Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Chunyue Feng"'
Autor:
Lu Li, Fei Liu, Chunyue Feng, Zhenjie Chen, Nan Zhang, Jianhua Mao, Xiangxiang Pan, Peifang Wei
Publikováno v:
Chinese Medical Journal, Vol 137, Iss 9, Pp 1044-1053 (2024)
Abstract. Over the past decade, mitochondrial dysfunction has been investigated as a key contributor to acute and chronic kidney disease. However, the precise molecular mechanisms linking mitochondrial damage to kidney disease remain elusive. The rec
Externí odkaz:
https://doaj.org/article/00e930eb9c704abc8c94142ca18a0e56
Autor:
Qing Ye, Hanyan Meng, Fang Ye, Haidong Fu, Jingjing Wang, Fei Liu, Huijun Shen, Yu Bao, Chunyue Feng, Xiaojing Zhang, Guoping Huang, Yi Xie, Xiujuan Zhu, Manli Zhao, Guoji Guo, Jianhua Mao
Publikováno v:
Clinical and Translational Medicine, Vol 14, Iss 4, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/91e9a061792540e3b290b184af2bec84
Publikováno v:
Kidney Diseases, Vol 7, Iss 5, Pp 343-349 (2021)
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disorder, accounting for approximately 5% of all ESRD cases worldwide. As a vasopressin receptor 2 antagonist, tolvaptan is the FDA-approved therapeu
Externí odkaz:
https://doaj.org/article/c47463bd88ad47b28ca7bf81d48cba96
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background 13q33–q34 microdeletions are rare chromosomal aberrations associated with a high risk of developmental disability, facial dysmorphism, cardiac defects and other malformation of organs. It is necessary to collect and report evide
Externí odkaz:
https://doaj.org/article/a7c9e45cd20e4f8dab65b732ecc0faa5
Autor:
Lingxia Zhang, Shugang Wang, Ruoque Mao, Haidong Fu, Jingjing Wang, Huijun Shen, Zhihong Lu, Junyi Chen, Yu Bao, Chunyue Feng, En Yin Lai, Qing Ye, Jianhua Mao
Publikováno v:
Genetics Research, Vol 2022 (2022)
Background. Both Lowe syndrome and Dent-2 disease are caused by variants in the OCRL gene. However, the reason why patients with similar OCRL gene mutations presented with different phenotypes remains uncertain. Methods. Children with hemizygous path
Externí odkaz:
https://doaj.org/article/22bfec9418fe4a10bd0b252efa00acf4
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
Autor:
Lingxia Zhang, Ke Huang, Shugang Wang, Haidong Fu, Jingjing Wang, Huijun Shen, Zhihong Lu, Junyi Chen, Yu Bao, Chunyue Feng, Guanping Dong, Jianhua Mao
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Gitelman syndrome (GS, OMIM 263800) is a genetic congenital tubulopathy associated with salt loss, which is characterized by hypokalemic metabolic toxicity, hypocalciuria, and hypomagnesemia. GS, which is typically detected in adolescence or adulthoo
Externí odkaz:
https://doaj.org/article/53a2ad1d18174b81b7cef198f606c629
Autor:
Xue He, Yueling Zhu, Haidong Fu, Chunyue Feng, Zhixia Liu, Weizhong Gu, Yanyan Jin, Binbin Yang, Huijun Shen
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
This report describes an 8-year-old male who presented with clinical manifestations including systemic edema, heavy proteinuria, hypoproteinemia, and persistent hypocomplementemia. Arachnoid cysts and focal nodular hyperplasia were also detected. Ima
Externí odkaz:
https://doaj.org/article/6f41ebc7b2334290951a2b1f07c2557f
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Epigenetic modifications including histone modifications and DNA and RNA modifications are involved in multiple biological processes and human diseases. One disease, kidney cancer, includes a common type of tumor, accounts for about 2% of all cancers
Externí odkaz:
https://doaj.org/article/60ce75b4cb204cef86a3624d9a7d869e
Publikováno v:
PeerJ, Vol 8, p e8599 (2020)
Background As a fundamental process internalizing molecules from the plasma membrane, endocytosis plays a crucial role in podocyte biology. Our previous study has identified that overexpression of Myole may enhance podocyte endocytosis. However, its
Externí odkaz:
https://doaj.org/article/7e111eb0ab9543c3b09311958bf61182