Related references
Note: Only part of the references are listed.Gene Therapy of Dominant CRX-Leber Congenital Amaurosis using Patient Stem Cell-Derived Retinal Organoids
Kamil Kruczek et al.
STEM CELL REPORTS (2021)
NASQAR: a web-based platform for high-throughput sequencing data analysis and visualization
Ayman Yousif et al.
BMC BIOINFORMATICS (2020)
Pluripotent stem cell-derived retinal organoids for disease modeling and development of therapies
Kamil Kruczek et al.
STEM CELLS (2020)
The single-cell transcriptional landscape of mammalian organogenesis
Junyue Cao et al.
NATURE (2019)
Comprehensive Integration of Single-Cell Data
Tim Stuart et al.
CELL (2019)
Deciphering retinal diseases through the generation of three dimensional stem cell-derived organoids: Concise Review
Ana Artero Castro et al.
STEM CELLS (2019)
Cone-rod homeobox CRX controls presynaptic active zone formation in photoreceptors of mammalian retina
Juthaporn Assawachananont et al.
HUMAN MOLECULAR GENETICS (2018)
Batch effects in single-cell RNA-sequencing data are corrected by matching mutual nearest neighbors
Laleh Haghverdi et al.
NATURE BIOTECHNOLOGY (2018)
A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis
M. T. Ibrahim et al.
SCIENTIFIC REPORTS (2018)
Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial
Stephen Russell et al.
LANCET (2017)
Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
Neruban Kumaran et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2017)
The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX, With Report of a Novel Macular Dystrophy Phenotype
Sarah Hull et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Otx2 ChIP-seq Reveals Unique and Redundant Functions in the Mature Mouse Retina
Alexander Samuel et al.
PLOS ONE (2014)
Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs
Xiufeng Zhong et al.
NATURE COMMUNICATIONS (2014)
Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy
Nicholas M. Tran et al.
PLOS GENETICS (2014)
CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors
Joseph C. Corbo et al.
GENOME RESEARCH (2010)
Regulation of photoreceptor gene expression by Crx-associated transcription factor network
Anne K. Hennig et al.
BRAIN RESEARCH (2008)
Leber congenital amaurosis: Genes, proteins and disease mechanisms
Anneke I. den Hollander et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2008)
Leber congenital amaurosis - A model for efficient genetic testing of heterogeneous disorders: LXIV Edward Jackson memorial lecture
Edwin M. Stone
AMERICAN JOURNAL OF OPHTHALMOLOGY (2007)
An overview of Leber congenital amaurosis: A model to understand human retinal development
RK Koenekoop
SURVEY OF OPHTHALMOLOGY (2004)