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Updated: Jun 10, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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基因和分子途径参与状细胞贫血病变的评估:生物信息学分析和未来的前景

Reza Maddah1, Sareh Etemad2, Bahareh Shateri Amiri3

  • 1Department of Bioprocess Engineering, Institute of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

Iranian journal of public health
|October 21, 2024
PubMed
概括

状细胞疾病 (SCD) 涉及有缺陷的全球蛋白链. 这项研究确定了SLC4A1和TOP2A等关键基因,这些基因对SCD病原和潜在的诊断标志物至关重要.

关键词:
基因基因 基因基因 基因基因分子路径的分子路径.病变的发生和发病.状细胞是一个状细胞.

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