X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (24) 24
index medicus (24) 24
ched2 (22) 22
anion transport proteins - genetics (21) 21
antiporters - genetics (20) 20
ophthalmology (17) 17
male (16) 16
mutation (16) 16
corneal dystrophies, hereditary - genetics (15) 15
female (14) 14
adult (10) 10
slc4a11 (10) 10
adolescent (9) 9
child, preschool (9) 9
pedigree (9) 9
child (8) 8
cornea (8) 8
dna mutational analysis (8) 8
gene (8) 8
harboyan syndrome (8) 8
chromosome-20 (7) 7
fuchs' endothelial dystrophy - genetics (7) 7
genetic disorders (7) 7
genetics & heredity (7) 7
mutations (7) 7
polymerase chain reaction (7) 7
young adult (7) 7
cell line (6) 6
congenital hereditary endothelial dystrophy (6) 6
hereditary endothelial dystrophy (6) 6
molecular sequence data (6) 6
phenotype (6) 6
amino acid sequence (5) 5
animals (5) 5
anion transport proteins - metabolism (5) 5
endothelium, corneal - pathology (5) 5
expression (5) 5
eye diseases (5) 5
genetic aspects (5) 5
antiporters - metabolism (4) 4
base sequence (4) 4
biochemistry & molecular biology (4) 4
cell-growth (4) 4
corneal dystrophies, hereditary (4) 4
corneal dystrophies, hereditary - diagnosis (4) 4
cotransporter (4) 4
deafness (4) 4
exons - genetics (4) 4
hearing loss, sensorineural - genetics (4) 4
hek293 cells (4) 4
linkage (4) 4
middle aged (4) 4
mutation - genetics (4) 4
sense organs (4) 4
audiometry (3) 3
ched (3) 3
cohort studies (3) 3
consanguinity (3) 3
corneal dystrophies, hereditary - surgery (3) 3
dystrophy ched2 (3) 3
endothelium (3) 3
endothelium, corneal (3) 3
endothelium, corneal - metabolism (3) 3
family (3) 3
gene expression (3) 3
gene mutations (3) 3
genes (3) 3
genetic linkage (3) 3
hearing loss, sensorineural - diagnosis (3) 3
india (3) 3
indian families (3) 3
medicine, research & experimental (3) 3
mice (3) 3
mutation, missense (3) 3
mutational spectrum (3) 3
perceptive deafness (3) 3
physiology (3) 3
proliferation (3) 3
research article (3) 3
transport (3) 3
2 siblings (2) 2
20p13 (2) 2
age (2) 2
ammonia (2) 2
analysis (2) 2
anion transport proteins - chemistry (2) 2
antiporters - chemistry (2) 2
apoptosis - genetics (2) 2
articles (2) 2
asian continental ancestry group - genetics (2) 2
blotting, western (2) 2
cell biology (2) 2
chromosome mapping (2) 2
codon, nonsense (2) 2
corneal dystrophies, hereditary - metabolism (2) 2
corneal dystrophies, hereditary - physiopathology (2) 2
corneal dystrophy (2) 2
corneal-dystrophy (2) 2
dna sequencing (2) 2
down-regulation (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, ISSN 0363-6143, 10/2013, Volume 305, Issue 7, pp. C716 - C727
Slc4a11, a member of the solute linked cotransporter 4 family that is comprised predominantly of bicarbonate transporters, was described as an electrogenic... 
borate | PHYSIOLOGY | CL-/HCO3-EXCHANGE | SLC4A11 | INTRACELLULAR PH REGULATION | BOVINE CORNEAL ENDOTHELIUM | CELL BIOLOGY | TRANSPORT | Na+ permeability | HEREDITARY ENDOTHELIAL DYSTROPHY | COTRANSPORTER | bicarbonate | MUTATIONS | KIDNEY | EXPRESSION | CHED2
Journal Article
Journal Article
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 10/2014, Volume 98, Issue 10, pp. 1460 - 1462
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 02/2012, Volume 33, Issue 2, pp. 419 - 428
Journal Article