X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (159) 159
humans (116) 116
ophthalmology (82) 82
animals (76) 76
mutation (64) 64
medicine (57) 57
female (53) 53
male (53) 53
research article (52) 52
retina (52) 52
eye diseases (50) 50
science (47) 47
sense organs (43) 43
genetic aspects (42) 42
multidisciplinary sciences (39) 39
inherited eye disorders (38) 38
genetics (37) 37
genetic structures (35) 35
biology (34) 34
eyes (33) 33
disease models, animal (32) 32
glaucoma (32) 32
mice (32) 32
retinal degeneration (32) 32
eye (31) 31
pedigree (29) 29
analysis (28) 28
cornea (28) 28
photoreceptors (27) 27
animal models (26) 26
genetic disorders (26) 26
degeneration (25) 25
proteins (25) 25
genes (24) 24
congenital diseases (23) 23
genetics & heredity (22) 22
middle aged (22) 22
retinitis pigmentosa (22) 22
adult (21) 21
inherited glaucoma (21) 21
dystrophy (20) 20
hereditary diseases (20) 20
retinal disorders (20) 20
united states--us (20) 20
apoptosis (19) 19
gene expression (19) 19
human genetics (19) 19
neurosciences (19) 19
optic nerve (18) 18
rodents (18) 18
disease (17) 17
diseases (17) 17
medicine and health sciences (17) 17
physiological aspects (17) 17
retinitis-pigmentosa (17) 17
biochemistry (16) 16
child (16) 16
corneal dystrophy (16) 16
dogs (16) 16
electroretinography (16) 16
gene therapy (16) 16
genomics (16) 16
inherited diseases (16) 16
medicine, research & experimental (16) 16
phenotype (16) 16
cell biology (15) 15
genomes (15) 15
medical research (15) 15
research (15) 15
age (14) 14
biology and life sciences (14) 14
blindness (14) 14
clinical genetics (14) 14
disorders, genetic (14) 14
gene mutations (14) 14
genetic diseases (14) 14
inherited retinal dystrophy (14) 14
neurology (14) 14
ocular system (14) 14
patients (14) 14
rats (14) 14
risk factors (14) 14
studies (14) 14
base sequence (13) 13
diagnosis (13) 13
disorders, inherited (13) 13
dna (13) 13
genotype (13) 13
molecular genetics (13) 13
mouse (13) 13
muridae (13) 13
neuroscience (13) 13
polymerase chain reaction (13) 13
transplantation (13) 13
aged (12) 12
child, preschool (12) 12
gene (12) 12
genetic diseases, inborn (12) 12
genetic predisposition to disease (12) 12
genetics of disease (12) 12
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (14) 14
UTL at Downsview - May be requested (3) 3
Online Resources - Online (2) 2
Collection Dvlpm't (Acquisitions) - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Gerstein Science - Reference (1) 1
Holland Bloorview Kids Rehabilitation - Reference (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
St. Michael's Hospital - Stacks (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 5, pp. e10707 - e10707
Background: Keratoplasty is the most effective treatment for corneal blindness, but suboptimal medical conditions and lack of qualified medical personnel and... 
