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Items: 1 to 20 of 68

1.

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.

2.

CMP‑N‑acetylneuraminic acid synthetase interacts with fragile X related protein 1.

Ma Y, Tian S, Wang Z, Wang C, Chen X, Li W, Yang Y, He S.

Mol Med Rep. 2016 Aug;14(2):1501-8. doi: 10.3892/mmr.2016.5438. Epub 2016 Jun 23.

3.

RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway.

Kenny P, Ceman S.

Int J Mol Sci. 2016 Jun 22;17(6). pii: E985. doi: 10.3390/ijms17060985. Review.

4.

Synaptic vesicle dynamic changes in a model of fragile X.

Broek JA, Lin Z, de Gruiter HM, van 't Spijker H, Haasdijk ED, Cox D, Ozcan S, van Cappellen GW, 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.

5.

Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.

Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, Fischer U, Dityatev A, Grabe HJ, Rujescu D, Fischer A, Ehrenreich H.

EMBO Mol Med. 2015 Nov 26;7(12):1565-79. doi: 10.15252/emmm.201505696.

6.

Comparison of Equivalence between Two Commercially Available S499-Phosphorylated FMRP Antibodies in Mice.

Reynolds CD, Smith GD, Jefferson TS, Lugo JN.

PLoS One. 2015 Nov 18;10(11):e0143134. doi: 10.1371/journal.pone.0143134. eCollection 2015.

7.

Global Analysis of mRNA, Translation, and Protein Localization: Local Translation Is a Key Regulator of Cell Protrusions.

Mardakheh FK, Paul A, Kümper S, Sadok A, Paterson H, Mccarthy A, Yuan Y, Marshall CJ.

Dev Cell. 2015 Nov 9;35(3):344-57. doi: 10.1016/j.devcel.2015.10.005.

8.

The RNA binding protein FXR1 is a new driver in the 3q26-29 amplicon and predicts poor prognosis in human cancers.

Qian J, Hassanein M, Hoeksema MD, Harris BK, Zou Y, Chen H, Lu P, Eisenberg R, Wang J, Espinosa A, Ji X, Harris FT, Rahman SM, Massion PP.

Proc Natl Acad Sci U S A. 2015 Mar 17;112(11):3469-74. doi: 10.1073/pnas.1421975112. Epub 2015 Mar 2.

9.

Fragile X mental retardation protein: A paradigm for translational control by RNA-binding proteins.

Chen E, Joseph S.

Biochimie. 2015 Jul;114:147-54. doi: 10.1016/j.biochi.2015.02.005. Epub 2015 Feb 17. Review.

10.

A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function.

Okray Z, de Esch CE, Van Esch H, Devriendt K, Claeys A, Yan J, Verbeeck J, Froyen G, Willemsen R, de Vrij FM, Hassan BA.

EMBO Mol Med. 2015 Feb 17;7(4):423-37. doi: 10.15252/emmm.201404576.

11.

The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice.

Lumaban JG, Nelson DL.

Hum Mol Genet. 2015 Apr 15;24(8):2175-84. doi: 10.1093/hmg/ddu737. Epub 2014 Dec 30.

12.

A feed-forward mechanism involving Drosophila fragile X mental retardation protein triggers a replication stress-induced DNA damage response.

Zhang W, Cheng Y, Li Y, Chen Z, Jin P, Chen D.

Hum Mol Genet. 2014 Oct 1;23(19):5188-96. doi: 10.1093/hmg/ddu241. Epub 2014 May 15.

13.

FMRP S499 is phosphorylated independent of mTORC1-S6K1 activity.

Bartley CM, O'Keefe RA, Bordey A.

PLoS One. 2014 May 7;9(5):e96956. doi: 10.1371/journal.pone.0096956. eCollection 2014.

14.

Fragile X mental retardation protein regulates translation by binding directly to the ribosome.

Chen E, Sharma MR, Shi X, Agrawal RK, Joseph S.

Mol Cell. 2014 May 8;54(3):407-17. doi: 10.1016/j.molcel.2014.03.023. Epub 2014 Apr 17.

15.

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.

16.

A novel role for the RNA-binding protein FXR1P in myoblasts cell-cycle progression by modulating p21/Cdkn1a/Cip1/Waf1 mRNA stability.

Davidovic L, Durand N, Khalfallah O, Tabet R, Barbry P, Mari B, Sacconi S, Moine H, Bardoni B.

PLoS Genet. 2013 Mar;9(3):e1003367. doi: 10.1371/journal.pgen.1003367. Epub 2013 Mar 21.

17.

Chromosomal fragility and human genetic disorders.

Baskaran S, Brahmachari V.

Indian J Clin Biochem. 2000 Aug;15(Suppl 1):145-57. doi: 10.1007/BF02867554.

18.

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

El Fatimy R, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, Khandjian EW.

PLoS One. 2012;7(6):e39338. doi: 10.1371/journal.pone.0039338. Epub 2012 Jun 21. Erratum in: PLoS One. 2012;7(9). doi:10.1371/annotation/05374d07-34cf-483f-80f4-ec87374cbeb6.

19.

Conservation of the RNA Transport Machineries and Their Coupling to Translation Control across Eukaryotes.

Vazquez-Pianzola P, Suter B.

Comp Funct Genomics. 2012;2012:287852. doi: 10.1155/2012/287852. Epub 2012 May 15.

20.

Circadian rhythm-dependent alterations of gene expression in Drosophila brain lacking fragile X mental retardation protein.

Xu S, Poidevin M, Han E, Bi J, Jin P.

PLoS One. 2012;7(5):e37937. doi: 10.1371/journal.pone.0037937. Epub 2012 May 24.

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