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Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.
scientific article published on 11 September 2013
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
title
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
main subject
gene therapy
0 references
Bardet-Biedl syndrome
1 reference
based on heuristic
inferred from title
author
Seongjin Seo
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Robert F. Mullins
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Alina V Dumitrescu
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Edwin M. Stone
series ordinal
7
1 reference
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Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Val C. Sheffield
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Arlene Drack
series ordinal
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
author name string
Sajag Bhattarai
series ordinal
4
1 reference
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Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Daniel Gratie
series ordinal
5
1 reference
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Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
Kai Wang
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
language of work or name
English
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publication date
11 September 2013
1 reference
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Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
number of pages
15
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inferred from page(s)
published in
Investigative Ophthalmology Visual Science
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
volume
54
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
issue
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
page(s)
6118-6132
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
describes a project that uses
ImageJ
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Europe PubMed Central
retrieved
11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3771708/fullTextXML
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Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null mice
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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement
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Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
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TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice
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6 September 2017
Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model.
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Functional analysis of BBS3 A89V that results in non-syndromic retinal degeneration
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Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome.
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Whirlin replacement restores the formation of the USH2 protein complex in whirlin knockout photoreceptors
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Equine infectious anemia viral vector-mediated codelivery of endostatin and angiostatin driven by retinal pigmented epithelium-specific VMD2 promoter inhibits choroidal neovascularization.
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BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly
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A simplified baculovirus-AAV expression vector system coupled with one-step affinity purification yields high-titer rAAV stocks from insect cells
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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
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6 September 2017
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome
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6 September 2017
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity
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6 September 2017
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
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6 September 2017
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
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6 September 2017
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
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ISCEV Standard for full-field clinical electroretinography (2008 update).
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Gene therapy restores vision in a canine model of childhood blindness
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3 September 2018
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PubMed
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retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1167/IOVS.13-11673
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
PMC publication ID
3771708
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
PubMed publication ID
23900607
1 reference
stated in
Europe PubMed Central
PMC publication ID
3771708
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23900607%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
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