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Items: 1 to 20 of 26

1.

Transcriptome-wide identification of NMD-targeted human mRNAs reveals extensive redundancy between SMG6- and SMG7-mediated degradation pathways.

Colombo M, Karousis ED, Bourquin J, Bruggmann R, Mühlemann O.

RNA. 2017 Feb;23(2):189-201. doi: 10.1261/rna.059055.116.

2.

Analysis of the Physiological Activities of Scd6 through Its Interaction with Hmt1.

Lien PT, Izumikawa K, Muroi K, Irie K, Suda Y, Irie K.

PLoS One. 2016 Oct 24;11(10):e0164773. doi: 10.1371/journal.pone.0164773.

3.

Who Regulates Whom? An Overview of RNA Granules and Viral Infections.

Poblete-Durán N, Prades-Pérez Y, Vera-Otarola J, Soto-Rifo R, Valiente-Echeverría F.

Viruses. 2016 Jun 28;8(7). pii: E180. doi: 10.3390/v8070180. Review.

5.

The feedback control of UPF3 is crucial for RNA surveillance in plants.

Degtiar E, Fridman A, Gottlieb D, Vexler K, Berezin I, Farhi R, Golani L, Shaul O.

Nucleic Acids Res. 2015 Apr 30;43(8):4219-35. doi: 10.1093/nar/gkv237.

6.

Phospho-dependent and phospho-independent interactions of the helicase UPF1 with the NMD factors SMG5-SMG7 and SMG6.

Chakrabarti S, Bonneau F, Schüssler S, Eppinger E, Conti E.

Nucleic Acids Res. 2014 Aug;42(14):9447-60. doi: 10.1093/nar/gku578.

7.

Identification and functional analysis of novel phosphorylation sites in the RNA surveillance protein Upf1.

Lasalde C, Rivera AV, León AJ, González-Feliciano JA, Estrella LA, Rodríguez-Cruz EN, Correa ME, Cajigas IJ, Bracho DP, Vega IE, Wilkinson MF, González CI.

Nucleic Acids Res. 2014 Feb;42(3):1916-29. doi: 10.1093/nar/gkt1049.

8.
9.

Selection of specific protein binders for pre-defined targets from an optimized library of artificial helicoidal repeat proteins (alphaRep).

Guellouz A, Valerio-Lepiniec M, Urvoas A, Chevrel A, Graille M, Fourati-Kammoun Z, Desmadril M, van Tilbeurgh H, Minard P.

PLoS One. 2013 Aug 27;8(8):e71512. doi: 10.1371/journal.pone.0071512.

10.

Comparison of EJC-enhanced and EJC-independent NMD in human cells reveals two partially redundant degradation pathways.

Metze S, Herzog VA, Ruepp MD, Mühlemann O.

RNA. 2013 Oct;19(10):1432-48. doi: 10.1261/rna.038893.113.

11.

Yeast hEST1A/B (SMG5/6)-like proteins contribute to environment-sensing adaptive gene expression responses.

Lai X, Beilharz T, Au WC, Hammet A, Preiss T, Basrai MA, Heierhorst J.

G3 (Bethesda). 2013 Oct 3;3(10):1649-59. doi: 10.1534/g3.113.006924.

12.

An unusual arrangement of two 14-3-3-like domains in the SMG5-SMG7 heterodimer is required for efficient nonsense-mediated mRNA decay.

Jonas S, Weichenrieder O, Izaurralde E.

Genes Dev. 2013 Jan 15;27(2):211-25. doi: 10.1101/gad.206672.112.

13.

NMD: a multifaceted response to premature translational termination.

Kervestin S, Jacobson A.

Nat Rev Mol Cell Biol. 2012 Nov;13(11):700-12. doi: 10.1038/nrm3454. Review.

14.

RNA degradation in Saccharomyces cerevisae.

Parker R.

Genetics. 2012 Jul;191(3):671-702. doi: 10.1534/genetics.111.137265. Review.

15.

Drosophila mutants show NMD pathway activity is reduced, but not eliminated, in the absence of Smg6.

Frizzell KA, Rynearson SG, Metzstein MM.

RNA. 2012 Aug;18(8):1475-86. doi: 10.1261/rna.032821.112.

16.

Functional analysis of the single Est1/Ebs1 homologue in Kluyveromyces lactis reveals roles in both telomere maintenance and rapamycin resistance.

Hsu M, Yu EY, Sprušanský O, McEachern MJ, Lue NF.

Eukaryot Cell. 2012 Jul;11(7):932-42. doi: 10.1128/EC.05319-11.

17.

The TPR-containing domain within Est1 homologs exhibits species-specific roles in telomerase interaction and telomere length homeostasis.

Sealey DC, Kostic AD, LeBel C, Pryde F, Harrington L.

BMC Mol Biol. 2011 Oct 18;12:45. doi: 10.1186/1471-2199-12-45.

18.

Quantitative fitness analysis shows that NMD proteins and many other protein complexes suppress or enhance distinct telomere cap defects.

Addinall SG, Holstein EM, Lawless C, Yu M, Chapman K, Banks AP, Ngo HP, Maringele L, Taschuk M, Young A, Ciesiolka A, Lister AL, Wipat A, Wilkinson DJ, Lydall D.

PLoS Genet. 2011 Apr;7(4):e1001362. doi: 10.1371/journal.pgen.1001362.

19.

Microtubule disruption targets HIF-1alpha mRNA to cytoplasmic P-bodies for translational repression.

Carbonaro M, O'Brate A, Giannakakou P.

J Cell Biol. 2011 Jan 10;192(1):83-99. doi: 10.1083/jcb.201004145.

20.

UPF1 association with the cap-binding protein, CBP80, promotes nonsense-mediated mRNA decay at two distinct steps.

Hwang J, Sato H, Tang Y, Matsuda D, Maquat LE.

Mol Cell. 2010 Aug 13;39(3):396-409. doi: 10.1016/j.molcel.2010.07.004.

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