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中文摘要
翻译
我们目前专注于分析染色体易位和机制涉及断裂和修复机制涉及易位。使用高分辨率显微镜结合机器学习,我们目前正在寻找新的方法来自动对患者样本进行易位评分,这些易位涉及我们在以前的出版物中绘制的CENP-A结构域,并使用可以破坏这些途径的小分子抑制剂。这些易位和扩增几乎发生在我们所检查的每次实体瘤中。我们已经显著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衰老组织。
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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