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A Precision Therapy Approach for Retinitis Pigmentosa 11 Using Splice-Switching Antisense Oligonucleotides to Restore the Open Reading Frame of PRPF31

International journal of molecular sciences, 2024-03, Vol.25 (6), p.3391

2024

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In vivo retinal imaging is associated with cognitive decline, blood-brain barrier disruption and neuroinflammation in type 2 diabetic mice

Frontiers in endocrinology (Lausanne), 2023-10, Vol.14, p.1224418

2023

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Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variant

Stem cell research, 2024-08, Vol.78, p.103461, Article 103461

2024

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Bioengineered Bruch's-like extracellular matrix promotes retinal pigment epithelial differentiation

Biochemistry and biophysics reports, 2017-07, Vol.10 (C), p.178-185

2017

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The current state of stem cell therapy for ocular disease

Experimental eye research, 2018-12, Vol.177, p.65-75

2018

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Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variant

Stem cell research, 2024-09, Vol.79, p.103492, Article 103492

2024

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Serum miRNA modulations indicate changes in retinal morphology

Frontiers in molecular neuroscience, 2023-03, Vol.16, p.1130249-1130249

2023

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Mitochondrial Dysfunction and Impaired Antioxidant Responses in Retinal Pigment Epithelial Cells Derived from a Patient with RCBTB1 -Associated Retinopathy

Cells (Basel, Switzerland), 2023-05, Vol.12 (10), p.1358

2023

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Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1

Stem cell research, 2021-07, Vol.54, p.102403-102403, Article 102403

2021

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mRNA transfection of mouse and human neural stem cell cultures

PloS one, 2013-12, Vol.8 (12), p.e83596-e83596

2013

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Recent Therapeutic Progress and Future Perspectives for the Treatment of Hearing Loss

Biomedicines, 2023-12, Vol.11 (12), p.3347

2023

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Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4

Stem cell research, 2020-10, Vol.48, p.101947-101947, Article 101947

2020

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TLR9 Ligand CpG-ODN Applied to the Injured Mouse Cornea Elicits Retinal Inflammation

The American journal of pathology, 2012, Vol.180 (1), p.209-220

2012

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Absence of clinical correlates of diabetic retinopathy in the Ins2Akita retina

Clinical & experimental ophthalmology, 2013-08, Vol.41 (6), p.582-592

2013

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Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200

Stem cell research, 2021-03, Vol.51, p.102154-102154, Article 102154

2021

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Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations

Stem cell research, 2019-10, Vol.40, p.101549-101549, Article 101549

2019

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Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461–10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene

Stem cell research, 2021-07, Vol.54, p.102439-102439, Article 102439

2021

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Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene

Stem cell research, 2021-01, Vol.50, p.102129-102129, Article 102129

2021

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Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene

Stem cell research, 2021-07, Vol.54, p.102448-102448, Article 102448

2021

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Generation of two induced pluripotent stem cell lines from a patient with dominant PRPF31 mutation and a related non-penetrant carrier

Stem cell research, 2019-01, Vol.34, p.101357-101357, Article 101357

2019

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Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy

Stem cell research, 2019-01, Vol.34, p.101352-101352, Article 101352

2019

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Roles of Eph receptors and ephrins in the normal and damaged adult CNS

Brain Research Reviews, 2006-09, Vol.52 (2), p.327-345

2006

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Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation

Stem cell research, 2018-08, Vol.31, p.147-151

2018

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Gene correction of the CLN3 c.175G>A variant in patient‐derived induced pluripotent stem cells prevents pathological changes in retinal organoids

Molecular genetics & genomic medicine, 2021-03, Vol.9 (3), p.e1601-n/a

2021

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Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation

Stem cell research, 2019-05, Vol.37, p.101452-101452, Article 101452

2019

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A Precision Therapy Approach for Retinitis Pigmentosa 11 Using Splice-Switching Antisense Oligonucleotides to Restore the Open Reading Frame of PRPF31

In vivo retinal imaging is associated with cognitive decline, blood-brain barrier disruption and neuroinflammation in type 2 diabetic mice

Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variant

Bioengineered Bruch's-like extracellular matrix promotes retinal pigment epithelial differentiation

The current state of stem cell therapy for ocular disease

Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variant

Serum miRNA modulations indicate changes in retinal morphology

Mitochondrial Dysfunction and Impaired Antioxidant Responses in Retinal Pigment Epithelial Cells Derived from a Patient with RCBTB1 -Associated Retinopathy

Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1

mRNA transfection of mouse and human neural stem cell cultures

Recent Therapeutic Progress and Future Perspectives for the Treatment of Hearing Loss

Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4

TLR9 Ligand CpG-ODN Applied to the Injured Mouse Cornea Elicits Retinal Inflammation

Absence of clinical correlates of diabetic retinopathy in the Ins2Akita retina

Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200

Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations

Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461–10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene

Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene

Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene

Generation of two induced pluripotent stem cell lines from a patient with dominant PRPF31 mutation and a related non-penetrant carrier

Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy

Roles of Eph receptors and ephrins in the normal and damaged adult CNS

Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation

Gene correction of the CLN3 c.175G>A variant in patient‐derived induced pluripotent stem cells prevents pathological changes in retinal organoids

Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation

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