Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Carol Eng"'
Autor:
Oliver Dorigo, Min Song, Hong Wu, Carol Eng, David Mulholland, Amer Karam, Kuang-Yui Michael Chen, Mirela Fekete, Gottfried E. Konecny, Chintda Santiskulvong
Supplementary Figures S1-S2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000cf18c56536764481348459b42ca66
https://doi.org/10.1158/1078-0432.22442108.v1
https://doi.org/10.1158/1078-0432.22442108.v1
Autor:
Oliver Dorigo, Min Song, Hong Wu, Carol Eng, David Mulholland, Amer Karam, Kuang-Yui Michael Chen, Mirela Fekete, Gottfried E. Konecny, Chintda Santiskulvong
Purpose: This study evaluates the effect of dual PI3K and mTOR inhibition using NVP-BEZ235 in preclinical models of ovarian cancer as a potential novel therapeutic strategy.Experimental Design: Inhibition of PI3K/Akt/mTOR signaling by NVP-BEZ235 was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::054110590ae9da05f5e64d717898dcd9
https://doi.org/10.1158/1078-0432.c.6518930.v1
https://doi.org/10.1158/1078-0432.c.6518930.v1
Publikováno v:
Journal of virology, vol 92, iss 18
How histone acetylation promotes transcription is not clearly understood. Here, we confirm an interaction between p300 and the adenovirus 2 large E1A activation domain (AD) and map the interacting regions in E1A by observing colocalization at an inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dffc20edb5efbda50fd00276396f54b
https://escholarship.org/uc/item/2js2d5dd
https://escholarship.org/uc/item/2js2d5dd
Publikováno v:
Journal of Innovation Management, Vol 10, Iss 3, Pp 1-25 (2022)
Studies have highlighted the benefits of external knowledge building as a means of heightening a firm’s innovation activities. Simultaneously supply chain scholars have highlighted the lack of focus on social facets at the micro behavioral level, a
Externí odkaz:
https://doaj.org/article/345e909c441549d0b0db9080b5e21ed0
Publikováno v:
Anticancer research. 32(2)
Pharmacological inhibition of the phosphoinositide 3-kinase (PI3K)/Akt pathway prevents G(1) cell cycle progression into S, resulting in G(1) accumulation. The hypothesis that this arrest might negatively impact on chemotherapeutic agents primarily e
Autor:
Chintda Santiskulvong, Oliver Dorigo, Gottfried E. Konecny, Kuang-Yui Michael Chen, Amer Karam, Hong Wu, Mirela Fekete, Carol Eng, David J. Mulholland, Min Song
Purpose: This study evaluates the effect of dual PI3K and mTOR inhibition using NVP-BEZ235 in preclinical models of ovarian cancer as a potential novel therapeutic strategy. Experimental Design: Inhibition of PI3K/Akt/mTOR signaling by NVP-BEZ235 was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e4aa79481f0e630bad20d9044c08651
https://europepmc.org/articles/PMC3078990/
https://europepmc.org/articles/PMC3078990/
Publikováno v:
Cytoskeleton.
Targeting of the PI3K (phosphoinositide3-kinase)/Akt/mTOR pathway in human ovarian cancer cells is a promising novel therapeutic strategy. We investigated the effects of cisplatin and the PI3K inhibitor LY294002 on invasion, migration and the express
Publikováno v:
Journal of Entrepreneurship, Management and Innovation, Vol 17, Iss 3, Pp 67-113 (2021)
PURPOSE: Firms do not continue and prosper purely on their own individual endeavors, as each firm is influenced by the activities of others, and thus direct and indirect relationships shape the firm’s strategic management. These relationships form
Externí odkaz:
https://doaj.org/article/2a361f7fd8d446878ca824334aa0341f
Autor:
Oliver Dorigo, Wing Yi Lung, Carol Eng, David T. Wang, Richard C. Koya, Chintda Santiskulvong, Sara Zabih
Publikováno v:
Cancer Research. 72:836-836
Introduction: Ovarian cancer is the most lethal of the gynecological malignancies and the 5th leading cause of cancer related deaths amongst women in the US. It is a chemotherapy-sensitive disease, and about 85% of patients respond to first line trea
Publikováno v:
Cell. 36(4)
Rodent cells transformed by adenovirus 2 (Ad2) express two highly related viral proteins of 289 and 243 amino acids encoded in early region 1A (E1A). Transformation studies were performed with adenovirus mutants that express only one or the other E1A