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Journal Abstract Search

828 related items for PubMed ID: 26419918

  • 1. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
    Sungur AÖ, Schwarting RK, Wöhr M.
    Autism Res; 2016 Jun; 9(6):696-709. PubMed ID: 26419918
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Ultrasonic vocalizations in Shank mouse models for autism spectrum disorders: detailed spectrographic analyses and developmental profiles.
    Wöhr M.
    Neurosci Biobehav Rev; 2014 Jun 30; 43():199-212. PubMed ID: 24726578
    [Abstract] [Full Text] [Related]

  • 4. Behavioral phenotypes and neurobiological mechanisms in the Shank1 mouse model for autism spectrum disorder: A translational perspective.
    Sungur AÖ, Schwarting RKW, Wöhr M.
    Behav Brain Res; 2018 Oct 15; 352():46-61. PubMed ID: 28963042
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 27(8):906-919. PubMed ID: 28500650
    [Abstract] [Full Text] [Related]

  • 6. Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder.
    Berg EL, Copping NA, Rivera JK, Pride MC, Careaga M, Bauman MD, Berman RF, Lein PJ, Harony-Nicolas H, Buxbaum JD, Ellegood J, Lerch JP, Wöhr M, Silverman JL.
    Autism Res; 2018 Apr 15; 11(4):587-601. PubMed ID: 29377611
    [Abstract] [Full Text] [Related]

  • 7. Characterization of early communicative behavior in mouse models of neurofibromatosis type 1.
    Maloney SE, Chandler KC, Anastasaki C, Rieger MA, Gutmann DH, Dougherty JD.
    Autism Res; 2018 Jan 15; 11(1):44-58. PubMed ID: 28842941
    [Abstract] [Full Text] [Related]

  • 8. SHANK1 and autism spectrum disorders.
    Gong X, Wang H.
    Sci China Life Sci; 2015 Oct 15; 58(10):985-90. PubMed ID: 26335738
    [Abstract] [Full Text] [Related]

  • 9. Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior.
    Wöhr M, Roullet FI, Hung AY, Sheng M, Crawley JN.
    PLoS One; 2011 Oct 15; 6(6):e20631. PubMed ID: 21695253
    [Abstract] [Full Text] [Related]

  • 10. SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
    Qiu S, Li Y, Bai Y, Shi J, Cui H, Gu Y, Ren Y, Zhao Q, Zhang K, Lu M, Wang Y, Li Y, Zhong W, Zhu X, Liu Y, Cheng Y, Qiao Y, Liu Y.
    Autism Res; 2019 Mar 15; 12(3):375-383. PubMed ID: 30629339
    [Abstract] [Full Text] [Related]

  • 11. Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.
    Brunner D, Kabitzke P, He D, Cox K, Thiede L, Hanania T, Sabath E, Alexandrov V, Saxe M, Peles E, Mills A, Spooren W, Ghosh A, Feliciano P, Benedetti M, Luo Clayton A, Biemans B.
    PLoS One; 2015 Mar 15; 10(8):e0134572. PubMed ID: 26273832
    [Abstract] [Full Text] [Related]

  • 12. Reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin.
    Mosienko V, Beis D, Alenina N, Wöhr M.
    Mol Autism; 2015 Mar 15; 6():13. PubMed ID: 25901271
    [Abstract] [Full Text] [Related]

  • 13. Dissociations in the neural substrates of language and social functioning in autism spectrum disorder.
    Crutcher J, Martin A, Wallace GL.
    Autism Res; 2018 Aug 15; 11(8):1175-1186. PubMed ID: 30365251
    [Abstract] [Full Text] [Related]

  • 14. Juvenile manifestation of ultrasound communication deficits in the neuroligin-4 null mutant mouse model of autism.
    Ju A, Hammerschmidt K, Tantra M, Krueger D, Brose N, Ehrenreich H.
    Behav Brain Res; 2014 Aug 15; 270():159-64. PubMed ID: 24855039
    [Abstract] [Full Text] [Related]

  • 15. Juvenile Shank3b deficient mice present with behavioral phenotype relevant to autism spectrum disorder.
    Balaan C, Corley MJ, Eulalio T, Leite-Ahyo K, Pang APS, Fang R, Khadka VS, Maunakea AK, Ward MA.
    Behav Brain Res; 2019 Jan 01; 356():137-147. PubMed ID: 30134148
    [Abstract] [Full Text] [Related]

  • 16. Altered postnatal developmental patterns of ultrasonic vocalizations in Dock4 knockout mice.
    Yang X, Guo D, Li K, Shi L.
    Behav Brain Res; 2021 May 21; 406():113232. PubMed ID: 33705839
    [Abstract] [Full Text] [Related]

  • 17. Effect of social odor context on the emission of isolation-induced ultrasonic vocalizations in the BTBR T+tf/J mouse model for autism.
    Wöhr M.
    Front Neurosci; 2015 May 21; 9():73. PubMed ID: 25852455
    [Abstract] [Full Text] [Related]

  • 18. Genetic control of social behavior: Lessons from mutant mice.
    Provenzano G, Chelini G, Bozzi Y.
    Behav Brain Res; 2017 May 15; 325(Pt B):237-250. PubMed ID: 27825935
    [Abstract] [Full Text] [Related]

  • 19. 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 May 15; 8():26. PubMed ID: 28638591
    [Abstract] [Full Text] [Related]

  • 20. Communication and social interaction in the cannabinoid-type 1 receptor null mouse: Implications for autism spectrum disorder.
    Fyke W, Premoli M, Echeverry Alzate V, López-Moreno JA, Lemaire-Mayo V, Crusio WE, Marsicano G, Wöhr M, Pietropaolo S.
    Autism Res; 2021 Sep 15; 14(9):1854-1872. PubMed ID: 34173729
    [Abstract] [Full Text] [Related]

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