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PUBMED FOR HANDHELDS

Journal Abstract Search


275 related items for PubMed ID: 28814801

  • 1. 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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  • 2. Abnormal electrophysiological phenotypes and sleep deficits in a mouse model of Angelman Syndrome.
    Copping NA, Silverman JL.
    Mol Autism; 2021 Feb 06; 12(1):9. PubMed ID: 33549123
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  • 3. 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. Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome.
    Colas D, Wagstaff J, Fort P, Salvert D, Sarda N.
    Neurobiol Dis; 2005 Nov 20; 20(2):471-8. PubMed ID: 15921919
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  • 6. Behavioral deficits in an Angelman syndrome model: effects of genetic background and age.
    Huang HS, Burns AJ, Nonneman RJ, Baker LK, Riddick NV, Nikolova VD, Riday TT, Yashiro K, Philpot BD, Moy SS.
    Behav Brain Res; 2013 Apr 15; 243():79-90. PubMed ID: 23295389
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  • 9. GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.
    Judson MC, Wallace ML, Sidorov MS, Burette AC, Gu B, van Woerden GM, King IF, Han JE, Zylka MJ, Elgersma Y, Weinberg RJ, Philpot BD.
    Neuron; 2016 Apr 06; 90(1):56-69. PubMed ID: 27021170
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  • 10. Seizure-like activity in a juvenile Angelman syndrome mouse model is attenuated by reducing Arc expression.
    Mandel-Brehm C, Salogiannis J, Dhamne SC, Rotenberg A, Greenberg ME.
    Proc Natl Acad Sci U S A; 2015 Apr 21; 112(16):5129-34. PubMed ID: 25848016
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  • 11. A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants.
    Sonzogni M, Wallaard I, Santos SS, Kingma J, du Mee D, van Woerden GM, Elgersma Y.
    Mol Autism; 2018 Apr 21; 9():47. PubMed ID: 30220990
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  • 12. Ube3a reinstatement mitigates epileptogenesis in Angelman syndrome model mice.
    Gu B, Carstens KE, Judson MC, Dalton KA, Rougié M, Clark EP, Dudek SM, Philpot BD.
    J Clin Invest; 2019 Jan 02; 129(1):163-168. PubMed ID: 30352049
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  • 13. Of mothers and myelin: Aberrant myelination phenotypes in mouse model of Angelman syndrome are dependent on maternal and dietary influences.
    Grier MD, Carson RP, Lagrange AH.
    Behav Brain Res; 2015 Sep 15; 291():260-267. PubMed ID: 26028516
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  • 14. Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes.
    Sonzogni M, Hakonen J, Bernabé Kleijn M, Silva-Santos S, Judson MC, Philpot BD, van Woerden GM, Elgersma Y.
    Mol Autism; 2019 Sep 15; 10():23. PubMed ID: 31143434
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  • 15. Ube3a loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice.
    Wallace ML, van Woerden GM, Elgersma Y, Smith SL, Philpot BD.
    J Neurophysiol; 2017 Jul 01; 118(1):634-646. PubMed ID: 28468997
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  • 16. Hypersociability in the Angelman syndrome mouse model.
    Stoppel DC, Anderson MP.
    Exp Neurol; 2017 Jul 01; 293():137-143. PubMed ID: 28411125
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  • 18. Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.
    DeLorey TM, Handforth A, Anagnostaras SG, Homanics GE, Minassian BA, Asatourian A, Fanselow MS, Delgado-Escueta A, Ellison GD, Olsen RW.
    J Neurosci; 1998 Oct 15; 18(20):8505-14. PubMed ID: 9763493
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