Molecular evolution of adeno-associated virus for enhanced glial gene delivery. - Test2 - elhamkhani - TriplyDB

Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

http://www.wikidata.org/entity/Q33492733

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A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cells E Pluribus Unum: 50 Years of Research, Millions of Viruses, and One Goal--Tailored Acceleration of AAV Evolution Biology and therapy of inherited retinal degenerative disease: insights from mouse models Glial promoter selectivity following AAV-delivery to the immature brain.Optogenetics.Dorsal raphe neuroinflammation promotes dramatic behavioral stress dysregulation AAV's anatomy: roadmap for optimizing vectors for translational success GFAP-driven GFP expression in activated mouse Müller glial cells aligning retinal blood vessels following intravitreal injection of AAV2/6 vectors An evolved adeno-associated viral variant enhances gene delivery and gene targeting in neural stem cells Engineering liver-detargeted AAV9 vectors for cardiac and musculoskeletal gene transfer.A NEW RECOMBINANT ADENO-ASSOCIATED VIRUS (AAV)-BASED RANDOM PEPTIDE DISPLAY LIBRARY SYSTEM: INFECTION-DEFECTIVE AAV1.9-3 AS A NOVEL DETARGETED PLATFORM FOR VECTOR EVOLUTION.Directed evolution of adeno-associated virus for enhanced gene delivery and gene targeting in human pluripotent stem cells.Directed evolution of novel adeno-associated viruses for therapeutic gene delivery.Adeno-associated virus: fit to serve Adeno-associated virus (AAV) vectors in gene therapy: immune challenges and strategies to circumvent them.Synthetic virology: engineering viruses for gene delivery An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina AAV-mediated, optogenetic ablation of Müller Glia leads to structural and functional changes in the mouse retina Gene therapy for the nervous system: challenges and new strategies.High capsid-genome correlation facilitates creation of AAV libraries for directed evolution Transforming growth factor α transforms astrocytes to a growth-supportive phenotype after spinal cord injury Enhanced selective gene delivery to neural stem cells in vivo by an adeno-associated viral variant Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rho(-/-) mouse Controlling AAV Tropism in the Nervous System with Natural and Engineered Capsids.The AAV vector toolkit: poised at the clinical crossroads Pulmonary Targeting of Adeno-associated Viral Vectors by Next-generation Sequencing-guided Screening of Random Capsid Displayed Peptide Libraries.A brain microvasculature endothelial cell-specific viral vector with the potential to treat neurovascular and neurological diseases.Optimization of design and production strategies for novel adeno-associated viral display peptide libraries.Creation of a cardiotropic adeno-associated virus: the story of viral directed evolution.Recent advances in RNA interference therapeutics for CNS diseases.CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypes Wnt Regulates Proliferation and Neurogenic Potential of Müller Glial Cells via a Lin28/let-7 miRNA-Dependent Pathway in Adult Mammalian Retinas.Improved Adeno-associated Viral Gene Transfer to Murine Glioma.Progress and prospects: Immunobiology of gene therapy for neurodegenerative disease: prospects and risks.Novel adeno-associated viral vectors for retinal gene therapy.Viral vectors for gene delivery to the central nervous system.Regenerative nanomedicine and the treatment of degenerative retinal diseases.The advent of AAV9 expands applications for brain and spinal cord gene delivery.A next step in adeno-associated virus-mediated gene therapy for neurological diseases: regulation and targeting.

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

http://www.wikidata.org/entity/Q33492733

description

2009 nî lūn-bûn

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2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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type

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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prefLabel

Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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Molecular Therapy

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Molecular evolution of adeno-associated virus for enhanced glial gene delivery.

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Jae-Hyung Jang

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James T Koerber

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Ryan Klimczak

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P2860

The atomic structure of adeno-associated virus (AAV-2), a vector for human gene therapy.

Safety and efficacy of gene transfer for Leber's congenital amaurosis

Directed evolution of adeno-associated virus to an infectious respiratory virus

Structure of Adeno-Associated Virus Serotype 8, a Gene Therapy Vector

Effect of gene therapy on visual function in Leber's congenital amaurosis

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

Sonic hedgehog regulates adult neural progenitor proliferation in vitro and in vivo

Expression and possible function of fibroblast growth factor 9 (FGF9) and its cognate receptors FGFR2 and FGFR3 in postnatal and adult retina

A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

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10.1038/MT.2009.184

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12

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