Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 293

1.

Altered surface mGluR5 dynamics provoke synaptic NMDAR dysfunction and cognitive defects in Fmr1 knockout mice.

Aloisi E, Le Corf K, Dupuis J, Zhang P, Ginger M, Labrousse V, Spatuzza M, Georg Haberl M, Costa L, Shigemoto R, Tappe-Theodor A, Drago F, Vincenzo Piazza P, Mulle C, Groc L, Ciranna L, Catania MV, Frick A.

Nat Commun. 2017 Oct 24;8(1):1103. doi: 10.1038/s41467-017-01191-2.

2.

RNA-binding proteins in neurodegeneration: mechanisms in aggregate.

Conlon EG, Manley JL.

Genes Dev. 2017 Aug 1;31(15):1509-1528. doi: 10.1101/gad.304055.117. Review. Erratum in: Genes Dev. 2017 Oct 1;31(19):2015.

PMID:
28912172
3.

Fragile X mental retardation protein regulates skeletal muscle stem cell activity by regulating the stability of Myf5 mRNA.

Fujita R, Zismanov V, Jacob JM, Jamet S, Asiev K, Crist C.

Skelet Muscle. 2017 Sep 7;7(1):18. doi: 10.1186/s13395-017-0136-8.

4.

Decreased surface expression of the δ subunit of the GABAA receptor contributes to reduced tonic inhibition in dentate granule cells in a mouse model of fragile X syndrome.

Zhang N, Peng Z, Tong X, Lindemeyer AK, Cetina Y, Huang CS, Olsen RW, Otis TS, Houser CR.

Exp Neurol. 2017 Nov;297:168-178. doi: 10.1016/j.expneurol.2017.08.008. Epub 2017 Aug 16.

PMID:
28822839
5.

Transcriptomic Analysis of Ribosome-Bound mRNA in Cortical Neurites In Vivo.

Ouwenga R, Lake AM, O'Brien D, Mogha A, Dani A, Dougherty JD.

J Neurosci. 2017 Sep 6;37(36):8688-8705. doi: 10.1523/JNEUROSCI.3044-16.2017. Epub 2017 Aug 8.

PMID:
28821669
6.

ESCRT-III Membrane Trafficking Misregulation Contributes To Fragile X Syndrome Synaptic Defects.

Vita DJ, Broadie K.

Sci Rep. 2017 Aug 17;7(1):8683. doi: 10.1038/s41598-017-09103-6.

7.

FXR1 regulates transcription and is required for growth of human cancer cells with TP53/FXR2 homozygous deletion.

Fan Y, Yue J, Xiao M, Han-Zhang H, Wang YV, Ma C, Deng Z, Li Y, Yu Y, Wang X, Niu S, Hua Y, Weng Z, Atadja P, Li E, Xiang B.

Elife. 2017 Aug 2;6. pii: e26129. doi: 10.7554/eLife.26129.

8.

A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms.

Lepeta K, Purzycka KJ, Pachulska-Wieczorek K, Mitjans M, Begemann M, Vafadari B, Bijata K, Adamiak RW, Ehrenreich H, Dziembowska M, Kaczmarek L.

EMBO Mol Med. 2017 Aug;9(8):1100-1116. doi: 10.15252/emmm.201707723.

9.

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
10.

Intrinsically disordered RGG/RG domains mediate degenerate specificity in RNA binding.

Ozdilek BA, Thompson VF, Ahmed NS, White CI, Batey RT, Schwartz JC.

Nucleic Acids Res. 2017 Jul 27;45(13):7984-7996. doi: 10.1093/nar/gkx460.

11.

RNA G-Quadruplexes in Biology: Principles and Molecular Mechanisms.

Fay MM, Lyons SM, Ivanov P.

J Mol Biol. 2017 Jul 7;429(14):2127-2147. doi: 10.1016/j.jmb.2017.05.017. Epub 2017 May 26. Review.

PMID:
28554731
12.

dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster.

Specchia V, D'Attis S, Puricella A, Bozzetti MP.

Int J Mol Sci. 2017 May 16;18(5). pii: E1066. doi: 10.3390/ijms18051066. Review.

13.

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
14.

Role of Splice Variants of Gtf2i, a Transcription Factor Localizing at Postsynaptic Sites, and Its Relation to Neuropsychiatric Diseases.

Shirai Y, Li W, Suzuki T.

Int J Mol Sci. 2017 Feb 15;18(2). pii: E411. doi: 10.3390/ijms18020411. Review.

15.

The tyrosine kinase receptor Tyro3 enhances lifespan and neuropeptide Y (Npy) neuron survival in the mouse anorexia (anx) mutation.

Kim DY, Yu J, Mui RK, Niibori R, Taufique HB, Aslam R, Semple JW, Cordes SP.

Dis Model Mech. 2017 May 1;10(5):581-595. doi: 10.1242/dmm.027433. Epub 2017 Jan 12.

16.

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.

17.

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.

18.

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.

19.

Scale Invariant Disordered Nanotopography Promotes Hippocampal Neuron Development and Maturation with Involvement of Mechanotransductive Pathways.

Schulte C, Ripamonti M, Maffioli E, Cappelluti MA, Nonnis S, Puricelli L, Lamanna J, Piazzoni C, Podestà A, Lenardi C, Tedeschi G, Malgaroli A, Milani P.

Front Cell Neurosci. 2016 Nov 18;10:267. eCollection 2016.

20.

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

Supplemental Content

Support Center