X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1038) 1038
Book Review (378) 378
Publication (112) 112
Book / eBook (44) 44
Book Chapter (21) 21
Conference Proceeding (7) 7
Magazine Article (3) 3
Newsletter (3) 3
Dissertation (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (924) 924
humans (829) 829
female (397) 397
male (395) 395
ophthalmology (348) 348
mutation (327) 327
animals (277) 277
adult (250) 250
dominant optic atrophy (216) 216
optic atrophy (210) 210
mitochondria (203) 203
neurosciences (198) 198
child (194) 194
mitochondrial dna (191) 191
middle aged (185) 185
clinical neurology (173) 173
gtp phosphohydrolases - genetics (163) 163
adolescent (162) 162
genetics & heredity (161) 161
genetic aspects (153) 153
eye diseases (145) 145
mitochondria - metabolism (133) 133
optic nerve (131) 131
pedigree (131) 131
optic atrophy, autosomal dominant - genetics (126) 126
cell biology (123) 123
dna, mitochondrial - genetics (120) 120
research (119) 119
opa1 (118) 118
biochemistry & molecular biology (117) 117
phenotype (115) 115
retina (115) 115
atrophy (112) 112
disease (110) 110
hereditary optic neuropathy (110) 110
glaucoma (108) 108
mice (107) 107
magnetic resonance imaging (102) 102
proteins (101) 101
gene (100) 100
apoptosis (99) 99
child, preschool (99) 99
retinal ganglion cells - pathology (99) 99
aged (98) 98
analysis (94) 94
diagnosis (94) 94
genetic structures (93) 93
abridged index medicus (89) 89
young adult (89) 89
neurology (88) 88
article (85) 85
genetics (84) 84
sense organs (84) 84
neuropathy (83) 83
mutations (79) 79
genes (78) 78
dna mutational analysis (77) 77
optic atrophy, autosomal dominant - pathology (76) 76
mitochondria - genetics (74) 74
medicine & public health (71) 71
mitochondria - pathology (71) 71
disease models, animal (70) 70
fusion (70) 70
mitochondrial diseases - genetics (70) 70
oxidative stress (70) 70
visual acuity (70) 70
infant (69) 69
mitochondrial proteins - genetics (69) 69
physiological aspects (69) 69
eye (68) 68
gtp phosphohydrolases - metabolism (66) 66
optic nerve - pathology (65) 65
medicine (64) 64
pediatrics (64) 64
tomography, optical coherence (62) 62
optic neuropathy (61) 61
optic atrophy - genetics (59) 59
gene mutations (57) 57
health aspects (57) 57
research article (57) 57
mutation - genetics (56) 56
neurodegeneration (56) 56
optic disk - pathology (56) 56
cytochrome-c release (55) 55
degeneration (55) 55
dynamin-related protein (55) 55
morphology (55) 55
electroretinography (54) 54
review (54) 54
molecular sequence data (53) 53
pathology (53) 53
children (52) 52
membrane proteins - genetics (51) 51
mouse model (51) 51
optic atrophy, hereditary, leber - genetics (51) 51
patients (51) 51
risk factors (51) 51
care and treatment (50) 50
mitochondrial proteins - metabolism (50) 50
optic atrophy, autosomal dominant - metabolism (49) 49
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (35) 35
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Gerstein Science - Reference (2) 2
UTL at Downsview - May be requested (2) 2
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Periodical Stacks (1) 1
Robarts - Stacks (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1089) 1089
German (3) 3
Spanish (3) 3
French (2) 2
Arabic (1) 1
Chinese (1) 1
Czech (1) 1
Italian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain, ISSN 0006-8950, 2/2008, Volume 131, Issue 2, pp. 338 - 351
Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organization and control of apoptosis, have been linked to non-syndromic... 
Chronic progressive external ophthalmoplegia | Dominant optic atrophy | Mitochondrial encephalomyopathy | Mitochondria | mtDNA multiple deletions | PROTEIN | mitochondria | NEUROSCIENCES | chronic progressive external ophthalmoplegia | R445H MUTATION | CLINICAL NEUROLOGY | mitochondrial encephalomyopathy | PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY | HEARING-LOSS | GENE | DISEASE | dominant optic atrophy | DEAFNESS | FISSION | DELETIONS | Ophthalmoplegia, Chronic Progressive External - pathology | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Mutation, Missense | DNA Mutational Analysis - methods | Ophthalmoplegia, Chronic Progressive External - genetics | DNA, Mitochondrial - genetics | Base Sequence | Muscle, Skeletal - chemistry | Adult | Female | Optic Atrophy, Autosomal Dominant - pathology | Child | Muscle, Skeletal - ultrastructure | Models, Molecular | Fibroblasts - pathology | Mitochondrial Myopathies - pathology | Syndrome | Magnetic Resonance Imaging | Point Mutation | Mitochondrial Myopathies - genetics | GTP Phosphohydrolases - genetics | Pedigree | Optic Atrophy, Autosomal Dominant - genetics | Aged | Index Medicus | Abridged Index Medicus | GTP Phosphohydrolases | Neurons and Cognition | DNA, Mitochondrial | Life Sciences | DNA Mutational Analysis | Fibroblasts | Optic Atrophy, Autosomal Dominant | Mitochondrial Myopathies | Ophthalmoplegia, Chronic Progressive External | Muscle, Skeletal
Journal Article
Brain, ISSN 0006-8950, 03/2010, Volume 133, Issue 3, pp. 771 - 786
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2015, Volume 47, Issue 8, pp. 926 - 932
Dominant optic atrophy (DOA)(1,2) and axonal peripheral neuropathy (Charcot-Marie-Tooth type 2, or CMT2)(3) are hereditary neurodegenerative disorders most... 
RECRUITMENT | CELLS | MITOCHONDRIAL DYNAMICS | FUSION | NEUROPATHY | ZEBRAFISH | UGO1P | OPA1 | GENETICS & HEREDITY | OUTER | GTPASE | Humans | Optic Atrophy, Autosomal Dominant - metabolism | Embryo, Nonmammalian - metabolism | Phosphate Transport Proteins - metabolism | Cercopithecus aethiops | Embryo, Nonmammalian - embryology | Male | Mitochondrial Proteins - genetics | Zebrafish - embryology | Charcot-Marie-Tooth Disease - genetics | RNA Interference | Mitochondrial Proteins - metabolism | HEK293 Cells | Muscle Proteins - metabolism | Female | Membrane Proteins - metabolism | Optic Atrophy, Autosomal Dominant - pathology | Phosphate Transport Proteins - genetics | Charcot-Marie-Tooth Disease - metabolism | Microscopy, Electron, Transmission | Genetic Predisposition to Disease - genetics | Animals, Genetically Modified | Membrane Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Sequence Analysis, DNA | Mitochondrial Membranes - metabolism | Muscle Proteins - genetics | Microscopy, Confocal | Exome - genetics | Animals | Pedigree | Embryo, Nonmammalian - ultrastructure | Zebrafish - metabolism | Optic Atrophy, Autosomal Dominant - genetics | Saccharomyces cerevisiae Proteins - metabolism | Protein Binding | Mutation | COS Cells | Development and progression | Genetic aspects | Optic atrophy | Gene mutations | Identification and classification | Health aspects | Proteins | Neurodegeneration | Genes | Neurological disorders | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 2468 - 6
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 02/2017, Volume 140, Issue 3, pp. 485 - 494
Journal Article
Brain, ISSN 0006-8950, 08/2010, Volume 133, Issue 8, pp. 2426 - 2438
Journal Article