X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3237) 3237
Publication (639) 639
Book Chapter (94) 94
Book / eBook (56) 56
Book Review (38) 38
Conference Proceeding (20) 20
Magazine Article (16) 16
Newspaper Article (8) 8
Dissertation (3) 3
Journal / eJournal (3) 3
Newsletter (2) 2
Trade Publication Article (2) 2
Data Set (1) 1
Government Document (1) 1
Presentation (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (2069) 2069
index medicus (1672) 1672
leber congenital amaurosis (1347) 1347
animals (1067) 1067
ophthalmology (1004) 1004
male (949) 949
female (844) 844
mutation (653) 653
mice (570) 570
genetics & heredity (568) 568
gene therapy (566) 566
retina (561) 561
lebers congenital amaurosis (548) 548
eye diseases (483) 483
sense organs (482) 482
retinal degeneration (469) 469
adult (456) 456
middle aged (440) 440
biochemistry & molecular biology (431) 431
genetic structures (422) 422
retinitis-pigmentosa (415) 415
blindness (413) 413
medicine, research & experimental (400) 400
article (391) 391
amaurosis fugax (386) 386
mutations (354) 354
eye proteins - genetics (353) 353
genetic aspects (339) 339
aged (334) 334
photoreceptors (332) 332
research (316) 316
gene-therapy (309) 309
disease models, animal (298) 298
electroretinography (293) 293
child (291) 291
retinitis pigmentosa (291) 291
disease (287) 287
leber congenital amaurosis - genetics (286) 286
dependovirus - genetics (273) 273
mouse model (273) 273
pedigree (272) 272
genetic therapy - methods (267) 267
adolescent (266) 266
retinitis pigmentosa - genetics (258) 258
genetics (252) 252
biotechnology & applied microbiology (250) 250
phenotype (250) 250
retinal degeneration - genetics (240) 240
amaurosis (237) 237
genes (230) 230
care and treatment (223) 223
degeneration (219) 219
genetic vectors (218) 218
leber's congenital amaurosis (215) 215
genetic therapy (212) 212
neurosciences (211) 211
proteins (211) 211
macular degeneration (207) 207
retina - metabolism (200) 200
health aspects (195) 195
gene (194) 194
clinical neurology (192) 192
congenital amaurosis (190) 190
mice, inbred c57bl (190) 190
research article (190) 190
dna mutational analysis (188) 188
analysis (187) 187
multidisciplinary sciences (181) 181
amaurosis fugax - etiology (177) 177
therapy (176) 176
expression (175) 175
child, preschool (172) 172
in-vivo (169) 169
cell biology (165) 165
gene expression (164) 164
physiological aspects (162) 162
retina - pathology (160) 160
risk factors (159) 159
cone-rod dystrophy (156) 156
visual cycle (156) 156
dystrophy (154) 154
mice, knockout (154) 154
genetic disorders (153) 153
vision (151) 151
molecular sequence data (148) 148
surgery (148) 148
cis-trans-isomerases (144) 144
medicine (144) 144
young adult (142) 142
rpe65 mutations (139) 139
carrier proteins - genetics (138) 138
genotype (138) 138
rpe65 (138) 138
gene transfer techniques (135) 135
eye proteins - metabolism (130) 130
diagnosis (129) 129
protein (127) 127
viruses (124) 124
visual acuity (120) 120
tomography, optical coherence (118) 118
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (31) 31
Collection Dvlpm't (Acquisitions) - Vendor file (12) 12
Gerstein Science - Stacks (12) 12
UTL at Downsview - May be requested (7) 7
UofT at Scarborough - Stacks (7) 7
OISE - Stacks (6) 6
UofT at Mississauga - Stacks (5) 5
New College (Ivey) - Stacks (3) 3
St. Michael's College (John M. Kelly) - 2nd Floor (3) 3
Victoria University E.J. Pratt - Stacks (3) 3
Online Resources - Online (2) 2
Thomas Fisher Rare Book - May be requested at Fisher (2) 2
Baycrest Hospital - Resident/Client Library (1) 1
Bridgepoint Health - Stacks (1) 1
Markham Stouffville Hospital - Stacks (1) 1
OISE - Bindery (1) 1
OISE - Periodical Stacks (1) 1
OISE - Storage (1) 1
Trinity College (John W Graham) - Stacks (1) 1
University College (Laidlaw) - Stacks (1) 1
UofT Schools - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3104) 3104
German (85) 85
Spanish (43) 43
French (39) 39
Korean (15) 15
Japanese (13) 13
Russian (10) 10
Italian (9) 9
Portuguese (8) 8
Polish (7) 7
Turkish (4) 4
Chinese (3) 3
Romanian (3) 3
Czech (2) 2
Danish (2) 2
Dutch (2) 2
Finnish (2) 2
Slovenian (2) 2
Swedish (2) 2
Persian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


eBook
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 09/2017, Volume 101, Issue 9, pp. 1147 - 1154
Journal Article
Human Gene Therapy, ISSN 1043-0342, 02/2016, Volume 27, Issue 2, pp. 134 - 147
Retinal degenerative diseases are a leading cause of irreversible blindness. Retinal cell death is the main cause of vision loss in genetic disorders such as... 
Reviews | PHOTORECEPTOR PRECURSORS | MEDICINE, RESEARCH & EXPERIMENTAL | RESTORES VISUAL RESPONSES | RETINAL PIGMENTED EPITHELIUM | PLURIPOTENT STEM-CELLS | CONE VIABILITY FACTOR | LEBER CONGENITAL AMAUROSIS | PHASE-I TRIAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | OPTIMIZED ALLOTOPIC EXPRESSION | MOUSE MODEL | GENETICS & HEREDITY | RETINITIS-PIGMENTOSA | Leber Congenital Amaurosis - pathology | Cell- and Tissue-Based Therapy - methods | Dependovirus - genetics | Retina - metabolism | Optogenetics - methods | Blindness - metabolism | Humans | Blindness - pathology | Leber Congenital Amaurosis - metabolism | Lentivirus - genetics | cis-trans-Isomerases - metabolism | Blindness - therapy | Leber Congenital Amaurosis - therapy | Genetic Vectors - chemistry | Genetic Vectors - metabolism | Retinitis Pigmentosa - genetics | Retinitis Pigmentosa - metabolism | Clinical Trials as Topic | Leber Congenital Amaurosis - genetics | Blindness - genetics | Macular Degeneration - metabolism | Macular Degeneration - congenital | cis-trans-Isomerases - genetics | Macular Degeneration - genetics | Macular Degeneration - therapy | Retinitis Pigmentosa - therapy | CRISPR-Cas Systems | Adenoviruses, Human - genetics | Retina - pathology | Retinitis Pigmentosa - pathology | Genetic Therapy - methods | Macular Degeneration - pathology | Macular degeneration | Therapy | Cell death | Retinal cells | Retinitis pigmentosa | Blindness | Disorders | Retinal degeneration | Retina | Retinitis | Age | Life Sciences
Journal Article
JAMA OPHTHALMOLOGY, ISSN 2168-6165, 10/2019, Volume 137, Issue 10, pp. 1123 - 1124
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 05/2015, Volume 372, Issue 20, pp. 1887 - 1897
Journal Article
2011, ISBN 9780547554884, 661
Book
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 9, pp. 975 - 977
Journal Article
Gene Therapy, ISSN 0969-7128, 2014, Volume 21, Issue 7, pp. 662 - 672
Journal Article