课题基金 / 基金详情

Targeting Eph receptors as anti-cancer therapy in malignant glioma.

Targeting Eph receptors as anti-cancer therapy in malignant glioma.
靶向 Eph 受体作为恶性神经胶质瘤的抗癌治疗。
批准号:
nhmrc : 552489
负责人:
Dr David Walker
金额:
$26.91万
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2009
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2009-01-01 至 2011-12-31

项目摘要

项目成果

Dr David Walker的其他基金

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中文摘要
翻译
恶性胶质瘤是脑癌最常见的形式,其特点是发病率和死亡率都很高。目前的治疗包括手术和辅助放化疗,但尽管有最好的护理,这种疾病的患者前景很差。对神经胶质瘤生物学的日益了解为改进治疗提供了前景。本研究旨在研究人类恶性神经胶质瘤动物模型中该疾病的治疗靶点。
英文摘要
Malignant gliomas are the commonest form of brain cancer and are characterised by a high degree of morbidity and mortality. Present treatment involves surgery and adjuvant chemoradiotherapy but despite best care the outlook for patients with this disease is poor. The increasing understanding of the biology of glioma offers the prospect of improved therapies. This proposal seeks to investigate a therapy target in this disease in animal models of human malignant glioma.
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会议论文
Developing sustainable Indigenous Health Worker led community oral health interventions.
  • 批准号:
    nhmrc : 571390
  • 项目类别:
    Early Career Fellowships
  • 资助金额:
    $22.97万
  • 财政年份:
    2009
  • 负责人:
    Dr David Walker
  • 依托单位:
Radiotherapy vs chemotherapy for low-grade gliomas stratified for genetic 1p loss: efficacy and quality of life benefits
  • 批准号:
    nhmrc : 509094
  • 项目类别:
    NHMRC Project Grants
  • 资助金额:
    $27.36万
  • 财政年份:
    2008
  • 负责人:
    Dr David Walker
  • 依托单位:
Sediment capture and deposition processes in coastal lagoons
  • 批准号:
    LP0883453
  • 项目类别:
    Linkage Projects
  • 资助金额:
    $5.85万
  • 财政年份:
    2008
  • 负责人:
    Dr David Walker
  • 依托单位:
Process evaluation of the training of Aboriginal health workers in rurual communities in basic oral health care
  • 批准号:
    nhmrc : 326239
  • 项目类别:
    NHMRC Postgraduate Scholarships
  • 资助金额:
    $9.74万
  • 财政年份:
    2005
  • 负责人:
    Dr David Walker
  • 依托单位:
国内基金
海外基金
Eph/Ephrin调控神经元活动促进胶质瘤进展的作用机制研究
Eph-Ephrin 信号通路通过调控 PVT→CeA 神经环路干预双相情感障碍共病睡眠障碍发生的机制研究
GRIP1突变通过Eph-ephrin受配体调控生发中心Tfh-B细胞互作和活化参与SLE发病机制研究
基于Eph/ephrin信号轴的ephrinB2高表达工程化细胞膜修饰支架介导大节段外周神经缺损修复及其材料生物学机制