Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Qianlei Zhao"'
Autor:
Tingting Chen, Yingying Hu, Liying Lu, Qianlei Zhao, Xiaoyue Tao, Bingqing Ding, Shangqin Chen, Jianghu Zhu, Xiaoling Guo, Zhenlang Lin
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Introduction: Hypoxic-ischemic encephalopathy (HIE) is a crucial cause of neonatal death and neurological sequelae, but currently there is no effective therapy drug for HIE. Both oxidative stress and apoptosis play critical roles in the pathological
Externí odkaz:
https://doaj.org/article/5f7c6bbe13ff46bebdcca1e00f05e690
Autor:
Xiucui Li, Shijia Bao, Wei Wang, Xulai Shi, Ying Hu, Feng Li, Qianlei Zhao, Feixia Zheng, Zhongdong Lin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
A series of neurological manifestations such as intellectual disability and epilepsy are closely related to hypomagnesemia. Cyclin M2 (CNNM2) proteins, as a member of magnesium (Mg2+) transporters, were found along the basolateral membrane of distal
Externí odkaz:
https://doaj.org/article/fd2550fd80e04575982cbb57e190107e
Publikováno v:
Metals, Vol 12, Iss 8, p 1263 (2022)
The fabrication of porous copper with ultrahigh porosity by adding 90% spacer content was an unsolved technical problem in the field. In this study, the green compacts placed on a layer wire mesh during the decomposition process of needlelike carbami
Externí odkaz:
https://doaj.org/article/8def453eaec34ac18c84c5486c4cb81b
Autor:
Qianlei Zhao, Tingting Chen, Chao Ni, Yingying Hu, Yan Nan, Wei Lin, Yanli Liu, Feixia Zheng, Xulai Shi, Zhongdong Lin, Jianghu Zhu, Zhenlang Lin
Publikováno v:
ACS Chemical Neuroscience. 13:2897-2912
The blood-brain barrier (BBB) is an important physiological barrier of the human body contributing to maintaining brain homeostasis and normal function. Hypoxic-ischemic (HI)-related brain injury is one of the main causes of neonatal acute morbidity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d9c039bf09c0c5ff1de76e7658406f
https://doi.org/10.1021/acschemneuro.2c00418
https://doi.org/10.1021/acschemneuro.2c00418
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 2; Pages: 473
Cerebral adrenoleukodystrophy (CALD) is a fatal genetic disease characterized by rapid, devastating neurological decline, with a narrow curative treatment window in the early stage. Non-canonical splice-site (NCSS) variants can easily be missed durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::764266b2096480675deaa41ca0323510
Autor:
Yingying Hu, Hongzhou Lin, Yan Nan, Qianlei Zhao, Tingting Chen, Xiaoyue Tao, Bingqing Ding, Liying Lu, Shangqin Chen, Jianghu Zhu, Xiaoling Guo, Zhenlang Lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bb94a9f6a1e57fa6694b54f0b4c2c3c
https://doi.org/10.2139/ssrn.4431348
https://doi.org/10.2139/ssrn.4431348
Autor:
Ying Hu, Zhenwei Liu, Feixia Zheng, Shiyu Fang, Zhongdong Lin, Qianlei Zhao, Feng Li, Xiucui Li
Publikováno v:
Acta Neurologica Belgica
To analyze the clinical characteristics and PRRT2 gene mutation of self-limited familial infantile epilepsy and evaluate the treatment responses of different antiepileptic drugs in self-limited familial infantile epilepsy. We reviewed the clinical fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1360f576be29297736906e7ffc28bc
https://doi.org/10.1007/s13760-020-01348-9
https://doi.org/10.1007/s13760-020-01348-9
Autor:
Ying Hu, Xu-Lai Shi, Feng Li, Shijia Bao, Wei Wang, Xiucui Li, Qianlei Zhao, Feixia Zheng, Zhongdong Lin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in Genetics
A series of neurological manifestations such as intellectual disability and epilepsy are closely related to hypomagnesemia. Cyclin M2 (CNNM2) proteins, as a member of magnesium (Mg2+) transporters, were found along the basolateral membrane of distal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0aa8139312e6a483217e76d99a4ccd
https://www.frontiersin.org/articles/10.3389/fgene.2021.705734/full
https://www.frontiersin.org/articles/10.3389/fgene.2021.705734/full
Autor:
Xiaoyu Wang, Shiyu Fang, Zhongdong Lin, Ying Hu, Zhenwei Liu, Feixia Zheng, Feng Li, Xiucui Li, Qianlei Zhao
Publikováno v:
Seizure. 91
Purpose: Self-limited familial infantile epilepsy (SFIE) is largely associated with variants in proline-rich transmembrane protein 2 (PRRT2). However, the detailed phenotype–genotype correlations are unclear, along with the efficacy of various anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c81bb56924c65036feebb2c0944af73
https://pubmed.ncbi.nlm.nih.gov/34298454
https://pubmed.ncbi.nlm.nih.gov/34298454
Publikováno v:
International immunopharmacology. 88
Background Neuroblastoma (NB) is one of the most common childhood tumors that is associated with a poor prognosis. Recently, immunotherapy has been recognized as an effective strategy in the treatment of NB patients. In this study, an immune-related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d1c06a44db36f096da4ba6bf6b95a85
https://pubmed.ncbi.nlm.nih.gov/33182060
https://pubmed.ncbi.nlm.nih.gov/33182060