KERATOCAN | SKELETAL-MUSCLE | REPAIR | CONFOCAL MICROSCOPY | BONE-MARROW | TISSUE | BIOLOGY | SPINAL-CORD | EXPRESSION | MARROW STROMAL CELLS | TRANSPLANTATION | Neonates | Collagens | Umbilical cords | Bone marrow | Mesenchymal stem cells | United States--US | Medical treatment | Stroma | Diseases | Nitric oxide | Stem cells | Taiwan | Spinal cord injuries | Mice | Umbilical cord | Mutation | Flow cytometry | Cornea | Transparency | Hydrogels | Mesenchyme | Medical services | Developing countries | Stem cell transplantation | Lamellae | Transplant rejection | Transplantation | Infections | Developing nations | Aldehyde dehydrogenase | Immunostaining | Hematopoietic stem cells | Developing countries--LDCs | Allografts | Corneal transplantation | Rodents | Medical personnel | CD34 antigen | Phenotypes | Congenital diseases | Light scattering | Neutrophils | Graft rejection | Microscopy | Collagen | Blindness | Liquid nitrogen | Muridae | Ohio | Chemokines | Apoptosis | stem cell transplantation | Nitrogen | Corneal Diseases - therapy | Stromal Cells - transplantation | Up-Regulation | Cell Proliferation | Stromal Cells - pathology | Humans | Umbilical Cord - cytology | Corneal Diseases - congenital | Dendritic Cells - pathology | Mesenchymal Stromal Cells - cytology | Flow Cytometry | Cell Shape | Cornea - pathology | Lumican | Aldehyde Dehydrogenase - metabolism | Corneal Diseases - pathology | Biomarkers - metabolism | Cell Separation | Cell Survival | Chondroitin Sulfate Proteoglycans - metabolism | Keratan Sulfate - metabolism | Proteoglycans - metabolism | Chondroitin Sulfate Proteoglycans - deficiency | Collagen - metabolism | Cornea - metabolism | Animals | Keratan Sulfate - deficiency | Mesenchymal Stem Cell Transplantation | Medical research | Genetic disorders | Corneal diseases | Sulfates | Gene mutations | Medicine, Experimental | Employee performance | Index Medicus | LDCs
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
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
Journal Article
The Ocular Surface, ISSN 1542-0124, 07/2005, Volume 3, Issue 3, pp. 155 - 166
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e95037 - e95037
Posterior amorphous corneal dystrophy (PACD) is a rare, autosomal dominant disorder affecting the cornea and iris. Next-generation sequencing of the previously... 
MOLECULAR CHARACTERIZATION | KERATOCAN | DECORIN | PLANA | GENE | MULTIDISCIPLINARY SCIENCES | MUTATION | SKIN FRAGILITY | KERATAN SULFATE | LUMICAN | FAMILY | Cornea | Animal models | Chromosomal deletions | Copy number | Genes | Genomics | Collagens | Genomes | Leucine | Gene deletion | Fibrillogenesis | Los Angeles California | Iris | Clonal deletion | Deletion | Chromosome 12 | Iowa City Iowa | Deoxyribonucleic acid--DNA | Library collections | Data analysis | Proteoglycans | United States--US | Chromosome deletion | California | Hereditary diseases | Haploinsufficiency | Pennsylvania | Medicine | Polymerase chain reaction | Genomic libraries | Corneal dystrophy | Mouse models | Collagen | Mutation | Dystrophy | Genetic testing | Chondroitin Sulfate Proteoglycans - genetics | Humans | Corneal Dystrophies, Hereditary - genetics | Proteoglycans - metabolism | Male | Corneal Dystrophies, Hereditary - metabolism | Keratan Sulfate - genetics | Small Leucine-Rich Proteoglycans | Pedigree | Female | High-Throughput Nucleotide Sequencing | Lumican | Genetic Linkage - genetics | Chromosomes, Human, Pair 12 - genetics | Decorin - genetics | Proteoglycans - genetics | Sequence Deletion - genetics | Gene mutations | Physiological aspects | Corneal diseases | Genetic aspects | Diagnosis | Research | Risk factors | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
OCULAR SURFACE, ISSN 1542-0124, 07/2005, Volume 3, Issue 3, pp. 155 - 166
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 02/2011, 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 | 2. X-linked endothelial corneal dystrophy | central cloudy dystrophy of Francxois | 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 | 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 | congenital hereditary endothelial 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
Journal Article
Journal Article
대한안과학회지, ISSN 0378-6471, 2002, Volume 43, Issue 12, pp. 2506 - 2512
Purpose: We collected genomic DNAs of Korean patients with inherited corneal disorders, and identified mutations of the BIGH3 gene related corneal dystrophies... 
Inherited corneal disease | BIGH3 gene | Mutation | Corneal dystrophy
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, pp. e49083 - e49083
Fuchs endothelial corneal dystrophy (FECD) is a common, familial disease of the corneal endothelium and is the leading indication for corneal transplantation.... 
