Expression and Prognostic Role of PLOD1 in Malignant Glioma

por Wang, Hao, Luo, Weijian, Dai, Limeng
Publicado 2020

Nonsmall cell lung cancer with rare exon 7 p.A289V mutation in the EGFR gene responds to Icotinib treatment: A case report

por Dai, Limeng, Su, Xuejiao, Lu, Lin, Lv, Donglai
Publicado 2018

E2F1 promotes cancer cell sensitivity to cisplatin by regulating the cellular DNA damage response through miR-26b in esophageal squamous cell carcinoma

por Zhang, Kun, Zhang, Bo, Bai, Yun, Dai, Limeng
Publicado 2020

microRNA-130b May Induce Cerebral Vasospasm after Subarachnoid Hemorrhage via Modulating Kruppel-like Factor 4

por Huang, Zewei, Hu, Jiliang, Xu, Jiongfu, Wang, Hao, Dai, Limeng
Publicado 2023

A Large Novel Deletion Downstream of PAX6 Gene in a Chinese Family with Ocular Coloboma

por Guo, Hong, Dai, Limeng, Huang, Yanming, Liao, Qiong, Bai, Yun
Publicado 2013

Monocarboxylate Transporter 1 May Benefit Cerebral Ischemia via Facilitating Lactate Transport From Glial Cells to Neurons

por Zhang, Mao, Wang, Yanyan, Bai, Yun, Dai, Limeng, Guo, Hong
Publicado 2022

X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions

por Zhao, Yuanyin, Li, Jia, Dai, Limeng, Ma, Yongyi, Bai, Yun, Guo, Hong
Publicado 2021

A case report of NPHP1 deletion in Chinese twins with nephronophthisis

por Chen, Feng, Dai, Limeng, Zhang, Jun, Li, Furong, Cheng, Jinbo, Zhao, Jinghong, Zhang, Bo
Publicado 2020

Deubiquitinating enzyme USP30 negatively regulates mitophagy and accelerates myocardial cell senescence through antagonism of Parkin

por Pan, Wei, Wang, Yaowen, Bai, Xinyu, Yin, Yuehui, Dai, Limeng, Zhou, Hong, Wu, Qin, Wang, Yan
Publicado 2021

Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth

por Wu, Yuanyuan, Chen, Xuedan, Liang, Yan, Li, Juan, Zhang, Kun, Dai, Limeng, Guan, Xingying, Wang, Kai, Bai, Yun
Publicado 2018

A Tiered Genetic Screening Strategy for the Molecular Diagnosis of Intellectual Disability in Chinese Patients

por Dai, Limeng, Zhang, Danyan, Wu, Zhifeng, Guan, Xingying, Ma, Mingfu, Li, Lianbing, Zhang, Yuping, Bai, Yun, Guo, Hong
Publicado 2021

Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families

por Dai, Limeng, Liu, Dan, Song, Min, Xu, Xueqing, Xiong, Gang, Yang, Kang, Zhang, Kun, Meng, Hui, Guo, Hong, Bai, Yun
Publicado 2014

A novel case of global developmental delay syndrome with microdeletion at 10p14–p15.3 and microduplication at 18p11.31–p11.32

por Zhang, Danyan, Zhu, Yijian, Feng, Xuefei, Dai, Limeng, Ma, Mingfu, Li, Lianbing, Guo, Hong, Zhao, Letian, Zhang, Yuping, Bai, Yun
Publicado 2019

Supt16 Haploinsufficiency Impairs PI3K/AKT/mTOR/Autophagy Pathway in Human Pluripotent Stem Cells Derived Neural Stem Cells

por Wang, Junwen, Wang, Ziyi, Dai, Limeng, Zhu, Xintong, Guan, Xingying, Wang, Junyi, Li, Jia, Zhang, Mao, Bai, Yun, Guo, Hong
Publicado 2023

PPARA genetic variants increase the risk for cardiac pumping function reductions following acute high‐altitude exposure: A self‐controlled study

por Yang, Jie, Liu, Chuan, Jihang, Zhang, Yu, Jie, Dai, Limeng, Ding, Xiaohan, Qiu, Youzhu, Yu, Sanjiu, Yang, Yuanqi, Wu, Yuzhang, Huang, Lan
Publicado 2019

Network Reconfiguration Among Cerebellar Visual, and Motor Regions Affects Movement Function in Spinocerebellar Ataxia Type 3

por Chen, Hui, Dai, Limeng, Zhang, Yuhan, Feng, Liu, Jiang, Zhenzhen, Wang, Xingang, Xie, Dongjing, Guo, Jing, Chen, Huafu, Wang, Jian, Liu, Chen
Publicado 2022

A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review

por Tan, Chengning, Dai, Limeng, Chen, Zhengqiong, Yang, Wuchen, Wang, Yali, Zeng, Cheng, Xiang, Zheng, Wang, Xiaojie, Zhang, Xiaomei, Ran, Qian, Guo, Hong, Li, Zhongjun, Chen, Li
Publicado 2020