Axonal transport of adeno-associated viral vectors is serotype-dependent. - Wikidata - thesis-toulmin - TriplyDB

Axonal transport of adeno-associated viral vectors is serotype-dependent.

Axonal transport of adeno-associated viral vectors is serotype-dependent.

http://www.wikidata.org/entity/Q41919978

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Biology of adeno-associated viral vectors in the central nervous system Gene delivery strategies to promote spinal cord repair Systemic AAV9 gene transfer in adult GM1 gangliosidosis mice reduces lysosomal storage in CNS and extends lifespan.Axonal transport of AAV9 in nonhuman primate brain.Convection-enhanced delivery of AAV2-PrPshRNA in prion-infected mice Gene transfer to the CNS using recombinant adeno-associated virus Age and lesion-induced increases of GDNF transgene expression in brain following intracerebral injections of DNA nanoparticles.Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain.Brain BLAQ: Post-hoc thick-section histochemistry for localizing optogenetic constructs in neurons and their distal terminals Angiotensin II type 1a receptors in subfornical organ contribute towards chronic intermittent hypoxia-associated sustained increase in mean arterial pressure.Double Virus Vector Infection to the Prefrontal Network of the Macaque Brain Presynaptic Inputs to Any CNS Projection Neuron Identified by Dual Recombinant Virus Infection In Vivo Selection Yields AAV-B1 Capsid for Central Nervous System and Muscle Gene Therapy Role of a Lateral Orbital Frontal Cortex-Basolateral Amygdala Circuit in Cue-Induced Cocaine-Seeking Behavior.Use of Adeno-Associated and Herpes Simplex Viral Vectors for In Vivo Neuronal Expression in Mice.Serotype-dependent transduction efficiencies of recombinant adeno-associated viral vectors in monkey neocortex Selective Manipulation of Neural Circuits Direct and retrograde transduction of nigral neurons with AAV6, 8, and 9 and intraneuronal persistence of viral particles Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector.Gene therapy for misfolding protein diseases of the central nervous system.Intraspinal AAV Injections Immediately Rostral to a Thoracic Spinal Cord Injury Site Efficiently Transduces Neurons in Spinal Cord and Brain.Transgene expression in target-defined neuron populations mediated by retrograde infection with adeno-associated viral vectors Intrapleural administration of AAV9 improves neural and cardiorespiratory function in Pompe disease.Adeno-associated Virus Vectors Efficiently Transduce Mouse and Rabbit Sensory Neurons Coinfected with Herpes Simplex Virus 1 following Peripheral Inoculation.An Intrabody Drug (rAAV6-INT41) Reduces the Binding of N-Terminal Huntingtin Fragment(s) to DNA to Basal Levels in PC12 Cells and Delays Cognitive Loss in the R6/2 Animal Model Adeno-associated virus type 6 is retrogradely transported in the non-human primate brain.New tricks for old dogmas: optogenetic and designer receptor insights for Parkinson's disease Gene therapy for the neurological manifestations in lysosomal storage disorders.Wallerian degeneration: an emerging axon death pathway linking injury and disease.Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy.Trans-neuronal transduction of spinal neurons following cortical injection and anterograde axonal transport of a bicistronic AAV1 vector Viral vector-based tools advance knowledge of basal ganglia anatomy and physiology.Lateral thalamic control of nociceptive response after whisker pad injection of varicella zoster virus.Cell-Specific Targeting of Genetically Encoded Tools for Neuroscience.Adeno-Associated Virus-Based Gene Therapy for CNS Diseases.MR-guided parenchymal delivery of adeno-associated viral vector serotype 5 in non-human primate brain.Genetic manipulation of specific neural circuits by use of a viral vector system.Gamma-Aminobutyric Acidergic Projections From the Dorsal Raphe to the Nucleus Accumbens Are Regulated by Neuromedin U.Pseudotyped Lentiviral Vectors for Retrograde Gene Delivery into Target Brain Regions.Spinal nociceptive circuit analysis with recombinant adeno-associated viruses: the impact of serotypes and promoters.

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P2860

Axonal transport of adeno-associated viral vectors is serotype-dependent.

http://www.wikidata.org/entity/Q41919978

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A P Kells

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E A Salegio

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G Mittermeyer

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P2860

Pathophysiology of chorea and bradykinesia in Huntington's disease.

Clades of Adeno-associated viruses are widely disseminated in human tissues.

AAV8, 9, Rh10, Rh43 vector gene transfer in the rat brain: effects of serotype, promoter and purification method

AAV hybrid serotypes: improved vectors for gene delivery

Promoters and regulatory elements that improve adeno-associated virus transgene expression in the brain.

Interventional MRI-guided putaminal delivery of AAV2-GDNF for a planned clinical trial in Parkinson's disease

HSV trafficking and development of gene therapy vectors with applications in the nervous system.

Rapid uncoating of vector genomes is the key to efficient liver transduction with pseudotyped adeno-associated virus vectors.

Transport and egress of herpes simplex virus in neurons.

Efficient gene therapy-based method for the delivery of therapeutics to primate cortex.

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3

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