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

DIPPER, a spatiotemporal proteomics atlas of human intervertebral discs for exploring ageing and degeneration dynamics

DIPPER,用于探索衰老和退化动态的人类椎间盘时空蛋白质组学图谱

Vivian Tam #, Peikai Chen #, Anita Yee, Nestor Solis, Theo Klein, Mateusz Kudelko, Rakesh Sharma, Wilson Cw Chan, Christopher M Overall, Lisbet Haglund, Pak C Sham, Kathryn Song Eng Cheah, Danny Chan

Knowledge-based analyses reveal new candidate genes associated with risk of hepatitis B virus related hepatocellular carcinoma

基于知识的分析揭示与乙肝病毒相关肝细胞癌风险相关的新候选基因

Deke Jiang, Jiaen Deng, Changzheng Dong, Xiaopin Ma, Qianyi Xiao, Bin Zhou, Chou Yang, Lin Wei, Carly Conran, S Lilly Zheng, Irene Oi-Lin Ng, Long Yu, Jianfeng Xu, Pak C Sham, Xiaolong Qi, Jinlin Hou, Yuan Ji, Guangwen Cao, Miaoxin Li

Mutations in Hnrnpa1 cause congenital heart defects

Hnrnpa1 突变导致先天性心脏缺陷

Zhe Yu, Paul Lf Tang, Jing Wang, Suying Bao, Joseph T Shieh, Alan Wl Leung, Zhao Zhang, Fei Gao, Sandra Yy Wong, Andy Lc Hui, Yuan Gao, Nelson Dung, Zhi-Gang Zhang, Yanhui Fan, Xueya Zhou, Yalun Zhang, Dana Sm Wong, Pak C Sham, Abid Azhar, Pui-Yan Kwok, Patrick Pl Tam, Qizhou Lian, Kathryn Se Cheah,

Dysfunction of Myosin Light-Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically-Engineered Rats

肌球蛋白轻链 4 (MYL4) 功能障碍可导致具有电、收缩和结构成分的遗传性心房心肌病:来自转基因大鼠的证据

Wenhui Peng, Miaoxin Li, Hailing Li, Kai Tang, Jianhui Zhuang, Jianguo Zhang, Jingjing Xiao, Hui Jiang, Dali Li, Yongchun Yu, Pak C Sham, Stanley Nattel, Yawei Xu

Tspyl2 Loss-of-Function Causes Neurodevelopmental Brain and Behavior Abnormalities in Mice

Tspyl2 功能丧失导致小鼠神经发育大脑和行为异常

Qi Li, Siu Yuen Chan, Kwun K Wong, Ran Wei, Yu On Leung, Abby Y Ding, Tomy C K Hui, Charlton Cheung, Siew E Chua, Pak C Sham, Ed X Wu, Grainne M McAlonan

Oncogenic mutation profiling in new lung cancer and mesothelioma cell lines

新肺癌和间皮瘤细胞系中的致癌突变谱分析

David Cl Lam ,Susan Y Luo ,Wen Deng ,Johnny Sh Kwan ,Jaime Rodriguez-Canales ,Annie Lm Cheung ,Grace Hw Cheng ,Chi-Ho Lin ,Ignacio I Wistuba ,Pak C Sham ,Thomas Sk Wan ,Sai-Wah Tsao

Genome-wide haplotype association mapping in mice identifies a genetic variant in CER1 associated with BMD and fracture in southern Chinese women

小鼠全基因组单倍型关联图谱鉴定出与中国南方女性骨密度和骨折相关的 CER1 基因变异

Paul L F Tang, Ching-Lung Cheung, Pak C Sham, Philip McClurg, Bob Lee, Shut-Yan Chan, David K Smith, Julian A Tanner, Andrew I Su, Kathryn S E Cheah, Annie W C Kung, You-Qiang Song