Rational Design of AAV Vectors For Efficient Transduction of Muller Cells

被引：0
|
作者：
Choudhury, Shreyasi [1 ]
Manek, Rachna [1 ]
White, Miranda [1 ]
Sun, Jinfeng [1 ]
Aslanidi, Georgiy [2 ]
Svrivistava, Arun [2 ]
Boye, Sanford L. [1 ]
Boye, Shannon Elizabeth [1 ]
机构：
[1] Univ Florida, Ophthalmol, Gainesville, FL USA
[2] Univ Florida, Pediat, Gainesville, FL USA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2015年 / 56卷 / 07期
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
3641
引用
收藏
页数：2
相关论文
共 50 条
  • [41] Efficient and Targeted Transduction of Nonhuman Primate Liver With Systemically Delivered Optimized AAV3B Vectors
    Li, Shaoyong
    Ling, Chen
    Zhong, Li
    Li, Mengxin
    Su, Qin
    He, Ran
    Tang, Qiushi
    Greiner, Dale L.
    Shultz, Leonard D.
    Brehm, Michael A.
    Flotte, Terence R.
    Mueller, Christian
    Srivastava, Arun
    Gao, Guangping
    MOLECULAR THERAPY, 2015, 23 (12) : 1867 - 1876
  • [42] AAV8 Vexosome Vectors Enhance Cell Transduction In Vitro and Outperform Conventional AAV8 Vectors in Liver-Transduction In Vivo in the Presence of Anti-AAV Neutralizing Antibodies
    Meliani, Amine
    Fitzpatrick, Zachary
    Charles, Severine
    Mu, Dakai
    Boisgerault, Florence
    Maguire, Casey A.
    Mingozzi, Federico
    MOLECULAR THERAPY, 2015, 23 : S125 - S126
  • [43] Capsid-modified Ad.AAV vectors for stable transduction of human hematopoietic cells.
    Lieber, A
    Shayakhmetov, DM
    Li, QL
    Stamatoyannopoulos, G
    BLOOD CELLS MOLECULES AND DISEASES, 2002, 28 (03) : 334 - 335
  • [44] Self-complementary AAV2 vectors improve transduction efficiency of corneal endothelial cells
    Gruenert, Anja Katharina
    Buening, Hildegard
    Schnoedt, Maria
    Schmeer, Marco
    Schleef, Martin
    Kruse, Friedrich E.
    Fuchsluger, Thomas Armin
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [45] Polymers for Improving the In Vivo Transduction Efficiency of AAV2 Vectors
    Moulay, Gilles
    Boutin, Sylvie
    Masurier, Carole
    Scherman, Daniel
    Kichler, Antoine
    PLOS ONE, 2010, 5 (12):
  • [46] Syngeneic AAV Pseudo-Vectors Potentiates Full Vector Transduction
    Wang, Qizhao
    Dong, Biao
    Pokiniewski, Katie A.
    Firrman, Jenni
    Wu, Zhongren
    Chin, Mario P. S.
    Diao, Yong
    Xu, Ruian
    Xiao, Weidong
    MOLECULAR THERAPY, 2016, 24 : S218 - S218
  • [47] Differential Transduction Profiles of AAV Vectors in a Mouse Model of Human Glycosylation
    Rao, Lavanya
    Albright, Blake H.
    Corriher, Travis
    Murlidharan, Giridhar
    Asokan, Aravind
    MOLECULAR THERAPY, 2015, 23 : S18 - S19
  • [48] Comparison of Transduction Efficiency of Tyrosine-Mutant AAV Vectors in Muscle
    Qiao, Chunping
    Zheng, Hui
    Yuan, Zhenhua
    Li, Jianbin
    Zhong, Li
    Srivastava, Arun
    Li, Juan
    Xiao, Xiao
    MOLECULAR THERAPY, 2009, 17 : S175 - S176
  • [49] A Short and Efficient Transduction Protocol for Mouse Hematopoietic Stem Cells with Lentiviral Vectors
    Fernandez-Garcia, Maria
    Mesa, Cristina
    Almarza, Elena
    Bueren, Juan
    Yanez, Rosa
    HUMAN GENE THERAPY METHODS, 2017, 28 (06) : 310 - 317
  • [50] Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors
    Eric M. Poeschla
    Flossie Wong-Staal
    David J. Looney
    Nature Medicine, 1998, 4 : 354 - 357
12345