Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Qingquan Gu"'
Autor:
Niaz Muhammad Khan, Basharat Hussain, Chenqing Zheng, Ayaz Khan, Muhammad Shareef Masoud, Qingquan Gu, Linhui Qiu, Naveed Altaf Malik, Muhammad Qasim, Muhammad Tariq, Junlei Chang
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Microcephaly (MCPH) is a genetically heterogeneous disorder characterized by non-progressive intellectual disability, small head circumference, and small brain size compared with the age- and sex-matched population. MCPH manifests as an isolated cond
Externí odkaz:
https://doaj.org/article/88c7182a27434a61a779b2a39ee93354
Autor:
Jing Du, Bing Sun, Kui Chen, Lang Zhang, Shubo Liu, Qingquan Gu, Li Fan, Nanming Zhao, Zhao Wang
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5530 (2009)
Metabolites of neural cells, is known to have a significant effect on the normal physiology and function of neurons in brain. However, whether they play a role in pathogenesis of neurodegenerative diseases is unknown. Here, we show that metabolites o
Externí odkaz:
https://doaj.org/article/4b9ce251c7594aad87ed4cc55af09fe4
Autor:
Jichang Huang, Chenqing Zheng, Rong Luo, Xin Cao, Mingjiang Liu, Qingquan Gu, Feng Li, Jinshu Li, Xiushan Wu, Zhenglin Yang, Xia Shen, Xiaoping Li
Publikováno v:
Free radical biologymedicine. 193(Pt 2)
Keshan disease is an endemic fatal dilated cardiomyopathy that can cause heart enlargement, heart failure, and cardiogenic death. Selenium deficiency is considered to be the main cause of Keshan disease. However, the molecular mechanism underlying Ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59f22462d5accd9b611b6b5999b692e8
https://pubmed.ncbi.nlm.nih.gov/36395956
https://pubmed.ncbi.nlm.nih.gov/36395956
Autor:
Wenlan Liu, Lilong Lin, Zhen-Ni Guo, Song Ta, Peng Zhang, Junlei Chang, Qingquan Gu, Feng-E Li, Zhihuan Li, Xianfang Rong, Yi Yang, Hang Jin, Chenqing Zheng, Yuan Zhang
Publikováno v:
CNS Neuroscience & Therapeutics
Aims The canonical Wnt signaling pathway plays an essential role in blood‐brain barrier integrity and intracerebral hemorrhage in preclinical stroke models. Here, we sought to explore the association between canonical Wnt signaling and hemorrhagic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e20cb80bf59697b3065a8bed8d673a
https://doi.org/10.1111/cns.13457
https://doi.org/10.1111/cns.13457
Autor:
Xiushan Wu, Jinshu Li, Zhenglin Yang, Xia Shen, Qingquan Gu, Jichang Huang, Rong Luo, Mingjiang Liu, Chenqing Zheng, Xiaoping Li
Keshan disease (KD), an endemic heart disease with multifocal necrosis and replacement fibrosis of the myocardium,is still a nightmare situation for human health. However, molecular mechanism in the pathogenesis of KD remains unclear. Herein, blood s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a18d51d00094b82954df94910664321a
https://doi.org/10.1101/2021.03.12.21253491
https://doi.org/10.1101/2021.03.12.21253491
Autor:
Min Xia, Haojing Shao, Chundi He, Zaixing Wang, Xing Fan, Gang Chen, Fusheng Zhou, Jianjun Liu, Tianhang Li, Junjun Shan, Xianyong Yin, Xuefeng Xie, Xinghua Gao, Renhua Wu, Yingrui Li, Shaowei Huang, Yu-Zhen Li, Xiaohang Zhao, Xueli Wu, Hui Cheng, Yang Li, Xin Jin, Ai-E Xu, Liping Wei, Xia Zhao, Fangzhen Tian, Yunqing Ren, Qi Cai, Lin Yang, Xianfa Tang, Hui Jiang, Jianzhong Zhang, Cheng Quan, Lin Dang, Xuejun Zhang, Bo Liang, Furen Zhang, Jianwen Han, Fengping Xu, Dongmei Shi, Guangdong Wen, Hongqing Tian, Xu Yang, Runsheng Chen, Yulin Sun, Liya Lin, Liangdan Sun, Huiling Fu, Sen Yang, Feng-Li Xiao, Jinhua Xu, Xiuyun Zhang, Yong Zhang, Baoqi Yang, Qingquan Gu, Xiaodong Zheng, Anping Zhang, Xianbo Zuo, Jun Wang, Qibin Li, Fang Wang, Junpu Mei, Cheng Zhou, Ying Qiu, Huayang Tang, Yong Cui, Hong Liu
Publikováno v:
Nature genetics. 46(1)
To explore the contribution of functional coding variants to psoriasis, we analyzed nonsynonymous single-nucleotide variants (SNVs) across the genome by exome sequencing in 781 psoriasis cases and 676 controls and through follow-up validation in 1,32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1c1d72fd2acd3ed300f3d4a9a2baf5
https://pubmed.ncbi.nlm.nih.gov/24212883
https://pubmed.ncbi.nlm.nih.gov/24212883
Autor:
Tingwei Sun, Qingquan Guo, Shaojuan Wu, Kui Su, Jingwen Lun, Yihan Zhang, Wen Tan, Haishan Zhao
Publikováno v:
Brazilian Archives of Biology and Technology, Vol 65 (2022)
Abstract The mushroom tyrosinase assay, B16-F10 mouse melanoma cell model, and zebrafish model are frequently used for high-throughput screening and are widely used for developing anti-hyperpigmentation compounds, although these systems cannot be com
Externí odkaz:
https://doaj.org/article/81e7a57378234be7abb950cf05cad9b8
Autor:
Wei Tan, Bo Cao, Wenqiu Xiao, Min Zhang, Shoushan Wang, Shilei Xie, Dong Xie, Faliang Cheng, Qingquan Guo, Peng Liu
Publikováno v:
Nanoscale Research Letters, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Surfactant-free and low Au loading Cu2O@Au and Au hollow cubes, based on electrodeposited Cu2O cubes as sacrificed templates, were prepared by means of a galvanic replacement reaction (GRR). The electrocatalytical performance of the as-prepa
Externí odkaz:
https://doaj.org/article/b70a1fe0a6db4e9197407e149f4ef2bc
Autor:
Lang Zhang, Bing Sun, Shubo Liu, Nanming Zhao, Li Fan, Zhao Wang, Kui Chen, Jing Du, Qingquan Gu
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5530 (2009)
PLoS ONE
PLoS ONE
Metabolites of neural cells, is known to have a significant effect on the normal physiology and function of neurons in brain. However, whether they play a role in pathogenesis of neurodegenerative diseases is unknown. Here, we show that metabolites o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a454ab4cffb35fe7c60b2c0537a6efe
https://doi.org/10.1371/journal.pone.0005530
https://doi.org/10.1371/journal.pone.0005530
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 32, Iss 2, Pp 324-331 (2018)
The present study aimed to describe the cDNA cloning of the cinnamate 4-hydroxylase (C4H) gene from ramie, predict the protein sequence and perform phylogenetic and structural analyses of this gene. C4H catalyses the hydroxylation of trans-cinnamic a
Externí odkaz:
https://doaj.org/article/c9ffe56a08a647afa9558e2db8f80bc6