Zobrazeno 1 - 10
of 303
pro vyhledávání: '"J. Lhomme"'
Publikováno v:
IRBM News. 34:150-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f001c74cc46d63ae9ba9e3a357a5ca2
https://doi.org/10.1016/j.irbmnw.2013.08.005
https://doi.org/10.1016/j.irbmnw.2013.08.005
Autor:
A. V. Ozhigin, Ben Gouldby, G.S. Shirshov, F. I. Rusadi, Marian Bubak, N. B. Melnikova, Alexander L. Pyayt, Robert Meijer, R.G. Belleman, Ilya I. Mokhov, J. Lhomme, Bernhard Lang, B.J. Broekhuijsen, Valeria V. Krzhizhanovskaya, Bartosz Balis
Publikováno v:
ICCS
Procedia Computer Science, 106-115, 4
Procedia Computer Science, 4, 106-115. Elsevier
Procedia Computer Science, 106-115, 4
Procedia Computer Science, 4, 106-115. Elsevier
We present a prototype of the flood early warning system (EWS) developed within the UrbanFlood FP7 project. The system monitors sensor networks installed in flood defenses (dikes, dams, embankments, etc.), detects sensor signal abnormalities, calcula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e4641a0a203b7a2f3c8b3ec2f876c3e
https://doi.org/10.1016/j.procs.2011.04.012
https://doi.org/10.1016/j.procs.2011.04.012
Publikováno v:
Journal of Hydrology. 299:203-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0c551be7c6e7bac7eb6f3e770b1f6d4
https://doi.org/10.1016/s0022-1694(04)00367-1
https://doi.org/10.1016/s0022-1694(04)00367-1
Publikováno v:
Bioconjugate Chemistry. 15:520-529
Selected sequences of oligodeoxyribonucleotides (ODNs) have been conjugated efficiently with distamycin-based peptides containing reactive cysteine and oxyamine functionalities at the C-terminus. The conjugation was performed easily within 30-60 min,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f4e2607387c13b31c24a75b0fec4769
https://doi.org/10.1021/bc0341730
https://doi.org/10.1021/bc0341730
Publikováno v:
Tetrahedron. 58:4291-4298
We describe the synthesis and DNA damaging activities of hybrid molecules in which a purine (adenine) is linked to an intercalating chromophore (acridine) by a polyamino linker. A DNA damaging agent, phenanthroline or para-nitrobenzamide, is tethered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f7a849828a55611dd56780a7364e823
https://doi.org/10.1016/s0040-4020(02)00345-9
https://doi.org/10.1016/s0040-4020(02)00345-9
Publikováno v:
The Journal of Organic Chemistry. 66:8222-8226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6becfdada97e8a4c57ae74dc054394c2
https://doi.org/10.1021/jo015811f
https://doi.org/10.1021/jo015811f
Publikováno v:
Magnetic Resonance in Chemistry. 37:73-76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c6c3e54e99282ce99534626b962b612
https://doi.org/10.1002/(sici)1097-458x(199901)37:1<73::aid-mrc402>3.0.co
https://doi.org/10.1002/(sici)1097-458x(199901)37:1<73::aid-mrc402>3.0.co
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:233-236
Cyclization of 8-bromo-9-alkylaminoethyl-adenine quantitatively affords a substituted imidazo[1,2-e]purine. The corresponding heterodimer, imidazo[1,2-e]purine-acridine, was prepared and its interaction with abasic site containing oligonucleotides wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2d4b95c9e43495dc9231a97966b5115
https://doi.org/10.1016/s0960-894x(98)00703-3
https://doi.org/10.1016/s0960-894x(98)00703-3
Publikováno v:
Scopus-Elsevier
The synthesis and characterisation of a new bifunctional Ru(II) complex are presented. This compound contains a metallic unit, photoreactive versus the guanines of DNA, and a new bifunctional ligand. An intramolecular luminescence quenching makes thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18d4b0dfb1cac4e5d42085619ce35787
https://doi.org/10.1016/s1387-7003(98)00092-6
https://doi.org/10.1016/s1387-7003(98)00092-6
Publikováno v:
Magnetic Resonance in Chemistry. 35:697-700
A combination of NMR techniques, including 13C and 1H DEPT, HMQC and HMBC experiments, was used to assign the structure of the compound formed by addition of aniline to 8H-pyrido[2,3,4-mn]acridine. From this NMR study, two structures were possible. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93de26429c1138fb374745938684f46f
https://doi.org/10.1002/(sici)1097-458x(199711)35:10<697::aid-omr156>3.0.co
https://doi.org/10.1002/(sici)1097-458x(199711)35:10<697::aid-omr156>3.0.co