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Journal Abstract Search

240 related items for PubMed ID: 11702207

  • 1. 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
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  • 2. Mutations of RPGR in X-linked retinitis pigmentosa (RP3).
    Vervoort R, Wright AF.
    Hum Mutat; 2002 May; 19(5):486-500. PubMed ID: 11968081
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  • 3. 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
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  • 7. Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa.
    Yokoyama A, Maruiwa F, Hayakawa M, Kanai A, Vervoort R, Wright AF, Yamada K, Niikawa N, Naōi N.
    Am J Med Genet; 2001 Dec 01; 104(3):232-8. PubMed ID: 11754050
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  • 13. Expression of crisp-1 mRNA splice variants in the rat epididymis, and comparative analysis of the rat and mouse crisp-1 gene regulatory regions.
    Roberts KP, Hoffman LB, Ensrud KM, Hamilton DW.
    J Androl; 2001 Dec 01; 22(1):157-63. PubMed ID: 11191082
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  • 14. Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa.
    Vervoort R, Lennon A, Bird AC, Tulloch B, Axton R, Miano MG, Meindl A, Meitinger T, Ciccodicola A, Wright AF.
    Nat Genet; 2000 Aug 01; 25(4):462-6. PubMed ID: 10932196
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  • 15. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
    Sharon D, Bruns GA, McGee TL, Sandberg MA, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 2000 Aug 01; 41(9):2712-21. PubMed ID: 10937588
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  • 17. Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts.
    Seim I, Collet C, Herington AC, Chopin LK.
    BMC Genomics; 2007 Aug 30; 8():298. PubMed ID: 17727735
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  • 20. Molecular characterization of the mouse gene encoding cellular retinaldehyde-binding protein.
    Kennedy BN, Huang J, Saari JC, Crabb JW.
    Mol Vis; 1998 Sep 04; 4():14. PubMed ID: 9736766
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