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Results: 1 to 20 of 62

1.

Rab-GDI complex dissociation factor expressed through translational frameshifting in filamentous ascomycetes.

Malagnac F, Fabret C, Prigent M, Rousset JP, Namy O, Silar P.

PLoS One. 2013 Sep 19;8(9):e73772. doi: 10.1371/journal.pone.0073772. eCollection 2013.

PMID:
24069231
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Sense from nonsense: therapies for premature stop codon diseases.

Bidou L, Allamand V, Rousset JP, Namy O.

Trends Mol Med. 2012 Nov;18(11):679-88. doi: 10.1016/j.molmed.2012.09.008. Epub 2012 Oct 17. Review.

PMID:
23083810
[PubMed - indexed for MEDLINE]
3.

Statistical analysis of readthrough levels for nonsense mutations in mammalian cells reveals a major determinant of response to gentamicin.

Floquet C, Hatin I, Rousset JP, Bidou L.

PLoS Genet. 2012;8(3):e1002608. doi: 10.1371/journal.pgen.1002608. Epub 2012 Mar 29.

PMID:
22479203
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

[Allele-specific therapy: suppression of nonsense mutations by readthrough inducers].

Floquet C, Rousset JP, Bidou L.

Med Sci (Paris). 2012 Feb;28(2):193-9. doi: 10.1051/medsci/2012282018. Epub 2012 Feb 27. Review. French.

PMID:
22377308
[PubMed - indexed for MEDLINE]
Free Article
5.

Readthrough of premature termination codons in the adenomatous polyposis coli gene restores its biological activity in human cancer cells.

Floquet C, Rousset JP, Bidou L.

PLoS One. 2011;6(8):e24125. doi: 10.1371/journal.pone.0024125. Epub 2011 Aug 31.

PMID:
21909382
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

[Rescue of nonsense mutated p53 by readthrough leads to apoptosis in cancers cells].

Floquet C, Rousset JP, Bidou L.

Med Sci (Paris). 2011 Jun-Jul;27(6-7):585-6. doi: 10.1051/medsci/2011276008. Epub 2011 Jul 1. French. No abstract available.

PMID:
21718640
[PubMed - indexed for MEDLINE]
Free Article
7.

A mutation within the C-terminal domain of Sup35p that affects [PSI+] prion propagation.

Kabani M, Cosnier B, Bousset L, Rousset JP, Melki R, Fabret C.

Mol Microbiol. 2011 Aug;81(3):640-58. doi: 10.1111/j.1365-2958.2011.07719.x. Epub 2011 Jun 16.

PMID:
21631606
[PubMed - indexed for MEDLINE]
8.

A viable hypomorphic allele of the essential IMP3 gene reveals novel protein functions in Saccharomyces cerevisiae.

Cosnier B, Kwapisz M, Hatin I, Namy O, Hermann-Le Denmat S, Morillon A, Rousset JP, Fabret C.

PLoS One. 2011 Apr 29;6(4):e19500. doi: 10.1371/journal.pone.0019500. Erratum in: PLoS One. 2011;6(5). doi:10.1371/annotation/18c67950-0fcc-4ba8-aa59-5d6a3e060c68.

PMID:
21559332
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A role for the universal Kae1/Qri7/YgjD (COG0533) family in tRNA modification.

El Yacoubi B, Hatin I, Deutsch C, Kahveci T, Rousset JP, Iwata-Reuyl D, Murzin AG, de Crécy-Lagard V.

EMBO J. 2011 Mar 2;30(5):882-93. doi: 10.1038/emboj.2010.363. Epub 2011 Feb 1.

PMID:
21285948
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Rescue of non-sense mutated p53 tumor suppressor gene by aminoglycosides.

Floquet C, Deforges J, Rousset JP, Bidou L.

Nucleic Acids Res. 2011 Apr;39(8):3350-62. doi: 10.1093/nar/gkq1277. Epub 2010 Dec 10.

