HuGE Literature Finder
Records 1-11
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Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndrome.
Journal of cellular biochemistry 2018 Sep . Mohanapriya Chinambedu Dhandapani, Vettriselvi Venkatesan, Nammalwar Bollam Rengaswamy, Gowrishankar Kalpana, Ekambaram Sudha, Sengutavan Prabha, Venkatachalam Perum |
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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 |
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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
Clinical journal of the American Society of Nephrology : CJASN 2015 Dec . Büscher Anja K, Beck Bodo B, Melk Anette, Hoefele Julia, Kranz Birgitta, Bamborschke Daniel, Baig Sabrina, Lange-Sperandio Bärbel, Jungraithmayr Theresa, Weber Lutz T, Kemper Markus J, Tönshoff Burkhard, Hoyer Peter F, Konrad Martin, Weber Stefanie, |
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NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
Nephrology (Carlton, Vic.) 2015 Nov . Guaragna Mara S, Cleto Thaís Lira, Souza Marcela Lopes, Lutaif Anna Cristina G B, de Castro Luiz Cláudio Gonçalves, Penido Maria Goretti Moreira Guimarães, Maciel-Guerra Andréa T, Belangero Vera M S, Guerra-Junior Gil, De Mello Maricilda |
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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 |
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Association between genetic polymorphisms of the NPHS1 gene and membranous glomerulonephritis in the Taiwanese population.
Clinica chimica acta; international journal of clinical chemistry 2010 May 411 (9-10): 714-8. Lo Wan-Yu, Chen Shih-Yin, Wang Huang-Joe, Shih Hung-Chang, Chen Cheng-Hsu, Tsai Chang-Hai, Tsai Fuu-J |
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[Association of NPHS1 gene polymorphism with IgA nephropathy].
Zhonghua yi xue za zhi 2009 Apr 89 (13): 881-5. Yu Lei, Li Gui-sen, Lü Ji-cheng, Wang Cai-li, Zhang Ho |
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NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
Iranian journal of kidney diseases 2009 Apr 3 (2): 99-102. Otukesh Hasan, Ghazanfari Behzad, Fereshtehnejad Seyed-Mohammad, Bakhshayesh Masoomeh, Hashemi Mehrdad, Hoseini Rozita, Chalian Majid, Salami Arezoo, Mehdipor Leila, Rahiminia Ays |
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NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.
Pediatric research 2007 Jan 61 (1): 117-22. Mao Jianhua, Zhang Yang, Du Lizhong, Dai Yuwen, Gu Weizhong, Liu Ai'min, Shang Shiqiang, Liang |
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Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).
Kidney international 2004 May 65 (5): 1856-63. Lahdenkari AT, Kestilä M, Holmberg C, Koskimies O, Jalanko H |
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Genetic polymorphism of NPHS1 modifies the clinical manifestations of Ig A nephropathy.
Laboratory investigation; a journal of technical methods and pathology 2003 Aug 83 (8): 1193-200. Narita Ichiei, Goto Shin, Saito Noriko, Song Jin, Kondo Daisuke, Omori Kentaro, Kawachi Hiroshi, Shimizu Fujio, Sakatsume Minoru, Ueno Mitsuhiro, Gejyo Fumita |
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- Page last updated:Sep 23, 2021
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