common... 
neurodegeneration | palmitoyl‐protein thioesterase‐1 | lysosomal storage disease | infantile neuronal ceroid lipofuscinosis | juvenile neuronal ceroid lipofuscinosis | batten disease
Journal Article