Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.
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The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.The pigmented epithelium, a bright partner against photoreceptor degeneration.CRISPR-Cas9-Based Genome Editing of Human Induced Pluripotent Stem Cells.Feeder-free differentiation of cells exhibiting characteristics of corneal endothelium from human induced pluripotent stem cells.Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy.Cellular regeneration strategies for macular degeneration: past, present and future.Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA.
P2860
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P2860
Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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name
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@en
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@nl
type
label
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@en
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@nl
prefLabel
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@en
Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@nl
P2093
P2860
P50
P1433
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Using CRISPR-Cas9 to Generate ...... nherited Retinal Degeneration.
@en
P2093
Chunhua Jiao
Darcey L Klaahsen
Erin R Burnight
George Q Daley
Jason W Ross
Jeaneen L Andorf
Jeremy M Hoffmann
Kristin R Anfinson
Malavika K Adur
Manav Gupta
P2860
P304
P356
10.1016/J.YMTHE.2017.05.015
P577
2017-06-12T00:00:00Z