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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 14, 2024. (Total: 232476Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Proteinuria and TRPC6[original query]
Lack of association between transient receptor potential cation channel 6 polymorphisms and primary membranous glomerulonephritis.
Renal failure 2010 Jul 32 (6): 666-72.
Chen Wen-Chi, Chen Shih-Yin, Chen Cheng-Hsu, Chen Huey-Yi, Lin Yi-Wen, Ho Tsung-Jung, Huang Yu-Chuen, Shen Jui-Lung, Tsai Fuu-Jen, Chen Yung-Hsia
TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Jan 27 (1): 205-9.
Mir Sevgi, Yavascan Onder, Berdeli Afig, Sozeri Bet
Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.
Contributions to nephrology 2013 181 91-100.
Zhang Qianying, Ma Jun, Xie Jingyuan, Wang Zhaohui, Zhu Bin, Hao Xu, Yang Li, Ren Hong, Chen N
TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy.
PloS one 2014 9 (7): e102065.
Hofstra Julia M, Coenen Marieke J H, Schijvenaars Mascha M V A P, Berden Jo H M, van der Vlag Johan, Hoefsloot Lies H, Knoers Nine V A M, Wetzels Jack F M, Nijenhuis T
Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2015 Jul .
Sun Z J, Ng K H, Liao P, Zhang Y, Ng J L, Liu I D, Tan P H, Chong S S C, Chan Y H, Liu J, Davila S, Heng C K, Jordan S C, Soong T W, Yap H
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2017 Feb .
Wang Fang, Zhang Yanqin, Mao Jianhua, Yu Zihua, Yi Zhuwen, Yu Li, Sun Jun, Wei Xiuxiu, Ding Fangrui, Zhang Hongwen, Xiao Huijie, Yao Yong, Tan Weizhen, Lovric Svjetlana, Ding Jie, Hildebrandt Friedhe
Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome.
Molecular biology reports 2021 Sep .
Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya
Genetic features and kidney morphological changes in women with X-linked Alport syndrome.
Journal of medical genetics 2023 5 .
Hongling Di, Qing Wang, Dandan Liang, Jiahui Zhang, Erzhi Gao, Chunxia Zheng, Xiaomin Yu, Zhihong L
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