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Results: 1 to 20 of 44

References for PMC Articles for PubMed (Select 20952458)

1.

Motor coordination in autism spectrum disorders: a synthesis and meta-analysis.

Fournier KA, Hass CJ, Naik SK, Lodha N, Cauraugh JH.

J Autism Dev Disord. 2010 Oct;40(10):1227-40. doi: 10.1007/s10803-010-0981-3.

PMID:
20195737
2.

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.

3.

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.

Li HH, Roy M, Kuscuoglu U, Spencer CM, Halm B, Harrison KC, Bayle JH, Splendore A, Ding F, Meltzer LA, Wright E, Paylor R, Deisseroth K, Francke U.

EMBO Mol Med. 2009 Apr;1(1):50-65. doi: 10.1002/emmm.200900003.

4.

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.

5.

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.

6.

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders.

Betancur C, Sakurai T, Buxbaum JD.

Trends Neurosci. 2009 Jul;32(7):402-12. doi: 10.1016/j.tins.2009.04.003. Epub 2009 Jun 21. Review.

PMID:
19541375
7.

Neural mechanisms of a genome-wide supported psychosis variant.

Esslinger C, Walter H, Kirsch P, Erk S, Schnell K, Arnold C, Haddad L, Mier D, Opitz von Boberfeld C, Raab K, Witt SH, Rietschel M, Cichon S, Meyer-Lindenberg A.

Science. 2009 May 1;324(5927):605. doi: 10.1126/science.1167768.

8.

Neurotransmitters drive combinatorial multistate postsynaptic density networks.

Coba MP, Pocklington AJ, Collins MO, Kopanitsa MV, Uren RT, Swamy S, Croning MD, Choudhary JS, Grant SG.

Sci Signal. 2009 Apr 28;2(68):ra19. doi: 10.1126/scisignal.2000102.

9.

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice.

Chadman KK, Gong S, Scattoni ML, Boltuck SE, Gandhy SU, Heintz N, Crawley JN.

Autism Res. 2008 Jun;1(3):147-58. doi: 10.1002/aur.22.

10.

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. Epub 2009 Feb 11.

PMID:
19243448
11.

Removal of FKBP12 enhances mTOR-Raptor interactions, LTP, memory, and perseverative/repetitive behavior.

Hoeffer CA, Tang W, Wong H, Santillan A, Patterson RJ, Martinez LA, Tejada-Simon MV, Paylor R, Hamilton SL, Klann E.

Neuron. 2008 Dec 10;60(5):832-45. doi: 10.1016/j.neuron.2008.09.037.

12.

Neuroligins and neurexins link synaptic function to cognitive disease.

Südhof TC.

Nature. 2008 Oct 16;455(7215):903-11. doi: 10.1038/nature07456. Review.

13.

Identifying autism loci and genes by tracing recent shared ancestry.

Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.

Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657. Erratum in: Science. 2010 Dec 24;330(6012):1746.

14.

Immune transcriptome alterations in the temporal cortex of subjects with autism.

Garbett K, Ebert PJ, Mitchell A, Lintas C, Manzi B, Mirnics K, Persico AM.

Neurobiol Dis. 2008 Jun;30(3):303-11. doi: 10.1016/j.nbd.2008.01.012. Epub 2008 Mar 10.

15.

Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.

Hung AY, Futai K, Sala C, Valtschanoff JG, Ryu J, Woodworth MA, Kidd FL, Sung CC, Miyakawa T, Bear MF, Weinberg RJ, Sheng M.

J Neurosci. 2008 Feb 13;28(7):1697-708. doi: 10.1523/JNEUROSCI.3032-07.2008.

16.

Structural variation of chromosomes in autism spectrum disorder.

Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.

Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17.

17.

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.

Jamain S, Radyushkin K, Hammerschmidt K, Granon S, Boretius S, Varoqueaux F, Ramanantsoa N, Gallego J, Ronnenberg A, Winter D, Frahm J, Fischer J, Bourgeron T, Ehrenreich H, Brose N.

Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1710-5. doi: 10.1073/pnas.0711555105. Epub 2008 Jan 28.

18.

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

Järvinen-Pasley A, Bellugi U, Reilly J, Mills DL, Galaburda A, Reiss AL, Korenberg JR.

Dev Psychopathol. 2008 Winter;20(1):1-35. doi: 10.1017/S0954579408000011. Review.

19.

Fragile X: translation in action.

Bear MF, Dölen G, Osterweil E, Nagarajan N.

Neuropsychopharmacology. 2008 Jan;33(1):84-7. Epub 2007 Oct 17. Review.

20.

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 5;318(5847):71-6. Epub 2007 Sep 6.

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