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Common circuit defect of excitatory-inhibitory balance in mouse models of autism.

Gogolla N, Leblanc JJ, Quast KB, Südhof TC, Fagiolini M, Hensch TK.

J Neurodev Disord. 2009 Jun;1(2):172-81. doi: 10.1007/s11689-009-9023-x.


Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autism.

Filice F, Vörckel KJ, Sungur AÖ, Wöhr M, Schwaller B.

Mol Brain. 2016 Jan 27;9:10. doi: 10.1186/s13041-016-0192-8.


Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities.

Wöhr M, Orduz D, Gregory P, Moreno H, Khan U, Vörckel KJ, Wolfer DP, Welzl H, Gall D, Schiffmann SN, Schwaller B.

Transl Psychiatry. 2015 Mar 10;5:e525. doi: 10.1038/tp.2015.19.


Reduced inhibitory gate in the barrel cortex of Neuroligin3R451C knock-in mice, an animal model of autism spectrum disorders.

Cellot G, Cherubini E.

Physiol Rep. 2014 Jul 16;2(7). pii: e12077. doi: 10.14814/phy2.12077.


Reduced susceptibility to induced seizures in the Neuroligin-3(R451C) mouse model of autism.

Hill-Yardin EL, Argyropoulos A, Hosie S, Rind G, Anderson P, Hannan AJ, O'Brien TJ.

Neurosci Lett. 2015 Mar 4;589:57-61. doi: 10.1016/j.neulet.2015.01.024.


Interneuron Transcriptional Dysregulation Causes Frequency-Dependent Alterations in the Balance of Inhibition and Excitation in Hippocampus.

Bartley AF, Lucas EK, Brady LJ, Li Q, Hablitz JJ, Cowell RM, Dobrunz LE.

J Neurosci. 2015 Nov 18;35(46):15276-90. doi: 10.1523/JNEUROSCI.1834-15.2015.


A single low dose of valproic acid in late prenatal life alters postnatal behavior and glutamic acid decarboxylase levels in the mouse.

Wei R, Li Q, Lam S, Leung J, Cheung C, Zhang X, Sham PC, Chua SE, McAlonan GM.

Behav Brain Res. 2016 Nov 1;314:190-8. doi: 10.1016/j.bbr.2016.08.006.


Distinct Defects in Synaptic Differentiation of Neocortical Neurons in Response to Prenatal Valproate Exposure.

Iijima Y, Behr K, Iijima T, Biemans B, Bischofberger J, Scheiffele P.

Sci Rep. 2016 Jun 6;6:27400. doi: 10.1038/srep27400.


Convergent synaptic and circuit substrates underlying autism genetic risks.

McGee A, Li G, Lu Z, Qiu S.

Front Biol (Beijing). 2014 Feb 1;9(2):137-150.


Shank1 regulates excitatory synaptic transmission in mouse hippocampal parvalbumin-expressing inhibitory interneurons.

Mao W, Watanabe T, Cho S, Frost JL, Truong T, Zhao X, Futai K.

Eur J Neurosci. 2015 Apr;41(8):1025-35. doi: 10.1111/ejn.12877.


Overexpression of Homer1a in the basal and lateral amygdala impairs fear conditioning and induces an autism-like social impairment.

Banerjee A, Luong JA, Ho A, Saib AO, Ploski JE.

Mol Autism. 2016 Feb 29;7:16. doi: 10.1186/s13229-016-0077-9.


Developmental regulation of GABAergic signalling in the hippocampus of neuroligin 3 R451C knock-in mice: an animal model of Autism.

Pizzarelli R, Cherubini E.

Front Cell Neurosci. 2013 Jun 4;7:85. doi: 10.3389/fncel.2013.00085.


Valproate-induced neurodevelopmental deficits in Xenopus laevis tadpoles.

James EJ, Gu J, Ramirez-Vizcarrondo CM, Hasan M, Truszkowski TL, Tan Y, Oupravanh PM, Khakhalin AS, Aizenman CD.

J Neurosci. 2015 Feb 18;35(7):3218-29. doi: 10.1523/JNEUROSCI.4050-14.2015.


Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function.

Etherton M, Földy C, Sharma M, Tabuchi K, Liu X, Shamloo M, Malenka RC, Südhof TC.

Proc Natl Acad Sci U S A. 2011 Aug 16;108(33):13764-9. doi: 10.1073/pnas.1111093108.


Autism-related neuroligin-3 mutation alters social behavior and spatial learning.

Jaramillo TC, Liu S, Pettersen A, Birnbaum SG, Powell CM.

Autism Res. 2014 Apr;7(2):264-72. doi: 10.1002/aur.1362.


Exploring the relationship between cortical GABA concentrations, auditory gamma-band responses and development in ASD: Evidence for an altered maturational trajectory in ASD.

Port RG, Gaetz W, Bloy L, Wang DJ, Blaskey L, Kuschner ES, Levy SE, Brodkin ES, Roberts TP.

Autism Res. 2016 Oct 1. doi: 10.1002/aur.1686.


A review on the current neuroligin mouse models.

Xu JY, Xia QQ, Xia J.

Sheng Li Xue Bao. 2012 Oct 25;64(5):550-62. Review.


A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice.

Burrows EL, Laskaris L, Koyama L, Churilov L, Bornstein JC, Hill-Yardin EL, Hannan AJ.

Mol Autism. 2015 Nov 14;6:62. doi: 10.1186/s13229-015-0055-7.


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;8(4):416-25. doi: 10.1111/j.1601-183X.2009.00487.x.


High resolution magnetic resonance imaging for characterization of the neuroligin-3 knock-in mouse model associated with autism spectrum disorder.

Kumar M, Duda JT, Hwang WT, Kenworthy C, Ittyerah R, Pickup S, Brodkin ES, Gee JC, Abel T, Poptani H.

PLoS One. 2014 Oct 9;9(10):e109872. doi: 10.1371/journal.pone.0109872.

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