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Article / Letter to editor
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2019
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Leiden University Medical Center (LUMC)
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Quinn, P.M.
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Wijnholds, J.
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Alves, C.H.
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Klooster, J.
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Pellissier, L.P.
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Vos, R.M.
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Buck, T.M.
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Jost, C.R.
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Koster, A.J.
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Quinn, P.M.; Buck, T.M.; Mulder, A.A.; Ohonin, C.; Alves, C.H.; Vos, R.M.; ... ; Wijnholds, J.
2019
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Muller Glia Are Targets of AAV5
Article / Letter to editor
metadata only
Quinn, P.M.; Mulder, A.A.; Alves, C.H.; Desrosiers, M.; Vries, S.I. de; Klooster, J.; ... ; Wijnholds, J.
2019
Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
Article / Letter to editor
metadata only
Quinn, P.M.; Alves, C.H.; Klooster, J.; Wijnholds, J.
2018
CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function
Article / Letter to editor
open access
Quinn, P.M.; Pellissier, L.P.; Wijnholds, J.
2017
The CRB1 Complex: Following the Trail of Crumbs to a Feasible Gene Therapy Strategy
Article / Letter to editor
open access
Buck, T.M.; Quinn, P.M.; Klooster, J.; Wijnholds, J.
2016
Ablation of Crb2 Specifically in Mouse Photoreceptors with Crb1 loss in Muller Cells Mimics Leber Congenital Amaurosis
Article / Letter to editor
metadata only
Quinn, P.M.; Wijnholds, J.
2016
Ablation of Crb1 and Crb2 Specifically in Mouse Muller Cells mimics early onset Retinitis Pigmentosa
Article / Letter to editor
metadata only
Pellissier, L.P.; Quinn, P.M.; Alves, C.H.; Vos, R.M.; Klooster, J.; Flannery, J.G.; ... ; Wijnholds, J.
2015
Gene therapy into photoreceptors and Muller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models
Article / Letter to editor
metadata only
Pellissier, L.P.; Alves, C.H.; Quinn, P.M.; Vos, R.M.; Tanimoto, N.; Lundvig, D.M.S.; ... ; Wijnholds, J.
2013
Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis
Article / Letter to editor
metadata only