Characterization of lentiviral vector-mediated gene transfer in adult mouse brain.
暂无分享,去创建一个
Zeger Debyser | Bart Nuttin | Veerle Baekelandt | B. de Strooper | B. Nuttin | V. Baekelandt | Z. Debyser | K. Eggermont | Bart De Strooper | Erwin Lauwers | Anje Claeys | Kristel Eggermont | E. Lauwers | Anje Claeys
[1] Philippe Colin,et al. The HIV-1 DNA flap stimulates HIV vector-mediated cell transduction in the brain , 2001, Nature Biotechnology.
[2] A. Hottinger,et al. Complete and Long-Term Rescue of Lesioned Adult Motoneurons by Lentiviral-Mediated Expression of Glial Cell Line-Derived Neurotrophic Factor in the Facial Nucleus , 2000, The Journal of Neuroscience.
[3] Hideki Mochizuki,et al. High-Titer Human Immunodeficiency Virus Type 1-Based Vector Systems for Gene Delivery into Nondividing Cells , 1998, Journal of Virology.
[4] B. Nuttin,et al. Lentiviral vector-mediated delivery of short hairpin RNA results in persistent knockdown of gene expression in mouse brain. , 2003, Human gene therapy.
[5] D. Trono,et al. A Third-Generation Lentivirus Vector with a Conditional Packaging System , 1998, Journal of Virology.
[6] Luc Montagnier,et al. HIV-1 Genome Nuclear Import Is Mediated by a Central DNA Flap , 2000, Cell.
[7] E. Poeschla,et al. Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors , 1998, Nature Medicine.
[8] A. Consiglio,et al. In vivo gene therapy of metachromatic leukodystrophy by lentiviral vectors: correction of neuropathology and protection against learning impairments in affected mice , 2001, Nature Medicine.
[9] F. Gage,et al. Bcl-xL protects adult septal cholinergic neurons from axotomized cell death. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[10] Y. Arsenijévic,et al. Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson's disease. , 2000, Human gene therapy.
[11] A. Kingsman,et al. Stable gene transfer to the nervous system using a non-primate lentiviral vector , 1999, Gene Therapy.
[12] D. C. Sterio. The unbiased estimation of number and sizes of arbitrary particles using the disector , 1984, Journal of microscopy.
[13] N. Blom,et al. In Vivo Protection of Nigral Dopamine Neurons by Lentiviral Gene Transfer of the Novel GDNF-Family Member Neublastin/Artemin , 2000, Molecular and Cellular Neuroscience.
[14] F. Gage,et al. Rescue from Photoreceptor Degeneration in therd Mouse by Human Immunodeficiency Virus Vector-Mediated Gene Transfer , 1999, Journal of Virology.
[15] D. Peterson,et al. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors , 1997, Nature Genetics.
[16] D. Trono,et al. Self-Inactivating Lentivirus Vector for Safe and Efficient In Vivo Gene Delivery , 1998, Journal of Virology.
[17] George Paxinos,et al. The Mouse Brain in Stereotaxic Coordinates , 2001 .
[18] AD Miller,et al. Enhanced in vitro and in vivo gene delivery using cationic agent complexed retrovirus vectors , 1998, Gene Therapy.
[19] R. J. Mullen,et al. NeuN, a neuronal specific nuclear protein in vertebrates. , 1992, Development.
[20] T. Hope,et al. Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element Enhances Expression of Transgenes Delivered by Retroviral Vectors , 1999, Journal of Virology.
[21] J. Ridet,et al. Lentiviral Vectors as a Gene Delivery System in the Mouse Midbrain: Cellular and Behavioral Improvements in a 6-OHDA Model of Parkinson's Disease Using GDNF , 2000, Experimental Neurology.
[22] B. Harder,et al. Lentivirus vectors encoding both central polypurine tract and posttranscriptional regulatory element provide enhanced transduction and transgene expression. , 2001, Human gene therapy.
[23] Luigi Naldini,et al. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo , 1997, Nature Biotechnology.
[24] A. Björklund,et al. Long-Term rAAV-Mediated Gene Transfer of GDNF in the Rat Parkinson's Model: Intrastriatal But Not Intranigral Transduction Promotes Functional Regeneration in the Lesioned Nigrostriatal System , 2000, The Journal of Neuroscience.
[25] P. Proost,et al. High‐level expression of active HIV‐1 integrase from a synthetic gene in human cells , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[26] M. King,et al. Neuron-Specific Transduction in the Rat Septohippocampal or Nigrostriatal Pathway by Recombinant Adeno-associated Virus Vectors , 1998, Experimental Neurology.
[27] T. Palmer,et al. Neurogenesis in the dentate gyrus of the adult rat: age-related decrease of neuronal progenitor proliferation , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[28] M. Halterman,et al. Lentivirus Vectors Using Human and Simian Immunodeficiency Virus Elements , 1999, Journal of Virology.
[29] Hanns Lochmüller,et al. The principles of gene therapy for the nervous system , 1996, Trends in Neurosciences.
[30] F. Gage,et al. In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral Vector , 1996, Science.
[31] B. de Strooper,et al. DNA-Dependent Protein Kinase Is Not Required for Efficient Lentivirus Integration , 2000, Journal of Virology.
[32] J. Bloch,et al. Lentiviral Gene Transfer to the Nonhuman Primate Brain , 1999, Experimental Neurology.
[33] L Naldini,et al. Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector , 1997, Journal of virology.
[34] I. Chen,et al. Lentiviral Vectors--the Promise of Gene Therapy Within Reach? , 1999, Science.
[35] J. Bloch,et al. Neurodegeneration prevented by lentiviral vector delivery of GDNF in primate models of Parkinson's disease. , 2000, Science.
[36] D. Trono,et al. Reversal of pathology in the entire brain of mucopolysaccharidosis type VII mice after lentivirus-mediated gene transfer. , 2000, Human gene therapy.
[37] L. Ailles,et al. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences , 2000, Nature Genetics.
[38] Fred H. Gage,et al. Development of a Self-Inactivating Lentivirus Vector , 1998, Journal of Virology.
[39] M. Dragunow,et al. Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective , 1999, Nature Medicine.
[40] C. Wilcox,et al. Characterization of Promoter Function and Cell-Type-Specific Expression from Viral Vectors in the Nervous System , 2000, Journal of Virology.
[41] G. Breese,et al. Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector , 1996, Brain Research.
[42] B. Pettmann,et al. Efficient Gene Transfer and Expression of Biologically Active Glial Cell Line‐Derived Neurotrophic Factor in Rat Motoneurons Transduced with Lentiviral Vectors , 2000 .