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

Novel variation in the CEL gene causing impaired fasting glucose in a Chinese pediatric patient: case report and literature review

中国一名儿童患者因CEL基因新变异导致空腹血糖受损:病例报告及文献综述

Su, Chang; Piao, Yurong; Chen, Congli; Wu, Di; Li, Rongmin; Sang, Yanmei

Single-center experience description of surgical management of diffuse congenital hyperinsulinism in a pediatric non-current cohort

单中心经验描述:对非当前儿科队列中弥漫性先天性高胰岛素血症的外科治疗

Li, Xiaoxiang; Chen, Congli; Ji, Yangmingyue; Wang, Yuxi; Sang, Yanmei

Targeted degradation of cell surface proteins through endocytosis triggered by cell-penetrating peptide-small molecule conjugates.

通过细胞穿透肽-小分子缀合物触发的内吞作用靶向降解细胞表面蛋白

He Wanyi, Chen Congli, Zheng Jiwei, Li Yanyan, Shi Huaihuai, Zhou Yimin, Li Meiqing, Gong Ping, Liu Ke, Shao Ximing, Yao Xiaojun, Li Hongchang, Chen Liang, Fang Lijing

Linker-free PROTACs efficiently induce the degradation of oncoproteins.

无连接子的PROTACs能有效诱导癌蛋白降解

Zhang Jianchao, Chen Congli, Chen Xiao, Liao Kefan, Li Fengming, Song Xiaoxiao, Liu Chaowei, Su Ming-Yuan, Sun Huiyong, Hou Tingjun, Tan Chris Soon Heng, Fang Lijing, Rao Hai

Bifunctional compounds for targeted degradation of carbonic anhydrase IX through integrin-facilitated lysosome degradation.

通过整合素促进溶酶体降解靶向降解碳酸酐酶 IX 的双功能化合物

He Wanyi, Chen Congli, Cai Runjie, Zheng Jiwei, Yao Mengyu, Shim Joong Sup, Kwok Hang Fai, Yao Xiaojun, Fang Lijing, Chen Liang

GCK Mutation Analysis and Clinical Profiles of Chinese Pediatric Patients with MODY2: Insights into Screening and Diagnosis

中国儿童MODY2患者的GCK基因突变分析及临床特征:对筛查和诊断的启示

Su, Chang; Piao, Yurong; Chen, Congli; Miao, Yuqi; Wu, Di; Sang, Yanmei

Distinct Amino Acid-Based PROTACs Target Oncogenic Kinases for Degradation in Non-Small Cell Lung Cancer (NSCLC)

基于独特氨基酸的 PROTAC 靶向致癌激酶,在非小细胞肺癌 (NSCLC) 中降解

Jianchao Zhang, Xiao Chen, Congli Chen, Fengming Li, Xiaoxiao Song, Chaowei Liu, Kefan Liao, Ming-Yuan Su, Chris Soon Heng Tan, Lijing Fang, Hai Rao

A synonymous KCNJ11 variant leading to MODY13: A case report and literature review

KCNJ11同义变异导致MODY13:病例报告及文献综述

Chen, Congli; Piao, Yurong; Sang, Yanmei

Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation

四例中国巴特综合征3型患者的临床、遗传特征及预后:进一步揭示基因型-表型相关性

Piao, Yurong; Chen, Congli; Wu, Di; Liu, Min; Li, Wenjing; Chen, Jiahui; Sang, Yanmei

Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population

中国3M综合征患者中发现新型OBSL1变异:c.458dupG突变可能是中国人群中的潜在热点突变

Piao, Yurong; Li, Rongmin; Wang, Yingjie; Chen, Congli; Sang, Yanmei