相关实验视频
Updated: Jun 25, 2025

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Iris Fixation via External Pentagram Suturing
Published on: May 5, 2022
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在中期维护期间的6 - 甲普林相关的阴侧阻塞综合征I:病例报告
Katie Voelz1,2, Gwendolyn Miller3, Cathy Lee-Miller1,2
1Department of Pediatrics.
Journal of pediatric hematology/oncology
|May 22, 2024
概括
在提奥普林治疗前,对TPMT和NUDT15酶的遗传查至关重要. 这一案例突显了6 - MP在未被诊断的酶功能障碍患者的严重并发症,强调了预防性基因检测的必要性.
科学领域:
- 药物基因组学 药物基因组学
- 在瘤学瘤学.
- 临床药理学 临床药理学
背景情况:
- 提奥普林类药物 (例如6 - 默卡普普林) 对于治疗免疫性疾病和恶性瘤至关重要.
- 氨酸S-甲基转移酶 (TPMT) 和努迪克斯-酶-15 (NUDT15) 酶对于氨酸代谢至关重要.
- 在TPMT和NUDT15的遗传变异可以导致药物代谢的改变和毒性风险的增加.
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