Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Meirong Liu"'
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundThe status of the sentinel lymph nodes (SLNs) is an important prognostic factor for many different types of cancer. The one-step nucleic acid amplification (OSNA) assay has emerged as a rapid intraoperative molecular diagnostic tool for LN
Externí odkaz:
https://doaj.org/article/e9b03e8ae3d34a60899cb94901325605
Case report: Comprehensive exploration of a novel PFKM mutation in glycogen storage disease Type VII
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Glycogen Storage Disease Type VII (GSD VII) is a rare glycogen metabolism disorder resulting from mutations in the PFKM gene, inherited in an autosomal recessive manner. It is characterized by exercise intolerance, muscle cramps, myoglobinuria, compe
Externí odkaz:
https://doaj.org/article/31eae076391745c3bf109e22c9f33123
Autor:
Kexin Jiao, Jialong Zhang, Qiuxiang Li, Xiaoqing Lv, Yanyan Yu, Bochen Zhu, Huahua Zhong, Xu’en Yu, Jia Song, Qing Ke, Fangyuan Qian, Xinghua Luan, Xiaojie Zhang, Xueli Chang, Liang Wang, Meirong Liu, Jihong Dong, Zhangyu Zou, Bitao Bu, Haishan Jiang
Publikováno v:
Journal of Medical Genetics; Nov2024, Vol. 61 Issue 11, p1053-1061, 9p
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Glutaric aciduria type II (GA II) is an autosomal recessive metabolic disorder of fatty acid, amino acid, and choline metabolism. The late-onset form of this disorder is caused by a defect in the mitochondrial electron transfer flavoprotein dehydroge
Externí odkaz:
https://doaj.org/article/3ac317bfea234c1b9af43cd6186baf16
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundWe aimed to investigate the biological mechanism and feature genes of Duchenne muscular dystrophy (DMD) by multi-omics and experimental verification strategy.MethodsWe integrated the transcriptomic and proteomic methods to find the differen
Externí odkaz:
https://doaj.org/article/2a78fbfa0ef646cf87327209460b48f0
Autor:
Zeya Yan, Feng Gu, Zilan Wang, Jiahao Meng, Xinyu Tao, Qiling Dai, Wei Wang, Meirong Liu, Zhong Wang
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundMultiple sclerosis (MS), an autoimmune disease, is characterized by inflammatory demyelinating lesions in the white matter of the central nervous system. Drugs targeting tyrosine kinase, a critical component of immune cell receptor signalin
Externí odkaz:
https://doaj.org/article/8ec727ce5dff45b5b4cff591bb60dc13
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Ataxia with oculomotor apraxia type 1 (AOA1) is a rare genetic disorder and is inherited in an autosomal recessive manner. It is mainly characterized by childhood-onset progressive cerebellar ataxia, with dysarthria and gait disturbance being the two
Externí odkaz:
https://doaj.org/article/78498275e14b45aba444f0074f74c67f
Publikováno v:
Chinese Journal of Lung Cancer, Vol 22, Iss 1, Pp 52-56 (2019)
Tyrosine kinase inhibitor (TKI) have been proved to be effective in the treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) sensitive mutation, which is superior to chemotherapy. However, the
Externí odkaz:
https://doaj.org/article/3b4fefef9b164b6694999c89b492d1e1
Autor:
Guannan Jiang, Xiang Li, Meirong Liu, Haiying Li, Haitao Shen, Juan liao, Wanchun You, Qi Fang, Gang Chen
Publikováno v:
Brain Research Bulletin. 197:31-41
Autor:
Yiren Qin, Xiaoyan Qian, Xue Luo, Yuanfang Li, Dapeng Wang, Jianhua Jiang, Quanquan Zhang, Meirong Liu, Junhua Xiao, Yan Zhang, Shanshan Diao, Hongru Zhao
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) has emerged as a novel biomarker for coronary atherosclerosis. However, the association between Lp-PLA2 and plaque vulnerability in atherosclerosis of cervicocerebral arteries remai
Externí odkaz:
https://doaj.org/article/5ec1559d68194d548f5429d830301271