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A comparison of some organizational characteristics of the mouse central retina and the human macula

PloS one, 2015-04, Vol.10 (4), p.e0125631-e0125631

2015

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Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies

PloS one, 2013-11, Vol.8 (11), p.e78496-e78496

2013

Volltextzugriff (PDF)

Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice

Nature communications, 2017-03, Vol.8 (1), p.14716-14716, Article 14716

2017

Volltextzugriff (PDF)

Long Non-Coding RNA MALAT1 Mediates Transforming Growth Factor Beta1-Induced Epithelial-Mesenchymal Transition of Retinal Pigment Epithelial Cells

PloS one, 2016-03, Vol.11 (3), p.e0152687-e0152687

2016

Volltextzugriff (PDF)

TGF-β1 induced transdifferentiation of rpe cells is mediated by TAK1

PloS one, 2015-04, Vol.10 (4), p.e0122229-e0122229

2015

Volltextzugriff (PDF)

Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma

Human molecular genetics, 2012-04, Vol.21 (8), p.1848-1860

2012

Volltextzugriff (PDF)

Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis

PloS one, 2013-11, Vol.8 (11), p.e79369-e79369

2013

Volltextzugriff (PDF)

Comparison of suprachoroidal drug delivery with subconjunctival and intravitreal routes using noninvasive fluorophotometry

PloS one, 2012-10, Vol.7 (10), p.e48188

2012

Volltextzugriff (PDF)

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan

PloS one, 2015-03, Vol.10 (3), p.e0119806-e0119806

2015

Volltextzugriff (PDF)

Nicotinamide Promotes Formation of Retinal Organoids From Human Pluripotent Stem Cells via Enhanced Neural Cell Fate Commitment

Frontiers in cellular neuroscience, 2022-06, Vol.16, p.878351-878351

2022

Volltextzugriff (PDF)

RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration

PloS one, 2014-04, Vol.9 (4), p.e95362-e95362

2014

Volltextzugriff (PDF)

Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration

PLoS genetics, 2020-12, Vol.16 (12), p.e1009259-e1009259

2020

Volltextzugriff (PDF)

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4413-4418

2007

Volltextzugriff (PDF)

Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss

PLoS genetics, 2010-05, Vol.6 (5), p.e1000955-e1000955

2010

Volltextzugriff (PDF)

Ablation of the proapoptotic genes CHOP or Ask1 does not prevent or delay loss of visual function in a P23H transgenic mouse model of retinitis pigmentosa

PloS one, 2014-02, Vol.9 (2), p.e83871-e83871

2014

Volltextzugriff (PDF)

The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome

PloS one, 2016-05, Vol.11 (5), p.e0155619-e0155619

2016

Volltextzugriff (PDF)

Suppression of experimental choroidal neovascularization by curcumin in mice

PloS one, 2012-12, Vol.7 (12), p.e53329

2012

Volltextzugriff (PDF)

A degenerative retinal process in HIV-associated non-infectious retinopathy

PloS one, 2013-09, Vol.8 (9), p.e74712-e74712

2013

Volltextzugriff (PDF)

Evaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogs

PloS one, 2013-04, Vol.8 (4), p.e60218-e60218

2013

Volltextzugriff (PDF)

Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina

Cell reports (Cambridge), 2016-10, Vol.17 (5), p.1399-1413

2016

Volltextzugriff (PDF)

Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15

PloS one, 2012-05, Vol.7 (5), p.e35865-e35865

2012

Volltextzugriff (PDF)

OCT Intensity of the Region between Outer Retina Band 2 and Band 3 as a Biomarker for Retinal Degeneration and Therapy

Bioengineering (Basel), 2024-05, Vol.11 (5), p.449

2024

Volltextzugriff (PDF)

Vigabatrin-induced retinal toxicity is partially mediated by signaling in rod and cone photoreceptors

PloS one, 2012-08, Vol.7 (8), p.e43889

2012

Volltextzugriff (PDF)

A constitutively active Gαi3 protein corrects the abnormal retinal pigment epithelium phenotype of Oa1-/- mice

PloS one, 2013-09, Vol.8 (9), p.e76240

2013

Volltextzugriff (PDF)

Extended duration of transgene expression from pegylated POD nanoparticles enables attenuation of photoreceptor degeneration

PloS one, 2013-11, Vol.8 (11), p.e82295

2013

Volltextzugriff (PDF)

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A comparison of some organizational characteristics of the mouse central retina and the human macula

Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies

Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice

Long Non-Coding RNA MALAT1 Mediates Transforming Growth Factor Beta1-Induced Epithelial-Mesenchymal Transition of Retinal Pigment Epithelial Cells

TGF-β1 induced transdifferentiation of rpe cells is mediated by TAK1

Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma

Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis

Comparison of suprachoroidal drug delivery with subconjunctival and intravitreal routes using noninvasive fluorophotometry

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan

Nicotinamide Promotes Formation of Retinal Organoids From Human Pluripotent Stem Cells via Enhanced Neural Cell Fate Commitment

RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration

Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss

Ablation of the proapoptotic genes CHOP or Ask1 does not prevent or delay loss of visual function in a P23H transgenic mouse model of retinitis pigmentosa

The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome

Suppression of experimental choroidal neovascularization by curcumin in mice

A degenerative retinal process in HIV-associated non-infectious retinopathy

Evaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogs

Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina

Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15

OCT Intensity of the Region between Outer Retina Band 2 and Band 3 as a Biomarker for Retinal Degeneration and Therapy

Vigabatrin-induced retinal toxicity is partially mediated by signaling in rod and cone photoreceptors

A constitutively active Gαi3 protein corrects the abnormal retinal pigment epithelium phenotype of Oa1-/- mice

Extended duration of transgene expression from pegylated POD nanoparticles enables attenuation of photoreceptor degeneration

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