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

Research hotspots and trends in therapeutic drug monitoring of anticancer drugs: a 1990-2024 bibliometric analysis

抗癌药物治疗药物监测的研究热点和趋势:1990-2024 年文献计量分析

Qian, Can; Yuan, Ting; Lu, Guanting; He, Miao; Li, Xin; Su, Huaiyu; Li, Chenglong

Tissue-resident memory T cells in diseases and therapeutic strategies

组织驻留记忆T细胞在疾病和治疗策略中的作用

Xie, Daoyuan; Lu, Guanting; Mai, Gang; Guo, Qiuyan; Xu, Guofeng

Tissue-resident memory T cells in urinary tract diseases

泌尿系统疾病中的组织驻留记忆T细胞

Xu, Guofeng; Li, Yuying; Lu, Guanting; Xie, Daoyuan

Tissue-Resident Memory T Cells in Rheumatoid Immune Diseases: Pathogenic Mechanisms and Therapeutic Strategies

类风湿性免疫疾病中的组织驻留记忆T细胞:致病机制和治疗策略

Tian, Yu; Zhang, Jie; Wu, Lianying; Zhang, Chi; Zheng, Fan; Yang, Yang; Lu, Guanting; Xie, Daoyuan

Metabolomics Insights into Gut Microbiota and Functional Constipation

代谢组学对肠道菌群和功能性便秘的深入研究

Zheng, Fan; Yang, Yong; Lu, Guanting; Tan, Joo Shun; Mageswary, Uma; Zhan, Yu; Ayad, Mina Ehab; Lee, Yeong-Yeh; Xie, Daoyuan

Protocol to study the effects of mutations near splicing sites on pre-mRNA splicing.

研究剪接位点附近突变对前体mRNA剪接影响的方案

Xie Daoyuan, Peng Qiongling, Tian Yu, Han Yangyun, Lu Guanting

A c.726C>G (p.Tyr242Ter) nonsense mutation-associated with splicing alteration (NASA) of WDR45 gene underlies β-propeller protein-associated neurodegeneration (BPAN).

WDR45 基因的 c.726C>G (p.Tyr242Ter) 无义突变与剪接改变 (NASA) 相关,是 β-螺旋桨蛋白相关神经退行性疾病 (BPAN) 的根本原因

Peng Qiongling, Cui Ying, Wu Jin, Wu Lianying, Liu Jiajia, Han Yangyun, Lu Guanting

Hepatic Tumor Stiffness Measured by Shear Wave Elastography Is Prognostic for HCC Progression Following Treatment With Anti-PD-1 Antibodies Plus Lenvatinib: A Retrospective Analysis of Two Independent Cohorts

剪切波弹性成像测量的肝肿瘤硬度可预测抗PD-1抗体联合乐伐替尼治疗后肝细胞癌的进展:两项独立队列的回顾性分析

Yuan, Guosheng; Xie, Fuli; Song, Yangda; Li, Qi; Li, Rong; Hu, Xiaoyun; Zang, Mengya; Cheng, Xiao; Lu, Guanting; Huang, Jing; Fan, Wenzhe; Rong, Xiaoxiang; Sun, Jian; Chen, Jinzhang

A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicing

同义变异通过影响前体mRNA剪接,导致一种罕见的维德曼-劳滕施特拉赫综合征,并伴有轻度贫血。

Peng, Qiongling; Zhang, Yan; Xian, Binqiang; Wu, Lianying; Ding, Jianying; Ding, Wuwu; Zhang, Xin; Ding, Bilan; Li, Ding; Wu, Jin; Hu, Xiaowu; Lu, Guanting

A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal Anomalies

一种导致神经发育障碍(伴有面部畸形和远端骨骼异常)的全新 ZMIZ1 致病变异

Lu, Guanting; Ma, Liya; Xu, Pei; Xian, Binqiang; Wu, Lianying; Ding, Jianying; He, Xiaoyan; Xia, Huiyun; Ding, Wuwu; Yang, Zhirong; Peng, Qiongling