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Development and preclinical validation of first-in-class dual inhibitors of the atypical MAP kinases ERK3 and ERK4

Development and preclinical validation of first-in-class dual inhibitors of the atypical MAP kinases ERK3 and ERK4
非典型 MAP 激酶 ERK3 和 ERK4 的一流双抑制剂的开发和临床前验证
批准号:
461610
负责人:
Meloche Sylvain
金额:
$69.66万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2022
资助国家:
加拿大
项目状态:
未结题
起止时间:
2022-03-01 至 2027-03-01

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中文摘要
翻译
蛋白激酶选择性化学抑制剂的开发对于了解蛋白激酶的作用机制和探索其在生理和疾病中的作用具有重要意义。这些化学工具对于验证潜在的药物靶点和
英文摘要
The development of selective chemical inhibitors of protein kinases is of key importance for understanding kinase mechanisms and exploring their roles in physiology and disease. These chemical tools are also essential to validate potential drug targets an
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Regulation, downstream targets and functional specificity of the MAP kinases ERK1 and ERK2
Targeting the degradation of the cyclin-dependent kinase inhibitor p21 as a novel approach to cancer therapy
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