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Journal Abstract Search

284 related items for PubMed ID: 28255463

  • 21. UPR activation specifically modulates glutamate neurotransmission in the cerebellum of a mouse model of autism.
    Trobiani L, Favaloro FL, Di Castro MA, Di Mattia M, Cariello M, Miranda E, Canterini S, De Stefano ME, Comoletti D, Limatola C, De Jaco A.
    Neurobiol Dis; 2018 Dec; 120():139-150. PubMed ID: 30201312
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  • 22. Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism.
    Wang L, Mirabella VR, Dai R, Su X, Xu R, Jadali A, Bernabucci M, Singh I, Chen Y, Tian J, Jiang P, Kwan KY, Pak C, Liu C, Comoletti D, Hart RP, Chen C, Südhof TC, Pang ZP.
    Mol Psychiatry; 2024 Jun; 29(6):1620-1635. PubMed ID: 36280753
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  • 25. A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
    Tabuchi K, Blundell J, Etherton MR, Hammer RE, Liu X, Powell CM, Südhof TC.
    Science; 2007 Oct 05; 318(5847):71-6. PubMed ID: 17823315
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  • 26. Abnormal Social Interactions in a Drosophila Mutant of an Autism Candidate Gene: Neuroligin 3.
    Yost RT, Robinson JW, Baxter CM, Scott AM, Brown LP, Aletta MS, Hakimjavadi R, Lone A, Cumming RC, Dukas R, Mozer B, Simon AF.
    Int J Mol Sci; 2020 Jun 29; 21(13):. PubMed ID: 32610435
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  • 28. Faster Gastrointestinal Transit, Reduced Small Intestinal Smooth Muscle Tone and Dysmotility in the Nlgn3R451C Mouse Model of Autism.
    Hosie S, Abo-Shaban T, Mou K, Balasuriya GK, Mohsenipour M, Alamoudi MU, Filippone RT, Belz GT, Franks AE, Bornstein JC, Nurgali K, Hill-Yardin EL.
    Int J Mol Sci; 2024 Jan 09; 25(2):. PubMed ID: 38255906
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  • 30. Targeting oxytocin receptor (Oxtr)-expressing neurons in the lateral septum to restore social novelty in autism spectrum disorder mouse models.
    Horiai M, Otsuka A, Hidema S, Hiraoka Y, Hayashi R, Miyazaki S, Furuse T, Mizukami H, Teruyama R, Tamura M, Bito H, Maejima Y, Shimomura K, Nishimori K.
    Sci Rep; 2020 Dec 17; 10(1):22173. PubMed ID: 33335150
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  • 33. Impaired cecal motility and secretion alongside expansion of gut-associated lymphoid tissue in the Nlgn3R451C mouse model of autism.
    Lee CYQ, Balasuriya GK, Herath M, Franks AE, Hill-Yardin EL.
    Sci Rep; 2023 Aug 04; 13(1):12687. PubMed ID: 37542090
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  • 35. Functional significance of rare neuroligin 1 variants found in autism.
    Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T.
    PLoS Genet; 2017 Aug 04; 13(8):e1006940. PubMed ID: 28841651
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  • 36. Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.
    Radyushkin K, Hammerschmidt K, Boretius S, Varoqueaux F, El-Kordi A, Ronnenberg A, Winter D, Frahm J, Fischer J, Brose N, Ehrenreich H.
    Genes Brain Behav; 2009 Jun 04; 8(4):416-25. PubMed ID: 19243448
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  • 38. 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 Jun 04; 10(8):e0134572. PubMed ID: 26273832
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  • 40. Mutations in neuroligin-3 in male mice impact behavioral flexibility but not relational memory in a touchscreen test of visual transitive inference.
    Norris RHC, Churilov L, Hannan AJ, Nithianantharajah J.
    Mol Autism; 2019 Jun 04; 10():42. PubMed ID: 31827744
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