Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Xinyu Kuang"'
Publikováno v:
IET Communications, Vol 18, Iss 19, Pp 1574-1587 (2024)
Abstract To address the concerns of energy supply and spectrum scarcity for wireless devices, energy harvesting cognitive radio networks have been proposed. To improve spectrum utilization, secondary users (SUs) access the licensed spectrum in underl
Externí odkaz:
https://doaj.org/article/82454379012c4bbeb97e27e8d2e42a84
Autor:
Liping Rong, Lizhi Chen, Jia Rao, Qian Shen, Guomin Li, Jialu Liu, Jianhua Mao, Chunyue Feng, Xiaowen Wang, Si Wang, Xinyu Kuang, Wenyan Huang, Qingshan Ma, Xiaorong Liu, Chen Ling, Rong Fu, Xiaojie Gao, Guixia Ding, Huandan Yang, Mei Han, Zhimin Huang, Qian Li, Qiuye Zhang, Yi Lin, Xiaoyun Jiang, Hong Xu
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Introduction: Few studies have addressed the genetic spectrum of NPHS1 variants in Chinese children with nephrotic syndrome. In this multicenter study, the clinical manifestations and features of NPHS1 variants in Chinese children with nephrotic synd
Externí odkaz:
https://doaj.org/article/d9ab4b91e9b24dce8f94058369ea3c78
Publikováno v:
International Journal of Genomics, Vol 2019 (2019)
This study is aimed at exploring the mechanism by which the −254C>G single nucleotide polymorphism (SNP) on the transient receptor potential cation channel 6 (TRPC6) gene promoter could increase its activation in steroid-resistant nephrotic syndrom
Externí odkaz:
https://doaj.org/article/483b89453d0a44b7a49ff67cc3f516cf
Autor:
Jian Gao, Fei Wang, Xinyu Kuang, Rong Chen, Jia Rao, Bin Wang, Wenyan Li, Haimei Liu, Qian Shen, Xiang Wang, Hong Xu
Publikováno v:
Annals of Saudi Medicine, Vol 36, Iss 4, Pp 252-257 (2016)
BACKGROUND: The illegal use of melamine in powdered baby formula resulted in a widespread outbreak of melamine-associated pediatric urolithiasis and kidney damage in China in 2008. We conducted this study because more needs to be known about the long
Externí odkaz:
https://doaj.org/article/3d828bbb8bb64158b0f2b155d0eec6e7
Publikováno v:
RAIRO - Operations Research. 56:395-414
This paper proposes an M/G/1 queueing model with bi-level randomized (p, N1, N2)-policy. That is, after all of the customers in the system are served, the server is closed down immediately. If N1(≥ 1) customers are accumulated in the queue, the ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ae7feb9db22efce262b1e6b4c8bc8d2
https://doi.org/10.1051/ro/2022008
https://doi.org/10.1051/ro/2022008
Autor:
Guixia Ding, Jialu Liu, Xiaojie Gao, Xiaowen Wang, Wen-Yan Huang, Lizhi Chen, Qian Li, Guomin Li, Jia Rao, Xiaoyun Jiang, Yi Lin, Mei Han, Rong Fu, Chunyue Feng, Hong Xu, Qian Shen, Huandan Yang, Qiuye Zhang, Xiaorong Liu, Xinyu Kuang, Zhimin Huang, Liping Rong, Si Wang, Chen Ling, Qingshan Ma, Jianhua Mao
Publikováno v:
Frontiers in Medicine
Frontiers in Medicine, Vol 8 (2021)
Frontiers in Medicine, Vol 8 (2021)
Introduction: Few studies have addressed the genetic spectrum of NPHS1 variants in Chinese children with nephrotic syndrome. In this multicenter study, the clinical manifestations and features of NPHS1 variants in Chinese children with nephrotic synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe7128c254554cfa444acc2f58166224
http://europepmc.org/articles/PMC8632042
http://europepmc.org/articles/PMC8632042
Autor:
Xinyu Kuang, Xiaoyan Qiu, Huajun Sun, Zhiling Li, Wenyan Huang, Hongxia Liu, Qi Zhao, Zhihu Jiang, Qinxia Xu
Publikováno v:
European Journal of Clinical Pharmacology. 75:1533-1540
The purpose of this study was to investigate the potential impact of CYP3A4, CYP3A5, and CYP3A7 polymorphisms on the concentration and efficacy of tacrolimus in a cohort of pediatric patients with nephrotic range proteinuria. Genetic variants includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b162a2d90b7ba54517b85b3f15f2a01e
https://doi.org/10.1007/s00228-019-02726-w
https://doi.org/10.1007/s00228-019-02726-w
Publikováno v:
Transl Pediatr
BACKGROUND: X-linked Alport syndrome (XLAS) is the most common form of Alport syndrome (AS), involves mutations in the COL4A5 gene encoding the type IV collagen a5 chain. In this research, we will report the analysis of the COL4A5 gene in a Chinese f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::786728d06d27e36aeb35c82c57cb051b
https://pubmed.ncbi.nlm.nih.gov/33209720
https://pubmed.ncbi.nlm.nih.gov/33209720
Autor:
Qinxia Xu, Xinyu Kuang, Wenyan Huang, Huajun Sun, Hongxia Liu, Xiaoyan Qiu, Qi Zhao, Zhihu Jiang, Zhiling Li
Publikováno v:
European Journal of Clinical Pharmacology. 77:1251-1252
The original publication of this paper contains two errors. We apologize for any inconvenience this may have caused.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5c78cc907b8a814af4205e236a3c860
https://doi.org/10.1007/s00228-020-02875-3
https://doi.org/10.1007/s00228-020-02875-3
Publikováno v:
Materials
The purpose of this study was to reveal that reconstructed soil composed of different types and proportions of materials has different effects on the growth of Melilotus officinalis, and to determine the most suitable formula of reconstructed soil ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ae8a0eaedee07cea16eef0db8856c97
https://pubmed.ncbi.nlm.nih.gov/31775275
https://pubmed.ncbi.nlm.nih.gov/31775275