日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Reactive oxygen species regulate adipose-osteogenic lineage commitment of human mesenchymal stem cells by modulating gene expression of C/EBP homology protein and aldo-keto reductase family 1 member A1.

活性氧通过调节 C/EBP 同源蛋白和醛酮还原酶家族 1 成员 A1 的基因表达来调节人类间充质干细胞的脂肪-骨谱系分化

Chiang Chen Hao, Kao Yu-Chieh, Lin Yi-Hui, Ma Yi-Shing, Wu Yu-Ting, Jian Bo-Yan, Wei Yau-Huei, Chen Chuan-Mu, Liou Ying-Ming

KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders

KCNQ2选择性过滤器突变导致Kv7.2 M电流功能障碍和构型改变,表现为癫痫性脑病和自闭症谱系障碍

Lee, Inn-Chi; Yang, Jiann-Jou; Liou, Ying-Ming; Wong, Swee-Hee

Early Blood Glucose Level Post-Admission Correlates with the Outcomes and Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy

新生儿缺氧缺血性脑病入院后早期血糖水平与预后及氧化应激相关

Lee, Inn-Chi; Yang, Jiann-Jou; Liou, Ying-Ming

Matrix metalloproteinase 1 1 G/2 G gene polymorphism is associated with acquired atrioventricular block via linking a higher serum protein level

基质金属蛋白酶1 1 G/2 G基因多态性与获得性房室传导阻滞相关,其机制是通过与较高的血清蛋白水平相关。

Chen, Jan-Yow; Chang, Kuan-Cheng; Liou, Ying-Ming

Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes

由KCNQ2突变导致的Kv7.2异源多聚体电流变化与长期神经发育结果相关。

Lee, Inn-Chi; Yang, Jiann-Jou; Wong, Swee-Hee; Liou, Ying-Ming; Li, Shuan-Yow

Transforming Growth Factor-β1 T869C Gene Polymorphism Is Associated with Acquired Sick Sinus Syndrome via Linking a Higher Serum Protein Level

转化生长因子-β1 T869C基因多态性与获得性病态鼻窦炎相关,其机制是通过关联较高的血清蛋白水平

Chen, Jan-Yow; Liu, Jiung-Hsiun; Wu, Hong-Dar Isaac; Lin, Kuo-Hung; Chang, Kuan-Cheng; Liou, Ying-Ming

Molecular targets for anti-oxidative protection of green tea polyphenols against myocardial ischemic injury

绿茶多酚抗氧化保护心肌缺血损伤的分子靶点

Hsieh, Shih-Rong; Cheng, Wei-Chen; Su, Yi-Min; Chiu, Chun-Hwei; Liou, Ying-Ming

Promoter polymorphism G-6A, which modulates angiotensinogen gene expression, is associated with non-familial sick sinus syndrome

启动子多态性G-6A可调节血管紧张素原基因表达,与非家族性病态窦房结综合征相关。

Chen, Jan-Yow; Liou, Ying-Ming; Wu, Hong-Dar Isaac; Lin, Kuo-Hung; Chang, Kuan-Cheng