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Items: 1 to 20 of 80

1.

RNA and microRNAs in fragile X mental retardation.

Jin P, Alisch RS, Warren ST.

Nat Cell Biol. 2004 Nov;6(11):1048-53. Review.

PMID:
15516998
2.

Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway.

Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, Nelson DL, Moses K, Warren ST.

Nat Neurosci. 2004 Feb;7(2):113-7.

PMID:
14703574
3.
4.

New insights into fragile X syndrome: from molecules to neurobehaviors.

Jin P, Warren ST.

Trends Biochem Sci. 2003 Mar;28(3):152-8. Review.

PMID:
12633995
5.

The Fragile X mental retardation protein.

Bardoni B, Schenck A, Mandel JL.

Brain Res Bull. 2001 Oct-Nov 1;56(3-4):375-82. Review.

PMID:
11719275
6.

The fragile X mental retardation protein, FMRP, recognizes G-quartets.

Darnell JC, Warren ST, Darnell RB.

Ment Retard Dev Disabil Res Rev. 2004;10(1):49-52. Review.

PMID:
14994288
7.

Sunrise at the synapse: the FMRP mRNP shaping the synaptic interface.

Antar LN, Bassell GJ.

Neuron. 2003 Feb 20;37(4):555-8. Review.

8.

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function.

Darnell JC, Jensen KB, Jin P, Brown V, Warren ST, Darnell RB.

Cell. 2001 Nov 16;107(4):489-99.

9.
10.

Fragile X mental retardation protein in learning-related synaptic plasticity.

Mercaldo V, Descalzi G, Zhuo M.

Mol Cells. 2009 Dec 31;28(6):501-7. doi: 10.1007/s10059-009-0193-x. Review.

11.

The fragile X syndrome: from molecular genetics to neurobiology.

Willemsen R, Oostra BA, Bassell GJ, Dictenberg J.

Ment Retard Dev Disabil Res Rev. 2004;10(1):60-7. Review.

PMID:
14994290
12.

The fragile X syndrome: exploring its molecular basis and seeking a treatment.

Bardoni B, Davidovic L, Bensaid M, Khandjian EW.

Expert Rev Mol Med. 2006 Apr 21;8(8):1-16. Review.

PMID:
16626504
13.

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.

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.

15.

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.

16.
17.

Role of microRNA pathway in mental retardation.

Qurashi A, Chang S, Peng J.

ScientificWorldJournal. 2007 Nov 2;7:146-54. Review.

18.

Differential translation and fragile X syndrome.

Vanderklish PW, Edelman GM.

Genes Brain Behav. 2005 Aug;4(6):360-84. Review.

19.

Translational regulation of the human achaete-scute homologue-1 by fragile X mental retardation protein.

Fähling M, Mrowka R, Steege A, Kirschner KM, Benko E, Förstera B, Persson PB, Thiele BJ, Meier JC, Scholz H.

J Biol Chem. 2009 Feb 13;284(7):4255-66. doi: 10.1074/jbc.M807354200.

20.

[Fragile X syndrome, a disease caused by defects in an RNA-binding protein].

Siomi MC, Siomi H.

Tanpakushitsu Kakusan Koso. 2003 Mar;48(4 Suppl):480-6. Review. Japanese. No abstract available.

PMID:
12696157
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