X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (350) 350
humans (302) 302
bestrophins (301) 301
eye proteins - genetics (234) 234
chloride channels - genetics (176) 176
ophthalmology (165) 165
animals (158) 158
male (145) 145
female (132) 132
mutation (132) 132
chloride channels (124) 124
bestrophin (119) 119
chloride channels - metabolism (102) 102
vitelliform macular dystrophy (100) 100
eye proteins - metabolism (99) 99
adult (90) 90
mice (88) 88
degeneration (85) 85
middle aged (83) 83
family (75) 75
gene (74) 74
electrooculography (69) 69
macular degeneration - genetics (69) 69
best-disease (68) 68
disease (68) 68
pedigree (68) 68
retinal-pigment epithelium (68) 68
tomography, optical coherence (68) 68
eye diseases (67) 67
child (65) 65
biochemistry & molecular biology (64) 64
protein (64) 64
vitelliform macular dystrophy - genetics (64) 64
vmd2 (63) 63
dna mutational analysis (60) 60
electroretinography (60) 60
phenotype (59) 59
mutations (58) 58
sense organs (58) 58
vmd2 gene (57) 57
article (53) 53
macular degeneration (52) 52
fluorescein angiography (50) 50
adolescent (49) 49
physiology (48) 48
genetics & heredity (47) 47
macular dystrophy (47) 47
aged (46) 46
ion channels (45) 45
retinal pigment epithelium (45) 45
channels (40) 40
membrane (40) 40
calcium - metabolism (39) 39
calcium (38) 38
genetic aspects (38) 38
mutation, missense (38) 38
optical coherence tomography (38) 38
research (38) 38
cell line (37) 37
molecular sequence data (37) 37
proteins (37) 37
cells (36) 36
patch-clamp techniques (35) 35
best1 (34) 34
gene expression (34) 34
retinal diseases - genetics (34) 34
vitelliform macular dystrophy - diagnosis (34) 34
cell biology (33) 33
visual acuity (33) 33
genotype (32) 32
best vitelliform macular dystrophy (31) 31
genetic structures (31) 31
retina (31) 31
retinal pigment epithelium - metabolism (31) 31
amino acid sequence (30) 30
fundus oculi (30) 30
neurosciences (30) 30
polymerase chain reaction (30) 30
child, preschool (29) 29
chloride channels - physiology (28) 28
expression (28) 28
retinal degeneration (28) 28
young adult (28) 28
analysis (27) 27
chlorides - metabolism (27) 27
eye diseases, hereditary - genetics (27) 27
eye proteins - chemistry (27) 27
abridged index medicus (26) 26
light peak (26) 26
visual acuity - physiology (26) 26
articles (25) 25
mouse bestrophin-2 (25) 25
research article (25) 25
identification (24) 24
multidisciplinary sciences (24) 24
cells, cultured (23) 23
electrophysiology (23) 23
gene mutations (23) 23
retinal degeneration - genetics (23) 23
best disease (22) 22
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (384) 384
German (9) 9
Chinese (3) 3
French (2) 2
Czech (1) 1
Italian (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Molecular Genetics, ISSN 0964-6906, 02/2013, Volume 22, Issue 3, pp. 593 - 607
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2015, Volume 112, Issue 20, pp. E2630 - E2639
Journal Article
Experimental Eye Research, ISSN 0014-4835, 04/2014, Volume 121, pp. 74 - 85
encodes Bestrophin-1 (Best1), a homo-oligomeric, integral membrane protein localized to the basolateral plasma membrane of the retinal pigment epithelium.... 
fluorescence resonance energy transfer | retinitis pigmentosa | MDCK | retinal pigment epithelium | vitelliform dystrophy | bestrophin | Fluorescence resonance energy transfer | Bestrophin | Retinitis pigmentosa | Vitelliform dystrophy | Retinal pigment epithelium | PROTEIN | BEST-DISEASE | VITELLIFORM MACULAR DYSTROPHY | PLASMA-MEMBRANE | CL-CHANNELS | VMD2 | MISSENSE MUTATIONS | POLARIZED EPITHELIUM | GENE | OPHTHALMOLOGY | CELL | Retinal Diseases - genetics | Vitelliform Macular Dystrophy - metabolism | Choroid Diseases - metabolism | Madin Darby Canine Kidney Cells - metabolism | Humans | Electrophysiology | Fluorescent Dyes - metabolism | Retinal Diseases - metabolism | Chloride Channels - genetics | Mutation, Missense | Retinal Degeneration - metabolism | Transfection | Bestrophins | Vitelliform Macular Dystrophy - genetics | Protein Multimerization - physiology | HEK293 Cells | Adenoviridae - genetics | Fluorescence Resonance Energy Transfer | Eye Proteins - genetics | Choroid Diseases - genetics | Green Fluorescent Proteins - metabolism | Gene Expression | Retinal Degeneration - genetics | Retinitis Pigmentosa - genetics | Retinitis Pigmentosa - metabolism | Blotting, Western | Eye Diseases, Hereditary - genetics | Chloride Channels - metabolism | Microscopy, Confocal | Patch-Clamp Techniques | Animals | Eye Proteins - metabolism | Dogs | Bacterial Proteins - metabolism | Eye Diseases, Hereditary - metabolism | Luminescent Proteins - metabolism | Oligomers | Exhibitions | Genetic aspects | Ophthalmology | Aquaporins | Index Medicus | Bestrophin, MDCK
Journal Article
Journal Article
Molecular Brain, ISSN 1756-6606, 2015, Volume 8, Issue 1, pp. 7 - 7
Journal Article
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 07/2019, Volume 60, Issue 8, pp. 2875 - 2887
PURPOSE. We previously found a dominant mutation, Rwhs, causing white spots on the retina accompanied by retinal folds. Here we identify the mutant gene to be... 
mouse models | genetic diseases | CRB1 | BESTROPHIN | FRIZZLED-RELATED PROTEIN | DEGENERATION | POSTERIOR MICROPHTHALMOS | MFRP | retina | CRUMBS HOMOLOG-1 | OPHTHALMOLOGY | GENOME-WIDE | RECESSIVE SYNDROME | RETINITIS-PIGMENTOSA | nanophthalmos
Journal Article
2019, ISBN 0444640320, Volume 160
The electrooculogram (EOG) measures the cornea-positive standing potential relative to the back of the eye. By attaching skin electrodes outside the eye near... 
Electrooculogram | Arden ratio | Adult vitelliform dystrophy | Pigment epithelium | Lipofuscin | Best disease | Bestrophin | Best1
Book Chapter
Bone, ISSN 8756-3282, 05/2019, Volume 122, pp. 193 - 198
Mandibular prognathism is a phenotype of facial deformity seen in populations around the world, but with higher incidence among East Asian populations. Five... 
Genetics | Mandibular prognathism | Bestrophin 3 | Endochondral growth | Japanese | Whole-exome sequencing | MICROSATELLITE | IDENTIFICATION | GENE | MALOCCLUSION | GROWTH | ENDOCRINOLOGY & METABOLISM | LINKAGE | GENOME-WIDE ASSOCIATION | Platelet-derived growth factor | Single nucleotide polymorphisms | Analysis | Genomics
Journal Article