Search Results - "Hauswirth, W.W"
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COMPARISON OF RAT RETINAL GANGLION CELLS TRANSDUCTION USING DIFFERENT HUMAN MINI-PROMOTERS COMPATIBLE WITH RAAV
Published in Cytotherapy (Oxford, England) (01-10-2022)Get full text
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42 - COMPARISON OF RAT RETINAL GANGLION CELLS TRANSDUCTION USING DIFFERENT HUMAN MINI-PROMOTERS COMPATIBLE WITH RAAV
Published in Cytotherapy (Oxford, England) (01-10-2022)Get full text
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COMPARISON OF RAT RETINAL GANGLION CELL TRANSDUCTION WITH DIFFERENT AMOUNT OF RAAV VECTOR
Published in Cytotherapy (Oxford, England) (01-10-2022)Get full text
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50 - COMPARISON OF RAT RETINAL GANGLION CELL TRANSDUCTION WITH DIFFERENT AMOUNT OF RAAV VECTOR
Published in Cytotherapy (Oxford, England) (01-10-2022)Get full text
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Modulation of the expression of the transcription factor Max in rat retinal ganglion cells by a recombinant adeno-associated viral vector
Published in Brazilian journal of medical and biological research (01-03-2005)“…Exclusion of the transcription factor Max from the nucleus of retinal ganglion cells is an early, caspase-independent event of programmed cell death following…”
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Tyrosine capsid-mutant AAV vectors for gene delivery to the canine retina from a subretinal or intravitreal approach
Published in Gene therapy (01-01-2014)“…Recombinant adeno-associated viruses are important vectors for retinal gene delivery. Currently utilized vectors have relatively slow onset, and for efficient…”
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Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus
Published in Gene therapy (01-08-2013)“…Usher 1 patients are born profoundly deaf and then develop retinal degeneration. Thus they are readily identified before the onset of retinal degeneration,…”
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Novel anti-VEGF chimeric molecules delivered by AAV vectors for inhibition of retinal neovascularization
Published in Gene therapy (01-01-2009)“…Vascular endothelial growth factor (VEGF) is important in pathological neovascularization, which is a key component of diseases such as the wet form of…”
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Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogs
Published in Gene therapy (01-02-2016)“…Delivery of therapeutic transgenes to retinal photoreceptors using adeno-associated virus (AAV) vectors has traditionally required subretinal injection…”
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Healthy and diseased corticospinal motor neurons are selectively transduced upon direct AAV2-2 injection into the motor cortex
Published in Gene therapy (01-03-2016)“…Direct gene delivery to the neurons of interest, without affecting other neuron populations in the cerebral cortex, represent a challenge owing to the…”
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Reduced retinal transduction and enhanced transgene-directed immunogenicity with intravitreal delivery of rAAV following posterior vitrectomy in dogs
Published in Gene therapy (01-06-2016)“…Adeno-associated virus (AAV) vector-based gene therapy is a promising treatment strategy for delivery of neurotrophic transgenes to retinal ganglion cells…”
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Efficient cochlear gene transfection in guinea-pigs with adeno-associated viral vectors by partial digestion of round window membrane
Published in Gene therapy (01-03-2012)“…The auditory portion of the inner ear, the cochlea, is an ideal organ for local gene transfection owing to its relative isolation. Various carriers have been…”
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AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa
Published in Gene therapy (01-08-2015)“…Loss of SPATA7 function causes the pathogenesis of Leber congenital amaurosis and retinitis pigmentosa. Spata7 knockout mice mimic human SPATA7 –related…”
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Mitochondrial DNA copy number in bovine oocytes and somatic cells
Published in Developmental biology (01-11-1982)“…Restriction endonuclease analysis and direct nucleotide sequencing of bovine mitochondrial DNA have revealed a high apparent rate of sequence divergence…”
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rAAV2 5 gene-targeting to rods:dose-dependent efficiency and complications associated with different promoters
Published in Gene therapy (01-09-2010)“…A prerequisite for using corrective gene therapy to treat humans with inherited retinal degenerative diseases that primarily affect rods is to develop viral…”
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AAV-mediated and pharmacological induction of Hsp70 expression stimulates survival of retinal ganglion cells following axonal injury
Published in Gene therapy (01-02-2015)“…We evaluated the effect of AAV2- and 17-AAG (17-N-allylamino-17-demethoxygeldanamycin)-mediated upregulation of Hsp70 expression on the survival of retinal…”
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Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency
Published in Gene therapy (01-07-2010)“…To test whether fast-acting, self-complimentary (sc), adeno-associated virus-mediated RPE65 expression prevents cone degeneration and/or restores cone…”
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Preservation of photoreceptor morphology and function in P23H rats using an allele independent ribozyme
Published in Experimental eye research (01-01-2007)“…To develop an allele independent ribozyme for the treatment of autosomal dominant retinitis pigmentosa (ADRP) associated with mutations in the rhodopsin ( RHO)…”
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Suppression of mouse rhodopsin expression in vivo by AAV mediated siRNA delivery
Published in Vision research (Oxford) (01-04-2007)“…The purpose of this study is to demonstrate that the expression of rhodopsin can be down regulated in vivo by AAV-delivered siRNA. This is the first step in an…”
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Heterogeneous mitochondrial DNA D-loop sequences in bovine tissue
Published in Cell (01-01-1984)“…Mitochondrial DNA from bovine tissue contains heterogeneous sequences located within an evolutionary conserved cytosine homopolymer sequence near the 5' end of…”
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