Peter M. Quinn
Leiden, ZH 2333ZA, Netherlands
Last Updated: 09/26/2026
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Found 11 publications
Ablating VHL in rod photoreceptors modulates RPE glycolysis and improves preclinical model of retinitis pigmentosa.
Journal: The Journal of clinical investigation
Published: August 07, 2024
Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina.
Journal: Life science alliance
Published: October 17, 2023
CRISPR/Cas therapeutic strategies for autosomal dominant disorders.
Journal: The Journal of clinical investigation
Published: May 02, 2022
Precision metabolome reprogramming for imprecision therapeutics in retinitis pigmentosa.
Journal: The Journal of clinical investigation
Published: July 14, 2020
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5.
Journal: Stem cell reports
Published: October 09, 2018
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Journal: Human molecular genetics
Published: August 08, 2018
CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function.
Journal: Human molecular genetics
Published: March 20, 2018
Production of iPS-Derived Human Retinal Organoids for Use in Transgene Expression Assays.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: December 01, 2017
The CRB1 Complex: Following the Trail of Crumbs to a Feasible Gene Therapy Strategy.
Journal: Frontiers in neuroscience
Published: December 21, 2016
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models.
Journal: Human molecular genetics
Published: December 09, 2014
Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosis.
Journal: PLoS genetics
Published: September 10, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026