标题
Adeno-Associated Virus Technologies and Methods for Targeted Neuronal Manipulation
作者
关键词
-
出版物
Frontiers in Neuroanatomy
Volume 13, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2019-11-26
DOI
10.3389/fnana.2019.00093
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Systemic AAV vectors for widespread and targeted gene delivery in rodents
- (2019) Rosemary C. Challis et al. Nature Protocols
- AAVcis-regulatory sequences are correlated with ocular toxicity
- (2019) Wenjun Xiong et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The GPI-Linked Protein LY6A Drives AAV-PHP.B Transport across the Blood-Brain Barrier
- (2019) Juliette Hordeaux et al. MOLECULAR THERAPY
- Comprehensive evaluation of ubiquitous promoters suitable for the generation of transgenic cynomolgus monkeys†
- (2019) Yasunari Seita et al. BIOLOGY OF REPRODUCTION
- A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency
- (2018) Julie Tordo et al. BRAIN
- Rationally designed AAV2 and AAVrh8R capsids provide improved transduction in the retina and brain
- (2018) Jennifer A. Sullivan et al. GENE THERAPY
- Widespread optogenetic expression in macaque cortex obtained with MR-guided, convection enhanced delivery (CED) of AAV vector to the thalamus
- (2018) Azadeh Yazdan-Shahmorad et al. JOURNAL OF NEUROSCIENCE METHODS
- In Vivo Selection of a Computationally Designed SCHEMA AAV Library Yields a Novel Variant for Infection of Adult Neural Stem Cells in the SVZ
- (2018) David S. Ojala et al. MOLECULAR THERAPY
- The Neurotropic Properties of AAV-PHP.B Are Limited to C57BL/6J Mice
- (2018) Juliette Hordeaux et al. MOLECULAR THERAPY
- Refined protocols of tamoxifen injection for inducible DNA recombination in mouse astroglia
- (2018) Hannah M. Jahn et al. Scientific Reports
- A MicroRNA-Based Gene-Targeting Tool for Virally Labeling Interneurons in the Rodent Cortex
- (2018) Marianna K. Keaveney et al. Cell Reports
- Emerging Issues in AAV-Mediated In Vivo Gene Therapy
- (2018) Pasqualina Colella et al. Molecular Therapy-Methods & Clinical Development
- Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems
- (2017) Ken Y Chan et al. NATURE NEUROSCIENCE
- Causal evidence for retina-dependent and -independent visual motion computations in mouse cortex
- (2017) Daniel Hillier et al. NATURE NEUROSCIENCE
- AAV-Mediated Anterograde Transsynaptic Tagging: Mapping Corticocollicular Input-Defined Neural Pathways for Defense Behaviors
- (2017) Brian Zingg et al. NEURON
- Cellular selectivity of AAV serotypes for gene delivery in neurons and astrocytes by neonatal intracerebroventricular injection
- (2017) Sean L. Hammond et al. PLoS One
- Adeno-Associated Viral Vectors Serotype 8 for Cell-Specific Delivery of Therapeutic Genes in the Central Nervous System
- (2017) Diego Pignataro et al. Frontiers in Neuroanatomy
- AAV-Mediated Astrocyte-Specific Gene Expression under Human ALDH1L1 Promoter in Mouse Thalamus
- (2017) Wuhyun Koh et al. Experimental Neurobiology
- Wiring and Molecular Features of Prefrontal Ensembles Representing Distinct Experiences
- (2016) Li Ye et al. CELL
- Brain endothelial cell‐targeted gene therapy of neurovascular disorders
- (2016) Serena Marchiò et al. EMBO Molecular Medicine
- Therapeutic rAAVrh10 MediatedSOD1Silencing in AdultSOD1G93AMice and Nonhuman Primates
- (2016) Florie Borel et al. HUMAN GENE THERAPY
- Strategies for targeting primate neural circuits with viral vectors
- (2016) Yasmine El-Shamayleh et al. JOURNAL OF NEUROPHYSIOLOGY
- Evaluation of AAV-mediated Gene Therapy for Central Nervous System Disease in Canine Mucopolysaccharidosis VII
- (2016) Brittney L Gurda et al. MOLECULAR THERAPY
- Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain
- (2016) Benjamin E Deverman et al. NATURE BIOTECHNOLOGY
- A viral strategy for targeting and manipulating interneurons across vertebrate species
- (2016) Jordane Dimidschstein et al. NATURE NEUROSCIENCE
- A Designer AAV Variant Permits Efficient Retrograde Access to Projection Neurons
- (2016) D. Gowanlock R. Tervo et al. NEURON
- rAAV-compatible MiniPromoters for restricted expression in the brain and eye
- (2016) Charles N. de Leeuw et al. Molecular Brain
- Recombinant Human Myelin-Associated Glycoprotein Promoter Drives Selective AAV-Mediated Transgene Expression in Oligodendrocytes
- (2016) Georg von Jonquieres et al. Frontiers in Molecular Neuroscience
- Potent spinal parenchymal AAV9-mediated gene delivery by subpial injection in adult rats and pigs
- (2016) Atsushi Miyanohara et al. Molecular Therapy-Methods & Clinical Development
- AAV9-mediated central nervous system–targeted gene delivery via cisterna magna route in mice
- (2016) Vera Lukashchuk et al. Molecular Therapy-Methods & Clinical Development
- 773. The TLR9-MyD88 Pathway Is Critical for Adaptive Immune Responses to AAV Vectors in Gene Therapy
- (2016) MOLECULAR THERAPY
- Evaluation of the expression pattern of rAAV2/1, 2/5, 2/7, 2/8, and 2/9 serotypes with different promoters in the mouse visual cortex
- (2015) Isabelle Scheyltjens et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Unique Glycan Signatures Regulate Adeno-Associated Virus Tropism in the Developing Brain
- (2015) Giridhar Murlidharan et al. JOURNAL OF VIROLOGY
- Comparative analyses of adeno-associated viral vector serotypes 1, 2, 5, 8 and 9 in marmoset, mouse and macaque cerebral cortex
- (2015) Akiya Watakabe et al. NEUROSCIENCE RESEARCH
- Neuroanatomy goes viral!
- (2015) Jonathan J. Nassi et al. Frontiers in Neuroanatomy
- Long-Term Two-Photon Calcium Imaging of Neuronal Populations with Subcellular Resolution in Adult Non-human Primates
- (2015) Osamu Sadakane et al. Cell Reports
- Adeno-Associated Virus Serotypes 1, 8, and 9 Share Conserved Mechanisms for Anterograde and Retrograde Axonal Transport
- (2014) Michael J. Castle et al. HUMAN GENE THERAPY
- Intrajugular Vein Delivery of AAV9-RNAi Prevents Neuropathological Changes and Weight Loss in Huntington's Disease Mice
- (2014) Brett D Dufour et al. MOLECULAR THERAPY
- Targeting cells with single vectors using multiple-feature Boolean logic
- (2014) Lief E Fenno et al. NATURE METHODS
- Genetic dissection of GABAergic neural circuits in mouse neocortex
- (2014) Hiroki Taniguchi Frontiers in Cellular Neuroscience
- A new era for functional labeling of neurons: activity-dependent promoters have come of age
- (2014) Takashi Kawashima et al. Frontiers in Neural Circuits
- Biodistribution of adeno-associated virus serotype 9 (AAV9) vector after intrathecal and intravenous delivery in mouse
- (2014) Daniel J. Schuster et al. Frontiers in Neuroanatomy
- Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magna
- (2014) Christian Hinderer et al. Molecular Therapy-Methods & Clinical Development
- Adeno-associated virus structural biology as a tool in vector development
- (2013) Lauren M Drouin et al. Future Virology
- Global CNS gene delivery and evasion of anti-AAV-neutralizing antibodies by intrathecal AAV administration in non-human primates
- (2013) S J Gray et al. GENE THERAPY
- Strong Cortical and Spinal Cord Transduction After AAV7 and AAV9 Delivery into the Cerebrospinal Fluid of Nonhuman Primates
- (2013) Lluis Samaranch et al. HUMAN GENE THERAPY
- AAV9-mediated Expression of a Non-self Protein in Nonhuman Primate Central Nervous System Triggers Widespread Neuroinflammation Driven by Antigen-presenting Cell Transduction
- (2013) Lluis Samaranch et al. MOLECULAR THERAPY
- Glial Promoter Selectivity following AAV-Delivery to the Immature Brain
- (2013) Georg von Jonquieres et al. PLoS One
- Analysis of Transduction Efficiency, Tropism and Axonal Transport of AAV Serotypes 1, 2, 5, 6, 8 and 9 in the Mouse Brain
- (2013) Dominik F. Aschauer et al. PLoS One
- Characterization of the Properties of Seven Promoters in the Motor Cortex of Rats and Monkeys After Lentiviral Vector-Mediated Gene Transfer
- (2013) Masae Yaguchi et al. Human Gene Therapy Methods
- Axonal transport of adeno-associated viral vectors is serotype-dependent
- (2012) E A Salegio et al. GENE THERAPY
- Correction of Pathological Accumulation of Glycosaminoglycans in Central Nervous System and Peripheral Tissues of MPSIIIA Mice Through Systemic AAV9 Gene Transfer
- (2012) Albert Ruzo et al. HUMAN GENE THERAPY
- The β-Globin Locus Control Region in Combination With the EF1α Short Promoter Allows Enhanced Lentiviral Vector-mediated Erythroid Gene Expression With Conserved Multilineage Activity
- (2012) Claudia A Montiel-Equihua et al. MOLECULAR THERAPY
- Merits of Combination Cortical, Subcortical, and Cerebellar Injections for the Treatment of Niemann-Pick Disease Type A
- (2012) Jie Bu et al. MOLECULAR THERAPY
- Visualization of Cortical Projection Neurons with Retrograde TET-Off Lentiviral Vector
- (2012) Akiya Watakabe et al. PLoS One
- The genome of self-complementary adeno-associated viral vectors increases Toll-like receptor 9-dependent innate immune responses in the liver
- (2011) A. T. Martino et al. BLOOD
- Immune Responses to AAV in Clinical Trials
- (2011) Federico Mingozzi et al. CURRENT GENE THERAPY
- Robust spinal motor neuron transduction following intrathecal delivery of AAV9 in pigs
- (2011) T Federici et al. GENE THERAPY
- Optimizing Promoters for Recombinant Adeno-Associated Virus-Mediated Gene Expression in the Peripheral and Central Nervous System Using Self-Complementary Vectors
- (2011) Steven J. Gray et al. HUMAN GENE THERAPY
