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Items: 1 to 20 of 79


RNA-associated protein 55 (RAP55) localizes to mRNA processing bodies and stress granules.

Yang WH, Yu JH, Gulick T, Bloch KD, Bloch DB.

RNA. 2006 Apr;12(4):547-54. Epub 2006 Feb 16.


Akt-mediated YB-1 phosphorylation activates translation of silent mRNA species.

Evdokimova V, Ruzanov P, Anglesio MS, Sorokin AV, Ovchinnikov LP, Buckley J, Triche TJ, Sonenberg N, Sorensen PH.

Mol Cell Biol. 2006 Jan;26(1):277-92.


CAR-1, a protein that localizes with the mRNA decapping component DCAP-1, is required for cytokinesis and ER organization in Caenorhabditis elegans embryos.

Squirrell JM, Eggers ZT, Luedke N, Saari B, Grimson A, Lyons GE, Anderson P, White JG.

Mol Biol Cell. 2006 Jan;17(1):336-44. Epub 2005 Nov 2.


A complex containing the Sm protein CAR-1 and the RNA helicase CGH-1 is required for embryonic cytokinesis in Caenorhabditis elegans.

Audhya A, Hyndman F, McLeod IX, Maddox AS, Yates JR 3rd, Desai A, Oegema K.

J Cell Biol. 2005 Oct 24;171(2):267-79.


A conserved RNA-protein complex component involved in physiological germline apoptosis regulation in C. elegans.

Boag PR, Nakamura A, Blackwell TK.

Development. 2005 Nov;132(22):4975-86. Epub 2005 Oct 12.


General translational repression by activators of mRNA decapping.

Coller J, Parker R.

Cell. 2005 Sep 23;122(6):875-86.


A role for the eIF4E-binding protein 4E-T in P-body formation and mRNA decay.

Ferraiuolo MA, Basak S, Dostie J, Murray EL, Schoenberg DR, Sonenberg N.

J Cell Biol. 2005 Sep 12;170(6):913-24. Erratum in: J Cell Biol. 2005 Oct 10;171(1):175.


Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies.

Brengues M, Teixeira D, Parker R.

Science. 2005 Oct 21;310(5747):486-9. Epub 2005 Sep 1.


Crystal structure and functional analysis of DEAD-box protein Dhh1p.

Cheng Z, Coller J, Parker R, Song H.

RNA. 2005 Aug;11(8):1258-70. Epub 2005 Jun 29.


Requirement for P granules and meiosis for accumulation of the germline RNA helicase CGH-1.

Navarro RE, Blackwell TK.

Genesis. 2005 Jul;42(3):172-80.


Stress granules and processing bodies are dynamically linked sites of mRNP remodeling.

Kedersha N, Stoecklin G, Ayodele M, Yacono P, Lykke-Andersen J, Fritzler MJ, Scheuner D, Kaufman RJ, Golan DE, Anderson P.

J Cell Biol. 2005 Jun 20;169(6):871-84.


Expression of rck/p54, a DEAD-box RNA helicase, in gametogenesis and early embryogenesis of mice.

Matsumoto K, Kwon OY, Kim H, Akao Y.

Dev Dyn. 2005 Jul;233(3):1149-56.


Moving messages: the intracellular localization of mRNAs.

St Johnston D.

Nat Rev Mol Cell Biol. 2005 May;6(5):363-75. Review.


A role for eIF4E and eIF4E-transporter in targeting mRNPs to mammalian processing bodies.

Andrei MA, Ingelfinger D, Heintzmann R, Achsel T, Rivera-Pomar R, L├╝hrmann R.

RNA. 2005 May;11(5):717-27.


The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules.

Wilczynska A, Aigueperse C, Kress M, Dautry F, Weil D.

J Cell Sci. 2005 Mar 1;118(Pt 5):981-92.


Processing bodies require RNA for assembly and contain nontranslating mRNAs.

Teixeira D, Sheth U, Valencia-Sanchez MA, Brengues M, Parker R.

RNA. 2005 Apr;11(4):371-82. Epub 2005 Feb 9.


The DNA/RNA-binding protein MSY2 marks specific transcripts for cytoplasmic storage in mouse male germ cells.

Yang J, Medvedev S, Reddi PP, Schultz RM, Hecht NB.

Proc Natl Acad Sci U S A. 2005 Feb 1;102(5):1513-8. Epub 2005 Jan 21.


RNA localization mechanisms in oocytes.

Kloc M, Etkin LD.

J Cell Sci. 2005 Jan 15;118(Pt 2):269-82. Review.

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