| P50 | author | Ania K Majewska | Q61162208 |
| | Brandon K. Harvey | Q64867341 |
| P2093 | author name string | Yu Zhang | |
| | Emily A Kelly | |
| | Cassandra E Lamantia | |
| | Rebecca L Lowery | |
| P2860 | cites work | Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity | Q39686097 |
| | Enhanced gene transfer efficiency in the murine striatum and an orthotopic glioblastoma tumor model, using AAV-7- and AAV-8-pseudotyped vectors | Q40238020 |
| | Adeno-associated virus vectors serotyped with AAV8 capsid are more efficient than AAV-1 or -2 serotypes for widespread gene delivery to the neonatal mouse brain | Q40329324 |
| | Adeno-associated virus-mediated gene transfer to the brain: duration and modulation of expression | Q40972848 |
| | Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 |
| | Remodeling of synaptic structure in sensory cortical areas in vivo. | Q42492164 |
| | Sindbis vector SINrep(nsP2S726): a tool for rapid heterologous expression with attenuated cytotoxicity in neurons | Q44237703 |
| | Self-complementary adeno-associated virus serotype 2 vector: global distribution and broad dispersion of AAV-mediated transgene expression in mouse brain | Q44686125 |
| | Recombinant AAV viral vectors pseudotyped with viral capsids from serotypes 1, 2, and 5 display differential efficiency and cell tropism after delivery to different regions of the central nervous system | Q45007196 |
| | Transduction characteristics of adeno-associated virus vectors expressing cap serotypes 7, 8, 9, and Rh10 in the mouse brain | Q45420843 |
| | Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivo | Q45709105 |
| | Neuron-specific transduction in the rat septohippocampal or nigrostriatal pathway by recombinant adeno-associated virus vectors | Q45756988 |
| | Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector | Q45769447 |
| | Comparative analysis of adeno-associated viral vector serotypes 1, 2, 5, 7, and 8 in mouse brain | Q45866495 |
| | A modified Sindbis vector for prolonged gene expression in neurons | Q73644371 |
| | Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus | Q24523073 |
| | Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy | Q24535690 |
| | Next-generation optical technologies for illuminating genetically targeted brain circuits | Q24649053 |
| | Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors | Q24682739 |
| | Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis | Q24684374 |
| | Diverse modes of axon elaboration in the developing neocortex | Q24814651 |
| | Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis | Q28213353 |
| | A custom-made two-photon microscope and deconvolution system | Q30654643 |
| | Axons and synaptic boutons are highly dynamic in adult visual cortex | Q33236808 |
| | Infectious clones and vectors derived from adeno-associated virus (AAV) serotypes other than AAV type 2. | Q33781976 |
| | Clades of Adeno-associated viruses are widely disseminated in human tissues. | Q34193756 |
| | Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo | Q34277742 |
| | Transduction profiles of recombinant adeno-associated virus vectors derived from serotypes 2 and 5 in the nigrostriatal system of rats | Q34436780 |
| | Selective and rapid uptake of adeno-associated virus type 2 in brain | Q34471578 |
| | Recombinant adeno-associated virus vector: use for transgene expression and anterograde tract tracing in the CNS | Q34472181 |
| | Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system. | Q35111738 |
| | Recombinant AAV-mediated gene delivery to the central nervous system. | Q35673387 |
| | Existence of transient functional double-stranded DNA intermediates during recombinant AAV transduction | Q35928797 |
| | Adeno-associated virus (AAV) vectors in the CNS. | Q36173003 |
| | dsAAV type 2-mediated gene transfer of MORS196A-EGFP into spinal cord as a pain management paradigm | Q36289075 |
| | Tropism and toxicity of adeno-associated viral vector serotypes 1, 2, 5, 6, 7, 8, and 9 in rat neurons and glia in vitro. | Q36541150 |
| | Gene therapy vectors based on adeno-associated virus type 1. | Q39550492 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 10 | |
| P1104 | number of pages | 15 | |
| P304 | page(s) | 674-688 | |
| P577 | publication date | 2009-09-01 | |
| P1433 | published in | Developmental Neurobiology | Q15716734 |
| P1476 | title | Rapid, long-term labeling of cells in the developing and adult rodent visual cortex using double-stranded adeno-associated viral vectors | |
| P478 | volume | 69 | |