HuGE Literature Finder
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Records 1-22
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Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
European journal of human genetics : EJHG 2015 Sep 23 (9): 1192-9. Bullich Gemma, Trujillano Daniel, Santín Sheila, Ossowski Stephan, Mendizábal Santiago, Fraga Gloria, Madrid Álvaro, Ariceta Gema, Ballarín José, Torra Roser, Estivill Xavier, Ars Elisab |
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Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure.
Nephron 2015 130 (3): 200-12. Stefanou Charalambos, Pieri Myrtani, Savva Isavella, Georgiou Georgia, Pierides Alkis, Voskarides Konstantinos, Deltas Constantin |
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Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Nov 29 (11): 2062-9. Laurin Louis-Philippe, Lu Mei, Mottl Amy K, Blyth Elizabeth R, Poulton Caroline J, Weck Karen |
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The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
International urology and nephrology 2014 Jul 46 (7): 1383-93. Lu Lu, Wan Heng, Yin Yi, Feng Wen-Jun, Wang Ming, Zou Yu-Cong, Huang Bo, Wang Dong-Tao, Shi Yin, Zhao Yan, Wei Lian- |
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Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
Bosnian journal of basic medical sciences / Udruz?enje basic?nih mediciniskih znanosti = Association of Basic Medical Sciences 2014 May 14 (2): 89-93. Bi?czak-Kuleta Agnieszka, Rubik Jacek, Litwin Mieczys?aw, Ryder Ma?gorzata, Lewandowska Klaudyna, Taryma-Le?niak Olga, Clark Jeremy S, Grenda Ryszard, Ciechanowicz Andrz |
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Gene-gene interactions in APOL1-associated nephropathy.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Mar 29 (3): 587-94. Divers Jasmin, Palmer Nicholette D, Lu Lingyi, Langefeld Carl D, Rocco Michael V, Hicks Pamela J, Murea Mariana, Ma Lijun, Bowden Donald W, Freedman Barry |
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R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
Iranian journal of kidney diseases 2013 Sep 7 (5): 399-403. Fotouhi Nikou, Ardalan Mohammadreza, Jabbarpour Bonyadi Mortaza, Abdolmohammadi Reza, Kamalifar Amir, Nasri Hamid, Einollahi Behz |
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The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation.
Annals of transplantation : quarterly of the Polish Transplantation Society 2013 18 436-42. Mohey Hesham, Thibaudin Lise, Laurent Blandine, Berthoux Franco |
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Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
Clinical nephrology 2012 Jul 78 (1): 47-53. Büscher Anja K, Konrad Martin, Nagel Mato, Witzke Oliver, Kribben Andreas, Hoyer Peter F, Weber Stefan |
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Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
Folia biologica 2012 58 (2): 64-8. Reiterová J, Safránková H, Obeidová L, St?krová J, Maixnerová D, Merta M, Tesa? |
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[The correlation between NPHS2 polymorphism and IgA nephropathy in northern Chinese patients].
Zhonghua nei ke za zhi [Chinese journal of internal medicine] 2011 Oct 50 (10): 10. Yu L, Lü JC, Li GS, Zhang H |
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Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
Journal of the American Society of Nephrology : JASN 2011 Mar 22 (3): 579-85. Jungraithmayr Therese C, Hofer Katrin, Cochat Pierre, Chernin Gil, Cortina Gerard, Fargue Sonja, Grimm Paul, Knueppel Tanja, Kowarsch Andreas, Neuhaus Thomas, Pagel Philipp, Pfeiffer Karl P, Schäfer Franz, Schönermarck Ulf, Seeman Tomas, Toenshoff Burkhard, Weber Stefanie, Winn Michelle P, Zschocke Johannes, Zimmerhackl Lothar |
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Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
Clinical journal of the American Society of Nephrology : CJASN 2011 Feb 6 (2): 344-54. Santín Sheila, Tazón-Vega Bárbara, Silva Irene, Cobo María Ángeles, Giménez Isabel, Ruíz Patricia, García-Maset Rafael, Ballarín José, Torra Roser, Ars Elisabet, |
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Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy.
Nephrology (Carlton, Vic.) 2009 Dec 14 (8): 728-34. Zhu Li, Yu Lei, Wang Chen-Dan, Lv Ji-Cheng, Li Gui-Sen, Zhang Hong, Wang Hai-Y |
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Eye involvement in children with primary focal segmental glomerulosclerosis.
Pediatric nephrology (Berlin, Germany) 2008 Mar 23 (3): 421-7. Ozaltin Fatih, Heeringa Saskia, Poyraz Ceren Erdogan, Bilginer Yelda, Kadayifcilar Sibel, Besbas Nesrin, Topaloglu Rezan, Ozen Seza, Hildebrandt Friedhelm, Bakkaloglu Ays |
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NPHS2 variation in focal and segmental glomerulosclerosis.
BMC nephrology 2008 9 (1): 13. Tonna Stephen J, Needham Alexander, Polu Krishna, Uscinski Andrea, Appel Gerald B, Falk Ronald J, Katz Avi, Al-Waheeb Salah, Kaplan Bernard S, Jerums George, Savige Judy, Harmon Jennifer, Zhang Kang, Curhan Gary C, Pollak Martin |
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NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2007 Dec 22 (12): 2031-40. Berdeli Afig, Mir Sevgi, Yavascan Onder, Serdaroglu Erkin, Bak Mustafa, Aksu Nejat, Oner Ayse, Anarat Ali, Donmez Osman, Yildiz Nurhan, Sever Lale, Tabel Yilmaz, Dusunsel Ruhan, Sonmez Ferah, Cakar Nilg |
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NPHS2 variation in sporadic focal segmental glomerulosclerosis.
Journal of the American Society of Nephrology : JASN 2007 Nov 18 (11): 2987-95. McKenzie Louise M, Hendrickson Sher L, Briggs William A, Dart Richard A, Korbet Stephen M, Mokrzycki Michelle H, Kimmel Paul L, Ahuja Tejinder S, Berns Jeffrey S, Simon Eric E, Smith Michael C, Trachtman Howard, Michel Donna M, Schelling Jeffrey R, Cho Monique, Zhou Yu C, Binns-Roemer Elizabeth, Kirk Gregory D, Kopp Jeffrey B, Winkler Cheryl |
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Lack of association between NPHS2 gene polymorphisms and sporadic IgA nephropathy.
Nephrology (Carlton, Vic.) 2007 Aug 12 (4): 371-5. Mao Jianhua, DU Lizhong, Gu Weizhong, Dai Yuwen, Liu Aimin, Xia Yonghui, Zhang Ya |
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Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis.
Archives of dermatological research 2007 Jun 299 (3): 151-5. Zhang Yang, Xudong Xu, Du Lizhong, Gu Weizhong, