Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Béatrice Jollès"'
Publikováno v:
Oligonucleotides. 14:191-198
Small interfering RNAs (siRNAs) are powerful tools in specifically silencing gene expression. Nevertheless, their efficiency can be limited when targeting proteins with an unusually long half-life, such as P-glycoprotein (P-gp), which is involved in
Publikováno v:
Antisense and Nucleic Acid Drug Development. 11:129-136
Minimally modified oligonucleotides belong to the second-generation antisense class. They are phosphodiester oligonucleotides with a minimum of phosphorothioate linkages in order to be protected against serum and cellular exonucleases and endonucleas
Publikováno v:
European Biophysics Journal. 26:277-281
An oligodeoxynucleotide has been synthesized, which mimics an ``antigene'' oligonucleotide with a polypyrimidic stretch on its 5′ side and is protected on its 3′ side against nucelases by a naturally forming and very stable hairpin, 5′GCGAAGC3
Autor:
Vérène Stierlé, Maria Duca, Ludovic Halby, Catherine Senamaud-Beaufort, Massimo L. Capobianco, Paola B. Arimondo, Béatrice Jollès, Alain Laigle
Publikováno v:
Molecular Pharmacology
Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2008, 73 (5), pp.1568-1577
Molecular pharmacology
73 (2008): 1568–1577. doi:10.1124/mol.107.042010
info:cnr-pdr/source/autori:Stierle, Verene (1); Duca, Maria (2); Halby, Ludovic (2); Senamaud-Beaufort, Catherine (2); Capobianco, Massimo L. (3); Laigle, Alain (1); Jolles, Beatrice (1); Arimondo, Paola B./titolo:Targeting MDR1 gene: Synthesis and cellular study of modified daunomycin-triplex-forming oligonucleotide conjugates able to inhibit gene expression in resistant cell lines/doi:10.1124%2Fmol.107.042010/rivista:Molecular pharmacology (Print)/anno:2008/pagina_da:1568/pagina_a:1577/intervallo_pagine:1568–1577/volume:73
Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2008, 73 (5), pp.1568-1577
Molecular pharmacology
73 (2008): 1568–1577. doi:10.1124/mol.107.042010
info:cnr-pdr/source/autori:Stierle, Verene (1); Duca, Maria (2); Halby, Ludovic (2); Senamaud-Beaufort, Catherine (2); Capobianco, Massimo L. (3); Laigle, Alain (1); Jolles, Beatrice (1); Arimondo, Paola B./titolo:Targeting MDR1 gene: Synthesis and cellular study of modified daunomycin-triplex-forming oligonucleotide conjugates able to inhibit gene expression in resistant cell lines/doi:10.1124%2Fmol.107.042010/rivista:Molecular pharmacology (Print)/anno:2008/pagina_da:1568/pagina_a:1577/intervallo_pagine:1568–1577/volume:73
Reversal of the multidrug-resistant (MDR) phenotype is very important for chemotherapy success. In fact, the expression of the MDR1 gene-encoded P-glycoprotein (P-gp) actively expels antitumor agents such as daunomycin (DNM) out of the cells, resulti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7afe2626028cdf85f24a7d412549b5c8
https://hal.archives-ouvertes.fr/hal-00449265
https://hal.archives-ouvertes.fr/hal-00449265
Publikováno v:
Biochimie
Biochimie, Elsevier, 2007, 89 (8), pp.1033-1036
Biochimie, Elsevier, 2007, 89 (8), pp.1033-1036
Effective silencing of MDR1, one of the genes involved in the multidrug resistance phenotype, can be achieved by the use of an efficient siRNA transfected into the doxorubicin-selected MCF7-R human cell line, alone or combined with a moderately effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed858da2f18d36a3537e72f223738c39
https://hal.archives-ouvertes.fr/hal-00449275
https://hal.archives-ouvertes.fr/hal-00449275
In the perspective of reversing multidrug resistance through antisense strategy while avoiding non-antisense effects of all-phosphorothioate oligonucleotides which non-specifically bind to proteins, a minimally modified antisense phosphodiester oligo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a1951872dff44b3cc31e64fd3ead99
https://hal.science/hal-00109048
https://hal.science/hal-00109048
Publikováno v:
Journal of Raman Spectroscopy
Journal of Raman Spectroscopy, Wiley, 2000, 31 (6), pp.481-484. ⟨10.1002/1097-4555(200006)31:63.0.CO;2-0⟩
Journal of Raman Spectroscopy, 2000, 31 (6), pp.481-484. ⟨10.1002/1097-4555(200006)31:63.0.CO;2-0⟩
Journal of Raman Spectroscopy, Wiley, 2000, 31 (6), pp.481-484. ⟨10.1002/1097-4555(200006)31:63.0.CO;2-0⟩
Journal of Raman Spectroscopy, 2000, 31 (6), pp.481-484. ⟨10.1002/1097-4555(200006)31:63.0.CO;2-0⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb0599579137eac072aea7a6b5e301d9
https://hal.archives-ouvertes.fr/hal-01596044
https://hal.archives-ouvertes.fr/hal-01596044
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 1997, 25, pp.4608-4613. ⟨10.1093/nar/25.22.4608⟩
Scopus-Elsevier
Nucleic Acids Research, 1997, 25, pp.4608-4613. ⟨10.1093/nar/25.22.4608⟩
Nucleic Acids Research, Oxford University Press, 1997, 25, pp.4608-4613. ⟨10.1093/nar/25.22.4608⟩
Scopus-Elsevier
Nucleic Acids Research, 1997, 25, pp.4608-4613. ⟨10.1093/nar/25.22.4608⟩
International audience; For the purposes of the antisense strategy oligodeoxyribonucleotides can be protected against serum and cell nuclease digestion by tagging at their 3′-end with a sequence naturally forming a very stable hairpin, d(GCGAAGC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35251651684608d27d9d872505d4e9dd
https://hal.archives-ouvertes.fr/hal-01480366/document
https://hal.archives-ouvertes.fr/hal-01480366/document
Publikováno v:
Journal of biomolecular structuredynamics. 14(1)
The four stranded form of polyriboinosinic acid, or poly(rl), formed under conditions of high ionic strength, has been studied principally by resonance Raman spectroscopy excited in the ultraviolet absorbent band of the hypoxanthine residues. UV Abso
Publikováno v:
Journal of Biomolecular Structure and Dynamics
Journal of Biomolecular Structure and Dynamics, 1996, 14 (3), pp.365-371. ⟨10.1080/07391102.1996.10508131⟩
Scopus-Elsevier
Journal of Biomolecular Structure and Dynamics, Taylor & Francis: STM, Behavioural Science and Public Health Titles, 1996, 14 (3), pp.365-371. ⟨10.1080/07391102.1996.10508131⟩
Journal of Biomolecular Structure and Dynamics, 1996, 14 (3), pp.365-371. ⟨10.1080/07391102.1996.10508131⟩
Scopus-Elsevier
Journal of Biomolecular Structure and Dynamics, Taylor & Francis: STM, Behavioural Science and Public Health Titles, 1996, 14 (3), pp.365-371. ⟨10.1080/07391102.1996.10508131⟩
International audience; In vitro degradation of antisense oligonucleotides protected or not on their 3′ side against enzymatic attack by a naturally forming hairpin has been studied by fluorescence resonance energy transfer (FRET). The two oligonuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b7ac47469debaf1d99cc3a9b1c546c4
https://hal.science/hal-01480966
https://hal.science/hal-01480966