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在儿科T细胞急性淋巴细胞白血病中解码线粒体功能障碍相关基因变异的诊断生物标志物

Yunfeng Lu1, Xi Yang2, Liying Liu3

  • 1Department of Pediatric Hematology and Oncology, Shandong Provincial Hospital affiliated to Shandong First Medical University, 324 Jing Wu Road, Jinan, 250021, China. ludoctorlu@163.com.

Scientific reports
|July 2, 2025
PubMed
概括

线粒体功能障碍是儿科T细胞急性淋巴细胞白血病 (T-ALL) 的关键. 这项研究确定了关键基因 (MDRDEGs),并开发了一种诊断模型,以改善儿科T-ALL检测和治疗.

关键词:
生物信息学分析机器学习是机器学习.线粒体功能障碍 线粒体功能障碍儿科瘤学 儿科瘤学在RNLS中使用RNLS.所有的T-ALL.在ULK1中,ULK1是ULK1.

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