- Adeno-Associated Virus Serotype 9 Transduction in the Central Nervous System of Nonhuman Primates
- (2011) Lluis Samaranch et al. HUMAN GENE THERAPY
- Several rAAV Vectors Efficiently Cross the Blood–brain Barrier and Transduce Neurons and Astrocytes in the Neonatal Mouse Central Nervous System
- (2011) Hongwei Zhang et al. MOLECULAR THERAPY
- Local and retrograde gene transfer into primate neuronal pathways via adeno-associated virus serotype 8 and 9
- (2011) Y. Masamizu et al. NEUROSCIENCE
- Innate Immune Responses to AAV Vectors
- (2011) Geoffrey L. Rogers et al. Frontiers in Microbiology
- Convection-enhanced delivery and systemic mannitol increase gene product distribution of AAV vectors 5, 8, and 9 and increase gene product in the adult mouse brain
- (2010) Nikisha Carty et al. JOURNAL OF NEUROSCIENCE METHODS
- Enhanced adenoviral gene delivery to motor and dorsal root ganglion neurons following injection into demyelinated peripheral nerves
- (2010) Yongjie Zhang et al. JOURNAL OF NEUROSCIENCE RESEARCH
- MicroRNA-regulated, Systemically Delivered rAAV9: A Step Closer to CNS-restricted Transgene Expression
- (2010) Jun Xie et al. MOLECULAR THERAPY
- Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
- (2010) Kevin D Foust et al. NATURE BIOTECHNOLOGY
- Efficient gene transfer into neurons in monkey brain by adeno-associated virus 8
- (2010) Yoshito Masamizu et al. NEUROREPORT
- Systematic Comparison of Constitutive Promoters and the Doxycycline-Inducible Promoter
- (2010) Jane Yuxia Qin et al. PLoS One
- Endothelial endothelin-1 over-expression using receptor tyrosine kinase tie-1 promoter leads to more severe vascular permeability and blood brain barrier breakdown after transient middle cerebral artery occlusion
- (2009) Justin W.C. Leung et al. BRAIN RESEARCH
- Transduction of Nonhuman Primate Brain with Adeno-Associated Virus Serotype 1: Vector Trafficking and Immune Response
- (2009) Piotr Hadaczek et al. HUMAN GENE THERAPY
- Differential Transduction Following Basal Ganglia Administration of Distinct Pseudotyped AAV Capsid Serotypes in Nonhuman Primates
- (2009) Hemraj B Dodiya et al. MOLECULAR THERAPY
- Preferential labeling of inhibitory and excitatory cortical neurons by endogenous tropism of adeno-associated virus and lentivirus vectors
- (2009) J.L. Nathanson et al. NEUROSCIENCE
- Short promoters in viral vectors drive selective expression in mammalian inhibitory neurons, but do not restrict activity to specific inhibitory cell-types
- (2009) Jason L. Nathanson Frontiers in Neural Circuits
- Expression of transgenes in midbrain dopamine neurons using the tyrosine hydroxylase promoter
- (2008) M S Oh et al. GENE THERAPY
- GFAPpromoter elements required for region-specific and astrocyte-specific expression
- (2008) Youngjin Lee et al. GLIA
- In Vitro and In Vivo Gene Therapy Vector Evolution via Multispecies Interbreeding and Retargeting of Adeno-Associated Viruses
- (2008) D. Grimm et al. JOURNAL OF VIROLOGY
- Expanded Repertoire of AAV Vector Serotypes Mediate Unique Patterns of Transduction in Mouse Brain
- (2008) Cassia N Cearley et al. MOLECULAR THERAPY
- Recombinant Adeno-associated Virus Transduction and Integration
- (2008) Brian R Schultz et al. MOLECULAR THERAPY
- Efficient Retrograde Neuronal Transduction Utilizing Self-complementary AAV1
- (2008) Edmund R Hollis II et al. MOLECULAR THERAPY
- Analysis of AAV Serotypes 1–9 Mediated Gene Expression and Tropism in Mice After Systemic Injection
- (2008) Carmela Zincarelli et al. MOLECULAR THERAPY
- Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes
- (2008) Kevin D Foust et al. NATURE BIOTECHNOLOGY
- High-level transgene expression in neurons by lentivirus with Tet-Off system
- (2008) Hiroyuki Hioki et al. NEUROSCIENCE RESEARCH
- AAV8, 9, Rh10, Rh43 Vector Gene Transfer in the Rat Brain: Effects of Serotype, Promoter and Purification Method
- (2007) Ronald L Klein et al. MOLECULAR THERAPY
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started