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Items: 1 to 20 of 166

1.

Systematic mapping of fragile X granules in the mouse brain reveals a potential role for presynaptic FMRP in sensorimotor functions.

Akins MR, Leblanc HF, Stackpole EE, Chyung E, Fallon JR.

J Comp Neurol. 2012 Nov 1;520(16):3687-706. doi: 10.1002/cne.23123.

2.

The FXG: a presynaptic fragile X granule expressed in a subset of developing brain circuits.

Christie SB, Akins MR, Schwob JE, Fallon JR.

J Neurosci. 2009 Feb 4;29(5):1514-24. doi: 10.1523/JNEUROSCI.3937-08.2009.

3.

N-myristoylation regulates the axonal distribution of the Fragile X-related protein FXR2P.

Stackpole EE, Akins MR, Fallon JR.

Mol Cell Neurosci. 2014 Sep;62:42-50. doi: 10.1016/j.mcn.2014.08.003. Epub 2014 Aug 7.

4.

Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains.

Akins MR, Berk-Rauch HE, Kwan KY, Mitchell ME, Shepard KA, Korsak LI, Stackpole EE, Warner-Schmidt JL, Sestan N, Cameron HA, Fallon JR.

Hum Mol Genet. 2017 Jan 1;26(1):192-209. doi: 10.1093/hmg/ddw381.

PMID:
28082376
5.

Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.

Higashimori H, Schin CS, Chiang MS, Morel L, Shoneye TA, Nelson DL, Yang Y.

J Neurosci. 2016 Jul 6;36(27):7079-94. doi: 10.1523/JNEUROSCI.1069-16.2016.

6.

Activity-dependent regulation of release probability at excitatory hippocampal synapses: a crucial role of fragile X mental retardation protein in neurotransmission.

Wang XS, Peng CZ, Cai WJ, Xia J, Jin D, Dai Y, Luo XG, Klyachko VA, Deng PY.

Eur J Neurosci. 2014 May;39(10):1602-12. doi: 10.1111/ejn.12546. Epub 2014 Mar 20.

7.

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.

Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA.

Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):949-56. doi: 10.1073/pnas.1423094112. Epub 2015 Jan 5.

8.

Abnormal presynaptic short-term plasticity and information processing in a mouse model of fragile X syndrome.

Deng PY, Sojka D, Klyachko VA.

J Neurosci. 2011 Jul 27;31(30):10971-82. doi: 10.1523/JNEUROSCI.2021-11.2011.

9.

Synaptic vesicle dynamic changes in a model of fragile X.

Broek JAC, Lin Z, de Gruiter HM, van 't Spijker H, Haasdijk ED, Cox D, Ozcan S, van Cappellen GWA, Houtsmuller AB, Willemsen R, de Zeeuw CI, Bahn S.

Mol Autism. 2016 Mar 1;7:17. doi: 10.1186/s13229-016-0080-1. eCollection 2016.

10.

Genetic upregulation of BK channel activity normalizes multiple synaptic and circuit defects in a mouse model of fragile X syndrome.

Deng PY, Klyachko VA.

J Physiol. 2016 Jan 1;594(1):83-97. doi: 10.1113/JP271031. Epub 2015 Nov 18.

11.

Cellular distribution of the fragile X mental retardation protein in the mouse brain.

Zorio DA, Jackson CM, Liu Y, Rubel EW, Wang Y.

J Comp Neurol. 2017 Mar 1;525(4):818-849. doi: 10.1002/cne.24100. Epub 2016 Sep 16.

12.

Fragile X granules are a family of axonal ribonucleoprotein particles with circuit-dependent protein composition and mRNA cargos.

Chyung E, LeBlanc HF, Fallon JR, Akins MR.

J Comp Neurol. 2018 Jan 1;526(1):96-108. doi: 10.1002/cne.24321. Epub 2017 Sep 20.

PMID:
28884477
13.

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
14.

Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome.

Centonze D, Rossi S, Mercaldo V, Napoli I, Ciotti MT, De Chiara V, Musella A, Prosperetti C, Calabresi P, Bernardi G, Bagni C.

Biol Psychiatry. 2008 May 15;63(10):963-73. Epub 2007 Oct 29.

PMID:
18028882
15.

Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.

El Fatimy R, Davidovic L, Tremblay S, Jaglin X, Dury A, Robert C, De Koninck P, Khandjian EW.

PLoS Genet. 2016 Jul 27;12(7):e1006192. doi: 10.1371/journal.pgen.1006192. eCollection 2016 Jul.

16.

The state of synapses in fragile X syndrome.

Pfeiffer BE, Huber KM.

Neuroscientist. 2009 Oct;15(5):549-67. doi: 10.1177/1073858409333075. Epub 2009 Mar 26. Review.

17.

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.

PMID:
22351071
18.

Proteomics, ultrastructure, and physiology of hippocampal synapses in a fragile X syndrome mouse model reveal presynaptic phenotype.

Klemmer P, Meredith RM, Holmgren CD, Klychnikov OI, Stahl-Zeng J, Loos M, van der Schors RC, Wortel J, de Wit H, Spijker S, Rotaru DC, Mansvelder HD, Smit AB, Li KW.

J Biol Chem. 2011 Jul 22;286(29):25495-504. doi: 10.1074/jbc.M110.210260. Epub 2011 May 19.

19.

Increasing our understanding of human cognition through the study of Fragile X Syndrome.

Cook D, Nuro E, Murai KK.

Dev Neurobiol. 2014 Feb;74(2):147-77. doi: 10.1002/dneu.22096. Epub 2013 Jul 30. Review.

20.

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.

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