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Journal Abstract Search

2034 related items for PubMed ID: 31704787

  • 1. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
    Gilbert J, O'Connor M, Templet S, Moghaddam M, Di Via Ioschpe A, Sinclair A, Zhu LQ, Xu W, Man HY.
    J Neurosci; 2020 Jan 02; 40(1):237-254. PubMed ID: 31704787
    [Abstract] [Full Text] [Related]

  • 2. Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism.
    Dhamne SC, Silverman JL, Super CE, Lammers SHT, Hameed MQ, Modi ME, Copping NA, Pride MC, Smith DG, Rotenberg A, Crawley JN, Sahin M.
    Mol Autism; 2017 Jan 02; 8():26. PubMed ID: 28638591
    [Abstract] [Full Text] [Related]

  • 3. Learning delays in a mouse model of Autism Spectrum Disorder.
    Rendall AR, Truong DT, Fitch RH.
    Behav Brain Res; 2016 Apr 15; 303():201-7. PubMed ID: 26873041
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  • 4. Heterozygous Nexmif female mice demonstrate mosaic NEXMIF expression, autism-like behaviors, and abnormalities in dendritic arborization and synaptogenesis.
    O'Connor M, Qiao H, Odamah K, Cerdeira PC, Man HY.
    Heliyon; 2024 Feb 15; 10(3):e24703. PubMed ID: 38322873
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  • 6. Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway.
    Bavley CC, Rice RC, Fischer DK, Fakira AK, Byrne M, Kosovsky M, Rizzo BK, Del Prete D, Alaedini A, Morón JA, Higgins JJ, D'Adamio L, Rajadhyaksha AM.
    J Neurosci; 2018 Mar 14; 38(11):2780-2795. PubMed ID: 29459374
    [Abstract] [Full Text] [Related]

  • 7. Repetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum Disorders.
    Wurzman R, Forcelli PA, Griffey CJ, Kromer LF.
    Behav Brain Res; 2015 Feb 01; 278():115-28. PubMed ID: 25281279
    [Abstract] [Full Text] [Related]

  • 8. Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity.
    Araujo DJ, Toriumi K, Escamilla CO, Kulkarni A, Anderson AG, Harper M, Usui N, Ellegood J, Lerch JP, Birnbaum SG, Tucker HO, Powell CM, Konopka G.
    J Neurosci; 2017 Nov 08; 37(45):10917-10931. PubMed ID: 28978667
    [Abstract] [Full Text] [Related]

  • 9. Decrease in endogenous brain allopregnanolone induces autism spectrum disorder (ASD)-like behavior in mice: A novel animal model of ASD.
    Ebihara K, Fujiwara H, Awale S, Dibwe DF, Araki R, Yabe T, Matsumoto K.
    Behav Brain Res; 2017 Sep 15; 334():6-15. PubMed ID: 28743598
    [Abstract] [Full Text] [Related]

  • 10. Repetitive behaviors in the Shank1 knockout mouse model for autism spectrum disorder: developmental aspects and effects of social context.
    Sungur AÖ, Vörckel KJ, Schwarting RK, Wöhr M.
    J Neurosci Methods; 2014 Aug 30; 234():92-100. PubMed ID: 24820912
    [Abstract] [Full Text] [Related]

  • 11. eIF4E/Fmr1 double mutant mice display cognitive impairment in addition to ASD-like behaviors.
    Huynh TN, Shah M, Koo SY, Faraud KS, Santini E, Klann E.
    Neurobiol Dis; 2015 Nov 30; 83():67-74. PubMed ID: 26306459
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  • 13. Aberrant cognitive phenotypes and altered hippocampal BDNF expression related to epigenetic modifications in mice lacking the post-synaptic scaffolding protein SHANK1: Implications for autism spectrum disorder.
    Sungur AÖ, Jochner MCE, Harb H, Kılıç A, Garn H, Schwarting RKW, Wöhr M.
    Hippocampus; 2017 Aug 30; 27(8):906-919. PubMed ID: 28500650
    [Abstract] [Full Text] [Related]

  • 14. Shank3B mutant mice display pitch discrimination enhancements and learning deficits.
    Rendall AR, Perrino PA, Buscarello AN, Fitch RH.
    Int J Dev Neurosci; 2019 Feb 30; 72():13-21. PubMed ID: 30385192
    [Abstract] [Full Text] [Related]

  • 15. Cell-Type-Specific Shank2 Deletion in Mice Leads to Differential Synaptic and Behavioral Phenotypes.
    Kim R, Kim J, Chung C, Ha S, Lee S, Lee E, Yoo YE, Kim W, Shin W, Kim E.
    J Neurosci; 2018 Apr 25; 38(17):4076-4092. PubMed ID: 29572432
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  • 17. Mouse Model of Chromosome 15q13.3 Microdeletion Syndrome Demonstrates Features Related to Autism Spectrum Disorder.
    Kogan JH, Gross AK, Featherstone RE, Shin R, Chen Q, Heusner CL, Adachi M, Lin A, Walton NM, Miyoshi S, Miyake S, Tajinda K, Ito H, Siegel SJ, Matsumoto M.
    J Neurosci; 2015 Dec 09; 35(49):16282-94. PubMed ID: 26658876
    [Abstract] [Full Text] [Related]

  • 18. Autism spectrum disorder traits in Slc9a9 knock-out mice.
    Yang L, Faraone SV, Zhang-James Y.
    Am J Med Genet B Neuropsychiatr Genet; 2016 Apr 09; 171B(3):363-76. PubMed ID: 26755066
    [Abstract] [Full Text] [Related]

  • 19. A Novel Human CAMK2A Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors.
    Stephenson JR, Wang X, Perfitt TL, Parrish WP, Shonesy BC, Marks CR, Mortlock DP, Nakagawa T, Sutcliffe JS, Colbran RJ.
    J Neurosci; 2017 Feb 22; 37(8):2216-2233. PubMed ID: 28130356
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