CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity

Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5

(2019) Peter M. Quinn et al.   Stem Cell Reports

CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function

(2018) Peter M Quinn et al.   HUMAN MOLECULAR GENETICS

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

(2018) Peter M Quinn et al.   HUMAN MOLECULAR GENETICS

CRB2 mutation causes autosomal recessive retinitis pigmentosa

(2018) Xue Chen et al.   EXPERIMENTAL EYE RESEARCH

Genotypic and Phenotypic Characteristics of CRB1 -Associated Retinal Dystrophies

(2017) Mays Talib et al.   OPHTHALMOLOGY

Role of the crumbs proteins in ciliogenesis, cell migration and actin organization

(2017) Elsa Bazellières et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes

(2017) Fabiana Louise Motta et al.   Scientific Reports

Expansion of phenotype and genotypic data in CRB2-related syndrome

(2016) Ryan E Lamont et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Defects of CRB2 Cause Steroid-Resistant Nephrotic Syndrome

(2015) Lwaki Ebarasi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

CRB2 Mutations Produce a Phenotype Resembling Congenital Nephrosis, Finnish Type, with Cerebral Ventriculomegaly and Raised Alpha-Fetoprotein

(2015) Anne Slavotinek et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models

(2015) Lucie P. Pellissier et al.   HUMAN MOLECULAR GENETICS

Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179

(2015) Koji M. Nishiguchi et al.   Nature Communications

CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice

(2014) Lucie P. Pellissier et al.   HUMAN MOLECULAR GENETICS

Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa

(2014) Celso Henrique Alves et al.   HUMAN MOLECULAR GENETICS

Müller glial cell reprogramming and retina regeneration

(2014) Daniel Goldman   NATURE REVIEWS NEUROSCIENCE

The CRB1 and adherens junction complex proteins in retinal development and maintenance

(2014) Celso Henrique Alves et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Correlation between SD-OCT, immunocytochemistry and functional findings in an animal model of retinal degeneration

(2014) Nicolás Cuenca et al.   Frontiers in Neuroanatomy

Specific tools for targeting and expression in Müller glial cells

(2014) Lucie P Pellissier et al.   Molecular Therapy-Methods & Clinical Development

Cone survival and preservation of visual acuity in an animal model of retinal degeneration

(2013) Ilaria Piano et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Microarray and Morphological Analysis of Early Postnatal CRB2 Mutant Retinas on a Pure C57BL/6J Genetic Background

(2013) Celso Henrique Alves et al.   PLoS One

Targeted Ablation of Crb1 and Crb2 in Retinal Progenitor Cells Mimics Leber Congenital Amaurosis

(2013) Lucie P. Pellissier et al.   PLoS Genetics

Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene

(2012) Celso Henrique Alves et al.   HUMAN MOLECULAR GENETICS

Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps

(2012) Frank G.A. Faas et al.   JOURNAL OF CELL BIOLOGY