PATHOGENESIS | APOPTOSIS | CTG REPEAT | UNFOLDED PROTEIN RESPONSE | MENTAL-RETARDATION | ENDOTHELIAL DYSTROPHY | MULTIDISCIPLINARY SCIENCES | INHERITANCE | PITT-HOPKINS-SYNDROME | MISSENSE MUTATIONS | HAPLOINSUFFICIENCY | Oregon | Cornea | Transcription factors | Laboratories | Intellectual disabilities | Pathogenesis | Transplantation | Biochemistry | Single-nucleotide polymorphism | Kinases | Repeated sequences | Gene sequencing | Proteins | Primers | DNA repeat expansion | Southern blotting | Expansion | Chromosomes | Deoxyribonucleic acid--DNA | Edema | Southern blot | United States--US | Health risks | Trinucleotide repeats | Data processing | Minnesota | Patients | Endothelium | White blood cells | Polymerase chain reaction | Corneal dystrophy | DNA | Dystrophy | Genetic testing | Molecular biology | DNA sequencing | Apoptosis | Polymorphism | DNA transcription | Blotting, Southern | Fuchs' Endothelial Dystrophy - genetics | Genetic Predisposition to Disease | Reproducibility of Results | Transcription Factor 4 | Humans | Middle Aged | Molecular Sequence Data | Male | Transcription Factors - genetics | Sequence Analysis, DNA | Case-Control Studies | Genome, Human - genetics | Microsatellite Repeats - genetics | Base Sequence | Alleles | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Aged, 80 and over | Trinucleotide Repeat Expansion - genetics | Female | Aged | Chromosomes, Human, Pair 18 - genetics | Genetic aspects | Single nucleotide polymorphisms | Genes | Analysis | Index Medicus | Deoxyribonucleic acid
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 5, pp. e10760 - e10760
Background: Mutations in a novel gene, UBIAD1, were recently found to cause the autosomal dominant eye disease Schnyder corneal dystrophy (SCD). SCD is... 
PROTEIN STRUCTURES | CHOLESTEROL | GENE | METABOLISM | MEMBRANE | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | CRYSTALLINE DYSTROPHY | TOPOLOGY PREDICTION | BLADDER | TRANSFERASE | Immunohistochemistry | Protein structure comparison | Detroit Michigan | Erinaceidae | Leukocytes (mononuclear) | Biochemistry | Proteins | Mitochondria | Surgery | Docking | Lipid metabolism | Membrane potential | Enzymes | Protein metabolism | Computer simulation | United States--US | Metabolism | Substrates | Membrane proteins | Pennsylvania | Molecular modelling | Mutation detection | Mutation | Protein structure | Maryland | Binding sites | Germany | Biotechnology | Cornea | Antibodies | Amino acids | Homology | Viruses | Lipids | Phospholipids | Urology | Genetic algorithms | Metabolites | Massachusetts | Ethnic groups | Peripheral blood mononuclear cells | Modelling | Lesions | Localization | Age | Lymphoblastoid cell lines | Inflammation | Phenolic compounds | Minority & ethnic groups | Cholesterol | Michigan | Medicine | Corneal dystrophy | Phenols | Dystrophy | Position (location) | Cancer | Mitochondria - enzymology | Demography | Cornea - enzymology | Humans | Corneal Dystrophies, Hereditary - enzymology | Corneal Dystrophies, Hereditary - genetics | Molecular Sequence Data | Corneal Dystrophies, Hereditary - pathology | Dimethylallyltranstransferase - genetics | Mitochondria - genetics | DNA Mutational Analysis | Base Sequence | Conserved Sequence | Cornea - pathology | Amino Acid Sequence | Models, Molecular | Linear Models | Mutant Proteins - metabolism | Cholesterol - metabolism | Mutation - genetics | Amino Acids | Protein Transport | Proteins - genetics | Mutant Proteins - chemistry | Family | Proteins - chemistry | Wildlife conservation | Analysis | Physiological aspects | Eye diseases | Genetic aspects | Ophthalmology | Native Americans | Index Medicus
Journal Article