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Chromosome Metabolism and Cancer

Chromosome Metabolism and Cancer
染色体代谢与癌症
批准号:
7812825
负责人:
Jonathan A Cooper
金额:
$21.44万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-11-15

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):本申请在通知no - od -09-058的支持下为另外两名博士后研究人员寻求资金,“NIH宣布为竞争性修订申请提供恢复法案资金”。我们已经确定了两名有价值的学员和优秀的导师,他们将在2011年3月31日结束的当前奖励期间加入培训计划。增加这些受训者将扩大研究和培训的范围,包括研究人类细胞核内染色体定位的调节机制和研究microRNA如何调节癌细胞中的基因表达。这两个项目都与癌症高度相关,两位候选人都非常合格。重要的是,其中一名学员是代表性不足的少数民族。如果获得资助,该奖项将通过为两名受训者提供大约18个月的就业机会(取决于奖项开始日期)来实现恢复法案的目标,并将帮助这些杰出的候选人在癌症生物学和染色体代谢方面的职业发展。
英文摘要
DESCRIPTION (provided by applicant): This application seeks funding for two additional postdoctoral research fellows under the aegis of Notice NOT-OD-09-058, "NIH Announces the Availability of Recovery Act Funds for Competitive Revision Applications". We have identified two worthy trainees and outstanding mentors who would be added to the Training Program for the duration of the current award, which ends 03/31/2011. Adding these trainees would expand the scope of the research and training to include studies on mechanisms that regulate chromosome location within the human cell nucleus and research on how microRNA's regulate gene expression in cancer cells. Both projects are highly cancer relevant, and both candidates are very highly qualified. Importantly, one of the trainees is an under-represented minority. If funded, this award would achieve the goals of the Recovery Act by providing employment to two trainees, for approximately 18 months (depending on the award start date), and would help these outstanding candidates forward in their careers in cancer biology and chromosome metabolism. RELEVANCE: Award of the requested supplement would allow the immediate funding of two excellent, qualified trainees and provide a lasting investment in the Nation's cancer research effort.
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Mechanisms of Purkinje cell migration
Regulation of cell migration and signaling by phosphotyrosine and ubiquitin
Regulation of cell migration and signaling by phosphotyrosine and ubiquitin
Regulation of cell migration and signaling by phosphotyrosine and ubiquitin
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