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Items: 1 to 20 of 351

1.

Post-transcriptional regulation of mouse neurogenesis by Pumilio proteins.

Zhang M, Chen D, Xia J, Han W, Cui X, Neuenkirchen N, Hermes G, Sestan N, Lin H.

Genes Dev. 2017 Aug 9. doi: 10.1101/gad.298752.117. [Epub ahead of print]

PMID:
28794184
2.

Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome.

Thomson SR, Seo SS, Barnes SA, Louros SR, Muscas M, Dando O, Kirby C, Wyllie DJA, Hardingham GE, Kind PC, Osterweil EK.

Neuron. 2017 Aug 2;95(3):550-563.e5. doi: 10.1016/j.neuron.2017.07.013.

3.

Proteomic analyses of nucleus laminaris identified candidate targets of the fragile X mental retardation protein.

Sakano H, Zorio DAR, Wang X, Ting YS, Noble WS, MacCoss MJ, Rubel EW, Wang Y.

J Comp Neurol. 2017 Oct 15;525(15):3341-3359. doi: 10.1002/cne.24281. Epub 2017 Jul 24.

PMID:
28685837
4.

Fragile X targeted pharmacotherapy: lessons learned and future directions.

Erickson CA, Davenport MH, Schaefer TL, Wink LK, Pedapati EV, Sweeney JA, Fitzpatrick SE, Brown WT, Budimirovic D, Hagerman RJ, Hessl D, Kaufmann WE, Berry-Kravis E.

J Neurodev Disord. 2017 Jun 12;9:7. doi: 10.1186/s11689-017-9186-9. eCollection 2017. Review.

5.

Fragile X mental retardation protein recognizes a G quadruplex structure within the survival motor neuron domain containing 1 mRNA 5'-UTR.

McAninch DS, Heinaman AM, Lang CN, Moss KR, Bassell GJ, Rita Mihailescu M, Evans TL.

Mol Biosyst. 2017 Jul 25;13(8):1448-1457. doi: 10.1039/c7mb00070g.

PMID:
28612854
6.

Reduced Lateral Inhibition Impairs Olfactory Computations and Behaviors in a Drosophila Model of Fragile X Syndrome.

Franco LM, Okray Z, Linneweber GA, Hassan BA, Yaksi E.

Curr Biol. 2017 Apr 24;27(8):1111-1123. doi: 10.1016/j.cub.2017.02.065. Epub 2017 Mar 30.

7.

Moving messages in the developing brain-emerging roles for mRNA transport and local translation in neural stem cells.

Pilaz LJ, Silver DL.

FEBS Lett. 2017 Jun;591(11):1526-1539. doi: 10.1002/1873-3468.12626. Epub 2017 Apr 6. Review.

PMID:
28304078
8.

Enhanced expression of ADCY1 underlies aberrant neuronal signalling and behaviour in a syndromic autism model.

Sethna F, Feng W, Ding Q, Robison AJ, Feng Y, Wang H.

Nat Commun. 2017 Feb 20;8:14359. doi: 10.1038/ncomms14359.

9.

New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.

Abekhoukh S, Sahin HB, Grossi M, Zongaro S, Maurin T, Madrigal I, Kazue-Sugioka D, Raas-Rothschild A, Doulazmi M, Carrera P, Stachon A, Scherer S, Drula Do Nascimento MR, Trembleau A, Arroyo I, Szatmari P, Smith IM, Milà M, Smith AC, Giangrande A, Caillé I, Bardoni B.

Dis Model Mech. 2017 Apr 1;10(4):463-474. doi: 10.1242/dmm.025809. Epub 2017 Feb 9.

10.

RNA G-quadruplexes and their potential regulatory roles in translation.

Song J, Perreault JP, Topisirovic I, Richard S.

Translation (Austin). 2016 Oct 4;4(2):e1244031. doi: 10.1080/21690731.2016.1244031. eCollection 2016. Review.

11.

RNA G-quadruplexes: emerging mechanisms in disease.

Cammas A, Millevoi S.

Nucleic Acids Res. 2017 Feb 28;45(4):1584-1595. doi: 10.1093/nar/gkw1280.

12.

Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene.

Barasoain M, Barrenetxea G, Huerta I, Télez M, Criado B, Arrieta I.

Genes (Basel). 2016 Dec 13;7(12). pii: E123. Review.

13.

Mammalian FMRP S499 Is Phosphorylated by CK2 and Promotes Secondary Phosphorylation of FMRP.

Bartley CM, O'Keefe RA, Blice-Baum A, Mihailescu MR, Gong X, Miyares L, Karaca E, Bordey A.

eNeuro. 2016 Nov 21;3(6). pii: ENEURO.0092-16.2016. eCollection 2016 Nov-Dec.

14.

Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP).

LaFauci G, Adayev T, Kascsak R, Brown WT.

Genes (Basel). 2016 Dec 9;7(12). pii: E121. Review.

15.

Dynamic mRNA Transport and Local Translation in Radial Glial Progenitors of the Developing Brain.

Pilaz LJ, Lennox AL, Rouanet JP, Silver DL.

Curr Biol. 2016 Dec 19;26(24):3383-3392. doi: 10.1016/j.cub.2016.10.040. Epub 2016 Dec 1.

PMID:
27916527
16.

Dysregulation of mRNA Localization and Translation in Genetic Disease.

Wang ET, Taliaferro JM, Lee JA, Sudhakaran IP, Rossoll W, Gross C, Moss KR, Bassell GJ.

J Neurosci. 2016 Nov 9;36(45):11418-11426. Review.

17.

Novel roles of amyloid-beta precursor protein metabolites in fragile X syndrome and autism.

Westmark CJ, Sokol DK, Maloney B, Lahiri DK.

Mol Psychiatry. 2016 Oct;21(10):1333-41. doi: 10.1038/mp.2016.134. Epub 2016 Aug 30. Review.

18.

Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome.

Tabolacci E, Palumbo F, Nobile V, Neri G.

Genes (Basel). 2016 Aug 17;7(8). pii: E49. doi: 10.3390/genes7080049. Review.

19.

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.

20.

Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP.

Majumder P, Chu JF, Chatterjee B, Swamy KB, Shen CJ.

Acta Neuropathol. 2016 Nov;132(5):721-738. Epub 2016 Aug 12.

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