Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tetyana, Denyssevych"'
Autor:
Linda Hamata, Tetyana Denyssevych, Brian Thiessen, Dawn Waterhouse, Sarah Jennings, Shirin Monfared, Sharon Smith, Mário L de Lemos
Publikováno v:
Journal of Oncology Pharmacy Practice. 15:45-52
Background. Neurotoxicity of intrathecal (IT) chemotherapy has been variously attributed to the preservatives, volume, osmolality, and pH of the preparations. There has been little evaluation of how different drug concentrations or diluents can affec
Autor:
Tetyana Denyssevych, Marcel B. Bally, Karen A. Gelmon, Hong Yan, Dana Masin, Corinna Warburton, Wieslawa H. Dragowska, Anne E. Wallis, Stephen Chia
Publikováno v:
Clinical Cancer Research. 10:2512-2524
Purpose: The purpose of this research was to assess the effects of single agent and combination treatment with trastuzumab and gefitinib on tumor growth and tumor microenvironment in two HER-2/neu overexpressing breast xenograft models, MDA-MB-435/LC
Autor:
Karen A. Gelmon, Marcel B. Bally, Tetyana Denyssevych, Stephen Chia, Norma Hudon, Dawn Waterhouse
Publikováno v:
Pharmaceutical research. 22(6)
We assessed the combination of doxorubicin or liposomal doxorubicin with trastuzumab for alterations in peak serum drug levels, as these agents are increasingly being paired in the treatment of aggressive breast cancer. We hypothesized that trastuzum
Autor:
Corinna, Warburton, Wieslawa H, Dragowska, Karen, Gelmon, Stephen, Chia, Hong, Yan, Dana, Masin, Tetyana, Denyssevych, Anne E, Wallis, Marcel B, Bally
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 10(7)
The purpose of this research was to assess the effects of single agent and combination treatment with trastuzumab and gefitinib on tumor growth and tumor microenvironment in two HER-2/neu overexpressing breast xenograft models, MDA-MB-435/LCC6(HER-2)
Publikováno v:
European journal of drug metabolism and pharmacokinetics. 27(2)
The MDR modulator, OC144-093, is a potential candidate for use in cancer therapy and exhibits potent biological activity in vitro and in vivo when combined with anticancer agents such as paclitaxel. Its inhibitory interaction with P-glycoprotein (Pgp
Autor:
Dawn N. Waterhouse, Tetyana Denyssevych, Norma Hudon, Stephen Chia, Karen A. Gelmon, Marcel B. Bally
Publikováno v:
Pharmaceutical Research; Jun2005, Vol. 22 Issue 6, p915-922, 8p