Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Daoqi Wu"'
Autor:
Lin Shi, Wenyi Tang, Hengci Zhang, Yunzhi Zhang, Haiping Yang, Daoqi Wu, Xiaoqin Li, Lu Liu, Lijie Liu, Xuelan Chen, Mo Wang
Publikováno v:
BMC Psychology, Vol 12, Iss 1, Pp 1-9 (2024)
Abstract Background Chronic kidney disease (CKD) is the third most common cause of death after cancer and heart disease. The continuous treatment of children with CKD was greatly challenged during the COVID-19 pandemic, which significantly impacted t
Externí odkaz:
https://doaj.org/article/14ccaea2759944e1961c9eafc4b41f7c
Autor:
Han Chan, Fenfen Ni, Bo Zhao, Huimin Jiang, Juanjuan Ding, Li Wang, Xiaowen Wang, Jingjing Cui, Shipin Feng, Xiaojie Gao, Xueying Yang, Huan Chi, Hao Lee, Xuelan Chen, Xiaoqin Li, Jia Jiao, Daoqi Wu, Gaofu Zhang, Mo Wang, Yupeng Cun, Xiongzhong Ruan, Haiping Yang, Qiu Li
Publikováno v:
Genes and Diseases, Vol 11, Iss 4, Pp 101126- (2024)
Dissecting the genetic components that contribute to the two main subphenotypes of steroid-sensitive nephrotic syndrome (SSNS) using genome-wide association studies (GWAS) strategy is important for understanding the disease. We conducted a multicente
Externí odkaz:
https://doaj.org/article/c0500a73e6dd4730b26acce64684be07
Autor:
Jia Jiao, Li Wang, Fenfen Ni, Mo Wang, Shipin Feng, Xiaojie Gao, Han Chan, Xueying Yang, Hao Lee, Huan Chi, Xuelan Chen, Daoqi Wu, Gaofu Zhang, Baohui Yang, Anshuo Wang, Qin Yang, Junli Wan, Sijie Yu, Xiaoqin Li, Mei Wang, Xiaofeng Chen, Xianying Mai, Xiongzhong Ruan, Haiping Yang, Qiu Li
Publikováno v:
Genes and Diseases, Vol 9, Iss 6, Pp 1662-1673 (2022)
Understanding the association between the genetic and clinical phenotypes in children with nephrotic syndrome (NS) of different etiologies is critical for early clinical guidance. We employed whole-exome sequencing (WES) to detect monogenic causes of
Externí odkaz:
https://doaj.org/article/3a664aabdee94df8a9a50673eaa071a6
Autor:
Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/d46b55f4cdf74c89bac6f7df53401fa6
Autor:
Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
ObjectiveCOQ8B nephropathy is a relatively rare autosomal recessive kidney disease characterized by proteinuria and a progressive deterioration of renal function, eventually leading to end-stage renal disease (ESRD). The objective is to study the cha
Externí odkaz:
https://doaj.org/article/93ca46fbb4e443929fd5c2cae7605ef3
Autor:
Hua-Ying Xiong, Yong-Qi Shi, Cheng Zhong, Qin Yang, Gaofu Zhang, Haiping Yang, Daoqi Wu, Yaxi Chen, Qiu Li, Mo Wang
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background:PAX2 is a nuclear transcription factor gene that is highly conserved among species. Variants within PAX2 could result in optic nerve colobomas and kidney hypoplasia. However, little clinical and genetic information is currently available a
Externí odkaz:
https://doaj.org/article/a83506c12e004d259389504ab6cade22
Autor:
Lin Shi, Hengci Zhang, Haiping Yang, Daoqi Wu, Xiaoqin Li, Yunzhi Zhang, Xuelan Chen, Mo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
To evaluate social support and loneliness as well as their association among caregivers of children with chronic kidney disease (CKD) from China during the coronavirus disease 2019 (COVID-19) pandemic. We collected data for caregivers of children wit
Externí odkaz:
https://doaj.org/article/d55ec74e2b2a4ad5aec47c8d37114e44
Autor:
Mo Wang, Han Chan, Hao Lee, Xia Yang, Jingzhi Wang, Xueying Yang, Chun Gan, Han Xiao, Qianqian Li, Jia Jiao, Daoqi Wu, Gaofu Zhang, Haiping Yang, Qiu Li
Publikováno v:
BMJ Open, Vol 9, Iss 8 (2019)
Introduction Idiopathic nephrotic syndrome (INS) is the most common glomerulopathy that results in childhood chronic kidney disease in China, but the relationships between different clinical phenotypes and immunological genetic variants observed in p
Externí odkaz:
https://doaj.org/article/057417a5ddb249918587154f39126f52
Autor:
Hua-Ying, Xiong, Yong-Qi, Shi, Cheng, Zhong, Qin, Yang, Gaofu, Zhang, Haiping, Yang, Daoqi, Wu, Yaxi, Chen, Qiu, Li, Mo, Wang
Publikováno v:
Frontiers in genetics. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8f46c791f1b1d3f1b21cd8712388d21
https://pubmed.ncbi.nlm.nih.gov/35444690
https://pubmed.ncbi.nlm.nih.gov/35444690
Autor:
Xuelan Chen, Xiaoqin Li, Yunzhi Zhang, Haiping Yang, Mo Wang, Lin Shi, Hengci Zhang, Daoqi Wu
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
To evaluate social support and loneliness as well as their association among caregivers of children with chronic kidney disease (CKD) from China during the coronavirus disease 2019 (COVID-19) pandemic. We collected data for caregivers of children wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94979ad816b0a1046961d1d844990d0d
https://doi.org/10.3389/fped.2020.570535
https://doi.org/10.3389/fped.2020.570535