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

Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia

多中心起源和基因流动塑造了东南亚β-地中海贫血突变的多样性

Zhang, Qianqian; Li, Jialong; Huang, Haoyang; Shang, Xuan; Ye, Yuhua; Zhang, Wei; Lin, Peng; Gong, Yi; Hoh, Boon-Peng; Luo, Qingming; Yan, Tizhen; Pan, Xinghua; Stoneking, Mark; Xu, Shuhua; Xu, Xiangmin; Deng, Lian

Correction: Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization

更正:研究肢带型肌营养不良症R8的基因型-表型相关性:临床严重程度、蛋白质生物学功能和蛋白质寡聚化的关联

Liang, Xiongda; Si, Jiameng; Xie, Hongting; Guan, Yuqing; Lin, Wanying; Lin, Zezhang; Zheng, Ganwei; Wei, Xiaofeng; Xiong, Xingbang; Zhuang, Zhengfei; Shang, Xuan

Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization.

研究肢带型肌营养不良症 R8 的基因型-表型相关性:临床严重程度、蛋白质生物学功能和蛋白质寡聚化的关联

Liang Xiongda, Si Jiameng, Xie Hongting, Guan Yuqing, Lin Wanying, Lin Zezhang, Zheng Ganwei, Wei Xiaofeng, Xiong Xingbang, Zhuang Zhengfei, Shang Xuan

Application value of long-read sequencing in full characterization of thalassemia-associated structural variations: identifying a novel large segmental duplication and literature review

长读长测序在全面表征地中海贫血相关结构变异中的应用价值:鉴定一种新的大片段重复及文献综述

Zhong, Zeyan; Zheng, Ganwei; Zhu, Dina; Liu, Yongqiong; Lin, Zezhang; Guan, Zhiyang; Xiong, Fu; Chen, Jianhong; Shang, Xuan

Clinical evaluation of target capture sequencing technique for noninvasive prenatal diagnosis of β-thalassemia: A prospective case series

靶向捕获测序技术在β-地中海贫血无创产前诊断中的临床评价:一项前瞻性病例系列研究

Chen, Yao; Liu, Danyong; Yang, Fang; Xiong, Li; Shang, Xuan; Liu, Siping; Li, Meng; Zhong, Mei

Successful treatment of depressed esophageal squamous papilloma with interferon- alpha 2a: A case report

干扰素-α-2a成功治疗凹陷性食管鳞状乳头状瘤:病例报告

Jiang, Jiong; Shi, Hai-Tao; Wu, Jie; Sha, Su-Mei; Cai, Shang-Xuan; Liu, Xin

Prognostic biomarker and clinical significance of PLOD gene family in clear cell renal cell carcinoma

PLOD基因家族在透明细胞肾细胞癌中的预后生物标志物及临床意义

Shang, Xuan; Liu, Liu; Yang, Zhenwei; Yan, Min; Ren, Ruimin; Guo, Kexin; Wang, Jie; Zhang, Wei; Chang, Jiasong; Li, Jialei; Cao, Jimin; Li, Guang; Gao, Lijuan

An unusual case of thalassemia intermedia with inheritable complex repeats detected by single-molecule optical mapping

通过单分子光学图谱检测到一例罕见的具有可遗传复杂重复序列的中间型地中海贫血病例

Zhang, Qianqian; Lin, Peng; Mao, Aiping; Liu, Yongqiong; Shang, Xuan; Wei, Xiaofeng; Li, Yuezhen; Lin, Bin; Xu, Xiangmin

High-sensitivity flip chip blue Mini-LEDs miniaturized optical instrument for non-invasive glucose detection

用于非侵入式血糖检测的高灵敏度倒装芯片蓝色迷你LED微型光学仪器

Ye, Zhi Ting; Tseng, Shen Fu; Tsou, Shang Xuan; Tsai, Chun Wei

Hb H Disease Caused by Uniparental Disomy: First Report of the α(T-Saudi)α Mutation in the Chinese Population

由单亲二体性引起的Hb H病:中国人群中首次报道α(T-Saudi)α突变

Wang, Ge; Xie, Hongting; Zhang, Jun; Huang, Peng; Liang, Min; Zhu, Dina; Zhang, Qianqian; Zhou, Yuqiu; Shang, Xuan