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Volumn 22, Issue 2, 2014, Pages 246-247

There must be a way out of here: Identifying a safe and efficient combination of promoter, transgene, and vector backbone for gene therapy of neurological disease

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DECARBOXYLASE; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; PARVOVIRUS VECTOR;

EID: 84893226252     PISSN: 15250016     EISSN: 15250024     Source Type: Journal    
DOI: 10.1038/mt.2013.297     Document Type: Note
Times cited : (3)

References (13)
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  • 4
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    • Samaranch, L, San Sebastian, W, Kells, AP, Salegio, EA, Heller, G, Bringas, JR et al. (2014). AAV9-mediated expression of a non-self protein in nonhuman primate central nervous system triggers widespread neuroinflammation driven by antigen-presenting cell transduction. Mol Ther 22: 329-337.
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  • 5
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    • Gene therapy for Parkinson′s disease: From non-human primates to humans
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  • 8
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    • One-year expression from high-capacity adenoviral vectors in the brains of animals with pre-existing antiadenoviral immunity: Clinical implications
    • Barcia, C, Jimenez-Dalmaroni, M, Kroeger, KM, Puntel, M, Rapaport, AJ, Larocque, D et al. (2007). One-year expression from high-capacity adenoviral vectors in the brains of animals with pre-existing antiadenoviral immunity: clinical implications. Mol Ther 15: 2154-2163.
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  • 9
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.