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Retinitis pigmentosa
scientific article (publication date: 18 November 2006)
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instance of
scholarly article
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review article
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Europe PubMed Central
title
Retinitis pigmentosa
(English)
1 reference
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PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
main subject
retinitis pigmentosa
0 references
author name string
Hartong DT
series ordinal
1
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
Berson EL
series ordinal
2
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
Dryja TP
series ordinal
3
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
language of work or name
English
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
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30 April 2017
publication date
18 November 2006
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
published in
The Lancet
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
volume
368
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
issue
9549
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
page(s)
1795-809
1 reference
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
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7 January 2021
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CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
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The epidemiology of retinitis pigmentosa in Denmark
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7 January 2021
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Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene
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BBS8 is rarely mutated in a cohort of 128 Bardet-Biedl syndrome families
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BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
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Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy
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Reading Performance in Patients with Retinitis Pigmentosa: A Study Using the MNREAD Charts
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Risk Factors for Genetic Typing and Detection in Retinitis Pigmentosa
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7 January 2021
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X-linked retinitis pigmentosa. Profile of clinical findings
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7 January 2021
based on heuristic
inferred from DOI database lookup
Contrast sensitivity in retinitis pigmentosa
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
A modified protocol for the assessment of visual function in patients with retinitis pigmentosa
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
The frequency of posterior subcapsular cataract in the hereditary retinal degenerations.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Histopathology of bone spicule pigmentation in retinitis pigmentosa
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
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Temporal aspects of the electroretinogram
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosa
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rates of change differ among measures of visual function in patients with retinitis pigmentosa
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Narrow-band filtering for monitoring low-amplitude cone electroretinograms in retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
The association between visual acuity and central retinal thickness in retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of ultrahigh- and standard-resolution optical coherence tomography for imaging macular pathology
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
A one-hit model of cell death in inherited neuronal degenerations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rate of visual field loss in retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Relationship between difficulty in performing daily activities and clinical measures of visual function in patients with retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Segregation of a mutation in CNGB1 encoding the beta-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CRB1 mutation spectrum in inherited retinal dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and histopathologic findings in clumped pigmentary retinal degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous tandem duplication within the gene encoding the beta-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense rhodopsin mutation in a family with recessive RP
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arrestin gene mutations in autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational spectrum in Usher syndrome type II.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The oligogenic properties of Bardet-Biedl syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel frameshift mutations in CRX associated with Leber congenital amaurosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cGMP-phosphodiesterase and its contribution to sensitivity regulation in retinal rods
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subunit stoichiometry of retinal rod cGMP phosphodiesterase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interaction of glutamic-acid-rich proteins with the cGMP signalling pathway in rod photoreceptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cGMP-gated channel and related glutamic acid-rich proteins interact with peripherin-2 at the rim region of rod photoreceptor disc membranes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glutamic acid-rich proteins of rod photoreceptors are natively unfolded
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanistic studies of ABCR, the ABC transporter in photoreceptor outer segments responsible for autosomal recessive Stargardt disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Visual cycle impairment in cellular retinaldehyde binding protein (CRALBP) knockout mice results in delayed dark adaptation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A palmitoylation switch mechanism in the regulation of the visual cycle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RPE65 is the isomerohydrolase in the retinoid visual cycle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A photic visual cycle of rhodopsin regeneration is dependent on Rgr.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tubby-like protein 1 (TULP1) interacts with F-actin in photoreceptor cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Crumbs, the Drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe retinal degeneration associated with disruption of semaphorin 4A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comprehensive proteomic analysis of the human spliceosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interactions in the network of Usher syndrome type 1 proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RPGR isoforms in photoreceptor connecting cilia and the transitional zone of motile cilia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of a ceramide kinase-like protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyclic guanosine monophosphate: elevation in degenerating photoreceptor cells of the C3H mouse retina