PMID:
21149266
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Translational errors: from yeast to new therapeutic targets.

Bidou L, Rousset JP, Namy O.

FEMS Yeast Res. 2010 Dec;10(8):1070-82. doi: 10.1111/j.1567-1364.2010.00684.x. Epub 2010 Oct 18. Review.

PMID:
20955199
[PubMed - indexed for MEDLINE]
12.

Nucleotide modifications in three functionally important regions of the Saccharomyces cerevisiae ribosome affect translation accuracy.

Baudin-Baillieu A, Fabret C, Liang XH, Piekna-Przybylska D, Fournier MJ, Rousset JP.

Nucleic Acids Res. 2009 Dec;37(22):7665-77. doi: 10.1093/nar/gkp816. Epub .

PMID:
19820108
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The paradox of viable sup45 STOP mutations: a necessary equilibrium between translational readthrough, activity and stability of the protein.

Kiktev D, Moskalenko S, Murina O, Baudin-Baillieu A, Rousset JP, Zhouravleva G.

Mol Genet Genomics. 2009 Jul;282(1):83-96. doi: 10.1007/s00438-009-0447-5. Epub 2009 Apr 16.

PMID:
19370360
[PubMed - indexed for MEDLINE]
14.

Molecular dissection of translation termination mechanism identifies two new critical regions in eRF1.

Hatin I, Fabret C, Rousset JP, Namy O.

Nucleic Acids Res. 2009 Apr;37(6):1789-98. doi: 10.1093/nar/gkp012. Epub 2009 Jan 27.

PMID:
19174561
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Epigenetic control of polyamines by the prion [PSI+].

Namy O, Galopier A, Martini C, Matsufuji S, Fabret C, Rousset JP.

Nat Cell Biol. 2008 Sep;10(9):1069-75. doi: 10.1038/ncb1766.

PMID:
19160487
[PubMed - indexed for MEDLINE]
16.

Ribosome performance is enhanced by a rich cluster of pseudouridines in the A-site finger region of the large subunit.

Piekna-Przybylska D, Przybylski P, Baudin-Baillieu A, Rousset JP, Fournier MJ.

J Biol Chem. 2008 Sep 19;283(38):26026-36. doi: 10.1074/jbc.M803049200. Epub 2008 Jul 8.

PMID:
18611858
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

[How translation termination factor eRF1 Euplotes does not recognise UGA stop codon].

Lekomtsev SA, Kolosov PM, Frolova LIu, Bidou L, Rousset JP, Kiselev LL.

Mol Biol (Mosk). 2007 Nov-Dec;41(6):1014-22. Russian.

PMID:
18318120
[PubMed - indexed for MEDLINE]
18.

A novel mutant of the Sup35 protein of Saccharomyces cerevisiae defective in translation termination and in GTPase activity still supports cell viability.

Fabret C, Cosnier B, Lekomtsev S, Gillet S, Hatin I, Le Maréchal P, Rousset JP.

BMC Mol Biol. 2008 Feb 11;9:22. doi: 10.1186/1471-2199-9-22.

PMID:
18267004
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes.

Allamand V, Bidou L, Arakawa M, Floquet C, Shiozuka M, Paturneau-Jouas M, Gartioux C, Butler-Browne GS, Mouly V, Rousset JP, Matsuda R, Ikeda D, Guicheney P.

J Gene Med. 2008 Feb;10(2):217-24.

PMID:
18074402
[PubMed - indexed for MEDLINE]
20.

Adding pyrrolysine to the Escherichia coli genetic code.

Namy O, Zhou Y, Gundllapalli S, Polycarpo CR, Denise A, Rousset JP, Söll D, Ambrogelly A.

FEBS Lett. 2007 Nov 13;581(27):5282-8. Epub 2007 Oct 23.

PMID:
17967457
[PubMed - indexed for MEDLINE]
Free Article

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