Takip et
Peter M.J. Quinn
Peter M.J. Quinn
Diğer adlarPeter Quinn, Peter M. Quinn
Assistant Professor of Ophthalmology, Perelman School of Medicine University of Pennsylvania
pennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
PINK1/PARKIN signalling in neurodegeneration and neuroinflammation.
PMJ Quinn, PI Moreira, AF Ambrósio, CH Alves
Acta Neuropathol Commun, 2020
3822020
Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis
LP Pellissier, CH Alves, PM Quinn, RM Vos, N Tanimoto, DMS Lundvig, ...
PLoS genetics 9 (12), e1003976, 2013
1032013
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5
PM Quinn, TM Buck, AA Mulder, C Ohonin, CH Alves, RM Vos, M Bialecka, ...
Stem Cell Reports, 2019
1022019
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models
LP Pellissier, PM Quinn, CH Alves, RM Vos, J Klooster, JG Flannery, ...
Human molecular genetics 24 (11), 3104-3118, 2015
962015
Organoids and organ chips in ophthalmology
N Manafi, F Shokri, K Achberger, M Hirayama, MH Mohammadi, ...
The Ocular Surface, 2020
692020
The CRB1 complex: following the trail of crumbs to a feasible gene therapy strategy
PM Quinn, LP Pellissier, J Wijnholds
Frontiers in neuroscience 11, 175, 2017
662017
Role of Oxidative Stress in Retinal Ganglion Cells degenerations
EYC Kang, PK Liu, YT Wen, PMJ Quinn, SR Levi, NK Wang, RK Tsai
Antioxidants, 2021
592021
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
PM Quinn, AA Mulder, CH Alves, M Desrosiers, SI de Vries, J Klooster, ...
Human Molecular Genetics, 2019
522019
CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function
PM Quinn, CH Alves, J Klooster, J Wijnholds
Human Molecular Genetics 27 (18), 2018
472018
Retinogenesis of the Human Fetal Retina: An Apical Polarity Perspective
PMJ Quinn, J Wijnholds
Genes, 2019
452019
The role of small molecules and their effect on the molecular mechanisms of early retinal organoid development
PE Wagstaff, A Heredero Berzal, CJF Boon, PMJ Quinn, A ten Asbroek, ...
International Journal of Molecular Sciences, 2021
332021
Production of iPS-derived human retinal organoids for use in transgene expression assays
PM Quinn, TM Buck, C Ohonin, HMM Mikkers, J Wijnholds
Retinal Gene Therapy: Methods and Protocols, 261-273, 2018
332018
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
WH Wu, YT Tsai, IW Huang, CH Cheng, CW Hsu, X Cui, J Ryu, ...
Molecular Therapy, 2022
272022
Prime Editing for Inherited Retinal Diseases
BLD Costa, SR Levi, E Eulau, YT Tsai, PMJ Quinn
Frontiers In Genome Editing, 2021
272021
Phase transition specified by a binary code patterns the vertebrate eye cup
R Balasubramanian, X Min, PMJ Quinn, Q Lo Giudice, C Tao, K Polanco, ...
Science Advances 7, 2021
192021
CRISPR/Cas therapeutic strategies for autosomal dominant disorders
SM Caruso, PMJ Quinn, BLD Costa, SH Tsang
The Journal of Clinical Investigation, 2022
182022
Impaired cholesterol efflux in retinal pigment epithelium of individuals with juvenile macular degeneration
Y Tsai, Y Li, J Ryu, P Su, C Cheng, W Wu, Y Li, PMJ Quinn, KW Leong, ...
The American Journal of Human Genetics, 2021
182021
Precision metabolome reprogramming for imprecision therapeutics in retinitis pigmentosa
S Caruso, J Ryu, PMJ Quinn, SH Tsang
The Journal of Clinical Investigation, 2020
162020
HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
Y Kong, PK Liu, Y Li, ND Nolan, PMJ Quinn, CW Hsu, LA Jenny, J Zhao, ...
EMBO Molecular Medicine, e16525, 2023
132023
Defining phenotype, tropism, and retinal gene therapy using adeno-associated viral vectors (AAV) in new-born Brown Norway rats with a spontaneous mutation in Crb1
N Boon, CH Alves, AA Mulder, CA Andriessen, TM Buck, PMJ Quinn, ...
International Journal of Molecular Sciences, 2021
132021
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