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Updated: Jan 16, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
07:00

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Published on: April 1, 2019

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协会研究SPARCL1 在缺血性中风中的基因多态性

Seong Shin Kwak1,2, Ki Ook Lee3, Chang Soo Ryu1,2

  • 1Department of Life Science, Graduate School, CHA University, 335 Pangyo-ro, Bundang-gu, Seongnam 13488, Republic of Korea.

Genes
|September 27, 2025
PubMed
概括

分泌的蛋白酸性和富含囊类1 (SPARCL1) 基因变异与缺血性中风风险有关. 这些SPARCL1多态可能作为预测中风和指导脑损伤治疗策略的潜在生物标志物.

关键词:
这就是SPARCL1的原因.热酸结合的结合缺血性中风 中风多形态主义的多态主义.

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