X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (489) 489
Publication (66) 66
Book / eBook (18) 18
Book Chapter (13) 13
Conference Proceeding (7) 7
Book Review (6) 6
Magazine Article (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (356) 356
male (236) 236
female (214) 214
ophthalmology (208) 208
index medicus (182) 182
electroretinography (175) 175
animals (162) 162
adult (147) 147
stationary night blindness (128) 128
night blindness - genetics (115) 115
mutation (113) 113
middle aged (112) 112
night blindness (100) 100
retina - pathology (93) 93
child (87) 87
mice (83) 83
adolescent (81) 81
retina (81) 81
night blindness - pathology (79) 79
pedigree (73) 73
sense organs (67) 67
retinal degeneration - genetics (65) 65
night blindness - etiology (64) 64
genetic structures (63) 63
visual acuity (61) 61
night blindness - physiopathology (60) 60
dark adaptation (58) 58
disease models, animal (56) 56
eye diseases (56) 56
night blindness - diagnosis (56) 56
retinal degeneration - pathology (55) 55
fundus oculi (54) 54
gene (53) 53
aged (52) 52
visual fields (51) 51
phenotype (48) 48
retinal degeneration (48) 48
child, preschool (47) 47
electroretinogram (47) 47
fluorescein angiography (47) 47
genetics & heredity (47) 47
mutations (47) 47
biochemistry & molecular biology (44) 44
photoreceptors (44) 44
retinitis pigmentosa - genetics (44) 44
dna mutational analysis (41) 41
retinitis pigmentosa (41) 41
neurosciences (40) 40
retinitis-pigmentosa (40) 40
genetic aspects (37) 37
research (36) 36
retina - physiopathology (36) 36
research article (35) 35
retinal degeneration - physiopathology (35) 35
article (34) 34
myopia - genetics (34) 34
retina - metabolism (34) 34
eye diseases, hereditary - genetics (33) 33
retinal cone photoreceptor cells - pathology (33) 33
analysis (31) 31
tomography, optical coherence (31) 31
light (29) 29
mice, inbred c57bl (29) 29
molecular sequence data (29) 29
night blindness - congenital (29) 29
genetic diseases, x-linked - genetics (28) 28
photoreceptor cells, vertebrate - pathology (28) 28
retinitis pigmentosa - pathology (28) 28
blindness (26) 26
night blindness - complications (26) 26
retinal degeneration - diagnosis (26) 26
medicine (25) 25
polymerase chain reaction (25) 25
proteins (25) 25
retinal rod photoreceptor cells - pathology (25) 25
syndrome (25) 25
physiological aspects (24) 24
retinal diseases - genetics (24) 24
genetics (23) 23
medicine & public health (23) 23
night blindness - metabolism (23) 23
retinal diseases - diagnosis (23) 23
disease (22) 22
dystrophy (22) 22
electroretinography - methods (22) 22
infant (22) 22
mice, knockout (22) 22
multidisciplinary sciences (22) 22
myopia - pathology (22) 22
vitamin a deficiency - complications (22) 22
young adult (22) 22
congenital stationary night blindness (21) 21
degeneration (21) 21
dominant retinitis-pigmentosa (21) 21
eye proteins - genetics (21) 21
genetic disorders (21) 21
genotype (21) 21
immunohistochemistry (21) 21
mouse (21) 21
rod (21) 21
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (11) 11
Regis College - Stacks (7) 7
Online Resources - Online (3) 3
UTL at Downsview - May be requested (3) 3
St. Augustine's Seminary - Stacks (2) 2
Trinity College (John W Graham) - Stacks (2) 2
Victoria University E.J. Pratt - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Stacks (1) 1
Knox College (Caven) - Stacks (1) 1
OISE - Stacks (1) 1
Regis College - Lonergan Research Institute (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Trinity College (John W Graham) - Storage (1) 1
Trinity College (John W Graham) - Wycliffe Storage (1) 1
UofT at Mississauga - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University E.J. Pratt - Storage (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (490) 490
French (6) 6
Japanese (6) 6
German (5) 5
Polish (4) 4
Spanish (3) 3
Hebrew (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 1011 - 1019
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 03/2017, Volume 58, Issue 3, pp. 1768 - 1778
PURPOSE. Mutations in LRIT3 lead to complete congenital stationary night blindness (cCSNB). Using a cCSNB mouse model lacking Lrit3 (nob6), we recently have... 
Retina | Congenital stationary night blindness | Multielectrode array | Electron microscopy | LRIT3 | METABOTROPIC GLUTAMATE-RECEPTOR | PHOTORECEPTOR SYNAPSES | congenital stationary night blindness | OUTER PLEXIFORM LAYER | MAMMALIAN RETINA | RETINAL GANGLION-CELLS | multielectrode array | retina | MGLUR6 | OPHTHALMOLOGY | electron microscopy | MOUSE RETINA | NORMAL LIGHT | STATIONARY NIGHT BLINDNESS | VISUAL RESPONSES | Immunohistochemistry | Synaptic Transmission - genetics | Night Blindness - metabolism | Humans | Male | Dendrites - ultrastructure | Retinal Cone Photoreceptor Cells - ultrastructure | Myopia - metabolism | Young Adult | Synapses - metabolism | DNA Mutational Analysis | Night Blindness - pathology | Female | Genetic Diseases, X-Linked - genetics | Membrane Proteins - metabolism | Retrospective Studies | Night Blindness - genetics | Electroretinography | Dendrites - metabolism | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary - pathology | Membrane Proteins - genetics | Myopia - pathology | Synapses - ultrastructure | Genetic Diseases, X-Linked - metabolism | Microscopy, Electron | Eye Diseases, Hereditary - genetics | Mice, Knockout | DNA - genetics | Myopia - genetics | Animals | Retinal Bipolar Cells - ultrastructure | Genetic Diseases, X-Linked - pathology | Mice | Mutation | Retinal Cone Photoreceptor Cells - metabolism | Eye Diseases, Hereditary - metabolism | Life Sciences | Human health and pathology | Sensory Organs | Visual Neuroscience
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, p. e0137072
Congenital stationary night blindness (CSNB) is a non-progressive, clinically and genetically heterogeneous disease of impaired night vision. We report a... 
