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Journal Abstract Search

336 related items for PubMed ID: 11895368

  • 1. Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.
    Miura K, Kishino T, Li E, Webber H, Dikkes P, Holmes GL, Wagstaff J.
    Neurobiol Dis; 2002 Mar; 9(2):149-59. PubMed ID: 11895368
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  • 2. Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.
    Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL.
    PLoS One; 2010 Aug 20; 5(8):e12278. PubMed ID: 20808828
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  • 5. The spectrum of mutations in UBE3A causing Angelman syndrome.
    Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL.
    Hum Mol Genet; 1999 Jan 20; 8(1):129-35. PubMed ID: 9887341
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  • 8. Impaired hippocampal plasticity and altered neurogenesis in adult Ube3a maternal deficient mouse model for Angelman syndrome.
    Mardirossian S, Rampon C, Salvert D, Fort P, Sarda N.
    Exp Neurol; 2009 Dec 20; 220(2):341-8. PubMed ID: 19782683
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  • 9. Molecular epigenetics of Angelman syndrome.
    Lalande M, Calciano MA.
    Cell Mol Life Sci; 2007 Apr 20; 64(7-8):947-60. PubMed ID: 17347796
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  • 10. Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.
    Yamasaki K, Joh K, Ohta T, Masuzaki H, Ishimaru T, Mukai T, Niikawa N, Ogawa M, Wagstaff J, Kishino T.
    Hum Mol Genet; 2003 Apr 15; 12(8):837-47. PubMed ID: 12668607
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  • 11. Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice.
    Born HA, Dao AT, Levine AT, Lee WL, Mehta NM, Mehra S, Weeber EJ, Anderson AE.
    Sci Rep; 2017 Aug 16; 7(1):8451. PubMed ID: 28814801
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  • 12. Angelman syndrome: how many genes to remain silent?
    Rougeulle C, Lalande M.
    Neurogenetics; 1998 Aug 16; 1(4):229-37. PubMed ID: 10732796
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  • 13. Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors.
    Heck DH, Zhao Y, Roy S, LeDoux MS, Reiter LT.
    Hum Mol Genet; 2008 Jul 15; 17(14):2181-9. PubMed ID: 18413322
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  • 14. Imprinting in Angelman and Prader-Willi syndromes.
    Jiang Y, Tsai TF, Bressler J, Beaudet AL.
    Curr Opin Genet Dev; 1998 Jun 15; 8(3):334-42. PubMed ID: 9691003
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  • 15. UBE3A/E6-AP mutations cause Angelman syndrome.
    Kishino T, Lalande M, Wagstaff J.
    Nat Genet; 1997 Jan 15; 15(1):70-3. PubMed ID: 8988171
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  • 16. The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.
    Sutcliffe JS, Jiang YH, Galijaard RJ, Matsuura T, Fang P, Kubota T, Christian SL, Bressler J, Cattanach B, Ledbetter DH, Beaudet AL.
    Genome Res; 1997 Apr 15; 7(4):368-77. PubMed ID: 9110176
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  • 18. Ube3a imprinting impairs circadian robustness in Angelman syndrome models.
    Shi SQ, Bichell TJ, Ihrie RA, Johnson CH.
    Curr Biol; 2015 Mar 02; 25(5):537-45. PubMed ID: 25660546
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  • 19. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.
    Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL.
    Nat Genet; 1997 Jan 02; 15(1):74-7. PubMed ID: 8988172
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  • 20. Towards a therapy for Angelman syndrome by targeting a long non-coding RNA.
    Meng L, Ward AJ, Chun S, Bennett CF, Beaudet AL, Rigo F.
    Nature; 2015 Feb 19; 518(7539):409-12. PubMed ID: 25470045
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