BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 22577079)

  • 1. Functional characterization of the human RPGR proximal promoter.
    Shu X; Simpson JR; Hart AW; Zeng Z; Patnaik SR; Gautier P; Murdoch E; Tulloch B; Wright AF
    Invest Ophthalmol Vis Sci; 2012 Jun; 53(7):3951-8. PubMed ID: 22577079
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A minimal murine Msx-1 gene promoter. Organization of its cis-regulatory motifs and their role in transcriptional activation in cells in culture and in transgenic mice.
    Takahashi T; Guron C; Shetty S; Matsui H; Raghow R
    J Biol Chem; 1997 Sep; 272(36):22667-78. PubMed ID: 9278425
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR Mutations.
    Beltran WA; Cideciyan AV; Boye SE; Ye GJ; Iwabe S; Dufour VL; Marinho LF; Swider M; Kosyk MS; Sha J; Boye SL; Peterson JJ; Witherspoon CD; Alexander JJ; Ying GS; Shearman MS; Chulay JD; Hauswirth WW; Gamlin PD; Jacobson SG; Aguirre GD
    Mol Ther; 2017 Aug; 25(8):1866-1880. PubMed ID: 28566226
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa.
    Kirschner R; Rosenberg T; Schultz-Heienbrok R; Lenzner S; Feil S; Roepman R; Cremers FP; Ropers HH; Berger W
    Hum Mol Genet; 1999 Aug; 8(8):1571-8. PubMed ID: 10401007
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A single, abbreviated RPGR-ORF15 variant reconstitutes RPGR function in vivo.
    Hong DH; Pawlyk BS; Adamian M; Sandberg MA; Li T
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):435-41. PubMed ID: 15671266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and characterization of a novel RPGR isoform in human retina.
    Neidhardt J; Glaus E; Barthelmes D; Zeitz C; Fleischhauer J; Berger W
    Hum Mutat; 2007 Aug; 28(8):797-807. PubMed ID: 17405150
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration.
    Wu Z; Hiriyanna S; Qian H; Mookherjee S; Campos MM; Gao C; Fariss R; Sieving PA; Li T; Colosi P; Swaroop A
    Hum Mol Genet; 2015 Jul; 24(14):3956-70. PubMed ID: 25877300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa.
    Fu J; Cheng J; Zhou Q; Wei C; Chen H; Lv H; Fu J
    Biosci Rep; 2019 Oct; 39(10):. PubMed ID: 31652454
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15.
    Thompson DA; Khan NW; Othman MI; Chang B; Jia L; Grahek G; Wu Z; Hiriyanna S; Nellissery J; Li T; Khanna H; Colosi P; Swaroop A; Heckenlively JR
    PLoS One; 2012; 7(5):e35865. PubMed ID: 22563472
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa.
    Fischer MD; McClements ME; Martinez-Fernandez de la Camara C; Bellingrath JS; Dauletbekov D; Ramsden SC; Hickey DG; Barnard AR; MacLaren RE
    Mol Ther; 2017 Aug; 25(8):1854-1865. PubMed ID: 28549772
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.
    Churchill JD; Bowne SJ; Sullivan LS; Lewis RA; Wheaton DK; Birch DG; Branham KE; Heckenlively JR; Daiger SP
    Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):1411-6. PubMed ID: 23372056
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP).
    Murga-Zamalloa C; Swaroop A; Khanna H
    Adv Exp Med Biol; 2010; 664():105-14. PubMed ID: 20238008
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
    Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel missense mutation of RPGR identified from retinitis pigmentosa affects splicing of the ORF15 region and causes loss of transcript heterogeneity.
    Liu YS; Pan JQ; Wan JF; Ren CY; Xu ZH; Pan XB; Gao RN; Liu SQ; Zhang JL; Yao QH; Wang JH; Li EM; Rao JH; Hou P; Chen JH
    Biochem Biophys Res Commun; 2020 Oct; 531(2):172-179. PubMed ID: 32788070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RPGR-associated retinal degeneration in human X-linked RP and a murine model.
    Huang WC; Wright AF; Roman AJ; Cideciyan AV; Manson FD; Gewaily DY; Schwartz SB; Sadigh S; Limberis MP; Bell P; Wilson JM; Swaroop A; Jacobson SG
    Invest Ophthalmol Vis Sci; 2012 Aug; 53(9):5594-608. PubMed ID: 22807293
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transcriptional regulation of the mouse PNRC2 promoter by the nuclear factor Y (NFY) and E2F1.
    Zhou D; Masri S; Ye JJ; Chen S
    Gene; 2005 Nov; 361():89-100. PubMed ID: 16181749
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements.
    Kirschner R; Erturk D; Zeitz C; Sahin S; Ramser J; Cremers FP; Ropers HH; Berger W
    Hum Genet; 2001 Sep; 109(3):271-8. PubMed ID: 11702207
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa.
    Zhao K; Wang L; Wang L; Wang L; Zhang Q; Wang Q
    Ophthalmic Genet; 2001 Sep; 22(3):187-94. PubMed ID: 11559860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The upstream region of the Rpe65 gene confers retinal pigment epithelium-specific expression in vivo and in vitro and contains critical octamer and E-box binding sites.
    Boulanger A; Liu S; Henningsgaard AA; Yu S; Redmond TM
    J Biol Chem; 2000 Oct; 275(40):31274-82. PubMed ID: 10896939
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: insights into X-linked Retinitis Pigmentosa and associated ciliopathies.
    He S; Parapuram SK; Hurd TW; Behnam B; Margolis B; Swaroop A; Khanna H
    Vision Res; 2008 Feb; 48(3):366-76. PubMed ID: 17904189
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.