Chemically Engineered AAV Vectors to Improve Biodistribution and Gene Transfer to the Central Nervous System

被引：0
|
作者：
Lefevre, Gaelle M. [1 ]
Burlot, Marie-Anne [1 ]
Brument, Nicole [1 ]
Jordi, Emmanuelle [1 ]
Ferry, Nicolas [1 ]
Blaettler, Thomas [1 ]
机构：
[1] Coave Therapeut, Paris, France
来源：
MOLECULAR THERAPY | 2022年 / 30卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q81 [生物工程学（生物技术）]; Q93 [微生物学];
学科分类号：
071005 ; 0836 ; 090102 ; 100705 ;
摘要：
994
引用
收藏
页码：464 / 464
页数：1
相关论文
共 50 条
  • [41] Characterization of delivery routes of AAV vectors for neonatal gene transfer
    Ogura, T
    Mizukami, H
    Mimuro, J
    Okada, T
    Hamada, H
    Kume, A
    Yoshikawa, H
    Sakata, Y
    Ozawa, K
    MOLECULAR THERAPY, 2004, 9 : S130 - S131
  • [42] Dual AAV vectors for efficient and safe retinal gene transfer
    Trapani, Ivana
    Auricchio, Alberto
    HUMAN GENE THERAPY, 2016, 27 (07) : A2 - A3
  • [43] Ocular gene transfer with self-complementary AAV vectors
    Yokoi, Katsutoshi
    Kachi, Shu
    Zhang, H. Steve
    Gregory, Philip D.
    Spratt, S. Kaye
    Samulski, R. Jude
    Campochiaro, Peter A.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2007, 48 (07) : 3324 - 3328
  • [44] NIDDK workshop on AAV vectors: Gene transfer into quiescent cells
    McKeon, C
    Samulski, RJ
    HUMAN GENE THERAPY, 1996, 7 (13) : 1615 - 1619
  • [45] Foamy virus as a gene transfer vector to the central nervous system
    Caprariello, A. V.
    Miller, R. H.
    Selkirk, S. M.
    GENE THERAPY, 2009, 16 (03) : 448 - 452
  • [46] THERAPEUTIC GENE-TRANSFER IN CENTRAL-NERVOUS-SYSTEM
    PESCHANSKI, M
    LISOVOSKI, F
    AKLI, S
    CAILLAUD, C
    WAHRMAN, P
    WEBERBENAROUS, A
    VIGNE, E
    STRATFORDPERRICAUDET, L
    PERRICAUDET, M
    KAHN, A
    NOUVELLE REVUE FRANCAISE D HEMATOLOGIE, 1993, 35 (03): : 299 - 300
  • [47] Foamy virus as a gene transfer vector to the central nervous system
    A V Caprariello
    R H Miller
    S M Selkirk
    Gene Therapy, 2009, 16 : 448 - 452
  • [48] DIRECT INVIVO GENE-TRANSFER TO THE CENTRAL-NERVOUS-SYSTEM USING REPLICATION DEFICIENT RECOMBINANT ADENOVIRUS VECTORS
    MASTRANGELI, A
    BAJOCCHI, G
    FELDMAN, SH
    CRYSTAL, RG
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 250 - 250
  • [49] Replication defective herpes simplex viral vectors and gene transfer to the nervous system
    Glorioso, J
    Fink, D
    Goins, W
    GENE DELIVERY SYSTEMS: A STATE-OF-THE-ART REVIEW, 1996, : 99 - 107
  • [50] DIRECT INVIVO GENE-TRANSFER TO EPENDYMAL CELLS IN THE CENTRAL-NERVOUS-SYSTEM USING RECOMBINANT ADENOVIRUS VECTORS
    BAJOCCHI, G
    FELDMAN, SH
    CRYSTAL, RG
    MASTRANGELI, A
    NATURE GENETICS, 1993, 3 (03) : 229 - 234
12345