| scholarly article | Q13442814 |
| P356 | DOI | 10.24272/J.ISSN.2095-8137.2017.015 |
| P724 | Internet Archive ID | zoological-research-2095-8137-3794 |
| P932 | PMC publication ID | 5396031 |
| P698 | PubMed publication ID | 28409504 |
| P2093 | author name string | Yang Wu | |
| Xin-Tian Hu | |||
| Na Zheng | |||
| Joshua D Rizak | |||
| Zheng-Hui Li | |||
| Dong-Dong Qin | |||
| Mei-Feng Yang | |||
| Shi-Hao Wu | |||
| Xiao-Bin He | |||
| Xia-Ping He | |||
| Lin-Heng Zhang | |||
| Hen Tang | |||
| Zhi-Xing Liao | |||
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| Comparative transduction efficiency of AAV vector serotypes 1-6 in the substantia nigra and striatum of the primate brain | Q33731226 | ||
| Differential transduction following basal ganglia administration of distinct pseudotyped AAV capsid serotypes in nonhuman primates | Q33731243 | ||
| Development of a self-inactivating lentivirus vector. | Q33784841 | ||
| Gene therapy in the CNS. | Q33837123 | ||
| Adeno-associated viral vectors as gene delivery vehicles | Q33941630 | ||
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| Immune response following intraocular delivery of recombinant viral vectors | Q34198445 | ||
| Selective and rapid uptake of adeno-associated virus type 2 in brain | Q34471578 | ||
| Gene delivery by lentivirus vectors | Q34688367 | ||
| Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection | Q34770058 | ||
| Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain | Q35006292 | ||
| Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system. | Q35111738 | ||
| Viral vectors for gene delivery to the nervous system | Q35120134 | ||
| Models of Parkinson's disease | Q35158085 | ||
| Adeno-associated virus serotype 9 transduction in the central nervous system of nonhuman primates | Q35892068 | ||
| Lentivirus-mediated gene transfer to the central nervous system: therapeutic and research applications | Q36366788 | ||
| Adeno-associated virus type 12 (AAV12): a novel AAV serotype with sialic acid- and heparan sulfate proteoglycan-independent transduction activity | Q36424146 | ||
| Serotype-dependent transduction efficiencies of recombinant adeno-associated viral vectors in monkey neocortex | Q36508670 | ||
| The 3'-untranslated region of CaMKII alpha is a cis-acting signal for the localization and translation of mRNA in dendrites | Q36690536 | ||
| Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection | Q36720691 | ||
| Immune responses to AAV vectors: overcoming barriers to successful gene therapy | Q36983740 | ||
| Adeno-associated virus (AAV) gene therapy for neurological disease | Q37998750 | ||
| The common marmoset as a novel animal model system for biomedical and neuroscience research applications | Q38032647 | ||
| Nuclear import defect of human immunodeficiency virus type 1 DNA flap mutants is not dependent on the viral strain or target cell type | Q38761998 | ||
| Opportunities and challenges in modeling human brain disorders in transgenic primates | Q38826903 | ||
| Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos. | Q39028341 | ||
| Gene therapy vectors based on adeno-associated virus type 1. | Q39550492 | ||
| Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity | Q39686097 | ||
| The human ubiquitin C promoter directs high ubiquitous expression of transgenes in mice | Q39716227 | ||
| Lentivirus-mediated expression of glutathione peroxidase: neuroprotection in murine models of Parkinson's disease | Q40397185 | ||
| Comparison of the ability of adeno-associated viral vectors pseudotyped with serotype 2, 5, and 8 capsid proteins to mediate efficient transduction of the liver in murine and nonhuman primate models | Q40418515 | ||
| Human immunodeficiency virus infection of cells arrested in the cell cycle | Q41531689 | ||
| 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 | Q41716240 | ||
| Comparative analyses of adeno-associated viral vector serotypes 1, 2, 5, 8 and 9 in marmoset, mouse and macaque cerebral cortex. | Q42186659 | ||
| Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
| Parkinson-like neurodegeneration induced by targeted overexpression of alpha-synuclein in the nigrostriatal system. | Q43940212 | ||
| Efficient transduction of non-human primate motor neurons after intramuscular delivery of recombinant AAV serotype 6. | Q44852051 | ||
| 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 | ||
| Efficient gene transduction of neurons by lentivirus with enhanced neuron-specific promoters. | Q45264367 | ||
| Transduction characteristics of adeno-associated virus vectors expressing cap serotypes 7, 8, 9, and Rh10 in the mouse brain | Q45420843 | ||
| Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area. | Q45858691 | ||
| Comparative analysis of adeno-associated viral vector serotypes 1, 2, 5, 7, and 8 in mouse brain | Q45866495 | ||
| Human CMV immediate-early enhancer: a useful tool to enhance cell-type-specific expression from lentiviral vectors | Q45872906 | ||
| Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2. | Q47341079 | ||
| Monosialoanglioside improves memory deficits and relieves oxidative stress in the hippocampus of rat model of Alzheimer's disease | Q48258142 | ||
| The human ubiquitin C promoter drives selective expression in principal neurons in the brain of a transgenic mouse line | Q48983644 | ||
| Gene transfer into the central nervous system in vivo using a recombinanat lentivirus vector. | Q52124625 | ||
| Transgenic mouse models of Alzheimer's disease | Q82647986 | ||
| P433 | issue | 2 | |
| P921 | main subject | rhesus macaque | Q156606 |
| P304 | page(s) | 88-95 | |
| P577 | publication date | 2017-03-01 | |
| P1433 | published in | Zoological Research | Q27714095 |
| P1476 | title | Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains | |
| P478 | volume | 38 |
| Q90732125 | AAV Gene Transfer with Tandem Promoter Design Prevents Anti-transgene Immunity and Provides Persistent Efficacy in Neonate Pompe Mice | cites work | P2860 |
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