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Tag aav [21 articles]

Recent papers classified by the tag aav.
  • AAV2-mediated delivery of human neurturin to the rat nigrostriatal system: Long-term efficacy and tolerability of CERE-120 for Parkinson's disease.
    Neurobiol Dis, Vol. 27, No. 1. (July 2007), pp. 67-76.
    by M Gasmi, EP Brandon, CD Herzog, A Wilson, KM Bishop, EK Hofer, JJ Cunningham, MA Printz, JH Kordower, RT Bartus
    posted to aav gdnf ntn pd by stevezhang on 2007-07-23 22:17:09 as ** along with 1 group SGMO_ZFP
  • Continuous low-level glial cell line-derived neurotrophic factor delivery using recombinant adeno-associated viral vectors provides neuroprotection and induces behavioral recovery in a primate model of Parkinson's disease.
    J Neurosci, Vol. 25, No. 4. (26 January 2005), pp. 769-777.
    posted to aav gdnf by stevezhang on 2006-06-20 19:18:35 as ** along with 1 group SGMO_ZFP
  • Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness.
    Mol Ther, Vol. 12, No. 6. (December 2005), pp. 1072-1082.
    posted to aav by stevezhang on 2007-03-16 19:57:03 as ** along with 1 group SGMO_ZFP
  • Midbrain injection of recombinant adeno-associated virus encoding rat glial cell line-derived neurotrophic factor protects nigral neurons in a progressive 6-hydroxydopamine-induced degeneration model of Parkinson's disease in rats.
    Proc Natl Acad Sci U S A, Vol. 94, No. 25. (9 December 1997), pp. 14083-14088.
    by RJ Mandel, SK Spratt, RO Snyder, SE Leff
    posted to aav gdnf by stevezhang on 2006-06-20 19:26:20 as ** along with 1 group SGMO_ZFP
  • Delayed delivery of AAV-GDNF prevents nigral neurodegeneration and promotes functional recovery in a rat model of Parkinson's disease.
    Gene Ther, Vol. 9, No. 6. (March 2002), pp. 381-389.
    posted to aav gdnf pd by stevezhang on 2006-06-18 08:06:06 as ** along with 1 group SGMO_ZFP
  • Striatal delivery of CERE-120, an AAV2 vector encoding human neurturin, enhances activity of the dopaminergic nigrostriatal system in aged monkeys.
    Mov Disord, Vol. 22, No. 8. (18 April 2007), pp. 1124-1132.
    by Christopher D D Herzog, Biplob Dass, James E E Holden, James Stansell, Mehdi Gasmi, Mark H H Tuszynski, Raymond T T Bartus, Jeffrey H H Kordower
    posted to aav ceregene gdnf monkey ntn pd by stevezhang on 2007-07-23 22:20:04 as ** along with 1 group SGMO_ZFP
  • Delivery of neurturin by AAV2 (CERE-120)-mediated gene transfer provides structural and functional neuroprotection and neurorestoration in MPTP-treated monkeys.
    Ann Neurol, Vol. 60, No. 6. (December 2006), pp. 706-715.
    by JH Kordower, CD Herzog, B Dass, RA Bakay, J Stansell, M Gasmi, RT Bartus
    posted to aav gdnf monkey ntn pd by stevezhang on 2007-07-23 22:18:22 as ** along with 1 group SGMO_ZFP
  • Neuroprotective effects of glial cell line-derived neurotrophic factor mediated by an adeno-associated virus vector in a transgenic animal model of amyotrophic lateral sclerosis.
    J Neurosci, Vol. 22, No. 16. (15 August 2002), pp. 6920-6928.
  • Recombinant adeno-associated viral vector-mediated glial cell line-derived neurotrophic factor gene transfer protects nigral dopamine neurons after onset of progressive degeneration in a rat model of Parkinson's disease.
    Exp Neurol, Vol. 160, No. 1. (November 1999), pp. 205-214.
    by RJ Mandel, RO Snyder, SE Leff
    posted to aav gdnf pd by stevezhang on 2006-08-26 02:18:46 as ** along with 1 group SGMO_ZFP
  • Striatal Delivery of Neurturin by CERE-120, an AAV2 Vector for the Treatment of Dopaminergic Neuron Degeneration in Parkinson's Disease.
    Mol Ther, Vol. 15, No. 1. (January 2007), pp. 62-68.
    by M Gasmi, CD Herzog, EP Brandon, JJ Cunningham, GA Ramirez, ET Ketchum, RT Bartus
    posted to aav gdnf ntn pd by stevezhang on 2007-07-23 22:16:24 as ** along with 1 group SGMO_ZFP
  • rAAV-asPLB transfer attenuates abnormal sarcoplasmic reticulum Ca(2+)-ATPase activity and cardiac dysfunction in rats with myocardial infarction.
