Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Renchao Li"'
Autor:
Weining Wang, Renchao Li
Publikováno v:
Neuroscience Research. 170:255-264
Neuropathic pain is a devastating disease and exists tolerance to current available analgesics. MicroRNAs were reported to be involved in the regulation of neuropathic pain, but the biological role of miR-216a-5p in neuropathic pain remains unclear.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8f7950970cc22d657265d9e32e9b9ff
https://doi.org/10.1016/j.neures.2020.08.001
https://doi.org/10.1016/j.neures.2020.08.001
Publikováno v:
Journal of the Association for Information Science and Technology. 71:183-195
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18b1a77a9472911fa108bbd4428c912c
https://doi.org/10.1002/asi.24227
https://doi.org/10.1002/asi.24227
Publikováno v:
Separation and Purification Technology. 197:401-406
The removal of organic persistent contaminants in the environment is a challenge due to their hydrophobic nature. In this work, the removal of 2,4-DCP based on the adsorption and Fenton oxidation was reported, where organobentonite (OB)-supported zer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61aa3009cbd8265cdb825b171ee31cf0
https://doi.org/10.1016/j.seppur.2018.01.032
https://doi.org/10.1016/j.seppur.2018.01.032
Publikováno v:
Chemical Engineering Journal. 264:587-594
Nanoscale zero-valent iron (nZVI) has received attention for its potential applications in contaminated site remediation due to its reactivity. However, it is still unclear how nZVI acts as a catalyst to generate sulfate radicals in heterogeneous Fen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92ce409046f6f0f0914cfe2f9d43a1cc
https://doi.org/10.1016/j.cej.2014.11.128
https://doi.org/10.1016/j.cej.2014.11.128
Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients
Autor:
Jitao Zhu, Wenhui Li, Sha Yu, Wei Lu, Qiong Xu, Sujuan Wang, Yanyan Qian, Qiufang Guo, Suzhen Xu, Yao Wang, Ping Zhang, Xuemei Zhao, Qi Ni, Renchao Liu, Xu Li, Bingbing Wu, Shuizhen Zhou, Huijun Wang
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Neurodevelopmental disorders (NDDs) have heterogeneity in both clinical characteristics and genetic factors. EBF3 is a recently discovered gene associated with a syndromic form of NDDs characterized by hypotonia, ataxia and facial features. In this s
Externí odkaz:
https://doaj.org/article/973b5253555a4ee8948d740b749af302
In this report, various iron-based nanoparticles (nZVI, n-Ni/Fe, n-Pd/Fe) were used for both heterogeneous Fenton oxidation of 2,4-dichlorophenol (2,4-DCP) and reductive dechlorination of 2,4-DCP in order to understand their roles in the Fenton oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2735cc03aefc36dd072545ce4b957bf4
https://hdl.handle.net/11541.2/111990
https://hdl.handle.net/11541.2/111990
Autor:
Yanyan Qian, Bingbing Wu, Renchao Liu, Yulan Lu, Ping Zhang, Caihong Shao, Ying Huang, Huijun Wang
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Congenital diarrhea diseases are a heterogeneous group of conditions and are the major cause of neonatal mortality worldwide. Proprotein convertase 1/3 (PC1/3) deficiency has been associated with severe malabsorptive diarrhea, obesity, and certain en
Externí odkaz:
https://doaj.org/article/06eb52559fba41d99bd8a2709ddde529
Autor:
Feifan Xiao, Xiuyun Liu, Yulan Lu, Bingbing Wu, Renchao Liu, Bo Liu, Kai Yan, Huiyao Chen, Guoqiang Cheng, Laishuan Wang, Qi Ni, Gang Li, Ping Zhang, Xiaomin Peng, Yun Cao, Chun Shen, Huijun Wang, Wenhao Zhou
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
The annular pancreas (AP) is a congenital anomaly of the pancreas that can cause acute abdominal pain and vomiting after birth. However, the genetic cause of AP is still unknown, and no study has reported AP in patients with 17q12 duplication. This s
Externí odkaz:
https://doaj.org/article/3d4b2deff4fd4194a8746c2c62bf209d
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Congenital myasthenic syndrome 22 (CMS22) is a rare autosomal recessive disorder due to isolated PREPL deficiency and characterized by neonatal hypotonia, muscular weakness, and feeding difficulties. Eight such cases have already
Externí odkaz:
https://doaj.org/article/844de8ef3f09496295b29017635a2a5f
Autor:
Sha Yu, Bingbing Wu, Yanyan Qian, Ping Zhang, Yulan Lu, Xinran Dong, Qing Wang, Xuemei Zhao, Renchao Liu, Wenhao Zhou, Huijun Wang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)
Abstract Background Rubinstein–Taybi syndrome (RSTS) is a rare genetic disease characterized by broad thumbs and halluces, facial dysmorphisms, short stature, and intellectual disability. RSTS is mainly caused by de novo variants in epigenetics‐a
Externí odkaz:
https://doaj.org/article/d8fe75c02ab0458b969982115b32afd5