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Items: 1 to 20 of 175

1.
2.

Analysis of domains affecting intracellular localization of the FMRP protein.

Bardoni B, Sittler A, Shen Y, Mandel JL.

Neurobiol Dis. 1997;4(5):329-36.

PMID:
9440121
3.

NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes.

Bardoni B, Willemsen R, Weiler IJ, Schenck A, Severijnen LA, Hindelang C, Lalli E, Mandel JL.

Exp Cell Res. 2003 Sep 10;289(1):95-107.

PMID:
12941608
4.

A nuclear role for the Fragile X mental retardation protein.

Fridell RA, Benson RE, Hua J, Bogerd HP, Cullen BR.

EMBO J. 1996 Oct 1;15(19):5408-14.

5.
6.

FMR1 protein: conserved RNP family domains and selective RNA binding.

Ashley CT Jr, Wilkinson KD, Reines D, Warren ST.

Science. 1993 Oct 22;262(5133):563-6.

PMID:
7692601
7.

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.

Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM.

J Neurosci. 1997 Mar 1;17(5):1539-47.

9.

A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein.

Bardoni B, Schenck A, Mandel JL.

Hum Mol Genet. 1999 Dec;8(13):2557-66.

PMID:
10556305
10.

Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.

Tamanini F, Bontekoe C, Bakker CE, van Unen L, Anar B, Willemsen R, Yoshida M, Galjaard H, Oostra BA, Hoogeveen AT.

Hum Mol Genet. 1999 May;8(5):863-9.

PMID:
10196376
11.

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.

Exp Neurol. 2004 Oct;189(2):343-53.

PMID:
15380484
12.

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 1;343 Pt 3:517-23.

13.

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.

Feng Y, Absher D, Eberhart DE, Brown V, Malter HE, Warren ST.

Mol Cell. 1997 Dec;1(1):109-18.

14.

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 1;15(9):1525-38. Epub 2006 Mar 28.

PMID:
16571602
15.

Evidence that fragile X mental retardation protein is a negative regulator of translation.

Laggerbauer B, Ostareck D, Keidel EM, Ostareck-Lederer A, Fischer U.

Hum Mol Genet. 2001 Feb 15;10(4):329-38.

PMID:
11157796
16.

Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.

Khandjian EW, Bardoni B, Corbin F, Sittler A, Giroux S, Heitz D, Tremblay S, Pinset C, Montarras D, Rousseau F, Mandel J.

Hum Mol Genet. 1998 Dec;7(13):2121-8.

PMID:
9817930
17.

In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein.

Piazzon N, Rage F, Schlotter F, Moine H, Branlant C, Massenet S.

J Biol Chem. 2008 Feb 29;283(9):5598-610. Epub 2007 Dec 19.

18.

Association of FMRP with ribosomal precursor particles in the nucleolus.

Willemsen R, Bontekoe C, Tamanini F, Galjaard H, Hoogeveen A, Oostra B.

Biochem Biophys Res Commun. 1996 Aug 5;225(1):27-33.

PMID:
8769090
19.

Biology of the fragile X mental retardation protein, an RNA-binding protein.

Khandjian EW.

Biochem Cell Biol. 1999;77(4):331-42. Review.

PMID:
10546896
20.

Fragile X mental retardation: misregulation of protein synthesis in the developing brain?

Feng Y.

Microsc Res Tech. 2002 May 1;57(3):145-7. Review.

PMID:
12112449

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