METABOTROPIC GLUTAMATE-RECEPTOR | LIGHT RESPONSE | RABBIT RETINA | MULTIDISCIPLINARY SCIENCES | DEPOLARIZING BIPOLAR | SYNAPTIC-TRANSMISSION | ROD BIPOLAR CELLS | GENE-EXPRESSION | FRAMESHIFT MUTATION | RETINITIS-PIGMENTOSA | MAMMALIAN RETINA | RGS Proteins - genetics | Night Blindness - metabolism | Humans | Heterotrimeric GTP-Binding Proteins - metabolism | Male | Heterotrimeric GTP-Binding Proteins - genetics | Myopia - metabolism | Night Blindness - pathology | RGS Proteins - metabolism | Female | Genetic Diseases, X-Linked - genetics | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Disease Models, Animal | Genetic Predisposition to Disease - genetics | Eye Diseases, Hereditary - pathology | Eye Diseases, Hereditary - physiopathology | Retina - physiopathology | Gene Expression Regulation | Retinal Cone Photoreceptor Cells - physiology | Proteoglycans - metabolism | Myopia - pathology | Presynaptic Terminals - physiology | Genetic Diseases, X-Linked - metabolism | Eye Diseases, Hereditary - genetics | Myopia - genetics | Animals | Calcium Channels, L-Type - genetics | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Dogs | Genetic Diseases, X-Linked - pathology | Presynaptic Terminals - metabolism | Calcium Channels, L-Type - metabolism | Retinal Cone Photoreceptor Cells - metabolism | Eye Diseases, Hereditary - metabolism | Proteoglycans - genetics | Immunohistochemistry | Veterinary colleges | Protein kinase C | Disease | Genes | Antibodies | Retina | Labelling | Rods | Nyctalopia | Veterinary medicine | Homozygosity | Modulators | Defects | Gene sequencing | Proteins | Signal transduction | Rodents | Bipolar cells | Synaptic ribbons | Dendrites | Terminals | University graduates | Night vision | Phenotypes | Congenital diseases | Immunomodulation | Gene expression | Electron microscopy | Spherules | Cones | Vision | Blindness | Photoreceptors | Mutation | Gene mapping | Stationary night blindness | Cellular structure | Pharmaceuticals
Journal Article
Journal of Neurophysiology, ISSN 0022-3077, 08/2017, Volume 118, Issue 2, pp. 845 - 854
Journal Article
Cellular Signalling, ISSN 0898-6568, 11/2013, Volume 25, Issue 11, pp. 2155 - 2162
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 03/2014, Volume 23, Issue 6, pp. 1538 - 1550
Journal Article
Molecular Brain, ISSN 1756-6606, 06/2016, Volume 9, Issue 1, p. 64
Background: Amyloid precursor protein knockout mice (APP-KO) have impaired differentiation of amacrine and horizontal cells. APP is part of a gene family and... 
Congenital stationary night blindness | Synaptopathy | Transcription | Amyloid precursor-like protein 2 | Differentiation | Amyloid precursor protein | Synapses | DEPOLARIZING BIPOLAR CELLS | LIGHT RESPONSE | APP-LIKE PROTEIN-2 | ALZHEIMERS-DISEASE | ROD BIPOLAR | NEUROSCIENCES | SYNAPSE FORMATION | RICH REPEAT PROTEIN | MUTATIONS | LINKED RETINITIS-PIGMENTOSA | DEVELOPING MOUSE RETINA | Retinal Bipolar Cells - pathology | Amyloid beta-Protein Precursor - chemistry | Amacrine Cells - metabolism | Presynaptic Terminals - ultrastructure | RNA, Messenger - metabolism | Neurogenesis | Synaptic Transmission | Complement System Proteins - metabolism | Gene Deletion | Amyloid beta-Protein Precursor - metabolism | Night Blindness - pathology | Genetic Diseases, X-Linked - genetics | Transcription, Genetic | Cell Differentiation | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Animals, Newborn | Amyloid beta-Protein Precursor - deficiency | Dendrites - metabolism | Photoreceptor Cells, Vertebrate - ultrastructure | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary - pathology | Eye Diseases, Hereditary - physiopathology | Mice, Inbred C57BL | RNA, Messenger - genetics | Myopia - pathology | Aging - pathology | Eye Diseases, Hereditary - genetics | Mice, Knockout | Myopia - genetics | Transcription Factors - metabolism | Amyloid beta-Protein Precursor - genetics | Animals | Myopia - physiopathology | Night Blindness - physiopathology | Retinal Bipolar Cells - ultrastructure | Genetic Diseases, X-Linked - pathology | Presynaptic Terminals - metabolism | Photoreceptor Cells, Vertebrate - metabolism | Photoreceptor Cells, Vertebrate - pathology | Night blindness | Glycoproteins | Genetic aspects | Research | Gene expression | Retinal diseases | Life Sciences
Journal Article