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

Prevalence of inherited metabolic disorders among newborns in Zhuzhou, a southern city in China

中国南方城市株洲新生儿遗传性代谢疾病患病率

Luo, Hunjin; Wang, Jiqing; Chen, Junfeng; Yi, Huijian; Yang, Xiaodong; Peng, Yao; Ni, Liu; Yang, Yi-Qiong; Zhang, Xiao-Min; Huang, Hongping

Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome

对一名特纳综合征患者罕见嵌合型X环染色体的特征分析

Luo, Hunjin; Ni, Liu; Yang, Yi-Qiong; Zhang, Xiao-Min; Huang, Hongping; Tan, Sainan; Ling, Chen; Liang, Li; Wang, Ling; Dan, Tang; Zhou, Shu-Xiang; Yang, Chunliu

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2

对一名患有2型瓦尔登堡综合征的患者中发现的MITF基因非终止突变进行功能分析

Sun, Jie; Hao, Ziqi; Luo, Hunjin; He, Chufeng; Mei, Lingyun; Liu, Yalan; Wang, Xueping; Niu, Zhijie; Chen, Hongsheng; Li, Jia-Da; Feng, Yong

LEF-1 Regulates Tyrosinase Gene Transcription In Vitro

LEF-1体外调控酪氨酸酶基因转录

Xueping Wang, Yalan Liu, Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Zhijie Niu, Jie Sun, Hunjin Luo, Jiada Li, Yong Feng

Identification of a novel anti-apoptotic E3 ubiquitin ligase that ubiquitinates antagonists of inhibitor of apoptosis proteins SMAC, HtrA2, and ARTS

鉴定出一种新型抗凋亡E3泛素连接酶,该酶可泛素化凋亡抑制蛋白SMAC、HtrA2和ARTS的拮抗剂。

Kim, Jung-Bin; Kim, So Youn; Kim, Byeong Mo; Lee, Hunjin; Kim, Insook; Yun, Jeanho; Jo, Yejin; Oh, Taeheun; Jo, Yongsam; Chae, Hee-Don; Shin, Deug Y

Disease-causing mutation in PKR2 receptor reveals a critical role of positive charges in the second intracellular loop for G-protein coupling and receptor trafficking

PKR2受体的致病突变揭示了第二个胞内环中正电荷在G蛋白偶联和受体转运中的关键作用。

Peng, Zhen; Tang, Yong; Luo, Hunjin; Jiang, Fang; Yang, Jiannan; Sun, Lin; Li, Jia-Da