253 related articles for article (PubMed ID: 16790844)
1. The fragile X mental retardation protein interacts with a distinct mRNA nuclear export factor NXF2.
Lai D; Sakkas D; Huang Y
RNA; 2006 Aug; 12(8):1446-9. PubMed ID: 16790844
[TBL] [Abstract][Full Text] [Related]
2. Fragile X mental retardation protein FMRP and the RNA export factor NXF2 associate with and destabilize Nxf1 mRNA in neuronal cells.
Zhang M; Wang Q; Huang Y
Proc Natl Acad Sci U S A; 2007 Jun; 104(24):10057-62. PubMed ID: 17548835
[TBL] [Abstract][Full Text] [Related]
3. The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.
Davidovic L; Bechara E; Gravel M; Jaglin XH; Tremblay S; Sik A; Bardoni B; Khandjian EW
Hum Mol Genet; 2006 May; 15(9):1525-38. PubMed ID: 16571602
[TBL] [Abstract][Full Text] [Related]
4. The C terminus of fragile X mental retardation protein interacts with the multi-domain Ran-binding protein in the microtubule-organising centre.
Menon RP; Gibson TJ; Pastore A
J Mol Biol; 2004 Oct; 343(1):43-53. PubMed ID: 15381419
[TBL] [Abstract][Full Text] [Related]
5. Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP.
Linder B; Plöttner O; Kroiss M; Hartmann E; Laggerbauer B; Meister G; Keidel E; Fischer U
Hum Mol Genet; 2008 Oct; 17(20):3236-46. PubMed ID: 18664458
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 16098134
[TBL] [Abstract][Full Text] [Related]
7. Fragile X mental retardation protein FMRP binds mRNAs in the nucleus.
Kim M; Bellini M; Ceman S
Mol Cell Biol; 2009 Jan; 29(1):214-28. PubMed ID: 18936162
[TBL] [Abstract][Full Text] [Related]
8. TAP/NXF1, the primary mRNA export receptor, specifically interacts with a neuronal RNA-binding protein HuD.
Saito K; Fujiwara T; Katahira J; Inoue K; Sakamoto H
Biochem Biophys Res Commun; 2004 Aug; 321(2):291-7. PubMed ID: 15358174
[TBL] [Abstract][Full Text] [Related]
9. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P.
Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL
Proc Natl Acad Sci U S A; 2001 Jul; 98(15):8844-9. PubMed ID: 11438699
[TBL] [Abstract][Full Text] [Related]
10. The fragile X mental retardation protein has nucleic acid chaperone properties.
Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL
Nucleic Acids Res; 2004; 32(7):2129-37. PubMed ID: 15096575
[TBL] [Abstract][Full Text] [Related]
11. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
Hu L; Chen Y; Evers S; Shen Y
Proteomics; 2005 Oct; 5(15):3979-90. PubMed ID: 16130171
[TBL] [Abstract][Full Text] [Related]
12. Identification of messenger RNAs and microRNAs associated with fragile X mental retardation protein.
Duan R; Jin P
Methods Mol Biol; 2006; 342():267-76. PubMed ID: 16957381
[TBL] [Abstract][Full Text] [Related]
13. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.
Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; Moine H
EMBO J; 2001 Sep; 20(17):4803-13. PubMed ID: 11532944
[TBL] [Abstract][Full Text] [Related]
14. NXF1/p15 heterodimers are essential for mRNA nuclear export in Drosophila.
Herold A; Klymenko T; Izaurralde E
RNA; 2001 Dec; 7(12):1768-80. PubMed ID: 11780633
[TBL] [Abstract][Full Text] [Related]
15. Methylation regulates the intracellular protein-protein and protein-RNA interactions of FMRP.
Dolzhanskaya N; Merz G; Aletta JM; Denman RB
J Cell Sci; 2006 May; 119(Pt 9):1933-46. PubMed ID: 16636078
[TBL] [Abstract][Full Text] [Related]
16. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse.
Bakker CE; de Diego Otero Y; Bontekoe C; Raghoe P; Luteijn T; Hoogeveen AT; Oostra BA; Willemsen R
Exp Cell Res; 2000 Jul; 258(1):162-70. PubMed ID: 10912798
[TBL] [Abstract][Full Text] [Related]
17. RNA-binding of the human cytomegalovirus transactivator protein UL69, mediated by arginine-rich motifs, is not required for nuclear export of unspliced RNA.
Toth Z; Lischka P; Stamminger T
Nucleic Acids Res; 2006; 34(4):1237-49. PubMed ID: 16500893
[TBL] [Abstract][Full Text] [Related]
18. Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P.
Tamanini F; Van Unen L; Bakker C; Sacchi N; Galjaard H; Oostra BA; Hoogeveen AT
Biochem J; 1999 Nov; 343 Pt 3(Pt 3):517-23. PubMed ID: 10527928
[TBL] [Abstract][Full Text] [Related]
19. New insights into fragile X syndrome: from molecules to neurobehaviors.
Jin P; Warren ST
Trends Biochem Sci; 2003 Mar; 28(3):152-8. PubMed ID: 12633995
[TBL] [Abstract][Full Text] [Related]
20. Fragile X mental retardation syndrome: structure of the KH1-KH2 domains of fragile X mental retardation protein.
Valverde R; Pozdnyakova I; Kajander T; Venkatraman J; Regan L
Structure; 2007 Sep; 15(9):1090-8. PubMed ID: 17850748
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]