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rhodopsin maturation antagonized by dominant rhodopsin mutants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rhodopsin C terminus, the site of mutations causing retinal disease, regulates trafficking by binding to ADP-ribosylation factor 4 (ARF4).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Saving cone cells in hereditary rod diseases: a possible role for rod-derived cone viability factor (RdCVF) therapy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of rod-derived cone viability factor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Supplemental vitamin A retards loss of ERG amplitude in retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vitamin A supplementation for retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Safety of <7500 RE (<25000 IU) vitamin A daily in adults with retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vitamin A intake and hip fractures among postmenopausal women
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum retinol levels and the risk of fracture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinoic acid embryopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chemistry and metabolism of lipids in the vertebrate retina
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electroretinographic Responses Following Vitamin A Therapy in A-Beta-Lipoproteinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Combined vitamin A and E therapy prevents retinal electrophysiological deterioration in abetalipoproteinaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Refsum's disease: management by diet and plasmapheresis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Light deprivation and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Light deprivation and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acetazolamide for treatment of chronic macular edema in retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Advances in night vision technology. A pocketscope for patients with retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improved mobility and independence of night-blind people using night-vision goggles.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improving nighttime mobility in persons with night blindness caused by retinitis pigmentosa: A comparison of two low-vision mobility devices.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Correlation of regenerable opsin with rod ERG signal in Rpe65-/- mice during development and aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In utero gene therapy rescues vision in a murine model of congenital blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene transfer in the RPE65 null mutation dog: relationship between construct volume, visual behavior and electroretinographic (ERG) results
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assessment of structure and function over a 3-year period after gene transfer in RPE65-/- dogs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photoreceptor cell rescue in retinal degeneration (rd) mice by in vivo gene therapy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rescue of photoreceptor function by AAV-mediated gene transfer in a mouse model of inherited retinal degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Encapsidated adenovirus mini-chromosome-mediated delivery of genes to the retina: application to the rescue of photoreceptor degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rescue from photoreceptor degeneration in the rd mouse by human immunodeficiency virus vector-mediated gene transfer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interference
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adenovirus-mediated delivery of rhodopsin-promoted bcl-2 results in a delay in photoreceptor cell death in the rd/rd mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of Bcl-2 protects against photoreceptor degeneration in retinal degeneration slow (rds) mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photoreceptor preservation in the S334ter model of retinitis pigmentosa by a novel estradiol analog
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinitis pigmentosa: rod photoreceptor rescue by a calcium-channel blocker in the rd mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transplantation of retinal pigment epithelial cells to immature and adult rat hosts: short- and long-term survival characteristics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photoreceptor repair in response to RPE transplants in RCS rats: outer segment regeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improvement of the pupillary light reflex of Royal College of Surgeons rats following RPE cell grafts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photoreceptor transplantation in retinitis pigmentosa: short-term follow-up
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GDF11 controls the timing of progenitor cell competence in developing retina
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal stem/progenitor properties of iris pigment epithelial cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel in vitro retinal differentiation model by co-culturing adult human bone marrow stem cells with retinal pigmented epithelium cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermal growth factor is a neuronal differentiation factor for retinal stem cells in vitro.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Embryonic stem cell-derived neural progenitors incorporate into degenerating retina and enhance survival of host photoreceptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal incorporation and differentiation of neural precursors derived from human embryonic stem cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transplantation of neuroblastic progenitor cells as a sheet preserves and restores retinal function.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Facile isolation and the characterization of human retinal stem cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vision change after sheet transplant of fetal retina with retinal pigment epithelium to a patient with retinitis pigmentosa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The artificial silicon retina microchip for the treatment of vision loss from retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Possible sources of neuroprotection following subretinal silicon chip implantation in RCS rats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thresholds for activation of rabbit retinal ganglion cells with relatively large, extracellular microelectrodes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Creating a meaningful visual perception in blind volunteers by optic nerve stimulation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct stimulation of optic nerve by electrodes implanted in optic disc of rabbit eyes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Feasibility of a visual prosthesis for the blind based on intracortical microstimulation of the visual cortex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of functional organization in human visual cortex: electrical cortical stimulation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Perceptual efficacy of electrical stimulation of human retina with a microelectrode array during short-term surgical trials
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Perceptual thresholds and electrode impedance in three retinal prosthesis subjects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2969740-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(06)69740-7
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
110101
OpenCitations bibliographic resource ID
110101
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
110101
PubMed ID
17113430
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17113430
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
110101
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