CORE--Shared Resources Animal Facility
核心--共享资源动物设施
基本信息
- 批准号:6990463
- 负责人:
- 金额:$ 6.51万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2004
- 资助国家:美国
- 起止时间:2004-06-28 至 2009-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): The mission of the Animal Resources Facility is to enable
Burnham Institute Cancer Center investigators to use small animals for biomedical research, a mission that has been and will continue to be critical to the success of the Cancer Center. The Facility operates as a centralized service in which most procedures are performed by trained Facility staff. This ensures a consistent standard of care, minimizes traffic through the Facility, and frees Cancer Center investigators from having to hire and train their own personnel for these tasks. The Facility provides three types of services: Mouse Genetics, Husbandry, and In Vivo Analysis. Mouse Genetics creates new lines of transgenic and gene knockout mice, Husbandry maintains and manages existing colonies of animals, and In Vivo Analysis helps to characterize the phenotypes of animals used for experimental studies. Current and projected cancer-related projects supported by the In Vivo Analysis service include the use of xenograft and transgenic mouse models to study mechanisms of tumor induction and progression, along with testing the efficacy of new agents for slowing tumor growth and metastasis. It is
envisioned that the Center's Drug Discovery Initiative will lead to the identification of new compounds that will need to be tested in vivo for activity against tumor growth and metastasis. To aid in the evaluation of these drugs, the In Vivo Analysis service will offer a centralized Tumor Analysis Core to establish and evaluate tumor onset and progression in transgenic and xenograft models. Specific Aims for this core will be to: 1) Offer consultation and information about the use of animal models, drug formulation, and drug administration; 2) Maintain two transgenic mouse colonies, TRAMP and MMTV-PyMT, for the respective study of prostate and mammary cancer. De novo tumorigenesis in these lines closely mimics that seen in human cases; 3) Maintain nude mice and stocks of MDA-MB-435 breast cancer and PC-3 prostate cancer cell lines for xenograft studies of drug effectiveness against human mammary and prostate tumors, respectively; 4) Initiate tumor growth (by breeding or xenografting) and
quantify tumor onset, growth, and metastasis in control and treated animals and ; 5) Collaborate with Informatics and Data Management Resources to maintain data archives for comparison of different drug trials.
描述(由申请人提供):动物资源基金的使命是使
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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William B. Stallcup其他文献
Correlation of surface antigens and cell type in cloned cell lines from the rat central nervous system.
大鼠中枢神经系统克隆细胞系表面抗原与细胞类型的相关性。
- DOI:
- 发表时间:
1976 - 期刊:
- 影响因子:3.7
- 作者:
William B. Stallcup;Melvin Cohn - 通讯作者:
Melvin Cohn
Agonist action of neostigmine on acetylcholine receptors of cultured mammalian muscle
- DOI:
10.1016/0006-8993(79)90550-x - 发表时间:
1979-08-24 - 期刊:
- 影响因子:
- 作者:
Robert J. Bloch;William B. Stallcup - 通讯作者:
William B. Stallcup
A Rapid Purification Procedure for Glyceraldehyde 3-Phosphate Dehydrogenase from Bakers' Yeast
- DOI:
10.1016/s0021-9258(19)44794-7 - 发表时间:
1972-10-01 - 期刊:
- 影响因子:
- 作者:
William B. Stallcup;Stephen C. Mockrin;D.E. Koshland - 通讯作者:
D.E. Koshland
Cai et al. reply
蔡等人的答复
- DOI:
10.1038/nature07917 - 发表时间:
2009-04-16 - 期刊:
- 影响因子:48.500
- 作者:
Chen-Leng Cai;Jody C. Martin;Yunfu Sun;Li Cui;Lianchun Wang;Kunfu Ouyang;Lei Yang;Lei Bu;Xingqun Liang;Xiaoxue Zhang;William B. Stallcup;Christopher P. Denton;Andrew McCulloch;Ju Chen;Sylvia M. Evans - 通讯作者:
Sylvia M. Evans
Specificity of adhesion between cloned neural cell lines
- DOI:
10.1016/0006-8993(77)90598-4 - 发表时间:
1977-05-13 - 期刊:
- 影响因子:
- 作者:
William B. Stallcup - 通讯作者:
William B. Stallcup
William B. Stallcup的其他文献
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{{ truncateString('William B. Stallcup', 18)}}的其他基金
Oligodendrocyte Maturation/Myelination in NG2 Null Mice
NG2 无效小鼠的少突胶质细胞成熟/髓鞘形成
- 批准号:
8056780 - 财政年份:2010
- 资助金额:
$ 6.51万 - 项目类别:
Ephrin-A3 in Neuron-Glia Communication
Ephrin-A3 在神经元-胶质细胞通讯中的作用
- 批准号:
7185423 - 财政年份:2006
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
6622932 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
7033823 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
7894844 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
8657813 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
9263044 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
NG2-PG in tumor vascularization and progression
NG2-PG 在肿瘤血管化和进展中的作用
- 批准号:
6881044 - 财政年份:2002
- 资助金额:
$ 6.51万 - 项目类别:
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