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Journal Abstract Search


306 related items for PubMed ID: 22427581

  • 1. Enhancement of rAAV2-mediated transgene expression in retina cells in vitro and in vivo by coadministration of low-dose chemotherapeutic drugs.
    Zhang S, Wu J, Wu X, Xu P, Tian Y, Yi M, Liu X, Dong X, Wolf F, Li C, Huang Q.
    Invest Ophthalmol Vis Sci; 2012 May 04; 53(6):2675-84. PubMed ID: 22427581
    [Abstract] [Full Text] [Related]

  • 2. Human blue-opsin promoter preferentially targets reporter gene expression to rat s-cone photoreceptors.
    Glushakova LG, Timmers AM, Pang J, Teusner JT, Hauswirth WW.
    Invest Ophthalmol Vis Sci; 2006 Aug 04; 47(8):3505-13. PubMed ID: 16877422
    [Abstract] [Full Text] [Related]

  • 3. Ultrasound-targeted microbubble destruction enhances AAV-mediated gene transfection in human RPE cells in vitro and rat retina in vivo.
    Li HL, Zheng XZ, Wang HP, Li F, Wu Y, Du LF.
    Gene Ther; 2009 Sep 04; 16(9):1146-53. PubMed ID: 19571889
    [Abstract] [Full Text] [Related]

  • 4. [Transduction efficacy of recombinant type 1 and type 2 adeno-associated virus in the retinal cells].
    Wu JH, Zhang SH, Liu Y, Chen XF, Xu P, Wu XB, Huang Q.
    Zhonghua Yi Xue Za Zhi; 2006 Oct 31; 86(40):2841-6. PubMed ID: 17200021
    [Abstract] [Full Text] [Related]

  • 5. AAV-mediated delivery of ciliary neurotrophic factor prolongs photoreceptor survival in the rhodopsin knockout mouse.
    Liang FQ, Dejneka NS, Cohen DR, Krasnoperova NV, Lem J, Maguire AM, Dudus L, Fisher KJ, Bennett J.
    Mol Ther; 2001 Feb 31; 3(2):241-8. PubMed ID: 11237681
    [Abstract] [Full Text] [Related]

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  • 7. Photoreceptor protection by iris pigment epithelial transplantation transduced with AAV-mediated brain-derived neurotrophic factor gene.
    Hojo M, Abe T, Sugano E, Yoshioka Y, Saigo Y, Tomita H, Wakusawa R, Tamai M.
    Invest Ophthalmol Vis Sci; 2004 Oct 31; 45(10):3721-6. PubMed ID: 15452082
    [Abstract] [Full Text] [Related]

  • 8. Neonatal systemic delivery of scAAV9 in rodents and large animals results in gene transfer to RPE cells in the retina.
    Joussemet B, Belbellaa B, Mendes-Madeira A, Bucher T, Briot-Nivard D, Dubreil L, Colle MA, Cherel Y, Moullier P, Rolling F.
    Exp Eye Res; 2011 Oct 31; 93(4):491-502. PubMed ID: 21723863
    [Abstract] [Full Text] [Related]

  • 9. Recombinant adeno-associated virus serotype 2 (rAAV2)-An efficient vector for gene delivery in condylar cartilage, glenoid fossa and TMJ disc in an experimental study in vivo.
    Li Q, Dai J, Rabie AB.
    Arch Oral Biol; 2009 Oct 31; 54(10):943-50. PubMed ID: 19683702
    [Abstract] [Full Text] [Related]

  • 10. Recombinant AAV-mediated delivery of a tet-inducible reporter gene to the rat retina.
    McGee Sanftner LH, Rendahl KG, Quiroz D, Coyne M, Ladner M, Manning WC, Flannery JG.
    Mol Ther; 2001 May 31; 3(5 Pt 1):688-96. PubMed ID: 11356074
    [Abstract] [Full Text] [Related]

