X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
female (8) 8
humans (8) 8
index medicus (8) 8
male (8) 8
aged (7) 7
fuchs' endothelial dystrophy - ethnology (7) 7
ophthalmology (6) 6
middle aged (5) 5
adult (4) 4
fuchs' endothelial dystrophy - genetics (4) 4
missense mutations (4) 4
prevalence (4) 4
african americans (3) 3
aged, 80 and over (3) 3
analysis (3) 3
asian continental ancestry group - genetics (3) 3
case-control studies (3) 3
fuchs' endothelial dystrophy - surgery (3) 3
genetic predisposition to disease - ethnology (3) 3
genotype (3) 3
incidence (3) 3
polymorphisms (3) 3
risk factors (3) 3
transcription factors - genetics (3) 3
united states - epidemiology (3) 3
association (2) 2
basic helix-loop-helix leucine zipper transcription factors - genetics (2) 2
biochemistry & molecular biology (2) 2
collagen type viii - genetics (2) 2
cornea (2) 2
endothelial dystrophy (2) 2
endothelium (2) 2
fuchs endothelial corneal dystrophy (2) 2
fuchs' endothelial dystrophy - pathology (2) 2
genetic predisposition to disease - genetics (2) 2
genome-wide association (2) 2
haplotypes (2) 2
inheritance (2) 2
keratoconus (2) 2
linkage (2) 2
linkage disequilibrium (2) 2
locus (2) 2
mutation (2) 2
protein (2) 2
retrospective studies (2) 2
risk (2) 2
tcf4 (2) 2
transcription factor 4 (2) 2
3-year outcomes (1) 1
abridged index medicus (1) 1
aldehyde dehydrogenase (1) 1
alleles (1) 1
anion transport proteins - genetics (1) 1
antiporters - genetics (1) 1
articles (1) 1
asian continental ancestry group - ethnology (1) 1
asian continental ancestry group - statistics & numerical data (1) 1
asian eyes (1) 1
base sequence (1) 1
bigh3 gene (1) 1
cell biology (1) 1
cell count (1) 1
cohort studies (1) 1
col8a2 (1) 1
col8a2 gene (1) 1
collagen (1) 1
complications (1) 1
continental population groups (1) 1
cornea - metabolism (1) 1
cornea - pathology (1) 1
cornea - physiology (1) 1
corneal diseases - ethnology (1) 1
corneal diseases - surgery (1) 1
corneal dystrophies, hereditary - ethnology (1) 1
corneal dystrophies, hereditary - genetics (1) 1
corneal endothelial cell loss - diagnosis (1) 1
corneal endothelial dystrophy (1) 1
corneal transplantation (1) 1
ctg18.1 trinucleotide repeat (1) 1
descemet stripping endothelial keratoplasty (1) 1
dimethylallyltranstransferase - genetics (1) 1
disease (1) 1
dna ligase atp (1) 1
dna ligase iii (1) 1
dna ligases - genetics (1) 1
dna mutational analysis (1) 1
dna repair (1) 1
dna replication (1) 1
dna-ligase-iii (1) 1
donor insertion device (1) 1
endothelium, corneal - pathology (1) 1
ethnic groups (1) 1
ethnicity (1) 1
europe - epidemiology (1) 1
european continental ancestry group - genetics (1) 1
european continental ancestry group - statistics & numerical data (1) 1
eye (1) 1
eye diseases (1) 1
factor-h polymorphism (1) 1
failure (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Cellular and Molecular Biology, ISSN 0145-5680, 2015, Volume 61, Issue 1, pp. 56 - 63
Journal Article
by Chae, H and Kim, M and Kim, Y and Kim, J and Kwon, A and Choi, H and Park, J and Jang, W and Lee, Y.S and Park, S.H and Kim, M.S
Clinical Genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 678 - 689
Corneal dystrophy typically refers to a group of rare hereditary disorders with a heterogeneous genetic background. A comprehensive molecular genetic analysis... 
posterior polymorphous corneal dystrophy | macular corneal dystrophy | molecular genetic analysis | Thiel–Behnke corneal dystrophy | Fuchs endothelial corneal dystrophy | granular corneal dystrophy | Schnyder corneal dystrophy | lattice corneal dystrophy | Korea | Molecular genetic analysis | Granular corneal dystrophy | Posterior polymorphous corneal dystrophy | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | IC3D CLASSIFICATION | MISSENSE MUTATIONS | COL8A2 GENE | HEREDITARY ENDOTHELIAL DYSTROPHY | GENETICS & HEREDITY | BIGH3 GENE | L527R MUTATION | TGFBI GENE-MUTATIONS | JAPANESE PATIENTS | PROTEIN FUNCTION | LATTICE | Sulfotransferases - genetics | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Corneal Dystrophies, Hereditary - genetics | Family Health | Male | Corneal Dystrophies, Hereditary - ethnology | Zinc Finger E-box-Binding Homeobox 1 - genetics | Transforming Growth Factor beta - genetics | Dimethylallyltranstransferase - genetics | DNA Mutational Analysis | Pedigree | Base Sequence | Adult | Female | Genetic Predisposition to Disease - ethnology | Aged | Mutation | Republic of Korea | Collagen Type VIII - genetics | Genetic aspects | Gene mutations | Analysis | Endothelium | Eye diseases | Cornea | Genetic disorders | Index Medicus
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.