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Adeno-Associated Virus Vector Genomes Persist as Episomal Chromatin in Primate Muscle

Journal of Virology, 2008-08, Vol.82 (16), p.7875-7885

2008

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Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates

PloS one, 2014-09, Vol.9 (9), p.e102538-10

2014

Volltextzugriff (PDF)

Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone–Rod Dystrophy

Molecular therapy, 2014-02, Vol.22 (2), p.265-277

2014

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Cross-Packaging of a Single Adeno-Associated Virus (AAV) Type 2 Vector Genome into Multiple AAV Serotypes Enables Transduction with Broad Specificity

Journal of Virology, 2002-01, Vol.76 (2), p.791-801

2002

Volltextzugriff (PDF)

Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates

Molecular therapy, 2009-03, Vol.17 (3), p.516-523

2009

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Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina

PloS one, 2014-01, Vol.9 (1), p.e86304-e86304

2014

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Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors

Molecular therapy, 2006-05, Vol.13 (5), p.967-975

2006

Volltextzugriff (PDF)

Preclinical studies on specific gene therapy for recessive retinal degenerative diseases

Current gene therapy, 2010-10, Vol.10 (5), p.389

2010

Volltextzugriff (PDF)

Adeno-associated viral vectors for retinal gene transfer and treatment of retinal diseases

Current gene therapy, 2005-06, Vol.5 (3), p.339

2005

Volltextzugriff (PDF)

Immune responses to gene product of inducible promoters

Current gene therapy, 2007-10, Vol.7 (5), p.334

2007

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Adeno-associated virus capsid serotype identification: Analytical methods development and application

Journal of virological methods, 2009-08, Vol.159 (2), p.167-177

2009

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Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis

Molecular therapy, 2018-01, Vol.26 (1), p.256-268

2018

Volltextzugriff (PDF)

In vivo gene regulation using tetracycline-regulatable systems

Advanced drug delivery reviews, 2009-07, Vol.61 (7), p.527-541

2009

Volltextzugriff (PDF)

AAV-mediated gene therapy for the treatment of retinal diseases

Current gene therapy, 2010-10, Vol.10 (5), p.318

Rolling, Fabienne

2010

Volltextzugriff (PDF)

AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs

Molecular therapy, 2016-05, Vol.24 (5), p.867-876

2016

Volltextzugriff (PDF)

Restoration of Vision in the pde6β-deficient Dog, a Large Animal Model of Rod-cone Dystrophy

Molecular therapy, 2012-11, Vol.20 (11), p.2019-2030

2012

Volltextzugriff (PDF)

Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate rats

Gene therapy, 2015-04, Vol.22 (4), p.316-324

2015

Volltextzugriff (PDF)

Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium

Gene therapy, 2007-02, Vol.14 (4), p.292-303

2007

Volltextzugriff (PDF)

Lack of Immunotoxicity After Regional Intravenous (RI) Delivery of rAAV to Nonhuman Primate Skeletal Muscle

Molecular therapy, 2010-01, Vol.18 (1), p.151-160

2010

Volltextzugriff (PDF)

Safety and Efficacy of Regional Intravenous (RI) Versus Intramuscular (IM) Delivery of rAAV1 and rAAV8 to Nonhuman Primate Skeletal Muscle

Molecular therapy, 2008-07, Vol.16 (7), p.1291-1299

2008

Volltextzugriff (PDF)

Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain

Molecular therapy, 2008-05, Vol.16 (5), p.916-923

2008

Volltextzugriff (PDF)

AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6[beta]-deficient Dogs

Molecular therapy, 2016-05, Vol.24 (5), p.867-876

2016

Volltextzugriff (PDF)

Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal delivery

Molecular therapy, 2003-06, Vol.7 (6), p.774-781

2003

Volltextzugriff (PDF)

Vitrectomy Before Intravitreal Injection of AAV2/2 Vector Promotes Efficient Transduction of Retinal Ganglion Cells in Dogs and Nonhuman Primates

Human gene therapy. Part B. Methods, 2016-06, Vol.27 (3), p.122

2016

Volltextzugriff (PDF)

Restoration of Vision in the pde6[beta]-deficient Dog, a Large Animal Model of Rod-cone Dystrophy

Molecular therapy, 2012-11, Vol.20 (11), p.2019

2012

Volltextzugriff (PDF)

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Adeno-Associated Virus Vector Genomes Persist as Episomal Chromatin in Primate Muscle

Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates

Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone–Rod Dystrophy

Cross-Packaging of a Single Adeno-Associated Virus (AAV) Type 2 Vector Genome into Multiple AAV Serotypes Enables Transduction with Broad Specificity

Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates

Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina

Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors

Preclinical studies on specific gene therapy for recessive retinal degenerative diseases

Adeno-associated viral vectors for retinal gene transfer and treatment of retinal diseases

Immune responses to gene product of inducible promoters

Adeno-associated virus capsid serotype identification: Analytical methods development and application

Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis

In vivo gene regulation using tetracycline-regulatable systems

AAV-mediated gene therapy for the treatment of retinal diseases

AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs

Restoration of Vision in the pde6β-deficient Dog, a Large Animal Model of Rod-cone Dystrophy

Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate rats

Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium

Lack of Immunotoxicity After Regional Intravenous (RI) Delivery of rAAV to Nonhuman Primate Skeletal Muscle

Safety and Efficacy of Regional Intravenous (RI) Versus Intramuscular (IM) Delivery of rAAV1 and rAAV8 to Nonhuman Primate Skeletal Muscle

Subretinal Delivery of Recombinant AAV Serotype 8 Vector in Dogs Results in Gene Transfer to Neurons in the Brain

AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6[beta]-deficient Dogs

Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal delivery

Vitrectomy Before Intravitreal Injection of AAV2/2 Vector Promotes Efficient Transduction of Retinal Ganglion Cells in Dogs and Nonhuman Primates

Restoration of Vision in the pde6[beta]-deficient Dog, a Large Animal Model of Rod-cone Dystrophy

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