Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laure-Anaïs Vincent"'
Autor:
Paul Le Baccon-Sollier, Yohan Malki, Morgane Maye, Lamiaa M. A. Ali, Laure Lichon, Pierre Cuq, Laure-Anaïs Vincent, Nicolas Masurier
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 935-949 (2020)
A series of 19 novel pyrido-imidazodiazepinones, with modulations of positions 2, 3 and 4 of the diazepine ring were synthesised and screened for their in vitro cytotoxic activities against two melanoma cell lines (A375 and MDA-MB-435) and for their
Externí odkaz:
https://doaj.org/article/6f35928d0f274a598d4cc9b50e2d5395
Autor:
Carine Deleuze-Masquéfa, Kamel Hadj Kaddour, Pierre Cuq, Zahraa Zghaib, Cindy Patinote, Mona Diab Assaf, Laure-Anaïs Vincent, Pierre-Antoine Bonnet, Romain M. Larive, Jean-François Guichou
Publikováno v:
European journal of medicinal chemistry. 212
The malignant transformation of melanocytes causes several thousand deaths each year, making melanoma an important public health concern. Melanoma is the most aggressive skin cancer, which incidence has regularly increased over the past decades. We d
Autor:
Lamiaa M. A. Ali, Pierre Cuq, Nicolas Masurier, Laure Lichon, Paul Le Baccon-Sollier, Yohan Malki, Laure-Anaïs Vincent, Morgane Maye
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 935-949 (2020)
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 935-949 (2020)
A series of 19 novel pyrido-imidazodiazepinones, with modulations of positions 2, 3 and 4 of the diazepine ring were synthesised and screened for their in vitro cytotoxic activities against two melanoma cell lines (A375 and MDA-MB-435) and for their
Autor:
Philippe Nirdé, Jean-Pierre Molès, Simon Galas, Myriam Richaud, Gilberte Marti-Mestres, Jean-Pierre Reynier, Paul Chambon, Hinda Dabboue, Laure-Anaïs Vincent
Publikováno v:
Altex-Heidelberg
Altex-Heidelberg-, Elsevier, 2018, 35, pp.123-125. ⟨10.14573/altex.1711101⟩
Altex-Heidelberg-, Elsevier, 2018, 35, pp.123-125. ⟨10.14573/altex.1711101⟩
International audience; 123 gation and subsequent differentiation into complex tissue-like structures with reproducible ratios of neurons, astrocytes and oligodendrocytes. The generated neurons elicit spontaneous calcium transients and stimuli-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3c7ba722fe79a1ca3a4d21d5980a711
https://hal.archives-ouvertes.fr/hal-01890127
https://hal.archives-ouvertes.fr/hal-01890127
Autor:
Laurence Vian, Lucie Rozkydalova, Kamel Hadj-Kaddour, Chaker Attaoua, Michel Bellis, Pierre Cuq, Laure-Anaïs Vincent
Publikováno v:
Fundamental & Clinical Pharmacology. 29:164-177
On account of its strong ability to become chemoresistant after a primary response to drugs, malignant melanoma (MM) remains a therapeutic challenge. This study focuses on acquired resistance to vinca alkaloids (VAs) using VA-resistant MM cell lines
Autor:
Nicole Bec, Jean-François Guichou, Georges Moarbess, Carine Deleuze-Masquéfa, Christian Larroque, Stéphanie Paniagua-Gayraud, Zahraa Zghaib, Mona Diab-Assaf, Pierre-Antoine Bonnet, Issam Kassab, Kamel Hadj-Kaddour, Pierre Cuq, Laure-Anaïs Vincent, Johanna Vappiani
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2016, 24 (11), pp.2433-2440. ⟨10.1016/j.bmc.2016.04.004⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2016, 24 (11), pp.2433-2440. ⟨10.1016/j.bmc.2016.04.004⟩
International audience; Microtubules are considered as important targets of anticancer therapy. EAPB0503 and its structural imidazo[1,2-a]quinoxaline derivatives are major microtubule-interfering agents with potent anticancer activity. In this study,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65724f03ac89ea6b2d087483f3e0fcfc
https://hal.umontpellier.fr/hal-02299123
https://hal.umontpellier.fr/hal-02299123
Autor:
Chaker Attaoua, Qiang Bai, Kamel Hadj-Kaddour, Aida Abdel Jaoued, John De Vos, Laure-Anaïs Vincent, Laurence Vian, Pierre Cuq
Publikováno v:
Fundamental & Clinical Pharmacology
Fundamental & Clinical Pharmacology, 2015, 29 (1), pp.62-71. ⟨10.1111/fcp.12093⟩
Fundamental and Clinical Pharmacology
Fundamental and Clinical Pharmacology, Wiley, 2015, 29 (1), pp.62-71. ⟨10.1111/fcp.12093⟩
Fundamental & Clinical Pharmacology, 2015, 29 (1), pp.62-71. ⟨10.1111/fcp.12093⟩
Fundamental and Clinical Pharmacology
Fundamental and Clinical Pharmacology, Wiley, 2015, 29 (1), pp.62-71. ⟨10.1111/fcp.12093⟩
International audience; On account of its extreme intrinsic resistance to apoptosis and of its strong ability to become chemoresistant after a primary response to drugs, malignant melanoma (MM) is still a therapeutic challenge. We previously showed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bef6e7a5837cff052132f5b104cababf
https://doi.org/10.1111/fcp.12093
https://doi.org/10.1111/fcp.12093