  • 11. Enhanced transduction and improved photoreceptor survival of retinal degeneration by the combinatorial use of rAAV2 with a lower dose of adenovirus.
    Wu J, Zhang S, Wu X, Dong X, Xu P, Liu X, Li C, Huang Q.
    Vision Res; 2008 Jul 31; 48(15):1648-54. PubMed ID: 18513780
    [Abstract] [Full Text] [Related]

  • 12. Ocular gene transfer with self-complementary AAV vectors.
    Yokoi K, Kachi S, Zhang HS, Gregory PD, Spratt SK, Samulski RJ, Campochiaro PA.
    Invest Ophthalmol Vis Sci; 2007 Jul 31; 48(7):3324-8. PubMed ID: 17591905
    [Abstract] [Full Text] [Related]

  • 13. Gene therapeutic prospects in early onset of severe retinal dystrophy: restoration of vision in RPE65 Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium.
    Rolling F, Le Meur G, Stieger K, Smith AJ, Weber M, Deschamps JY, Nivard D, Mendes-Madeira A, Provost N, Péréon Y, Cherel Y, Ali RR, Hamel C, Moullier P, Rolling F.
    Bull Mem Acad R Med Belg; 2006 Jul 31; 161(10-12):497-508; discussion 508-9. PubMed ID: 17503728
    [Abstract] [Full Text] [Related]

  • 14. Distinctive gene transduction efficiencies of commonly used viral vectors in the retina.
    Zhang SH, Wu JH, Wu XB, Dong XY, Liu XJ, Li CY, Qian-Huang.
    Curr Eye Res; 2008 Jan 31; 33(1):81-90. PubMed ID: 18214745
    [Abstract] [Full Text] [Related]

  • 15. [Liposome-mediated gene transfer into retina].
    Wang F, Xia X, Hu H, Li L, Tian Y, Chen X, Huang Q.
    Zhonghua Yan Ke Za Zhi; 2002 Sep 31; 38(9):520-2. PubMed ID: 12410968
    [Abstract] [Full Text] [Related]

  • 16. Does recombinant adeno-associated virus-vectored proximal region of mouse rhodopsin promoter support only rod-type specific expression in vivo?
    Glushakova LG, Timmers AM, Issa TM, Cortez NG, Pang J, Teusner JT, Hauswirth WW.
    Mol Vis; 2006 Apr 07; 12():298-309. PubMed ID: 16617297
    [Abstract] [Full Text] [Related]

  • 17. AAV-mediated expression of CNTF promotes long-term survival and regeneration of adult rat retinal ganglion cells.
    Leaver SG, Cui Q, Plant GW, Arulpragasam A, Hisheh S, Verhaagen J, Harvey AR.
    Gene Ther; 2006 Sep 07; 13(18):1328-41. PubMed ID: 16708079
    [Abstract] [Full Text] [Related]

  • 18. Efficiency of lentiviral transduction during development in normal and rd mice.
    Pang J, Cheng M, Haire SE, Barker E, Planelles V, Blanks JC.
    Mol Vis; 2006 Jul 11; 12():756-67. PubMed ID: 16862069
    [Abstract] [Full Text] [Related]

  • 19. Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina.
    Bainbridge JW, Mistry A, Schlichtenbrede FC, Smith A, Broderick C, De Alwis M, Georgiadis A, Taylor PM, Squires M, Sethi C, Charteris D, Thrasher AJ, Sargan D, Ali RR.
    Gene Ther; 2003 Aug 11; 10(16):1336-44. PubMed ID: 12883530
    [Abstract] [Full Text] [Related]

  • 20. Post-injury delivery of rAAV2-CNTF combined with short-term pharmacotherapy is neuroprotective and promotes extensive axonal regeneration after optic nerve trauma.
    Hellström M, Pollett MA, Harvey AR.
    J Neurotrauma; 2011 Dec 11; 28(12):2475-83. PubMed ID: 21861632
    [Abstract] [Full Text] [Related]


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