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- 2020
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Mark
Clinical phenotype and course of PDE6A-associated retinitis pigmentosa disease, characterized in preparation for a gene supplementation trial
(
- Contribution to journal › Article
- 2018
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Mark
Combination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration
2018) In Proceedings of the National Academy of Sciences of the United States of America 115(13). p.2997-3006(
- Contribution to journal › Article
- 2016
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Mark
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
(
- Contribution to journal › Article
- 2014
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Mark
Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration.
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- Contribution to journal › Article
- 2013
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Mark
Phenotypic map of porcine retinal ganglion cells
(
- Contribution to journal › Article
- 2010
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Mark
A community standard format for the representation of protein affinity reagents
(
- Contribution to journal › Article
- 2009
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Mark
PKG activity causes photoreceptor cell death in two retinitis pigmentosa models
(
- Contribution to journal › Article
- 2008
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Mark
Identification of paracrine neuroprotective candidate proteins by a functional assay-driven proteomics approach
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- Contribution to journal › Article
- 2007
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Mark
Excessive activation of poly(ADP-ribose) polymerase contributes to inherited photoreceptor degeneration in the retinal degeneration 1 mouse.
(
- Contribution to journal › Article
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Mark
ProteomeBinders: planning a European resource of affinity reagents for analysis of the human proteome
(
- Contribution to journal › Debate/Note/Editorial