X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (13784) 13784
Book Review (2482) 2482
Publication (1578) 1578
Book Chapter (206) 206
Book / eBook (158) 158
Newsletter (101) 101
Conference Proceeding (62) 62
Newspaper Article (21) 21
Dissertation (11) 11
Magazine Article (3) 3
Reference (3) 3
Trade Publication Article (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (12125) 12125
humans (8224) 8224
animals (6739) 6739
male (3642) 3642
mice (3228) 3228
female (3196) 3196
cell biology (2615) 2615
biochemistry & molecular biology (2192) 2192
mutation (2031) 2031
proteins (1984) 1984
ophthalmology (1959) 1959
adult (1847) 1847
membrane proteins - genetics (1770) 1770
neurosciences (1755) 1755
middle aged (1608) 1608
membrane proteins - metabolism (1557) 1557
expression (1236) 1236
research (1208) 1208
skeletal-muscle (1167) 1167
aged (1135) 1135
gene (1124) 1124
rats (1075) 1075
genetics & heredity (1073) 1073
article (1064) 1064
molecular sequence data (1026) 1026
muscular dystrophy (1002) 1002
analysis (993) 993
membrane proteins (993) 993
child (989) 989
cells (982) 982
physiological aspects (956) 956
cells, cultured (944) 944
adolescent (920) 920
protein (913) 913
muscle, skeletal - metabolism (902) 902
membrane (883) 883
phenotype (881) 881
immunohistochemistry (876) 876
amino acid sequence (865) 865
multidisciplinary sciences (860) 860
clinical neurology (843) 843
membranes (835) 835
genetic aspects (828) 828
gene expression (827) 827
cell membrane - metabolism (802) 802
mice, inbred c57bl (771) 771
physiology (749) 749
muscular dystrophies - genetics (746) 746
mutations (725) 725
abridged index medicus (721) 721
dystrophin (718) 718
research article (712) 712
cell line (711) 711
muscular-dystrophy (702) 702
disease models, animal (691) 691
mice, knockout (652) 652
duchenne muscular-dystrophy (647) 647
muscles (636) 636
signal transduction (608) 608
child, preschool (604) 604
skeletal muscle (604) 604
biophysics (602) 602
biology (598) 598
disease (598) 598
genes (590) 590
muscle, skeletal - pathology (589) 589
pedigree (583) 583
localization (577) 577
pathology (576) 576
rodents (576) 576
calcium - metabolism (570) 570
medicine (566) 566
sense organs (554) 554
eye diseases (549) 549
muscular dystrophies - metabolism (547) 547
membrane glycoproteins - genetics (543) 543
protein binding (541) 541
calcium (539) 539
biochemistry (524) 524
life sciences (518) 518
microscopy, electron (517) 517
base sequence (515) 515
genetics (511) 511
utrophin (499) 499
membrane glycoproteins - metabolism (497) 497
medicine, research & experimental (487) 487
aged, 80 and over (485) 485
apoptosis (484) 484
dysferlin (478) 478
plasma-membrane (478) 478
retina (473) 473
cell membranes (467) 467
blotting, western (464) 464
cytoskeletal proteins - genetics (463) 463
dystrophin - metabolism (463) 463
cytoskeletal proteins - metabolism (462) 462
dystrophy (461) 461
muscle (457) 457
cornea (453) 453
muscular dystrophies - pathology (451) 451
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (102) 102
UofT at Mississauga - Stacks (18) 18
UTL at Downsview - May be requested (12) 12
Collection Dvlpm't (Acquisitions) - Closed Orders (6) 6
UofT at Scarborough - Stacks (6) 6
Collection Dvlpm't (Acquisitions) - Vendor file (5) 5
Online Resources - Online (4) 4
Earth Sciences (Noranda) - Stacks (2) 2
Engineering & Comp. Sci. - Reference (2) 2
Chemistry (A D Allen) - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Cancelled Order (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Physics - Stacks (1) 1
Toronto East General Hospital - Stacks (1) 1
UofT at Mississauga - Reference (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (13767) 13767
German (102) 102
Japanese (85) 85
French (76) 76
Russian (44) 44
Spanish (38) 38
Chinese (17) 17
Polish (13) 13
Korean (10) 10
Italian (7) 7
Portuguese (7) 7
Serbian (3) 3
Turkish (3) 3
Czech (2) 2
Dutch (2) 2
Ukrainian (2) 2
Finnish (1) 1
Hebrew (1) 1
Slovak (1) 1
Slovenian (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, 02/2015, Volume 34, Issue 2, pp. 117 - 159
PURPOSE:To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information.... 
