AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption.
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Dystrophin Dp71 Isoforms Are Differentially Expressed in the Mouse Brain and Retina: Report of New Alternative Splicing and a Novel Nomenclature for Dp71 Isoforms.Glial fibrillary acidic protein promoter determines transgene expression in satellite glial cells following intraganglionic adeno-associated virus delivery in adult rats.
P2860
AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@en
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@nl
type
label
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@en
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@nl
prefLabel
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@en
AAV-mediated gene therapy in D ...... ation and oedema reabsorption.
@nl
P2093
P2860
P50
P356
P1476
AAV-mediated gene therapy in D ...... ration and oedema reabsorption
@en
P2093
Abdoulaye Sene
Alvaro Rendon
Audrey Giocanti-Aurégan
Brahim El Mathari
Cecilia Montañez
Jorge Aragón
Marie Darche
Michel Paques
Ophélie Vacca
Peggy Barbe
P2860
P304
P356
10.1093/HMG/DDW159
P577
2016-06-10T00:00:00Z