    Eur J Heart Fail (18 December 2007)
    by Xiao-Yan Y Zhao, Shen-Jiang J Hu, Jiang Li, Yun Mou, Ka Bian, Jian Sun, Zhao-Hui H Zhu
    posted to aav chf pln by stevezhang on 2007-12-23 01:21:51 as ***
  • AAV-mediated knockdown of phospholamban leads to improved contractility and calcium handling in cardiomyocytes.
    J Gene Med (7 December 2007)
    by Lourdes M M Andino, Morihiko Takeda, Hideko Kasahara, Andrew Jakymiw, Barry J J Byrne, Alfred S S Lewin
    posted to aav pln sirna by stevezhang on 2008-01-15 12:49:39 as **
  • Intramuscular injection of AAV-GDNF results in sustained expression of transgenic GDNF, and its delivery to spinal motoneurons by retrograde transport.
    Neurosci Res, Vol. 45, No. 1. (January 2003), pp. 33-40.
  • Treatment of human disease by adeno-associated viral gene transfer.
    Hum Genet, Vol. 119, No. 6. (July 2006), pp. 571-603.
    by KH Warrington, RW Herzog
    posted to aav human treatment by schmoutz on 2007-08-21 22:23:02 as read along with 1 group Neuroscience
  • Long-term pharmacologically regulated expression of erythropoietin in primates following AAV-mediated gene transfer
    Blood, Vol. 105, No. 4. (15 February 2005), pp. 1424-1430.
    by Victor M Rivera, Guang-Ping Gao, Rebecca L Grant, Michael A Schnell, Philip W Zoltick, Leonard W Rozamus, Tim Clackson, James M Wilson
    posted to aav gene regulated therapy v10 by lyndallsarkies on 2008-05-17 12:01:16 as **
  • Gene Therapy Strategies for Duchenne Muscular Dystrophy Utilizing Recombinant Adeno-associated Virus Vectors
    Mol Ther, Vol. 13, No. 2. (February 2006), pp. 241-249.
    by Michael J Blankinship, Paul Gregorevic, Jeffrey S Chamberlain
    posted to aav dmd gene therapy v12 by lyndallsarkies on 2008-05-18 10:19:44 as **
  • AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
    Blood, Vol. 101, No. 8. (15 April 2003), pp. 2963-2972.
    by Catherine S Manno, Amy J Chew, Sylvia Hutchison, Peter J Larson, Roland W Herzog, Valder R Arruda, Shing J Tai, Margaret V Ragni, Arthur Thompson, Margareth Ozelo, Linda B Couto, Debra G Leonard, Frederick A Johnson, Alan Mcclelland, Ciaran Scallan, Erik Skarsgard, Alan W Flake, Mark A Kay, Katherine A High, Bertil Glader
    posted to aav delivery factor hemophiliacs human ix of to v11 viral by lyndallsarkies on 2008-05-17 20:45:57 as **
  • Long-term persistence of gene expression from adeno-associated virus serotype 5 in the mouse airways
    Gene Therapy, Vol. aop, No. current.
    by SG Sumner-Jones, LA Davies, A Varathalingam, DR Gill, SC Hyde,
    posted to aav delivery lungs to v9 by lyndallsarkies on 2008-05-17 09:57:52 as **
  • The packaging capacity of adeno-associated virus (AAV) and the potential for wild-type-plus AAV gene therapy vectors
    FEBS Letters, Vol. 407, No. 1. (21 April 1997), pp. 78-84.
    by Paul L Hermonat, Gerald J Quirk, Brian M Bishop, Li Han
    posted to aav by lisaxlee on 2007-08-07 16:44:54 as **
  • Cone-specific expression using a human red opsin promoter in recombinant AAV
    Vision Research, Vol. 48, No. 3. (February 2008), pp. 332-338.
    by Qiuhong Li, Adrian M Timmers, John Guy, Jijing Pang, William W Hauswirth
    posted to aav opsin promoter by breden to the group guppyopsinnih on 2008-04-15 23:02:59 as **
  • Versatility of AAV vectors for retinal gene transfer
    Vision Research, Vol. 48, No. 3. (February 2008), pp. 353-359.
    by Enrico M Surace, Alberto Auricchio
    posted to aav gene retinal transfer by breden to the group guppyopsinnih on 2008-04-15 23:05:00 as **
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