Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Gaofu, Zhang"'
Autor:
Xueting Cheng, Jiahuan Chen, Xueying Yang, Han Chan, Xia Yang, Jia Jiao, Anshuo Wang, Gaofu Zhang, Xuelan Chen, Xiaoqin Li, Mo Wang, Baohui Yang, Haiping Yang, Qiu Li
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-14 (2024)
Abstract Background Steroid-resistant nephrotic syndrome (SRNS) are monogenic in some cases, however, there are still no clear guidelines on genetic testing in the clinical practice of SRNS in children. Methods Three hundred thirty-two children were
Externí odkaz:
https://doaj.org/article/cbc3ec2642694ae9a825d410c3f22e4f
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:
Qilin Chen, Huimin Jiang, Rong Ding, Jinjie Zhong, Longfei Li, Junli Wan, Xiaoqian Feng, Liping Peng, Xia Yang, Han Chen, Anshuo Wang, Jia Jiao, Qin Yang, Xuelan Chen, Xiaoqin Li, Lin Shi, Gaofu Zhang, Mo Wang, Haiping Yang, Qiu Li
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Nephrotic syndrome (NS) is a relatively rare and serious presentation of IgA nephropathy (IgAN) (NS-IgAN). Previous research has suggested that the pathogenesis of NS-IgAN may involve circulating immune imbalance and kidney injury; however, this has
Externí odkaz:
https://doaj.org/article/d5503b70c6594198a04226abbd6a8428
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:
Xixi Yu, Jiacheng Li, Chengrong Tao, Jia Jiao, Junli Wan, Cheng Zhong, Qin Yang, Yongqi Shi, Gaofu Zhang, Haiping Yang, Qiu Li, Mo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundImmunoglobulin A nephropathy (IgAN) is one of the most common kidney diseases leading to renal injury. Of pediatric cases, 25%–30% progress into end-stage kidney disease (ESKD) in 20–25 years. Therefore, predicting and intervening in Ig
Externí odkaz:
https://doaj.org/article/6b18208e8ff949579ca7172d10a4d7fb
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, Gaofu Zhang, Li Wang, Zhijuan Li, Qian Shen, Yuhong Li, Hongtao Zhu, Yue Du, Liangzhong Sun, Bo Zhao, Lijun Zhao, Haidong Fu, Xiaoyan Li, Xiaojie Gao, Sheng Hao, Juanjuan Ding, Zongwen Chen, Zhiquan Xu, Xiaorong Liu, Yuhong Tao, Aihua Zhang, Qiu Li, Mo Wang
Publikováno v:
Frontiers in Public Health, Vol 10 (2022)
BackgroundThere is great mental stress due to the coronavirus disease 2019 (COVID-19) pandemic. However, there are no detailed psychological studies of the children with chronic kidney disease (CKD) and their guardians during the COVID-19 pandemic.Ob
Externí odkaz:
https://doaj.org/article/1821b2ea856f44fa9f8c774241bbd011
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Background Immune dysregulation, polyendocrinopathy, enteropathy, X‐linked (IPEX) syndrome is a monogenic immunodeficiency disease caused by forkhead box protein3 (FOXP3) mutation. The kidney is commonly involved in IPEX syndrome, but ther
Externí odkaz:
https://doaj.org/article/b238904f957d4de18ff367375dcfa7f9
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