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Results: 1 to 20 of 203

Similar articles for PubMed (Select 17881655)

1.

The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.

Davidovic L, Jaglin XH, Lepagnol-Bestel AM, Tremblay S, Simonneau M, Bardoni B, Khandjian EW.

Hum Mol Genet. 2007 Dec 15;16(24):3047-58. Epub 2007 Sep 19.

2.

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.

3.

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.

PMID:
16098134
4.

The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.

Davidovic L, Bechara E, Gravel M, Jaglin XH, Tremblay S, Sik A, Bardoni B, Khandjian EW.

Hum Mol Genet. 2006 May 1;15(9):1525-38. Epub 2006 Mar 28.

5.

Dynamic association of the fragile X mental retardation protein as a messenger ribonucleoprotein between microtubules and polyribosomes.

Wang H, Dictenberg JB, Ku L, Li W, Bassell GJ, Feng Y.

Mol Biol Cell. 2008 Jan;19(1):105-14. Epub 2007 Oct 31.

6.
7.

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.

PMID:
16631377
9.

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.

Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM.

J Neurosci. 1997 Mar 1;17(5):1539-47.

10.

Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells.

Schrier M, Severijnen LA, Reis S, Rife M, van't Padje S, van Cappellen G, Oostra BA, Willemsen R.

Exp Neurol. 2004 Oct;189(2):343-53.

PMID:
15380484
12.

Myosin Va is required for the transport of fragile X mental retardation protein (FMRP) granules.

Lindsay AJ, McCaffrey MW.

Biol Cell. 2014 Feb;106(2):57-71. doi: 10.1111/boc.201200076. Epub 2014 Jan 8.

PMID:
24175909
13.
14.

The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain.

Aschrafi A, Cunningham BA, Edelman GM, Vanderklish PW.

Proc Natl Acad Sci U S A. 2005 Feb 8;102(6):2180-5. Epub 2005 Jan 31.

15.

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.

Mazroui R, Huot ME, Tremblay S, Filion C, Labelle Y, Khandjian EW.

Hum Mol Genet. 2002 Nov 15;11(24):3007-17.

16.

Identification of FMRP-associated mRNAs using yeast three-hybrid system.

Zou K, Liu J, Zhu N, Lin J, Liang Q, Brown WT, Shen Y, Zhong N.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):769-77. doi: 10.1002/ajmg.b.30678.

PMID:
18163424
17.

The transport of Staufen2-containing ribonucleoprotein complexes involves kinesin motor protein and is modulated by mitogen-activated protein kinase pathway.

Jeong JH, Nam YJ, Kim SY, Kim EG, Jeong J, Kim HK.

J Neurochem. 2007 Sep;102(6):2073-84. Epub 2007 Jun 22.

PMID:
17587311
18.

Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors.

Nakamoto M, Nalavadi V, Epstein MP, Narayanan U, Bassell GJ, Warren ST.

Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15537-42. Epub 2007 Sep 19.

19.
20.

Identification of mRNA/protein (mRNP) complexes containing Puralpha, mStaufen, fragile X protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor.

Ohashi S, Koike K, Omori A, Ichinose S, Ohara S, Kobayashi S, Sato TA, Anzai K.

J Biol Chem. 2002 Oct 4;277(40):37804-10. Epub 2002 Jul 29.

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