X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (288) 288
Book / eBook (42) 42
Newspaper Article (38) 38
Publication (27) 27
Book Review (13) 13
Dissertation (6) 6
Book Chapter (2) 2
Conference Proceeding (2) 2
Magazine Article (1) 1
Streaming Audio (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (155) 155
humans (142) 142
male (87) 87
female (81) 81
ophthalmology (62) 62
genetics & heredity (52) 52
middle aged (47) 47
aged (41) 41
mutation (41) 41
adult (37) 37
animals (37) 37
pedigree (36) 36
genetics (33) 33
genetic aspects (32) 32
gene (30) 30
neurosciences (29) 29
mutations (28) 28
eye proteins - genetics (27) 27
eye diseases (26) 26
mice (26) 26
genes (25) 25
research (25) 25
biochemistry & molecular biology (24) 24
phenotype (24) 24
dna mutational analysis (23) 23
macular degeneration (23) 23
adolescent (22) 22
analysis (22) 22
gene expression (22) 22
research article (22) 22
physiological aspects (21) 21
retina (21) 21
risk factors (21) 21
macular degeneration - genetics (20) 20
retinitis pigmentosa - genetics (20) 20
sense organs (20) 20
pseudoxanthoma elasticum - genetics (19) 19
case-control studies (18) 18
genotype (18) 18
aged, 80 and over (17) 17
pseudoxanthoma elasticum (17) 17
abridged index medicus (16) 16
chromosome mapping (16) 16
degeneration (16) 16
disease (16) 16
expression (16) 16
identification (16) 16
medicine (16) 16
genetic linkage (15) 15
prevalence (15) 15
article (14) 14
child (14) 14
multidrug resistance-associated proteins - genetics (14) 14
pseudoxanthoma elasticum - pathology (14) 14
abcc6 (13) 13
amino acid sequence (13) 13
epidemiology (13) 13
glaucoma (13) 13
history (13) 13
molecular sequence data (13) 13
protein (13) 13
x chromosome (13) 13
base sequence (12) 12
cohort studies (12) 12
genetic structures (12) 12
polymerase chain reaction (12) 12
polymorphism, single nucleotide (12) 12
population (12) 12
proteins (12) 12
transporter (12) 12
age (11) 11
genetic predisposition to disease (11) 11
heterozygote (11) 11
medical research (11) 11
photoreceptors (11) 11
science (11) 11
eye (10) 10
family (10) 10
health aspects (10) 10
linkage analysis (10) 10
localization (10) 10
medicine, general & internal (10) 10
multidisciplinary sciences (10) 10
retinal pigment epithelium (10) 10
retinitis-pigmentosa (10) 10
young adult (10) 10
biology (9) 9
cells (9) 9
electroretinography (9) 9
follow-up studies (9) 9
genetic research (9) 9
genomics (9) 9
mice, inbred c57bl (9) 9
mutation - genetics (9) 9
psychology (9) 9
retina - metabolism (9) 9
retinal-pigment epithelium (9) 9
retinitis pigmentosa (9) 9
atp-binding cassette transporters - genetics (8) 8
blindness (8) 8
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (25) 25
UTL at Downsview - May be requested (12) 12
UofT at Mississauga - Stacks (6) 6
Collection Dvlpm't (Acquisitions) - Vendor file (4) 4
Gerstein Science - Stacks (3) 3
Victoria University E.J. Pratt - Stacks (3) 3
Criminology - Stacks (2) 2
OISE - Stacks (2) 2
Online Resources - Online (2) 2
Pontifical Inst. Mediaeval Studies - Library use only (2) 2
UofT at Scarborough - Stacks (2) 2
Aerospace - Stacks (1) 1
Architecture Landscape (Shore + Moffat) - Stacks (1) 1
Art - Reference (1) 1
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Knox College (Caven) - Stacks (1) 1
New College (Ivey) - Stacks (1) 1
OISE - Missing (1) 1
Robarts - Reference (1) 1
Royal Ontario Museum - Stacks (1) 1
St. Augustine's Seminary - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Trinity College (John W Graham) - Oversize (1) 1
Trinity College (John W Graham) - Stacks (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
Victoria University E.J. Pratt - Reference (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 (380) 380
French (3) 3
German (2) 2
Norwegian (2) 2
Dutch (1) 1
Icelandic (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cornea, ISSN 0277-3740, 06/2019, Volume 38, Issue 6, pp. 718 - 722
PURPOSE:Brittle cornea syndrome (BCS) is a rare recessive disorder affecting connective tissues, most prominently in the eye. Pathogenic mutations causing BCS... 
