X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (37) 37
humans (26) 26
ophthalmology (19) 19
corneal dystrophies, hereditary - genetics (18) 18
female (16) 16
male (16) 16
article (13) 13
animals (12) 12
mice (12) 12
mutation (11) 11
pedigree (11) 11
cornea (10) 10
research article (9) 9
adult (8) 8
corneal dystrophy (8) 8
dystrophy (8) 8
family (8) 8
gene (8) 8
middle aged (8) 8
research (8) 8
adolescent (7) 7
cells, cultured (7) 7
eye diseases (7) 7
gene expression (7) 7
mutations (7) 7
transcription factors - genetics (7) 7
apoptosis (6) 6
biochemistry & molecular biology (6) 6
cell biology (6) 6
child (6) 6
corneal diseases (6) 6
corneal dystrophies, hereditary - diagnosis (6) 6
corneal dystrophies, hereditary - metabolism (6) 6
dna mutational analysis (6) 6
endothelial cells (6) 6
expression (6) 6
genetic aspects (6) 6
identification (6) 6
mice, inbred c57bl (6) 6
multidisciplinary sciences (6) 6
phenotype (6) 6
zeb1 (6) 6
abridged index medicus (5) 5
biology and life sciences (5) 5
central-nervous-system (5) 5
corneal endothelium (5) 5
endothelium, corneal - metabolism (5) 5
gene-expression (5) 5
genetics & heredity (5) 5
heterozygote (5) 5
in-vitro (5) 5
medicine (5) 5
medicine and health sciences (5) 5
neurosciences (5) 5
polymerase chain reaction (5) 5
proteins (5) 5
aged (4) 4
cornea - pathology (4) 4
corneal dystrophies, hereditary - pathology (4) 4
deoxyribonucleic acid (4) 4
deoxyribonucleic acid--dna (4) 4
dna (4) 4
dna copy number variations (4) 4
endothelium (4) 4
gene expression regulation (4) 4
gene mutations (4) 4
genes (4) 4
genetics (4) 4
genomics (4) 4
homeodomain proteins - genetics (4) 4
linkage (4) 4
mice, knockout (4) 4
phenotypes (4) 4
polymorphism, single nucleotide (4) 4
promoter regions, genetic (4) 4
protein (4) 4
risk factors (4) 4
science (4) 4
young adult (4) 4
zinc finger e-box-binding homeobox 1 (4) 4
anatomy (3) 3
angiogenesis (3) 3
articles (3) 3
base sequence (3) 3
cell growth (3) 3
cell line (3) 3
cells (3) 3
child, preschool (3) 3
chromosomes (3) 3
classification (3) 3
copy number (3) 3
corneal topography (3) 3
encephalomyelitis, autoimmune, experimental - immunology (3) 3
encephalomyelitis, autoimmune, experimental - pathology (3) 3
epithelial-mesenchymal transition (3) 3
exclusion (3) 3
experimental autoimmune encephalomyelitis (3) 3
gene frequency (3) 3
gene identification and analysis (3) 3
genetic loci (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Immunology, ISSN 0022-1767, 06/2007, Volume 178, Issue 12, pp. 8158 - 8167
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 12/2013, Volume 131, Issue 12, p. 1583
  The identification of steep corneal curvatures in a significant percentage of patients with posterior polymorphous corneal dystrophy (PPCD) confirms this... 
Cornea | Classification | Eye diseases | Mutation | Ophthalmology
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 04/2015, Volume 36, Issue 2, pp. 145 - 148
Journal Article
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 6, pp. e0157418 - e0157418
Purpose To report identification of a COL17A1 mutation in a family with a corneal dystrophy previously mapped to chromosome 10q23-q24. Methods Whole-exome... 
EXCLUSION | COLLAGEN | GENE | MULTIDISCIPLINARY SCIENCES | XVII | BEHNKE CORNEAL-DYSTROPHY | INDIVIDUAL PHENOTYPIC VARIANCES | CDB2 | PREDICTION | FAMILY | Autoantigens - metabolism | Epithelial Cells - metabolism | Alternative Splicing | Cytoskeletal Proteins - genetics | Humans | Corneal Dystrophies, Hereditary - genetics | Male | Epithelium, Corneal - pathology | Autoantigens - genetics | Case-Control Studies | Exome | Corneal Dystrophies, Hereditary - pathology | Genes, Dominant | Female | Gene Expression | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Gene Frequency | Non-Fibrillar Collagens - genetics | Epithelial Cells - pathology | Chromosome Mapping | Corneal Dystrophies, Hereditary - diagnosis | Corneal Dystrophies, Hereditary - metabolism | Sequence Analysis, DNA | Non-Fibrillar Collagens - metabolism | Phenotype | Pedigree | Alleles | Epithelium, Corneal - metabolism | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | Cornea | Epithelial cells | Genes | Genomes | Gene sequencing | Proteins | Chromosome 10 | Genetics | Growth factors | Chromosomes | Deoxyribonucleic acid--DNA | Erosion | Phenotypes | Erosion mechanisms | Filtration | Splicing | Medicine | Gene frequency | Corneal dystrophy | Collagen | Dynamin | Dystrophy | Genetic testing | DNA sequencing | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e95037 - e95037
Journal Article
Revista Mexicana de Oftalmología, ISSN 0187-4519, 07/2019, Volume 93, Issue 4
Journal Article