PubMed for id: 411940

Year	Number of Results
1991	1
1993	7
1994	1
1995	3
1996	2
1997	1
1998	1
1999	2
2001	5
2002	2
2004	1
2006	1
2008	1
2009	1
2010	1
2012	1
2014	3
2015	1
2024	0

1

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. Myrick LK, et al. Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):949-56. doi: 10.1073/pnas.1423094112. Epub 2015 Jan 5. Proc Natl Acad Sci U S A. 2015. PMID: 25561520 Free PMC article.

2

MOV10 and FMRP regulate AGO2 association with microRNA recognition elements.

Kenny PJ, Zhou H, Kim M, Skariah G, Khetani RS, Drnevich J, Arcila ML, Kosik KS, Ceman S. Kenny PJ, et al. Cell Rep. 2014 Dec 11;9(5):1729-1741. doi: 10.1016/j.celrep.2014.10.054. Epub 2014 Nov 20. Cell Rep. 2014. PMID: 25464849 Free PMC article.

3

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

Corominas R, Yang X, Lin GN, Kang S, Shen Y, Ghamsari L, Broly M, Rodriguez M, Tam S, Wanamaker SA, Fan C, Yi S, Tasan M, Lemmens I, Kuang X, Zhao N, Malhotra D, Michaelson JJ, Vacic V, Calderwood MA, Roth FP, Tavernier J, Horvath S, Salehi-Ashtiani K, Korkin D, Sebat J, Hill DE, Hao T, Vidal M, Iakoucheva LM. Corominas R, et al. Nat Commun. 2014 Apr 11;5:3650. doi: 10.1038/ncomms4650. Nat Commun. 2014. PMID: 24722188 Free PMC article.

4

Fragile X syndrome due to a missense mutation.

Myrick LK, Nakamoto-Kinoshita M, Lindor NM, Kirmani S, Cheng X, Warren ST. Myrick LK, et al. Eur J Hum Genet. 2014 Oct;22(10):1185-9. doi: 10.1038/ejhg.2013.311. Epub 2014 Jan 22. Eur J Hum Genet. 2014. PMID: 24448548 Free PMC article.

5

FMRP targets distinct mRNA sequence elements to regulate protein expression.

Ascano M Jr, Mukherjee N, Bandaru P, Miller JB, Nusbaum JD, Corcoran DL, Langlois C, Munschauer M, Dewell S, Hafner M, Williams Z, Ohler U, Tuschl T. Ascano M Jr, et al. Nature. 2012 Dec 20;492(7429):382-6. doi: 10.1038/nature11737. Epub 2012 Dec 12. Nature. 2012. PMID: 23235829 Free PMC article.

6

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.

Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. Collins SC, et al. Am J Med Genet A. 2010 Oct;152A(10):2512-20. doi: 10.1002/ajmg.a.33626. Am J Med Genet A. 2010. PMID: 20799337 Free PMC article.

7

A novel function for fragile X mental retardation protein in translational activation.

Bechara EG, Didiot MC, Melko M, Davidovic L, Bensaid M, Martin P, Castets M, Pognonec P, Khandjian EW, Moine H, Bardoni B. Bechara EG, et al. PLoS Biol. 2009 Jan 20;7(1):e16. doi: 10.1371/journal.pbio.1000016. PLoS Biol. 2009. PMID: 19166269 Free PMC article.

8

The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer.

Didiot MC, Tian Z, Schaeffer C, Subramanian M, Mandel JL, Moine H. Didiot MC, et al. Nucleic Acids Res. 2008 Sep;36(15):4902-12. doi: 10.1093/nar/gkn472. Epub 2008 Jul 24. Nucleic Acids Res. 2008. PMID: 18653529 Free PMC article.

9

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. Antar LN, et al. Mol Cell Neurosci. 2006 May-Jun;32(1-2):37-48. doi: 10.1016/j.mcn.2006.02.001. Epub 2006 May 2. Mol Cell Neurosci. 2006. PMID: 16631377

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. Schrier M, et al. Exp Neurol. 2004 Oct;189(2):343-53. doi: 10.1016/j.expneurol.2004.05.039. Exp Neurol. 2004. PMID: 15380484

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