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A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.

Dictenberg JB, Swanger SA, Antar LN, Singer RH, Bassell GJ.

Dev Cell. 2008 Jun;14(6):926-39. doi: 10.1016/j.devcel.2008.04.003.


Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses.

Antar LN, Li C, Zhang H, Carroll RC, Bassell GJ.

Mol Cell Neurosci. 2006 May-Jun;32(1-2):37-48. Epub 2006 May 2.


Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein.

Kao DI, Aldridge GM, Weiler IJ, Greenough WT.

Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15601-6. doi: 10.1073/pnas.1010564107. Epub 2010 Aug 16.


Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis.

De Rubeis S, Fernández E, Buzzi A, Di Marino D, Bagni C.

Adv Exp Med Biol. 2012;970:517-51. doi: 10.1007/978-3-7091-0932-8_23. Review.


Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome.

Gross C, Nakamoto M, Yao X, Chan CB, Yim SY, Ye K, Warren ST, Bassell GJ.

J Neurosci. 2010 Aug 11;30(32):10624-38. doi: 10.1523/JNEUROSCI.0402-10.2010.


Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons.

Levenga J, Buijsen RA, Rifé M, Moine H, Nelson DL, Oostra BA, Willemsen R, de Vrij FM.

Neurobiol Dis. 2009 Aug;35(2):241-50. doi: 10.1016/j.nbd.2009.05.004. Epub 2009 May 21.


Excessive astrocyte-derived neurotrophin-3 contributes to the abnormal neuronal dendritic development in a mouse model of fragile X syndrome.

Yang Q, Feng B, Zhang K, Guo YY, Liu SB, Wu YM, Li XQ, Zhao MG.

PLoS Genet. 2012;8(12):e1003172. doi: 10.1371/journal.pgen.1003172. Epub 2012 Dec 27.


Single-Molecule Imaging of PSD-95 mRNA Translation in Dendrites and Its Dysregulation in a Mouse Model of Fragile X Syndrome.

Ifrim MF, Williams KR, Bassell GJ.

J Neurosci. 2015 May 6;35(18):7116-30. doi: 10.1523/JNEUROSCI.2802-14.2015.


Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons.

Antar LN, Dictenberg JB, Plociniak M, Afroz R, Bassell GJ.

Genes Brain Behav. 2005 Aug;4(6):350-9.


Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome.

Zeier Z, Kumar A, Bodhinathan K, Feller JA, Foster TC, Bloom DC.

Gene Ther. 2009 Sep;16(9):1122-9. doi: 10.1038/gt.2009.83. Epub 2009 Jul 2.


Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.

Iliff AJ, Renoux AJ, Krans A, Usdin K, Sutton MA, Todd PK.

Hum Mol Genet. 2013 Mar 15;22(6):1180-92. doi: 10.1093/hmg/dds525. Epub 2012 Dec 18.


Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome.

Till SM, Wijetunge LS, Seidel VG, Harlow E, Wright AK, Bagni C, Contractor A, Gillingwater TH, Kind PC.

Hum Mol Genet. 2012 May 15;21(10):2143-56. doi: 10.1093/hmg/dds030. Epub 2012 Feb 9.


Fragile X syndrome: From protein function to therapy.

Bagni C, Oostra BA.

Am J Med Genet A. 2013 Nov;161A(11):2809-21. doi: 10.1002/ajmg.a.36241. Epub 2013 Sep 24. Review.


Fragile X mental retardation protein regulates the levels of scaffold proteins and glutamate receptors in postsynaptic densities.

Schütt J, Falley K, Richter D, Kreienkamp HJ, Kindler S.

J Biol Chem. 2009 Sep 18;284(38):25479-87. doi: 10.1074/jbc.M109.042663. Epub 2009 Jul 28.


Transport of fragile X mental retardation protein via granules in neurites of PC12 cells.

De Diego Otero Y, Severijnen LA, van Cappellen G, Schrier M, Oostra B, Willemsen R.

Mol Cell Biol. 2002 Dec;22(23):8332-41.


Delayed stabilization of dendritic spines in fragile X mice.

Cruz-Martín A, Crespo M, Portera-Cailliau C.

J Neurosci. 2010 Jun 9;30(23):7793-803. doi: 10.1523/JNEUROSCI.0577-10.2010.


Modulation of dendritic spines and synaptic function by Rac1: a possible link to Fragile X syndrome pathology.

Bongmba OY, Martinez LA, Elhardt ME, Butler K, Tejada-Simon MV.

Brain Res. 2011 Jul 5;1399:79-95. doi: 10.1016/j.brainres.2011.05.020. Epub 2011 May 17. Erratum in: Brain Res. 2011 Nov 14;1423:114-5.

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