Zobrazeno 1 - 10
of 709
pro vyhledávání: '"M E Dolan"'
Autor:
Amy L. Stark, Wendy B. London, Navin Pinto, Sharon J. Diskin, Nancy J. Cox, M E Dolan, Susan L. Cohn, Hae Kyung Im, Nirav N. Antao, Eric R. Gamazon, Jamie Myers, Anuar Konkashbaev, John M. Maris, Susan M. Ludeman
Publikováno v:
Clinical pharmacology and therapeutics
High-risk neuroblastoma is an aggressive malignancy, with high rates of treatment failure. We evaluated genetic variants associated with in vitro sensitivity to two derivatives of cyclophosphamide for association with clinical response in a separate
Publikováno v:
Cancer Research. 73:P3-15
Chemotherapy-induced peripheral neuropathy is the major dose-limiting toxicity for several anti-cancer drugs including taxanes, platinating agents and microtubule inhibitors. In general, animal models have been used to study neuropathy. Our goals are
Autor:
Hitoshi Zembutsu, Eric P. Winer, Nancy J. Cox, M E Dolan, Claudia Wing, Mark J. Ratain, Michiaki Kubo, Chidiamara Njoku, Eric R. Gamazon, Dorothy Watson, Clifford A. Hudis, Yusuke Nakamura, Ivo D. Shterev, Kouros Owzar, Heather E. Wheeler, Chen Jiang, Deanna L. Kroetz, Robert Michael Baldwin, Lawrence N. Shulman, Uchenna O. Njiaju
Publikováno v:
Clinical Cancer Research. 19:491-499
Purpose: We sought to show the relevance of a lymphoblastoid cell line (LCL) model in the discovery of clinically relevant genetic variants affecting chemotherapeutic response by comparing LCL genome-wide association study (GWAS) results to clinical
Autor:
Lidija K. Gorsic, Dana Ziliak, Heather E. Wheeler, Yujia Wen, M E Dolan, Rong Stephanie Huang
Publikováno v:
Pharmacogenetics and Genomics. 21:476-488
Aim To determine whether cellular apoptosis is a suitable phenotypic trait for pharmacogenomics studies by evaluating caspase 3/7-mediated activity in lymphoblastoid cell lines after treatment with six chemotherapeutic agents: 5′-deoxyfluorouridine
Autor:
Eric R. Gamazon, Emily O. Kistner, Wei Zhang, Shiwei Duan, Rong Stephanie Huang, Nancy J. Cox, M E Dolan
Publikováno v:
Pharmacogenetics and Genomics. 20:269-273
We have developed Pharmacogenomics And Cell database (PACdb), a results database that makes available relationships between single nucleotide polymorphisms, gene expression, and cellular sensitivity to various drugs in cell-based models to help deter
Autor:
Xu, Junfeng1,2,3,4,5 (AUTHOR), Lou, Xin1,2,3,4,5 (AUTHOR), Wang, Fei1,2,3,4,5 (AUTHOR), Zhang, Wuhu1,2,3,4,5 (AUTHOR), Xu, Xiaowu1,2,3,4,5 (AUTHOR), Ye, Zeng1,2,3,4,5 (AUTHOR), Zhuo, Qifeng1,2,3,4,5 (AUTHOR), Wang, Yan1,2,3,4,5 (AUTHOR), Jing, Desheng1,2,3,4,5 (AUTHOR), Fan, Guixiong1,2,3,4,5 (AUTHOR), Chen, Xuemin6 (AUTHOR), Zhang, Yue6 (AUTHOR), Zhou, Chenjie1,2,3,4,5 (AUTHOR), Chen, Jie1,2,3,4,5 (AUTHOR) chenjie@fudanpci.org, Qin, Yi1,2,3,4,5 (AUTHOR) qinyi@fudanpci.org, Yu, Xianjun1,2,3,4,5 (AUTHOR) yuxianjun@fudanpci.org, Ji, Shunrong1,2,3,4,5 (AUTHOR) jishunrong@fudanpci.org
Publikováno v:
Advanced Science. 9/18/2024, Vol. 11 Issue 35, p1-21. 21p.
Publikováno v:
Clinical Pharmacology & Therapeutics. 92:425-427
The use of cell-based models has emerged as a promising means to discover and validate pharmacologic phenotype-genotype relationships. The availability of large-scale genome studies in both human and model systems is now allowing us unprecedented opp
Publikováno v:
Bone Marrow Transplantation. 27:1201-1209
The ability to culture CD34+ stem cells, while maintaining their pluripotency, is essential for manipulations such as gene transfection for therapeutic trials. Human peripheral blood (PB) CD34+ cells (> or = 90% purity) were cultured for up to 4 days
Publikováno v:
Gene Therapy. 8:384-390
Introduction of foreign genes into human CD34(+) hematopoietic precursor cells offers a means to correct inborn errors or to protect human stem cells from chemotherapeutic damage. Electroporation is a non-chemical, nonviral, highly reproducible means
Autor:
M E Dolan, Reginald B. Ewesuedo
Publikováno v:
Cancer Chemotherapy and Pharmacology. 46:150-155
Purpose: O6-Benzylguanine (BG) is a modulator of the DNA repair protein, O6-alkylguanine-DNA alkyltransferase (AGT). BG is converted in mice, rats and humans to an equally active, yet longer-lived metabolite, O6-benzyl-8-oxoguanine (8-oxo-BG) by CYP1