Fleck corneal dystrophy | Cornea | Epithelial and subepithelial dystrophies | Descemetmembrane | Posterior amorphous corneal dystrophy | Confocal microscopy | Cornea pathology | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | Stromal dystrophies | Hereditary disease | Epithelial basement membranedystrophy | Pre-Descemet corneal dystrophy | Histopathology | Keratoconus | Congenital corneal endothelial dystrophy and X-linked endothelialdystrophy | Bowman membrane | Subepithelialmucinous corneal dystrophy | Endothelial dystrophies | Genetics | Schnyder corneal dystrophy | Gelatinousdrop-like corneal dystrophy | Fuchsendothelial corneal dystrophy | Epithelial-stromal TGFBI dystrophies | Lisch epithelial corneal dystrophy | Stroma | Histology | Meesmann dystrophy | Epithelium | Endothelium | Genetic disease | Epithelial recurrent erosion dystrophies | Posteror polymorphous corneal dystrophy | Centralcloudy dystrophy of François | Granular corneal dystrophy type 1 | Granular corneal dystrophy type 2 | TGFBI | Reis-Bücklers corneal dystrophy | Congenital stromal corneal dystrophy | Cornea dystrophy | cornea | endothelial dystrophies | histology | epithelial basement membrane dystrophy | genetic disease | epithelial and subepithelial dystrophies | central cloudy dystrophy of Francois | macular corneal dystrophy | subepithelial mucinous corneal dystrophy | cornea pathology | stroma | FRANCOIS | congenital corneal endothelial dystrophy and X-linked endothelial dystrophy | posteror polymorphous corneal dystrophy | DISEASE | epithelium | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy | pre-Descemet corneal dystrophy | histopathology | INDIVIDUAL PHENOTYPIC VARIANCES | FAMILY | epithelial recurrent erosion dystrophies | granular corneal dystrophy type 1 | granular corneal dystrophy type 2 | genetics | cornea dystrophy | UBIAD1 GENE | MUTATIONS | Descemet membrane | endothelium | hereditary disease | epithelial-stromal TGFBI dystrophies | keratoconus | posterior amorphous corneal dystrophy | congenital stromal corneal dystrophy | stromal dystrophies | fleck corneal dystrophy | confocal microscopy | gelatinous drop-like corneal dystrophy | EDEMA | OPHTHALMOLOGY | LINKAGE | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | International Classification of Diseases | Corneal Dystrophies, Hereditary - classification | Corneal Dystrophies, Hereditary - pathology | Humans | Index Medicus
Journal Article
CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 12/2007, Volume 16, Issue 23, pp. 2816 - 2833
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 05/2013, Volume 201, Issue 4, pp. 499 - 510
The muscular dystrophies are a group of heterogeneous genetic diseases characterized by progressive degeneration and weakness of skeletal muscle. Since the... 
SKELETAL-MUSCLE | ALPHA-DYSTROGLYCAN | ABNORMAL GLYCOSYLATION | ALPHA-7-BETA-1 INTEGRIN | 3 UNTRANSLATED REGION | WALKER-WARBURG-SYNDROME | NITRIC-OXIDE | DILATED CARDIOMYOPATHY | MYOTONIC-DYSTROPHY | MEMBRANE REPAIR | CELL BIOLOGY | Dystrophin | Utrophin | Analysis | Muscular dystrophy | Musculoskeletal system | Genotype & phenotype | Neuromuscular diseases | Genes | Reviews
Journal Article
Ophthalmology, ISSN 0161-6420, 2006, Volume 113, Issue 8, pp. 1392 - 1400.e4
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 01/2011, Volume 228, pp. S1 - S39
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | central cloudy dystrophy of Francxois | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | HELIX TERMINATION MOTIF | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | Fuchs endothelial corneal dystrophy posterior | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | polymorphous corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Ophthalmology, ISSN 0161-6420, 2009, Volume 116, Issue 4, pp. 771 - 782.e1
Journal Article
Journal of Cataract & Refractive Surgery, ISSN 0886-3350, 07/2018, Volume 44, Issue 7, pp. 864 - 870
To compare the corneal endothelial cell loss and central corneal thickness (CCT) after conventional phacoemulsification surgery or femtosecond laser–assisted... 
CLASSIFICATION-SYSTEM-III | SURGERY | KERATOPLASTY | RISK-FACTORS | SOFT-SHELL TECHNIQUE | MEMBRANE | PHACOEMULSIFICATION | OPHTHALMOLOGY | INTRAOCULAR-LENS IMPLANTATION | EXTRACELLULAR-MATRIX | CELL LOSS | THICKNESS | Cataract | Ophthalmology | Surgery | Endothelium
Journal Article
Journal Article
Journal Article