Zobrazeno 1 - 4
of 4
pro vyhledávání: '"MESH: Naphthalimides"'
Autor:
Kai Lee Yap, Anthony Ting, Tiffany Siew Joo Lim, Vaidehi Krishnan, Etienne Schwob, Chee Seng Cheng, Léon Dirick, Hong Hwa Lim, Uttam Surana, San Ling Si-Hoe
Publikováno v:
Cell Cycle
Cell Cycle, Taylor & Francis, 2014, 6 (13), pp.1621-1630. ⟨10.4161/cc.6.13.4373⟩
ResearcherID
Cell Cycle, Taylor & Francis, 2014, 6 (13), pp.1621-1630. ⟨10.4161/cc.6.13.4373⟩
ResearcherID
International audience; DNA replication checkpoint is activated in response to replication stresses. It maintains the integrity of stalled replication forks and prevents premature segregation of largely unreplicated chromosomes. In budding yeast, Mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac08ee66d5cf6a6e796354277e76585
https://hal.archives-ouvertes.fr/hal-03044284
https://hal.archives-ouvertes.fr/hal-03044284
Autor:
David Martín-Oliva, F. Javier Oliver, Mariano Ruiz de Almodóvar, José Antonio Muñoz-Gámez, José Manuel Rodríguez-Vargas, Antonio Almendros, Rosa Quiles-Pérez, Josiane Ménissier-de Murcia, Gilbert de Murcia, Rocío Aguilar-Quesada
Publikováno v:
Autophagy
Autophagy, Taylor & Francis, 2009, 5 (1), pp.61-74. ⟨10.4161/auto.5.1.7272⟩
Autophagy, Taylor & Francis, 2009, 5 (1), pp.61-74. ⟨10.4161/auto.5.1.7272⟩
Autophagy is a lysosome-dependent degradative pathway frequently activated in tumor cells treated with chemotherapy or radiation. PARP-1 has been implicated in different pathways leading to cell death and its inhibition potentiates chemotherapy-induc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6af02a2a797b5a9e42b1b711d42af94
https://hal.archives-ouvertes.fr/hal-02371531
https://hal.archives-ouvertes.fr/hal-02371531
Publikováno v:
Drug Metabolism and Disposition
Drug Metabolism and Disposition, American Society for Pharmacology and Experimental Therapeutics (ASPET), 2008, 36 (12), pp.2556-63. ⟨10.1124/dmd.108.023333⟩
Drug Metabolism and Disposition, 2008, 36 (12), pp.2556-63. ⟨10.1124/dmd.108.023333⟩
Drug Metabolism and Disposition, American Society for Pharmacology and Experimental Therapeutics (ASPET), 2008, 36 (12), pp.2556-63. ⟨10.1124/dmd.108.023333⟩
Drug Metabolism and Disposition, 2008, 36 (12), pp.2556-63. ⟨10.1124/dmd.108.023333⟩
International audience; This study was designed to analyze the effects of the Ca2+/calmodulin-dependent protein kinase kinase (CaMKK) inhibitor STO-609 (7-oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic acid) toward the aryl hydrocarbon re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec862dc842f585fe7a07b4b531b607ce
https://pubmed.ncbi.nlm.nih.gov/18755850
https://pubmed.ncbi.nlm.nih.gov/18755850
Autor:
J M Ruiz de Almodóvar, F. Javier Oliver, Ana Cañuelo, José Antonio Muñoz-Gámez, Gilbert de Murcia, David Martín-Oliva, Rocío Aguilar-Quesada, M. Isabel Núñez, M. Teresa Valenzuela
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2005, 386 (Pt 1), pp.119-25. ⟨10.1042/BJ20040776⟩
Biochemical Journal, Portland Press, 2005, 386 (Pt 1), pp.119-25. ⟨10.1042/BJ20040776⟩
p53 deficiency confers resistance to doxo (doxorubicin), a clinically active and widely used antitumour anthracycline antibiotic. The purpose of the present study was to investigate the reversal mechanism of doxo resistance by the potent PARP [poly(A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f0e349143e197743920f1589b40effc
https://hal.archives-ouvertes.fr/hal-02371526
https://hal.archives-ouvertes.fr/hal-02371526