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Titlebook: Gene Delivery and Therapy for Neurological Disorders; Xuenong Bo,Joost Verhaagen Book 2015 Springer Science+Business Media New York 2015 A

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發(fā)表于 2025-3-25 06:22:13 | 只看該作者
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發(fā)表于 2025-3-25 07:41:30 | 只看該作者
https://doi.org/10.1007/978-0-387-47672-8y for treating neurological disorders with AAV vectors, with much anticipation for moving these treatments forward to aid patients and families affected by these terrible diseases. In this chapter, we will detail the protocols used for stereotaxic AAV infusion into the brain of mice, cats, sheep, and nonhuman primates.
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發(fā)表于 2025-3-25 22:15:32 | 只看該作者
Child Justice Administration in Africaiency and broad tropism. This chapter discusses lentiviral vectors properties and applications in gene therapy for neurodegenerative diseases, presenting some of the recent progress in this field. We also present the materials and methods necessary to generate high-titer lentiviral vectors. Methods
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https://doi.org/10.1007/978-3-319-05071-3ter, we summarize the latest studies on viral vector-mediated gene deliveries in animal models of spinal cord injury. Most of the studies reported so far are aimed at delivery of molecules that prevent cell death, or increase intrinsic regenerating state of injured neurons, or modify the CNS environ
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發(fā)表于 2025-3-26 19:40:45 | 只看該作者
Suitable Families and Parents in Lawistration. This chapter also illustrates the methods of constructing AAV vectors with hypoxia-inducible gene expression, generating the mouse permanent distal middle cerebral artery occlusion (pMCAO) model, standard assays to analyze brain injury and gene transfer, and effective behavior tests for t
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