Pakistan | Humans | Joint Instability - genetics | Child, Preschool | Female | Male | Skin Abnormalities - genetics | Mutation | Transcription Factors - genetics | Eye Abnormalities - genetics | Joint Instability - congenital | Child | Gene mutations | Corneal diseases | Genetic aspects | Diagnosis | Pakistanis | Identification and classification | Health aspects | Index Medicus
Journal Article
LIPIDS IN HEALTH AND DISEASE, ISSN 1476-511X, 01/2019, Volume 18, Issue 1, pp. 2 - 2
Journal Article
by Verhoeven, Virginie J. M and Hysi, Pirro G and Wojciechowski, Robert and Fan, Qiao and Guggenheim, Jeremy A and Höhn, René and Macgregor, Stuart and Hewitt, Alex W and Nag, Abhishek and Cheng, Ching-Yu and Yonova-Doing, Ekaterina and Zhou, Xin and Ikram, M. Kamran and Buitendijk, Gabriëlle H. S and McMahon, George and Kemp, John P and Pourcain, Beate St and Simpson, Claire L and Mäkelä, Kari-Matti and Lehtimäki, Terho and Kähönen, Mika and Paterson, Anew D and Hosseini, S. Mohsen and Wong, Hoi Suen and Xu, Liang and Jonas, Jost B and Pärssinen, Olavi and Wedenoja, Juho and Yip, Shea Ping and Ho, Daniel W. H and Pang, Chi Pui and Chen, Li Jia and Burdon, Kathryn P and Craig, Jamie E and Klein, Barbara E. K and Klein, Ronald and Haller, Toomas and Metspalu, Anes and Khor, Chiea-Chuen and Tai, E.-Shyong and Aung, Tin and Vithana, Eranga and Tay, Wan-Ting and Barathi, Veluchamy A and Chen, Peng and Li, Ruoying and Liao, Jiemin and Zheng, Yingfeng and Ong, Rick T and Döring, Angela and Evans, David M and Timpson, Nicholas J and Verkerk, Annemieke J. M. H and Meitinger, Thomas and Raitakari, Olli and Hawthorne, Felicia and Spector, Tim D and Karssen, Lennart C and Pirastu, Mario and Murgia, Federico and Ang, Wei and Mishra, Aniket and Montgomery, Grant W and Pennell, Craig E and Cumberland, Phillippa M and Cotlarciuc, Ioana and Mitchell, Paul and Wang, Jie Jin and Schache, Maria and Janmahasathian, Sarayut and Igo, Robert P and Lass, Jonathan H and Chew, Emily and Iyengar, Sudha K and Gorgels, Theo G. M. F and Rudan, Igor and Hayward, Caroline and Wright, Alan F and Polasek, Ozren and Vatavuk, Zoran and Wilson, James F and Fleck, Brian and Zeller, Tanja and Mirshahi, Alireza and Müller, Christian and Uitterlinden, Ané G and Rivadeneira, Fernando and Vingerling, Johannes R and Hofman, Albert and Oostra, Ben A and Amin, Najaf and Bergen, Arthur A. B and teo, Yik-Ying and Rahi, Jugnoo S and Vitart, Veronique and Williams, Cathy and Baird, Paul N and Wong, Tien-Yin and Oexle, Konrad and Pfeiffer, Norbert and ... and Fuchs' Genetics Multi-Ctr Study Gr and Diabet Control Complications Trial and WTCCC2 and CREAM and Consortium for Refractive Error and Myopia (CREAM) and Fuchs' Genetics Multi-Center Study Group and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and Wellcome Trust Case Control Consortium 2 (WTCCC2) and The Fuchs' Genetics Multi-Center Study Group and The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 3, pp. 314 - 318
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2013, Volume 110, Issue 50, pp. 20206 - 20211
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Proteins | Rodents | Blindness | Gene expression | Cells | Index Medicus | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
Retina, ISSN 0275-004X, 09/2015, Volume 35, Issue 9, pp. e57 - e58
Journal Article
Experimental Eye Research, ISSN 0014-4835, 04/2014, Volume 121
Journal Article
Retina, ISSN 0275-004X, 09/2015, Volume 35, Issue 9, pp. e57 - e58
Journal Article
by van Koolwijk, Leonieke M. E and Ramdas, Wishal D and Ikram, M. Kamran and Jansonius, Nomdo M and Pasutto, Francesca and Hysi, Pirro G and Macgregor, Stuart and Janssen, Sarah F and Hewitt, Alex W and Viswanathan, Ananth C and ten Brink, Jacoline B and Hosseini, S. Mohsen and Amin, Najaf and Despriet, Dominiek D. G and Willemse-Assink, Jacqueline J. M and Kramer, Rogier and Rivadeneira, Fernando and Struchalin, Maksim and Aulchenko, Yurii S and Weisschuh, Nicole and Zenkel, Matthias and Mardin, Christian Y and Gramer, Eugen and Welge-Lüssen, Ulrich and Montgomery, Grant W and Carbonaro, Francis and Young, Terri L and Bellenguez, Céline and McGuffin, Peter and Foster, Paul J and Topouzis, Fotis and Mitchell, Paul and Wang, Jie Jin and Wong, Tien Y and Czudowska, Monika A and Hofman, Albert and Uitterlinden, Ane G and Wolfs, Roger C. W and de Jong, Paulus T. V. M and Oostra, Ben A and Paterson, Anew D and Mackey, David A and Bergen, Arthur A. B and Reis, Ané and Hammond, Christopher J and Vingerling, Johannes R and Lemij, Hans G and Klaver, Caroline C. W and van Duijn, Cornelia M and Donnelly, Peter and Barroso, Ines and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Deloukas, Panos and Duncanson, Auey and Jankowski, Janusz and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N.-A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Wood, Nicholas W and Spencer, Chris C. A and Band, Gavin and Freeman, Colin and Hellenthal, Garrett and Giannoulatou, Eleni and Pirinen, Matti and Pearson, Richard and Strange, Amy and Su, Zhan and Vukcevic, Damjan and Langford, Cordelia and Hunt, Sarah E and Edkins, Sarah and Gwilliam, Rhian and Blackburn, Hannah and Bumpstead, Suzannah J and nov, Serge and Gillman, Matthew and Gray, Emma and Hammond, Naomi and Jayakumar, Alagurevathi and McCann, Owen T and Liddle, Jennifer and Potter, Simon C and Ravinarajah, Radhi and Ricketts, Michelle and Waller, Matthew and Weston, Paul and Widaa, Sara and Whittaker, Pamela and McCarthy, Mark I and DCCT-EDIC Res Grp and Wellcome Trust Case Control and Wellcome Trust Case Control Consortium 2 and DCCT/EDIC Research Group and The DCCT/EDIC Research Group
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 5, pp. e1002611 - e1002611
Journal Article