Core C. Cell Culture and Animal Models Core Core C, the Cell Culture and Animal Models Core, is an integrated, dedicated, essential component of the Program, which will provide materials and services to all four Projects of the Program. This Core supports the Projects by providing specialized cell culture facilities, resources and expertise, by maintaining active and frozen stocks of cell lines used by the Projects, by providing training in cell culture techniques when needed by researchersin the Projects, and by assisting with cell culture experiments or performing cell culture experiments when desired by the Program Leaders. In addition, the Core will oversee an SPF animal facility in which studies with mice can be performed. This colony is suitable for long term studies of genetically altered mice, immune deficient (nude) mice and mice immunosuppressed by irradiation and/or drug treatments. The equipment, supplies, and expertise needed to monitor animals for tumor development and to implant, measure,and treat tumors will be available in this Core facility. When desired by the Project Leaders, the Core will maintain mouse strains and animal tumor model systems, will train Project staff in the techniques used with these model systems, and will participate in the design, performance, and analysisof experiments using these mouse model systems.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
3P01CA129186-05S1
Application #
8518513
Study Section
Special Emphasis Panel (ZCA1-GRB-S)
Project Start
Project End
Budget Start
2011-08-01
Budget End
2013-07-31
Support Year
5
Fiscal Year
2012
Total Cost
$6,917
Indirect Cost
$2,751
Name
Yale University
Department
Type
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Zhu, Rui; Baumann, Raymond P; Penketh, Philip G et al. (2013) Hypoxia-selective O6-alkylguanine-DNA alkyltransferase inhibitors: design, synthesis, and evaluation of 6-(benzyloxy)-2-(aryldiazenyl)-9H-purines as prodrugs of O6-benzylguanine. J Med Chem 56:1355-9
Zhu, Rui; Baumann, Raymond P; Patridge, Eric et al. (2013) Chloroethylating and methylating dual function antineoplastic agents display superior cytotoxicity against repair proficient tumor cells. Bioorg Med Chem Lett 23:1853-9
Daley, James M; Niu, Hengyao; Sung, Patrick (2013) Roles of DNA helicases in the mediation and regulation of homologous recombination. Adv Exp Med Biol 767:185-202
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