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Journal Abstract Search

828 related items for PubMed ID: 26419918

  • 21. 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
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  • 22. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.
    El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H.
    Behav Brain Res; 2013 Aug 15; 251():41-9. PubMed ID: 23183221
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  • 23. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.
    Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, Wang H.
    Mol Psychiatry; 2022 Jul 15; 27(7):2985-2998. PubMed ID: 35388181
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  • 24. Communication Impairment in Ultrasonic Vocal Repertoire during the Suckling Period of Cd157 Knockout Mice: Transient Improvement by Oxytocin.
    Lopatina OL, Furuhara K, Ishihara K, Salmina AB, Higashida H.
    Front Neurosci; 2017 Jul 15; 11():266. PubMed ID: 28566999
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  • 28. ASD symptoms in toddlers and preschoolers: An examination of sex differences.
    Ros-Demarize R, Bradley C, Kanne SM, Warren Z, Boan A, Lajonchere C, Park J, Carpenter LA.
    Autism Res; 2020 Jan 15; 13(1):157-166. PubMed ID: 31747131
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  • 29. 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 15; 83():67-74. PubMed ID: 26306459
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  • 31. Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in mice.
    Qin Y, Zhang XY, Liu Y, Ma Z, Tao S, Li Y, Peng R, Wang F, Wang J, Feng J, Qiu Z, Jin L, Wang H, Gong X.
    Transl Psychiatry; 2023 Oct 25; 13(1):329. PubMed ID: 37880287
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  • 35. CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
    Katayama Y, Nishiyama M, Shoji H, Ohkawa Y, Kawamura A, Sato T, Suyama M, Takumi T, Miyakawa T, Nakayama KI.
    Nature; 2016 Sep 29; 537(7622):675-679. PubMed ID: 27602517
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  • 39. 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.
    Yang M, Mahrt EJ, Lewis F, Foley G, Portmann T, Dolmetsch RE, Portfors CV, Crawley JN.
    Autism Res; 2015 Oct 29; 8(5):507-21. PubMed ID: 25663600
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  • 40. Autism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlations.
    Oberman LM, Boccuto L, Cascio L, Sarasua S, Kaufmann WE.
    Orphanet J Rare Dis; 2015 Aug 27; 10():105. PubMed ID: 26306707
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