BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

526 related articles for article (PubMed ID: 16123399)

  • 1. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.
    Pawlyk BS; Smith AJ; Buch PK; Adamian M; Hong DH; Sandberg MA; Ali RR; Li T
    Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3039-45. PubMed ID: 16123399
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Retinal degeneration is slowed in transgenic rats by AAV-mediated delivery of FGF-2.
    Lau D; McGee LH; Zhou S; Rendahl KG; Manning WC; Escobedo JA; Flannery JG
    Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3622-33. PubMed ID: 11006261
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
    Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR
    Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gene therapy for detached retina by adeno-associated virus vector expressing glial cell line-derived neurotrophic factor.
    Wu WC; Lai CC; Chen SL; Xiao X; Chen TL; Tsai RJ; Kuo SW; Tsao YP
    Invest Ophthalmol Vis Sci; 2002 Nov; 43(11):3480-8. PubMed ID: 12407159
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoter.
    Khani SC; Pawlyk BS; Bulgakov OV; Kasperek E; Young JE; Adamian M; Sun X; Smith AJ; Ali RR; Li T
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):3954-61. PubMed ID: 17724172
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 47(8):3505-13. PubMed ID: 16877422
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 12():298-309. PubMed ID: 16617297
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.
    Zhao Y; Hong DH; Pawlyk B; Yue G; Adamian M; Grynberg M; Godzik A; Li T
    Proc Natl Acad Sci U S A; 2003 Apr; 100(7):3965-70. PubMed ID: 12651948
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rescue of photoreceptor function by AAV-mediated gene transfer in a mouse model of inherited retinal degeneration.
    Jomary C; Vincent KA; Grist J; Neal MJ; Jones SE
    Gene Ther; 1997 Jul; 4(7):683-90. PubMed ID: 9282169
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long-term evaluation of retinal function in Prph2Rd2/Rd2 mice following AAV-mediated gene replacement therapy.
    Schlichtenbrede FC; da Cruz L; Stephens C; Smith AJ; Georgiadis A; Thrasher AJ; Bainbridge JW; Seeliger MW; Ali RR
    J Gene Med; 2003 Sep; 5(9):757-64. PubMed ID: 12950066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa.
    Liang FQ; Aleman TS; Dejneka NS; Dudus L; Fisher KJ; Maguire AM; Jacobson SG; Bennett J
    Mol Ther; 2001 Nov; 4(5):461-72. PubMed ID: 11708883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ribozyme knockdown of the gamma-subunit of rod cGMP phosphodiesterase alters the ERG and retinal morphology in wild-type mice.
    Liu J; Timmers AM; Lewin AS; Hauswirth WW
    Invest Ophthalmol Vis Sci; 2005 Oct; 46(10):3836-44. PubMed ID: 16186371
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis.
    Roman AJ; Boye SL; Aleman TS; Pang JJ; McDowell JH; Boye SE; Cideciyan AV; Jacobson SG; Hauswirth WW
    Mol Vis; 2007 Sep; 13():1701-10. PubMed ID: 17960108
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Retinal degeneration in tulp1-/- mice: vesicular accumulation in the interphotoreceptor matrix.
    Hagstrom SA; Duyao M; North MA; Li T
    Invest Ophthalmol Vis Sci; 1999 Nov; 40(12):2795-802. PubMed ID: 10549638
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration.
    Schlichtenbrede FC; MacNeil A; Bainbridge JW; Tschernutter M; Thrasher AJ; Smith AJ; Ali RR
    Gene Ther; 2003 Mar; 10(6):523-7. PubMed ID: 12621456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 3(2):241-8. PubMed ID: 11237681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Predominant rod photoreceptor degeneration in Leber congenital amaurosis.
    van der Spuy J; Munro PM; Luthert PJ; Preising MN; Bek T; Heegaard S; Cheetham ME
    Mol Vis; 2005 Jul; 11():542-53. PubMed ID: 16052170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Knockdown of wild-type mouse rhodopsin using an AAV vectored ribozyme as part of an RNA replacement approach.
    Gorbatyuk MS; Pang JJ; Thomas J; Hauswirth WW; Lewin AS
    Mol Vis; 2005 Aug; 11():648-56. PubMed ID: 16145542
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Brain-derived neurotrophic factor gene delivery to muller glia preserves structure and function of light-damaged photoreceptors.
    Gauthier R; Joly S; Pernet V; Lachapelle P; Di Polo A
    Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3383-92. PubMed ID: 16123443
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cone-specific expression using a human red opsin promoter in recombinant AAV.
    Li Q; Timmers AM; Guy J; Pang J; Hauswirth WW
    Vision Res; 2008 Feb; 48(3):332-8. PubMed ID: 17905404
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.