TRANSGENIC CORE
转基因核心
基本信息
- 批准号:6946249
- 负责人:
- 金额:$ 10万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-07-01 至 2010-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The ability to produce defined changes in individual genes through transgenic and gene knockout
technologies has provided investigators with powerful tools for understanding the role of specific genes and their corresponding proteins in a variety of biological processes and with the ability to monitor changes in genomic integrity in virtually every cell and tissue type, including post mitotic tissues. Sophisticated methods of regulating gene expression with molecular switches (e.g., tetracycline binary system of gene regulation, Cre recombinase-mediated regulation of sequences flanked by lox P sites) combined with transgenic and gene knockout technologies are facilitating investigations into the roles of specific genes in aging in adult
animals by bypassing embryonic expression. Most recently, RNAi has been shown to be a powerful method for studying the role of specific genes and their corresponding proteins and can be used in conjunction with transgenic technology to produce animals in which reduced abundance of specific proteins can be achieved. These genetic manipulations can be used with traditional methods of studying aging (e.g., lifespan studies, cross-sectional pathology studies) to test directly the role of specific genes in aging. The major function of the Transgenic Core is to make genetically manipulated rodents for aging studies. This Core is essential for investigators interested in studying the roles of specific genes in aging and age-related diseases. Accordingly, the Specific Aims of the Transgenic Core are: 1. To produce and identify transgenic founder mice and rats. 2. To assist investigators in the production of mice carrying gene knockouts. 3. To provide educational activities for students, postdoctoral fellows, investigators, and laboratory personnel engaged in using transgenic rodents. 4. To implement new technologies for generating genetically engineered rodents as the need arises.
通过转基因和基因敲除在单个基因中产生确定变化的能力
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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Christi A Walter其他文献
Christi A Walter的其他文献
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{{ truncateString('Christi A Walter', 18)}}的其他基金
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10436348 - 财政年份:2020
- 资助金额:
$ 10万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10646448 - 财政年份:2020
- 资助金额:
$ 10万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10264033 - 财政年份:2020
- 资助金额:
$ 10万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10091650 - 财政年份:2020
- 资助金额:
$ 10万 - 项目类别:
Tumor Suppressors Mediate a Reduction in Male Gamete Quality with Aging
肿瘤抑制剂介导雄性配子质量随着衰老而降低
- 批准号:
9564362 - 财政年份:2017
- 资助金额:
$ 10万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8195926 - 财政年份:2010
- 资助金额:
$ 10万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
7930438 - 财政年份:2010
- 资助金额:
$ 10万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8259063 - 财政年份:2010
- 资助金额:
$ 10万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8397515 - 财政年份:2010
- 资助金额:
$ 10万 - 项目类别:
Base Excision Repair, Genetic Integrity & Health Span
碱基切除修复、遗传完整性
- 批准号:
7109417 - 财政年份:2004
- 资助金额:
$ 10万 - 项目类别: