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Items: 1 to 20 of 162

1.

SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.

Durand CM, Perroy J, Loll F, Perrais D, Fagni L, Bourgeron T, Montcouquiol M, Sans N.

Mol Psychiatry. 2012 Jan;17(1):71-84. doi: 10.1038/mp.2011.57.

2.

Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.

Arons MH, Thynne CJ, Grabrucker AM, Li D, Schoen M, Cheyne JE, Boeckers TM, Montgomery JM, Garner CC.

J Neurosci. 2012 Oct 24;32(43):14966-78. doi: 10.1523/JNEUROSCI.2215-12.2012.

3.

The PSD protein ProSAP2/Shank3 displays synapto-nuclear shuttling which is deregulated in a schizophrenia-associated mutation.

Grabrucker S, Proepper C, Mangus K, Eckert M, Chhabra R, Schmeisser MJ, Boeckers TM, Grabrucker AM.

Exp Neurol. 2014 Mar;253:126-37. doi: 10.1016/j.expneurol.2013.12.015.

PMID:
24382453
4.

Vasodilator-stimulated phosphoprotein (VASP) induces actin assembly in dendritic spines to promote their development and potentiate synaptic strength.

Lin WH, Nebhan CA, Anderson BR, Webb DJ.

J Biol Chem. 2010 Nov 12;285(46):36010-20. doi: 10.1074/jbc.M110.129841.

5.

SHANK3 gene mutations associated with autism facilitate ligand binding to the Shank3 ankyrin repeat region.

Mameza MG, Dvoretskova E, Bamann M, Hönck HH, Güler T, Boeckers TM, Schoen M, Verpelli C, Sala C, Barsukov I, Dityatev A, Kreienkamp HJ.

J Biol Chem. 2013 Sep 13;288(37):26697-708. doi: 10.1074/jbc.M112.424747.

6.

Linkage of the actin cytoskeleton to the postsynaptic density via direct interactions of Abp1 with the ProSAP/Shank family.

Qualmann B, Boeckers TM, Jeromin M, Gundelfinger ED, Kessels MM.

J Neurosci. 2004 Mar 10;24(10):2481-95. Erratum in: J Neurosci. 2004 Apr 14;24(15):following 3849.

7.

Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.

Roussignol G, Ango F, Romorini S, Tu JC, Sala C, Worley PF, Bockaert J, Fagni L.

J Neurosci. 2005 Apr 6;25(14):3560-70.

8.

Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.

Cochoy DM, Kolevzon A, Kajiwara Y, Schoen M, Pascual-Lucas M, Lurie S, Buxbaum JD, Boeckers TM, Schmeisser MJ.

Mol Autism. 2015 Apr 29;6:23. doi: 10.1186/s13229-015-0020-5.

9.

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.

Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsäter H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T.

Nat Genet. 2007 Jan;39(1):25-7.

10.

The actin-binding protein Abp1 controls dendritic spine morphology and is important for spine head and synapse formation.

Haeckel A, Ahuja R, Gundelfinger ED, Qualmann B, Kessels MM.

J Neurosci. 2008 Oct 1;28(40):10031-44. doi: 10.1523/JNEUROSCI.0336-08.2008.

11.

Postsynaptic PDLIM5/Enigma Homolog binds SPAR and causes dendritic spine shrinkage.

Herrick S, Evers DM, Lee JY, Udagawa N, Pak DT.

Mol Cell Neurosci. 2010 Feb;43(2):188-200. doi: 10.1016/j.mcn.2009.10.009.

12.

Myosin IIb controls actin dynamics underlying the dendritic spine maturation.

Koskinen M, Bertling E, Hotulainen R, Tanhuanpää K, Hotulainen P.

Mol Cell Neurosci. 2014 Jul;61:56-64. doi: 10.1016/j.mcn.2014.05.008.

PMID:
24938665
13.

Cortactin-binding protein 2 modulates the mobility of cortactin and regulates dendritic spine formation and maintenance.

Chen YK, Hsueh YP.

J Neurosci. 2012 Jan 18;32(3):1043-55. doi: 10.1523/JNEUROSCI.4405-11.2012.

14.
15.

The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

Fujii R, Okabe S, Urushido T, Inoue K, Yoshimura A, Tachibana T, Nishikawa T, Hicks GG, Takumi T.

Curr Biol. 2005 Mar 29;15(6):587-93.

16.

Vezatin is essential for dendritic spine morphogenesis and functional synaptic maturation.

Danglot L, Freret T, Le Roux N, Narboux Nême N, Burgo A, Hyenne V, Roumier A, Contremoulins V, Dauphin F, Bizot JC, Vodjdani G, Gaspar P, Boulouard M, Poncer JC, Galli T, Simmler MC.

J Neurosci. 2012 Jun 27;32(26):9007-22. doi: 10.1523/JNEUROSCI.3084-11.2012.

17.
18.

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.

Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T.

PLoS Genet. 2014 Sep 4;10(9):e1004580. doi: 10.1371/journal.pgen.1004580.

19.

PTEN knockdown alters dendritic spine/protrusion morphology, not density.

Haws ME, Jaramillo TC, Espinosa F, Widman AJ, Stuber GD, Sparta DR, Tye KM, Russo SJ, Parada LF, Stavarache M, Kaplitt M, Bonci A, Powell CM.

J Comp Neurol. 2014 Apr 1;522(5):1171-90. doi: 10.1002/cne.23488.

20.

Contribution of SHANK3 mutations to autism spectrum disorder.

Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW.

Am J Hum Genet. 2007 Dec;81(6):1289-97.

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