Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Abdullah Mayati"'
Autor:
Abdullah Mayati, Normand Podechard, Manuelle Rineau, Lydie Sparfel, Dominique Lagadic-Gossmann, Olivier Fardel, Eric Le Ferrec
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Exposure to environmental polycyclic aromatic hydrocarbons (PAHs), such as benzo(a)pyrene (B(a)P), has been linked to several health-threatening risks. PAHs were also shown to hinder adrenergic receptor (ADR) responses. As we previously demo
Externí odkaz:
https://doaj.org/article/c8613d3a23d14ba8b04f0210cc5654ff
Autor:
Abdullah Mayati, Amélie Moreau, Elodie Jouan, Marie Febvre-James, Claire Denizot, Yannick Parmentier, Olivier Fardel
Publikováno v:
Pharmaceutics, Vol 10, Iss 4, p 246 (2018)
The HepaRG cell line is a highly differentiated human hepatoma cell line, displaying the expression of various drug transporters. However, functional expression of nucleoside transporters remains poorly characterized in HepaRG cells, although these t
Externí odkaz:
https://doaj.org/article/a331245c50974f2b832089b411af91e9
Autor:
Abdullah Mayati, Arnaud Bruyere, Amélie Moreau, Elodie Jouan, Claire Denizot, Yannick Parmentier, Olivier Fardel
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0144667 (2015)
Ro 31-8220 is a potent protein kinase C (PKC) inhibitor belonging to the chemical class of bisindolylmaleimides (BIMs). Various PKC-independent effects of Ro 31-8220 have however been demonstrated, including inhibition of the ATP-binding cassette dru
Externí odkaz:
https://doaj.org/article/d1d8ff9d690c455688926235c6547d1d
Autor:
Elodie Jouan, Marc Le Vée, Abdullah Mayati, Claire Denizot, Yannick Parmentier, Olivier Fardel
Publikováno v:
Pharmaceutics, Vol 8, Iss 2, p 12 (2016)
In vitro evaluation of P-glycoprotein (P-gp) inhibitory potential is now a regulatory issue during drug development, in order to predict clinical inhibition of P-gp and subsequent drug–drug interactions. Assays for this purpose, commonly based on P
Externí odkaz:
https://doaj.org/article/b195d41d987e48fe8fd614d50fe54910
Autor:
Bruno Stieger, Claire Denizot, Amélie Moreau, Yannick Parmentier, Olivier Fardel, Abdullah Mayati
Publikováno v:
European Journal of Pharmaceutical Sciences
European Journal of Pharmaceutical Sciences, Elsevier, 2017, 106, pp.302--312. ⟨10.1016/j.ejps.2017.06.010⟩
European Journal of Pharmaceutical Sciences, 2017, 106, pp.302--312. ⟨10.1016/j.ejps.2017.06.010⟩
European Journal of Pharmaceutical Sciences, Elsevier, 2017, 106, pp.302--312. ⟨10.1016/j.ejps.2017.06.010⟩
European Journal of Pharmaceutical Sciences, 2017, 106, pp.302--312. ⟨10.1016/j.ejps.2017.06.010⟩
International audience; The catecholamine epinephrine is known to repress expression of hepatic drug metabolizing enzymes such as cytochromes P-450. The present study was designed to determine whether epinephrine may also target expression of main he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d0961a28c93c795593ea8c92e61222
https://doi.org/10.5167/uzh-138404
https://doi.org/10.5167/uzh-138404
Autor:
Olivier Fardel, Yannick Parmentier, Marc Le Vee, Claire Denizot, Abdullah Mayati, Elodie Jouan
Publikováno v:
Pharmaceutics
Pharmaceutics, 2016, 8 (2), pp.12. ⟨10.3390/pharmaceutics8020012⟩
Pharmaceutics, Vol 8, Iss 2, p 12 (2016)
Pharmaceutics; Volume 8; Issue 2; Pages: 12
Pharmaceutics, 2016, 8 (2), pp.12. ⟨10.3390/pharmaceutics8020012⟩
Pharmaceutics, Vol 8, Iss 2, p 12 (2016)
Pharmaceutics; Volume 8; Issue 2; Pages: 12
International audience; In vitro evaluation of P-glycoprotein (P-gp) inhibitory potential is now a regulatory issue during drug development, in order to predict clinical inhibition of P-gp and subsequent drug-drug interactions. Assays for this purpos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cca241d6bb4f7f36ff863a6954f44682
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01305488
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01305488
Autor:
Dominique Lagadic-Gossmann, Jørn A. Holme, Johan Øvrevik, Olivier Fardel, Eric Le Ferrec, Abdullah Mayati
Publikováno v:
Toxicology in Vitro
Toxicology in Vitro, 2014, 28 (6), pp.1153-7. ⟨10.1016/j.tiv.2014.05.012⟩
Toxicology in Vitro, Elsevier, 2014, 28 (6), pp.1153-7. ⟨10.1016/j.tiv.2014.05.012⟩
Toxicology in Vitro, 2014, 28 (6), pp.1153-7. ⟨10.1016/j.tiv.2014.05.012⟩
Toxicology in Vitro, Elsevier, 2014, 28 (6), pp.1153-7. ⟨10.1016/j.tiv.2014.05.012⟩
Nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) are widespread environmental pollutants, generated from reactions between PAHs and nitrogen oxides during combustion processes. In the present study we have investigated the mechanisms of CXCL8 (IL-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d1a89629353cdeabfb9607ca6ac3770
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01058607/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01058607/document
Autor:
Arnaud Courtois, Nicolas Levoin, Philippe Uriac, Monique N'Diaye, Dominique Lagadic-Gossmann, Hervé Paris, Eric Le Ferrec, Olivier Fardel, Abdullah Mayati
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, 2012, 287 (6), pp.4041-52. ⟨10.1074/jbc.M111.319970⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2012, 287 (6), pp.4041-52. ⟨10.1074/jbc.M111.319970⟩
Journal of Biological Chemistry, 2012, 287 (6), pp.4041-52. ⟨10.1074/jbc.M111.319970⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2012, 287 (6), pp.4041-52. ⟨10.1074/jbc.M111.319970⟩
International audience; Polycyclic aromatic hydrocarbons (PAHs) such as benzo(a)pyrene (B(a)P) are widely distributed environmental contaminants, known as potent ligands of the aryl hydrocarbon receptor (AhR). These chemicals trigger an early and tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b997b1dffb255b2fd9b4bee2619dfca
https://hal.science/hal-00682497
https://hal.science/hal-00682497
Publikováno v:
Environmental Toxicology
Environmental Toxicology, Wiley, 2011, 27 (9), pp.556-562. ⟨10.1002/tox.20675⟩
Environmental Toxicology, 2011, 27 (9), pp.556-562. ⟨10.1002/tox.20675⟩
Environmental Toxicology, Wiley, 2011, 27 (9), pp.556-562. ⟨10.1002/tox.20675⟩
Environmental Toxicology, 2011, 27 (9), pp.556-562. ⟨10.1002/tox.20675⟩
International audience; Polycyclic aromatic hydrocarbons (PAHs) such as benzo(a)pyrene (B(a)P) constitute a major family of widely-distributed environmental toxic contaminants, known as potent ligands of the aryl hydrocarbon receptor (AhR). B(a)P has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e64f47224be0a5ea005bbcc2b13167a
https://hal.archives-ouvertes.fr/hal-00680889
https://hal.archives-ouvertes.fr/hal-00680889