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Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication.

Bozdagi O, Sakurai T, Papapetrou D, Wang X, Dickstein DL, Takahashi N, Kajiwara Y, Yang M, Katz AM, Scattoni ML, Harris MJ, Saxena R, Silverman JL, Crawley JN, Zhou Q, Hof PR, Buxbaum JD.

Mol Autism. 2010 Dec 17;1(1):15. doi: 10.1186/2040-2392-1-15.


Validating γ oscillations and delayed auditory responses as translational biomarkers of autism.

Gandal MJ, Edgar JC, Ehrlichman RS, Mehta M, Roberts TP, Siegel SJ.

Biol Psychiatry. 2010 Dec 15;68(12):1100-6. doi: 10.1016/j.biopsych.2010.09.031.


NMDA receptor hypofunction in the dentate gyrus and impaired context discrimination in adult Fmr1 knockout mice.

Eadie BD, Cushman J, Kannangara TS, Fanselow MS, Christie BR.

Hippocampus. 2012 Feb;22(2):241-54. doi: 10.1002/hipo.20890. Epub 2010 Nov 3.


Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome.

Feyder M, Karlsson RM, Mathur P, Lyman M, Bock R, Momenan R, Munasinghe J, Scattoni ML, Ihne J, Camp M, Graybeal C, Strathdee D, Begg A, Alvarez VA, Kirsch P, Rietschel M, Cichon S, Walter H, Meyer-Lindenberg A, Grant SG, Holmes A.

Am J Psychiatry. 2010 Dec;167(12):1508-17. doi: 10.1176/appi.ajp.2010.10040484. Epub 2010 Oct 15.


Sociability and motor functions in Shank1 mutant mice.

Silverman JL, Turner SM, Barkan CL, Tolu SS, Saxena R, Hung AY, Sheng M, Crawley JN.

Brain Res. 2011 Mar 22;1380:120-37. doi: 10.1016/j.brainres.2010.09.026. Epub 2010 Sep 21.


Functional rescue of excitatory synaptic transmission in the developing hippocampus in Fmr1-KO mouse.

Meredith RM, de Jong R, Mansvelder HD.

Neurobiol Dis. 2011 Jan;41(1):104-10. doi: 10.1016/j.nbd.2010.08.026. Epub 2010 Sep 15.


Characterization and reversal of synaptic defects in the amygdala in a mouse model of fragile X syndrome.

Suvrathan A, Hoeffer CA, Wong H, Klann E, Chattarji S.

Proc Natl Acad Sci U S A. 2010 Jun 22;107(25):11591-6. doi: 10.1073/pnas.1002262107. Epub 2010 Jun 7.


Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.

Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U, Endris V, Roberts W, Szatmari P, Pinto D, Bonin M, Riess A, Engels H, Sprengel R, Scherer SW, Rappold GA.

Nat Genet. 2010 Jun;42(6):489-91. doi: 10.1038/ng.589. Epub 2010 May 16.


Linkage and candidate gene studies of autism spectrum disorders in European populations.

Holt R, Barnby G, Maestrini E, Bacchelli E, Brocklebank D, Sousa I, Mulder EJ, Kantojärvi K, Järvelä I, Klauck SM, Poustka F, Bailey AJ, Monaco AP; EU Autism MOLGEN Consortium.

Eur J Hum Genet. 2010 Sep;18(9):1013-9. doi: 10.1038/ejhg.2010.69. Epub 2010 May 5. Erratum in: Eur J Hum Genet. 2010 Sep;18(9):1020. Parr, Jeremy [added].


Diminished prevalence but preserved synaptic distribution of N-methyl-D-aspartate receptor subunits in the methyl CpG binding protein 2(MeCP2)-null mouse brain.

Maliszewska-Cyna E, Bawa D, Eubanks JH.

Neuroscience. 2010 Jul 14;168(3):624-32. doi: 10.1016/j.neuroscience.2010.03.065. Epub 2010 Apr 7.


Mechanism-based approaches to treating fragile X.

Dölen G, Carpenter RL, Ocain TD, Bear MF.

Pharmacol Ther. 2010 Jul;127(1):78-93. doi: 10.1016/j.pharmthera.2010.02.008. Epub 2010 Mar 18. Review.


NR1 knockdown mice as a representative model of the glutamate hypothesis of schizophrenia.

Ramsey AJ.

Prog Brain Res. 2009;179:51-8. doi: 10.1016/S0079-6123(09)17906-2. Epub 2009 Nov 20. Review.


Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.

Blundell J, Blaiss CA, Etherton MR, Espinosa F, Tabuchi K, Walz C, Bolliger MF, Südhof TC, Powell CM.

J Neurosci. 2010 Feb 10;30(6):2115-29. doi: 10.1523/JNEUROSCI.4517-09.2010.


Abnormal neural oscillations and synchrony in schizophrenia.

Uhlhaas PJ, Singer W.

Nat Rev Neurosci. 2010 Feb;11(2):100-13. doi: 10.1038/nrn2774. Review.


The female urine sniffing test: a novel approach for assessing reward-seeking behavior in rodents.

Malkesman O, Scattoni ML, Paredes D, Tragon T, Pearson B, Shaltiel G, Chen G, Crawley JN, Manji HK.

Biol Psychiatry. 2010 May 1;67(9):864-71. doi: 10.1016/j.biopsych.2009.10.018. Epub 2009 Dec 24.


Repetitive self-grooming behavior in the BTBR mouse model of autism is blocked by the mGluR5 antagonist MPEP.

Silverman JL, Tolu SS, Barkan CL, Crawley JN.

Neuropsychopharmacology. 2010 Mar;35(4):976-89. doi: 10.1038/npp.2009.201. Epub 2009 Dec 23.


Generation and characterization of FMR1 knockout zebrafish.

den Broeder MJ, van der Linde H, Brouwer JR, Oostra BA, Willemsen R, Ketting RF.

PLoS One. 2009 Nov 19;4(11):e7910. doi: 10.1371/journal.pone.0007910.


Altered neuroligin expression is involved in social deficits in a mouse model of the fragile X syndrome.

Dahlhaus R, El-Husseini A.

Behav Brain Res. 2010 Mar 17;208(1):96-105. doi: 10.1016/j.bbr.2009.11.019. Epub 2009 Nov 20.


MPEP reduces seizure severity in Fmr-1 KO mice over expressing human Abeta.

Westmark CJ, Westmark PR, Malter JS.

Int J Clin Exp Pathol. 2009 Oct 10;3(1):56-68.


Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.

Etherton MR, Blaiss CA, Powell CM, Südhof TC.

Proc Natl Acad Sci U S A. 2009 Oct 20;106(42):17998-8003. doi: 10.1073/pnas.0910297106. Epub 2009 Oct 12.

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