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/vufind/Search/Results?lookfor=%22RLBP1%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22RLBP1%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
Search /vufind/Search2/Results?lookfor=%22RLBP1%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
PubPharm (20)
1
Explore the safety and efficacy of subretinal administration of CPK850 gene therapy in patients with retinitis pigmentosa caused by mutations in the RLBP1 gene : An open-label first-in-human single ascending dose study to explore the safety, tolerability and efficacy of subretinal administration of CPK850 gene therapy in patients with retinitis pigmentosa caused by mutations in the RLBP1 gene
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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2
Explore the safety and efficacy of subretinal administration of CPK850 gene therapy in patients with retinitis pigmentosa caused by mutations in the RLBP1 gene : An open-label first-in-human single ascending dose study to explore the safety, tolerability and efficacy of subretinal administration of CPK850 gene therapy in patients with retinitis pigmentosa caused by mutations in the RLBP1 gene
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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3
The rhodopsin-retinochrome system for retinal re-isomerization predates the origin of cephalopod eyes
enthalten in:
BMC ecology and evolution
| 2021
von
Vöcking, O.
|
Leclère, L.
|
Hausen, H.
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4
Retinitis Punctata Albescens and RLBP1-Allied Phenotypes : Phenotype-Genotype Correlation and Natural History in the Aim of Gene Therapy
enthalten in:
Ophthalmology science
| 2021
von
Bocquet, B.
|
El Alami Trebki, H.
|
Roux, A.
| +14
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5
A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens
enthalten in:
European journal of ophthalmology
| 2021
von
Torres-Costa, S.
|
Ferreira, C.
|
Grangeia, A.
| +4
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6
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant : Insights from Molecular Modeling
enthalten in:
International journal of molecular sciences
| 2021
von
Donato, L.
|
Abdalla, E.
|
Scimone, C.
| +5
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7
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling
in:
International Journal of Molecular Sciences
| 2021
von
Luigi Donato
|
Ebtesam Mohamed Abdalla
|
Concetta Scimone
| +5
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8
The rhodopsin-retinochrome system for retinal re-isomerization predates the origin of cephalopod eyes
in:
BMC Ecology and Evolution
| 2021
von
Oliver Vöcking
|
Lucas Leclère
|
Harald Hausen
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9
Progress in treating inherited retinal diseases : Early subretinal gene therapy clinical trials and candidates for future initiatives
enthalten in:
Progress in retinal and eye research
| 2020
von
Garafalo, A.
|
Cideciyan, A.
|
Héon, E.
| +6
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10
Qualitative Interviews to Better Understand the Patient Experience and Evaluate Patient-Reported Outcomes (PRO) in RLBP1 Retinitis Pigmentosa (RLBP1 RP)
enthalten in:
Advances in therapy
| 2020
von
Green, J.
|
Tolley, C.
|
Bentley, S.
| +9
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Acta ophthalmologica
2
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WHO International Clinical Trials Registry Plat...
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1
BMC Ecology and Evolution
1
BMC ecology and evolution
1
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Alle anzeigen ...
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Thema
13
Journal Article
13
RLBP1
6
Carrier Proteins
6
retinitis pigmentosa
5
11-cis-retinal-binding protein
5
Research Support, Non-U.S. Gov't
5
retinitis punctata albescens
4
CRALBP
3
Research Support, N.I.H., Extramural
3
visual cycle
2
610
2
AAV
2
Bothnia dystrophy
2
Chemistry
2
EC 3.6.5.2
2
Frameshift mutation
2
Genetics
2
Geographical-area related mutation
2
Medical Condition: retinitis pigmentosa caused ...
2
Mollusk
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Erscheinungszeitraum
11
2020-
8
2010-2019
1
2000-2009
Erscheinungsjahr(e)
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Sprache
20
Englisch
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