X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1350) 1350
Book Review (229) 229
Publication (205) 205
Book Chapter (31) 31
Book / eBook (24) 24
Conference Proceeding (15) 15
Newspaper Article (14) 14
Magazine Article (4) 4
Reference (2) 2
Trade Publication Article (2) 2
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1203) 1203
humans (944) 944
male (575) 575
ophthalmology (522) 522
animals (513) 513
female (508) 508
stationary night blindness (499) 499
night blindness - genetics (448) 448
electroretinography (406) 406
mutation (365) 365
adult (347) 347
retina (271) 271
pedigree (269) 269
mice (257) 257
night blindness (256) 256
middle aged (228) 228
adolescent (218) 218
child (200) 200
sense organs (189) 189
gene (184) 184
biochemistry & molecular biology (178) 178
genetic structures (175) 175
genetics & heredity (174) 174
night blindness - physiopathology (172) 172
retinitis pigmentosa - genetics (163) 163
molecular sequence data (159) 159
eye diseases (142) 142
neurosciences (139) 139
night blindness - congenital (139) 139
retinal degeneration - genetics (131) 131
photoreceptors (128) 128
mutations (126) 126
genetic aspects (125) 125
retinitis pigmentosa (122) 122
dna mutational analysis (121) 121
phenotype (121) 121
dark adaptation (119) 119
amino acid sequence (118) 118
research (117) 117
night blindness - diagnosis (114) 114
electroretinogram (112) 112
visual acuity (110) 110
retinal degeneration (109) 109
analysis (108) 108
myopia - genetics (107) 107
genetic linkage (104) 104
disease models, animal (101) 101
visual fields (101) 101
aged (100) 100
blindness (98) 98
x chromosome (98) 98
fundus oculi (95) 95
retinitis-pigmentosa (95) 95
child, preschool (94) 94
article (93) 93
light (93) 93
base sequence (92) 92
abridged index medicus (90) 90
genes (90) 90
rhodopsin (90) 90
polymerase chain reaction (89) 89
proteins (88) 88
mice, inbred c57bl (87) 87
rhodopsin - genetics (85) 85
congenital stationary night blindness (82) 82
eye proteins - genetics (82) 82
retina - physiopathology (82) 82
genetics (80) 80
eye diseases, hereditary - genetics (77) 77
genetic disorders (75) 75
research article (75) 75
genetic diseases, x-linked - genetics (73) 73
medicine & public health (73) 73
retina - metabolism (71) 71
multidisciplinary sciences (70) 70
genotype (68) 68
retina - pathology (68) 68
fluorescein angiography (67) 67
mice, knockout (65) 65
chromosome mapping (63) 63
gene expression (63) 63
retinal degeneration - physiopathology (63) 63
bipolar cells (62) 62
dominant retinitis-pigmentosa (62) 62
retinal diseases - genetics (62) 62
expression (61) 61
night blindness - metabolism (61) 61
nyctalopia (61) 61
photic stimulation (61) 61
protein (60) 60
signal transduction (59) 59
calcium channels, l-type - genetics (58) 58
photoreceptor (58) 58
calcium channels - genetics (57) 57
night blindness - complications (57) 57
retinitis pigmentosa - physiopathology (57) 57
vision (57) 57
genes, recessive (56) 56
rhodopsin - metabolism (56) 56
cell biology (55) 55
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (12) 12
Regis College - Stacks (6) 6
Trinity College (John W Graham) - Stacks (5) 5
UofT at Scarborough - Stacks (5) 5
Victoria University E.J. Pratt - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (4) 4
Knox College (Caven) - Stacks (4) 4
St. Michael's College (John M. Kelly) - 3rd Floor (4) 4
UTL at Downsview - May be requested (4) 4
Gerstein Science - Stacks (3) 3
St. Augustine's Seminary - Stacks (3) 3
OISE - Stacks (2) 2
Online Resources - Online (2) 2
UofT at Mississauga - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
Robarts - Storage (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Trinity College (John W Graham) - Storage (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University E.J. Pratt - Reference (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1347) 1347
German (18) 18
French (14) 14
Chinese (7) 7
Japanese (5) 5
Spanish (3) 3
Czech (2) 2
Polish (2) 2
Dutch (1) 1
Hebrew (1) 1
Italian (1) 1
Romanian (1) 1
Russian (1) 1
Slovenian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature genetics, ISSN 1061-4036, 2000, Volume 26, Issue 3, pp. 319 - 323
Journal Article
Journal Article
Journal of Neurophysiology, ISSN 0022-3077, 08/2017, Volume 118, Issue 2, pp. 845 - 854
Journal Article
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 04/2003, Volume 44, Issue 4, pp. 1663 - 1672
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 03/2014, Volume 23, Issue 6, pp. 1538 - 1550
Journal Article
Journal Article
Molecular Brain, ISSN 1756-6606, 06/2016, Volume 9, Issue 1, pp. 64 - 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 | Index Medicus | Life Sciences
Journal Article