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Journal Abstract Search


715 related items for PubMed ID: 17940072

  • 1. The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology.
    Dindot SV, Antalffy BA, Bhattacharjee MB, Beaudet AL.
    Hum Mol Genet; 2008 Jan 01; 17(1):111-8. PubMed ID: 17940072
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  • 3. Maternal Loss of Ube3a Impairs Experience-Driven Dendritic Spine Maintenance in the Developing Visual Cortex.
    Kim H, Kunz PA, Mooney R, Philpot BD, Smith SL.
    J Neurosci; 2016 Apr 27; 36(17):4888-94. PubMed ID: 27122043
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  • 4. 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 27; 9(2):149-59. PubMed ID: 11895368
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  • 7. Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a.
    Sato M, Stryker MP.
    Proc Natl Acad Sci U S A; 2010 Mar 23; 107(12):5611-6. PubMed ID: 20212164
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  • 10. Enhanced Nociception in Angelman Syndrome Model Mice.
    McCoy ES, Taylor-Blake B, Aita M, Simon JM, Philpot BD, Zylka MJ.
    J Neurosci; 2017 Oct 18; 37(42):10230-10239. PubMed ID: 28931574
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  • 11. 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 18; 220(2):341-8. PubMed ID: 19782683
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  • 12. Loss of Angelman Syndrome Protein E6AP Disrupts a Novel Antagonistic Estrogen-Retinoic Acid Transcriptional Crosstalk in Neurons.
    El Hokayem J, Weeber E, Nawaz Z.
    Mol Neurobiol; 2018 Sep 18; 55(9):7187-7200. PubMed ID: 29388081
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  • 13. Loss of dopaminergic neurons and resulting behavioural deficits in mouse model of Angelman syndrome.
    Mulherkar SA, Jana NR.
    Neurobiol Dis; 2010 Dec 18; 40(3):586-92. PubMed ID: 20696245
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  • 14. UBE3A/E6-AP regulates cell proliferation by promoting proteasomal degradation of p27.
    Mishra A, Godavarthi SK, Jana NR.
    Neurobiol Dis; 2009 Oct 18; 36(1):26-34. PubMed ID: 19591933
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  • 15. Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model.
    Silva-Santos S, van Woerden GM, Bruinsma CF, Mientjes E, Jolfaei MA, Distel B, Kushner SA, Elgersma Y.
    J Clin Invest; 2015 May 18; 125(5):2069-76. PubMed ID: 25866966
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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 18; 7(4):368-77. PubMed ID: 9110176
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  • 18. 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 18; 15(1):74-7. PubMed ID: 8988172
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  • 19. Activity-dependent changes in MAPK activation in the Angelman Syndrome mouse model.
    Filonova I, Trotter JH, Banko JL, Weeber EJ.
    Learn Mem; 2014 Jan 16; 21(2):98-104. PubMed ID: 24434871
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  • 20. Angelman syndrome - insights into a rare neurogenetic disorder.
    Buiting K, Williams C, Horsthemke B.
    Nat Rev Neurol; 2016 Oct 16; 12(10):584-93. PubMed ID: 27615419
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