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中文摘要
翻译
我们目前的重点是分析染色体易位,以及易位所涉及的断裂和修复机制。使用高分辨率显微镜与机器学习相结合,我们目前正在寻找新的方法来自动对涉及我们在以前的出版物中映射的CENP-A结构域的患者样本的易位进行评分,并使用可以破坏这些途径的小分子抑制剂。这些移位和扩增几乎在我们检查过的每一次实体瘤中都会发生。我们已经显著地扩大了我们的工作范围,包括成人胶质母细胞瘤和来自人类患者的老化组织。
英文摘要
We are currently focused on analysis of chromosome translocations and mechanisms involved in the breaks and repair machinery involved in the translocations. Using high resolution microscopy coupled to machine learning, we are currently finding new ways to automatically score patient samples for translocations involving the CENP-A domain we mapped in previous publications, and using small molecule inhibitors that can disrupt these pathways. These translocations and amplifications occur in virtually every time of solid tumor we have examined. We have expanded our work significantly to include adult glioblastomas and aging tissues derived from human patients.
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Analysis of centromere identity and structure in human cells
  • 批准号:
    7966218
  • 项目类别:
  • 资助金额:
    $31.78万
  • 财政年份:
    --
  • 负责人:
    YAMINI P DALAL
  • 依托单位:
Genome wide profiling of histone variants in tumors
  • 批准号:
    8938009
  • 项目类别:
  • 资助金额:
    $36.81万
  • 财政年份:
    --
  • 负责人:
    YAMINI P DALAL
  • 依托单位:
Analysis of centromere identity and structure in human cells
  • 批准号:
    8553040
  • 项目类别:
  • 资助金额:
    $30.55万
  • 财政年份:
    --
  • 负责人:
    YAMINI P DALAL
  • 依托单位:
Analysis of centromere identity and structure in human cells
  • 批准号:
    10014571
  • 项目类别:
  • 资助金额:
    $47.33万
  • 财政年份:
    --
  • 负责人:
    YAMINI P DALAL
  • 依托单位:
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