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

Multi-Scale Transcriptomic Sequencing Data Analysis Reveals LINC00467 is Associated with Malignant Progression in Breast Cancer: An In Silico and In Vitro Study

多尺度转录组测序数据分析揭示LINC00467与乳腺癌恶性进展相关:一项计算机模拟和体外研究

Zha, Hui; Li, Chao; Chen, Jia; Bo, Hao; Hu, Zhaolan; Qin, Zailong; Guo, Jie; Yuan, Junbin

Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene

对由NDUFAF6基因双等位基因功能缺失变异引起的Leigh综合征中国患者的临床和遗传分析

Yang, Qi; Zhang, Qiang; Zhou, Xunzhao; Qin, Zailong; Liang, Xuanjing; Yi, Sheng; Zhang, Shujie; Lu, Weiliang; Yi, Shang; Luo, Jingsi

Characterization of a novel inherited splice-site variant in MAPK8IP3 expands the genetic and phenotypic spectrum of neurodevelopmental disorders

对MAPK8IP3中一种新型遗传剪接位点变异的鉴定,拓展了神经发育障碍的遗传和表型谱。

Yi, Sheng; Yang, Qi; Song, Xiong; Huang, Limei; Yi, Shang; Qin, Zailong; Luo, Jingsi

Clinical and Genetic Analysis of SMARCC2-Related Diseases in Three Chinese Patients

三例中国SMARCC2相关疾病患者的临床和基因分析

Ou, Shan; Zhang, Shujie; Yang, Qi; Zhang, Qiang; Zhou, Xunzhao; Zhang, Qinle; Rong, Xiuliang; Qi, Nana; Qian, Jiale; Xi, Bibing; Lin, Ranran; Wei, Shengkai; Su, Jingyu; Qin, Zailong; Luo, Jingsi

Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasia

COG5基因中导致胎儿水肿和骨骼发育不良的新型复合杂合变异

Yang, Qi; He, Wei; Zhang, Qiang; Yi, Sheng; Zhou, Xunzhao; Wang, Linlin; Yi, Shang; Qin, Zailong; Luo, Jingsi

[Retracted] Gambogic acid suppresses colon cancer cell activity in vitro

【已撤稿】藤黄酸在体外抑制结肠癌细胞活性

Zhou, Zailong; Ma, Jian

Targeting the LINC01272-FUS signal axis inhibits the migration and invasion of testicular germ cell tumors.

靶向 LINC01272-FUS 信号轴可抑制睾丸生殖细胞肿瘤的迁移和侵袭。

Zhao Xueheng, Cao Jian, Xue Lei, Fan Liqing, Zhu Fang, Qin Zailong, Chen Ziyi, Liu Zhizhong, Shu Jinhui, Bo Hao

Case Report: Cabezas syndrome caused by CUL4B gene mutations in two unrelated Chinese boys

病例报告:两名互不相关的中国男孩因CUL4B基因突变而患上卡贝萨斯综合征

Lin, Li; Yang, Qi; Zhang, Shujie; Zhou, Xunzhao; Li, Xiaoling; Yi, Sheng; Zhang, Qiang; Yi, Shang; He, Sheng; Qin, Zailong; Luo, Jingsi

ASXL3 gene variants causing Bainbridge-Ropers syndrome: clinical and genetic analysis of four Chinese patients

ASXL3基因变异导致Bainbridge-Ropers综合征:四例中国患者的临床和遗传分析

Yang, Qi; Zhang, Qiang; Zhou, Xunzhao; Yi, Shang; Qin, Zailong; Yi, Sheng; He, Sheng; Luo, Jingsi

Ensemble learning for microbiome-based caries diagnosis: multi-group modeling and biological interpretation from salivary and plaque metagenomic data

基于微生物组的龋病诊断集成学习:唾液和牙菌斑宏基因组数据的多组建模和生物学解释

Wei, Fangqiao; Wu, Zailong; Li, Guanghui; Sun, Xiangyu; Shi, Xiangru; Tan, Lei; Ai, Tianxiang; Qu, Long; Zheng, Shuguo