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Items: 1 to 20 of 144

1.

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction.

Sowers LP, Loo L, Wu Y, Campbell E, Ulrich JD, Wu S, Paemka L, Wassink T, Meyer K, Bing X, El-Shanti H, Usachev YM, Ueno N, Manak JR, Shepherd AJ, Ferguson PJ, Darbro BW, Richerson GB, Mohapatra DP, Wemmie JA, Bassuk AG.

Mol Psychiatry. 2013 Oct;18(10):1077-89. doi: 10.1038/mp.2013.71. Epub 2013 May 28. Erratum in: Mol Psychiatry. 2014 Jun;19(6):742. Manak, R J [corrected to Manak, J R].

2.

The non-canonical Wnt ligand Wnt5a rescues morphological deficits in Prickle2-deficient hippocampal neurons.

Sowers LP, Mouw TJ, Ferguson PJ, Wemmie JA, Mohapatra DP, Bassuk AG.

Mol Psychiatry. 2013 Oct;18(10):1049. doi: 10.1038/mp.2013.119. No abstract available.

PMID:
24056908
3.

Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.

Mohn JL, Alexander J, Pirone A, Palka CD, Lee SY, Mebane L, Haydon PG, Jacob MH.

Mol Psychiatry. 2014 Oct;19(10):1133-42. doi: 10.1038/mp.2014.61. Epub 2014 Jun 17.

4.

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.

5.

Defective motile cilia in Prickle2-deficient mice.

Sowers LP, Yin T, Mahajan VB, Bassuk AG.

J Neurogenet. 2014 Mar-Jun;28(1-2):146-52. doi: 10.3109/01677063.2014.885966. Epub 2014 Apr 7.

PMID:
24708399
6.

Impaired synaptic clustering of postsynaptic density proteins and altered signal transmission in hippocampal neurons, and disrupted learning behavior in PDZ1 and PDZ2 ligand binding-deficient PSD-95 knockin mice.

Nagura H, Ishikawa Y, Kobayashi K, Takao K, Tanaka T, Nishikawa K, Tamura H, Shiosaka S, Suzuki H, Miyakawa T, Fujiyoshi Y, Doi T.

Mol Brain. 2012 Dec 26;5:43. doi: 10.1186/1756-6606-5-43.

7.

PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders.

Paemka L, Mahajan VB, Skeie JM, Sowers LP, Ehaideb SN, Gonzalez-Alegre P, Sasaoka T, Tao H, Miyagi A, Ueno N, Takao K, Miyakawa T, Wu S, Darbro BW, Ferguson PJ, Pieper AA, Britt JK, Wemmie JA, Rudd DS, Wassink T, El-Shanti H, Mefford HC, Carvill GL, Manak JR, Bassuk AG.

PLoS One. 2013 Dec 3;8(12):e80737. doi: 10.1371/journal.pone.0080737. eCollection 2013.

8.

Mutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in Mice.

Zheng F, Kasper LH, Bedford DC, Lerach S, Teubner BJ, Brindle PK.

PLoS One. 2016 Jan 5;11(1):e0146366. doi: 10.1371/journal.pone.0146366. eCollection 2016.

9.

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.

Morice E, Farley S, Poirier R, Dallerac G, Chagneau C, Pannetier S, Hanauer A, Davis S, Vaillend C, Laroche S.

Neurobiol Dis. 2013 Oct;58:156-68. doi: 10.1016/j.nbd.2013.05.016. Epub 2013 Jun 3.

PMID:
23742761
10.

Increased Dosage of High-Affinity Kainate Receptor Gene grik4 Alters Synaptic Transmission and Reproduces Autism Spectrum Disorders Features.

Aller MI, Pecoraro V, Paternain AV, Canals S, Lerma J.

J Neurosci. 2015 Oct 7;35(40):13619-28. doi: 10.1523/JNEUROSCI.2217-15.2015.

11.

SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth.

Corradi A, Fadda M, Piton A, Patry L, Marte A, Rossi P, Cadieux-Dion M, Gauthier J, Lapointe L, Mottron L, Valtorta F, Rouleau GA, Fassio A, Benfenati F, Cossette P.

Hum Mol Genet. 2014 Jan 1;23(1):90-103. doi: 10.1093/hmg/ddt401. Epub 2013 Aug 15.

12.

Prickle2 is localized in the postsynaptic density and interacts with PSD-95 and NMDA receptors in the brain.

Hida Y, Fukaya M, Hagiwara A, Deguchi-Tawarada M, Yoshioka T, Kitajima I, Inoue E, Watanabe M, Ohtsuka T.

J Biochem. 2011 Jun;149(6):693-700. doi: 10.1093/jb/mvr023. Epub 2011 Feb 15.

PMID:
21324980
13.

Repetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum Disorders.

Wurzman R, Forcelli PA, Griffey CJ, Kromer LF.

Behav Brain Res. 2015 Feb 1;278:115-28. doi: 10.1016/j.bbr.2014.09.012. Epub 2014 Oct 2.

14.

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. Epub 2014 Mar 11.

15.

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.

16.

Impaired hippocampus-dependent spatial flexibility and sociability represent autism-like phenotypes in GluK2 mice.

Micheau J, Vimeney A, Normand E, Mulle C, Riedel G.

Hippocampus. 2014 Sep;24(9):1059-69. doi: 10.1002/hipo.22290. Epub 2014 Apr 30.

PMID:
24753134
17.

CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation.

Tanabe Y, Fujita-Jimbo E, Momoi MY, Momoi T.

J Neurochem. 2015 Aug;134(4):783-93. doi: 10.1111/jnc.13168. Epub 2015 Jun 3.

18.

A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.

Martin PM, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok PY, Moon RT, Cheyette BN.

Transl Psychiatry. 2013 Sep 3;3:e301. doi: 10.1038/tp.2013.75.

19.

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies.

Shimamoto C, Ohnishi T, Maekawa M, Watanabe A, Ohba H, Arai R, Iwayama Y, Hisano Y, Toyota T, Toyoshima M, Suzuki K, Shirayama Y, Nakamura K, Mori N, Owada Y, Kobayashi T, Yoshikawa T.

Hum Mol Genet. 2014 Dec 15;23(24):6495-511. doi: 10.1093/hmg/ddu369. Epub 2014 Jul 15. Erratum in: Hum Mol Genet. 2015 Apr 15;24(8):2409.

20.

Learning delays in a mouse model of Autism Spectrum Disorder.

Rendall AR, Truong DT, Fitch RH.

Behav Brain Res. 2016 Apr 15;303:201-7. doi: 10.1016/j.bbr.2016.02.006. Epub 2016 Feb 9.

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