Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Alain Laigle"'
Publikováno v:
Biochemical Pharmacology. 70:1424-1430
MDR1 overexpression is one form of the multidrug resistance (MDR) phenotype, which can be acquired by patients initially responsive to chemotherapy. Because of the high toxicity of the inhibitors of P-glycoprotein (P-gp), the protein encoded by MDR1,
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
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 15:107-117
Resonance Raman spectra excited at 257 nm are reported for the complexes of the Nickel, Cobalt and Zinc derivatives of Tetrakis(4-N-methylpyridyl)porphine with poly(dA.dT)2, poly(dA)poly(dT), poly(dG.dC)2 and poly(dG).poly(dC). These spectra are inte
Autor:
Laurence Gallois, Arlette Garnier-Suillerot, Alain Laigle, Marina M.-L. Fiallo, Waldemar Priebe
Publikováno v:
European Journal of Biochemistry. 241:879-887
Anthracyclines are potent anticancer agents. Their use is limited by the problem of multidrug resistance (MDR) associated with a decreased intracellular accumulation of drug correlated with the presence, in the membrane of resistant cells, of the P-g
Publikováno v:
Chemico-Biological Interactions. 101:49-58
Anthracyclines remain today the medications of choice against a wide spectrum of human cancers. Anthracyclines are fluorescent molecules and microfluorimetric methods are often used to determine their cellular distribution. The use of microspectroflu
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
Autor:
Pierre-Yves Turpin, Jean-Pierre Ballini, P. Vigny, Alain Laigle, C. Amirand, L. Chinsky, M. Duquesne, Franck Sureau
Publikováno v:
Applied Spectroscopy. 44:1047-1051
Ultraviolet-excited resonance Raman spectra have been obtained for the first time for microsamples of dAMP deoxymononucleotide and DNA and for the nuclear DNA of a single living T47D cultured cell. The spectral variations observed in changing the exc
Publikováno v:
Photochemistry and Photobiology. 51:519-525
The resonance Raman spectra of water-soluble porphyrins, Cu(TMpy-P4) and Ni(TMpy-P4), and their mixtures with DNA, Poly(dG-dC).Poly(dG-dC), and Poly(dA-dT).Poly(dA-dT) were measured using 426 nm pulsed laser excitation (and 556 nm for some applicatio