Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Abdelaziz Elass"'
Autor:
Dharmendra Singh, Bennaceur Ouaki, Nassima Radouane, Michael Depriester, Abdelhak Hadj-Sahraoui, Lucette Tidahy, Abdelkrim Maaroufi, Abdelaziz Elass, Benoit Duponchel
Publikováno v:
Journal of the Chinese Chemical Society. 68:1456-1465
Publikováno v:
The Journal of Physical Chemistry B. 102:4233-4239
The vibrational spectra of the arabinonucleoside 9-β-d-arabinofuranosyladenine, ara-A, are reported. Ara-A is of interest because of its antiviral activity. An accurate knowledge of the vibrational modes is a valuable help for the elucidation of dru
Autor:
Gérard Vergoten, Dominique Legrand, Elisabeth Elass-Rochard, Abdelaziz Elass, Geneviève Spik, Joël Mazurier
Publikováno v:
Quantitative Structure-Activity Relationships. 15:94-101
Human lactoferrin displays considerable structural homology with transferrins of other species. However, lactoferrins and transferrins play distinct biological roles and bind to specific cell receptors. Previous reports have shown that residues 4 - 5
Publikováno v:
Quantitative Structure-Activity Relationships. 15:382-388
Two series of compounds structurally related to phenolphthalein and triphenylalkyl carboxylic acid were tested as inhibitors of bilirubin glucuronidation catalyzed by rat liver microsomal UDP-glucuronosyltransferase, and analyzed by the CoMFA method
Autor:
Elisabeth Elass-Rochard, Abdelaziz Elass, Joël Mazurier, Gérard Vergoten, Geneviève Spik, Dominique Legrand
Publikováno v:
Quantitative Structure-Activity Relationships. 15:102-107
It has previously been established that all or part of residues 4 - 52 of human lactoferrin interact with the specific T-lymphocyte receptor. Furthermore, the preliminary study using classical quantitative structure-affinity relationships (QSAR) mode
Publikováno v:
ChemInform. 30
Autor:
Jean-Claude Ziegler, Abdelaziz Elass, Alain Cartier, Eric Battaglia, Mourad Said, Sylvie Fournel-Gigleux, Gérard Vergoten, Jacques Magdalou, Marie-Hélène Livertoux, Virginie Cano
Publikováno v:
Journal of biochemical and molecular toxicology. 12(1)
A series of potent and competitive inhibitors of UDP-glucuronosyltransferase derived from 7,7,7-triphenylheptanoic acid has been synthesized in order to probe the active site of the isozyme involved in the glucuronidation of the endogenous toxic comp
Autor:
Dominique Legrand, Gérard Vergoten, Joël Mazurier, Geneviève Spik, Pierrette Maes, Elisabeth Rochard, Jean Montreuil, Abdelaziz Elass
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 1992, 31 (38), pp.9243-51
Biochemistry, 1992, 31 (38), pp.9243-51
Biochemistry, American Chemical Society, 1992, 31 (38), pp.9243-51
Biochemistry, 1992, 31 (38), pp.9243-51
International audience; Fluorescein isothiocyanate derivatization of the human lactotransferrin on Lys-264 inhibits the binding of the protein of human PHA-activated lymphocytes [Legrand, D., Mazurier, J., Maes, P., Rochard, E., Montreuil, J., & Spik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3075af22e7f4d05b5ac65c6cf6ebbb63
https://hal.archives-ouvertes.fr/hal-00484422
https://hal.archives-ouvertes.fr/hal-00484422
Publikováno v:
HETEROCYCLES. 51:2213