X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (31) 31
humans (27) 27
mutation (25) 25
retinitis pigmentosa - genetics (22) 22
retinitis pigmentosa (21) 21
eye proteins - genetics (19) 19
eys (19) 19
ophthalmology (19) 19
female (18) 18
male (18) 18
ortholog (18) 18
identification (17) 17
dna mutational analysis (16) 16
pedigree (15) 15
adult (12) 12
eys gene (12) 12
genetics & heredity (12) 12
gene (11) 11
middle aged (11) 11
aged (9) 9
genetic aspects (9) 9
photoreceptors (9) 9
recessive retinitis-pigmentosa (9) 9
genes (8) 8
genes, recessive (8) 8
research article (8) 8
retinal degeneration (8) 8
retinitis pigmentosa - pathology (8) 8
abundance (7) 7
analysis (7) 7
cone-rod dystrophy (7) 7
eye diseases (7) 7
genetics (7) 7
henri ey (7) 7
marine water (7) 7
phenotype (7) 7
retinitis (7) 7
stock assessment (7) 7
animals (6) 6
base sequence (6) 6
eyes (6) 6
genetic structures (6) 6
polymerase chain reaction (6) 6
prediction (6) 6
retina (6) 6
ane (5) 5
barents sea (5) 5
case-control studies (5) 5
clupea harengus (5) 5
echo surv eys (5) 5
exons (5) 5
extracellular matrix proteins - genetics (5) 5
families (5) 5
fish catch statistics (5) 5
fishery management (5) 5
genomics (5) 5
greenland (5) 5
jan mayen (5) 5
japanese patients (5) 5
mallotus villosus (5) 5
micromesistius poutassou (5) 5
molecular sequence data (5) 5
mutations (5) 5
norway (5) 5
optical coherence tomography (5) 5
patients (5) 5
pne (5) 5
prevalence (5) 5
recruitment (5) 5
retinitis pigmentosa - diagnosis (5) 5
disease (4) 4
dystrophy (4) 4
electroretinography (4) 4
eye proteins - metabolism (4) 4
fundus oculi (4) 4
genetic research (4) 4
genetic variation (4) 4
life sciences (4) 4
medicine (4) 4
population (4) 4
proteins (4) 4
science (4) 4
tomography, optical coherence (4) 4
amino acid sequence (3) 3
asian continental ancestry group - genetics (3) 3
autosomal recessive (3) 3
biochemistry & molecular biology (3) 3
biodiversity conservation (3) 3
biology and life sciences (3) 3
cell biology (3) 3
chromosome segregation - genetics (3) 3
developmental biology (3) 3
drosophila proteins - genetics (3) 3
ecology (3) 3
exons - genetics (3) 3
eye (3) 3
eyes shut homolog (3) 3
eys mutations (3) 3
family (3) 3
gene frequency (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


DFO Atlantic fisheries research document, Volume 96/8., 44, [4]
The overal TAC has been caught in both years since the remaining individual SFA quotas were lifted in 1994. With one TAC the fishery has concentrated in a... 
landing statistics | biomass | fishery surv eys | licenses | by catch | marine water | shellfish catch statistics | Scotian Shelf | abundance | ANW | Pandalus borealis | stock assessment
Book
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 05/2019, Volume 60, Issue 6, pp. 2049 - 2063
PURPOSE. To assess the phenotypic variability and natural course of inherited retinal diseases (IRDs) caused by EYS mutations. METHODS. Multiethnic cohort... 
ORTHOLOG | RECESSIVE RETINITIS-PIGMENTOSA | macular dystrophy | IDENTIFICATION | inherited retinal disease | GENE | retinitis pigmentosa | OPHTHALMOLOGY | cone-rod dystrophy | MUTATIONS | JAPANESE PATIENTS | EYS | PROGRESSION
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2018, Volume 176, Issue 12, pp. 2695 - 2703
Whole exome sequencing (WES) has become routine in clinical practice, especially in studies of recessive hereditary diseases in inbred consanguineous families,... 
CNV | WES | EYS | haplotyping | ORTHOLOG | ISRAELI | HOMOZYGOSITY | GENE | DISEASE | GENETICS & HEREDITY | BARDET-BIEDL-SYNDROME | LINKAGE | SMART | Nonsense mutation | Retinitis pigmentosa | Exons | Nyctalopia | Gene deletion | Hereditary diseases | Electroretinograms | Retinography | DNA microarrays | Clonal deletion | Inbreeding | Retinitis | Mutation
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2017, Volume 10, Issue 2, pp. 325 - 328
Dear Editor, I am Dr.Ji-Hong Wu,from the Department of Ophthalmology,Eye&ENT Hospital of Fudan University,China.I write to present a case report of retinitis... 
EYS MUTATIONS | PHENOTYPE | OPHTHALMOLOGY | IDENTIFICATION | EXUDATIVE VITREORETINOPATHY | FZD4
Journal Article
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 04/2011, Volume 32, Issue 4, pp. E2091 - E2103
Autosomal-recessive retinitis pigmentosa (arRP) is a genetically heterogeneous group of disorders to which a novel gene, C2orf71, was recently associated. The... 
USH2A GENE | EYS GENE | SERVER | GENETICS & HEREDITY | RECESSIVE RETINITIS-PIGMENTOSA | Rod-cone dystrophies | Autosomal-recessive retinitis pigmentosa | C2orf71
Journal Article
Seminars in Ophthalmology, ISSN 0882-0538, 05/2018, Volume 33, Issue 4, pp. 560 - 565
Purpose: EYS and USH2A are the most common causative genes for retinitis pigmentosa (RP) in Japan. We determined the clinical outcomes for USH2A-related... 
hearing impairment | genetic disorder | non-syndromic retinitis pigmentosa | rod-cone dysfunction | EYS gene | GENOTYPE-PHENOTYPE CORRELATION | POPULATION | FREQUENT | 2299DELG | SYNDROME TYPE-II | LARGE COHORT | LONG ISOFORM | GENE | SYNDROME TYPE-2 | OPHTHALMOLOGY | SPECTRUM | Index Medicus
Journal Article
Journal Article
Journal Article