Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jérôme Trzcionka"'
Autor:
Noureddine Belmadoui, Jérôme Trzcionka, Cecilia Paris, Virginie Lhiaubet-Vallet, Miguel A. Miranda, Maria J. Climent
Publikováno v:
ChemBioChem. 8:402-407
Cyclobutane pyrimidine dimers (CPD) and (6-4) photoproducts are among the main UV-induced DNA lesions. Both types of damage are mostly repaired in prokaryotes by photolyase enzymes. The repair mechanism of (6-4) photolyases has still not been fully e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::737470b845f77e9034a5930e78b18f28
https://doi.org/10.1002/cbic.200600394
https://doi.org/10.1002/cbic.200600394
Autor:
Nadia Chouini-Lalanne, Miguel A. Miranda, Virginie Lhiaubet-Vallet, Jérôme Trzcionka, Susana Encinas
Publikováno v:
The Journal of Physical Chemistry B. 108:14148-14153
The detailed triplet state characteristics of 2-(4-acetylphenyl)isoindolin-1-one (kINP), a N-phenylphthalimidine (PPI) derivative, have been studied in fluid solution at room temperature. The attac...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c913b57f1485b84fddfee51beffd634
https://doi.org/10.1021/jp0498926
https://doi.org/10.1021/jp0498926
Publikováno v:
Photochemical & Photobiological Sciences. 3:226-230
The in vitro photosensitizing activity of indoprofen, a non-steroidal anti-inflammatory drug, toward DNA has been studied by gel sequencing experiments using (32)P-end labelled synthetic oligonucleotides in phosphate buffered solution. Upon irradiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4cad3fa6330803174a49b9d384aeda2
https://doi.org/10.1039/b307719e
https://doi.org/10.1039/b307719e
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2014, 22 (17), pp.4711-4716. ⟨10.1016/j.bmc.2014.07.010⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2014, 22 (17), pp.4711-4716. ⟨10.1016/j.bmc.2014.07.010⟩
International audience; DNA damage under oxidative stress leads to oxidation of guanine base. The identification of the resulting guanine lesions in cellular DNA is difficult due to the sensitivity of the primary oxidation products to hydrolysis and/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18fa7b1c7d32b43bfe5aac7c83f3ad50
https://hal.archives-ouvertes.fr/hal-02007975
https://hal.archives-ouvertes.fr/hal-02007975
Autor:
Karen Torres, Luis E. Piñero-Santiago, Carmelo Garcia, Jaysika Leguillú, Miguel A. Miranda, Jérôme Trzcionka, Virginie Lhiaubet-Vallet, Rolando Oyola
Publikováno v:
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
instname
Unwanted photoinduced responses are well-known adverse effects of most promazine drugs, including levomepromazine (LPZ, Levoprome((R)) or Nozinan((R))). This drug is indicated in psychiatry primarily for the treatment of schizophrenia and other schiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::240697f27b3ff1d1aaadb8a42ada6864
https://doi.org/10.1111/php.12147
https://doi.org/10.1111/php.12147
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2013, 37 (11), pp.3581. ⟨10.1039/C3NJ01004J⟩
New Journal of Chemistry, Royal Society of Chemistry, 2013, 37 (11), pp.3581. ⟨10.1039/C3NJ01004J⟩
International audience; The cationic manganese porphyrin (Mn-TMPyP) was activated by an oxygen atom donor KHSO5 (oxone) to form a high-valent manganese-oxo species (MnV[double bond, length as m-dash]O) in aqueous buffer. The high-valent MnV[double bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66e8a88dfa02bcbed39e7cb92046e357
https://hal.archives-ouvertes.fr/hal-02908762
https://hal.archives-ouvertes.fr/hal-02908762
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 2008, 47, pp.4788-4799. ⟨10.1021/bi7022199⟩
Biochemistry, American Chemical Society, 2008, 47, pp.4788-4799. ⟨10.1021/bi7022199⟩
We investigated the incorporation of oxidatively modified guanine residues in DNA using three DNA polymerases, Escherichia coli Kf exo+, Kf exo-, and Taq DNA polymerase. We prepared nucleoside 5'-triphosphates with modified bases (dN (ox)TP) includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8e645da059859d58688582b40def814
https://hal.archives-ouvertes.fr/hal-00276125
https://hal.archives-ouvertes.fr/hal-00276125
Publikováno v:
Photochemicalphotobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology. 4(3)
The photophysical properties of indoprofen photoproducts have been examined in various solvents by absorbance and emission spectroscopies in relation with their photosensitizing properties. The photophysical properties of 2-[4-(1-hydroxy)ethylphenyl]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b72e4f9f91e8b9c401fd5fbdd07905f
https://pubmed.ncbi.nlm.nih.gov/15738999
https://pubmed.ncbi.nlm.nih.gov/15738999
Publikováno v:
New Journal of Chemistry. 29:570
The excited states of 2-methylisoindolin-1-one (INS) have been investigated by absorbance spectroscopy and theoretical calculations performed at the TDDFT level and compared with those of three related compounds involved in DNA photosensitization: in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643301a118b7fce346f1005c48a4c518
https://doi.org/10.1039/b415876h
https://doi.org/10.1039/b415876h
Autor:
Miguel A. Miranda, Susana Encinas, Virginie Lhiaubet-Vallet, Jérôme Trzcionka, Nadia Chouini-Lalanne
Publikováno v:
Photochemistry and Photobiology. 77:487
The photophysical properties and photochemistry of indoprofen (INP) have been investigated. Absorption and emission spectroscopies in phosphate buffer, ethanol and ether show that INP photophysics is dominated by a singlet-singlet transition of pipi*
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::855aada9e31c6be7c20ee7a5d8a8838d
https://doi.org/10.1562/0031-8655(2003)077<0487:pappoi>2.0.co
https://doi.org/10.1562/0031-8655(2003)077<0487:pappoi>2.0.co