Suppr超能文献

相似文献

1
Viral vectors for in vivo gene transfer in Parkinson's disease: properties and clinical grade production.
Exp Neurol. 2008 Jan;209(1):58-71. doi: 10.1016/j.expneurol.2007.08.008. Epub 2007 Aug 24.
2
Gene therapeutic strategies for neuroprotection: implications for Parkinson's disease.
Exp Neurol. 1997 Mar;144(1):58-68. doi: 10.1006/exnr.1996.6389.
3
Adeno-associated viral vectors for clinical gene transfer studies.
Curr Gene Ther. 2005 Jun;5(3):311-21. doi: 10.2174/1566523054065066.
5
Viral vectors in the treatment of Parkinson's disease.
Mov Disord. 2000 Jan;15(1):9-17. doi: 10.1002/1531-8257(200001)15:1<9::aid-mds1004>3.0.co;2-5.
6
Viral vectors for gene therapy in Parkinson's disease.
Rev Neurosci. 2001;12(1):69-78. doi: 10.1515/revneuro.2001.12.1.69.
8
Long-Term Follow-Up of a Phase I/II Study of ProSavin, a Lentiviral Vector Gene Therapy for Parkinson's Disease.
Hum Gene Ther Clin Dev. 2018 Sep;29(3):148-155. doi: 10.1089/humc.2018.081.
9
Viral vectors for gene transfer: a review of their use in the treatment of human diseases.
Drugs. 2000 Aug;60(2):249-71. doi: 10.2165/00003495-200060020-00002.
10
Gene therapy for Parkinson's disease using recombinant adeno-associated viral vectors.
Expert Opin Biol Ther. 2005 May;5(5):663-71. doi: 10.1517/14712598.5.5.663.

引用本文的文献

1
Intracerebral lentiviral ABCD1 gene therapy in an early disease onset ALD mouse model.
Gene Ther. 2023 Feb;30(1-2):18-30. doi: 10.1038/s41434-022-00355-0. Epub 2022 Jul 6.
2
Adeno-Associated Virus Expression of α-Synuclein as a Tool to Model Parkinson's Disease: Current Understanding and Knowledge Gaps.
Aging Dis. 2021 Jul 1;12(4):1120-1137. doi: 10.14336/AD.2021.0517. eCollection 2021 Jul.
3
Advantages and Recent Developments of Autologous Cell Therapy for Parkinson's Disease Patients.
Front Cell Neurosci. 2020 Apr 3;14:58. doi: 10.3389/fncel.2020.00058. eCollection 2020.
4
Endothelial cell-targeted pVEGF165 polyplex plays a pivotal role in inhibiting intimal thickening after vascular injury.
Int J Nanomedicine. 2015 Sep 10;10:5751-68. doi: 10.2147/IJN.S88109. eCollection 2015.
8
Gene therapy for misfolding protein diseases of the central nervous system.
Neurotherapeutics. 2013 Jul;10(3):498-510. doi: 10.1007/s13311-013-0191-8.
9
Optimizing NTS-polyplex as a tool for gene transfer to cultured dopamine neurons.
PLoS One. 2012;7(12):e51341. doi: 10.1371/journal.pone.0051341. Epub 2012 Dec 26.
10
Gene therapy for Parkinson's disease.
Parkinsons Dis. 2012;2012:757305. doi: 10.1155/2012/757305. Epub 2012 Mar 25.

本文引用的文献

2
AAV vector integration sites in mouse hepatocellular carcinoma.
Science. 2007 Jul 27;317(5837):477. doi: 10.1126/science.1142658.
5
Preparation and titration of CsCl-banded adenovirus stocks.
Methods Mol Med. 2007;130:223-35. doi: 10.1385/1-59745-166-5:223.
6
Comparative analysis of adeno-associated viral vector serotypes 1, 2, 5, 7, and 8 in mouse brain.
Hum Gene Ther. 2007 Mar;18(3):195-206. doi: 10.1089/hum.2006.178.
8
Assays to evaluate the genotoxicity of retroviral vectors.
Mol Ther. 2006 Oct;14(4):459-60. doi: 10.1016/j.ymthe.2006.08.003. Epub 2006 Aug 21.
9
A novel human artificial chromosome gene expression system using herpes simplex virus type 1 vectors.
EMBO Rep. 2006 Sep;7(9):911-8. doi: 10.1038/sj.embor.7400768. Epub 2006 Aug 11.
10
Effective high-capacity gutless adenoviral vectors mediate transgene expression in human glioma cells.
Mol Ther. 2006 Sep;14(3):371-81. doi: 10.1016/j.ymthe.2006.05.006. Epub 2006 Jun 23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验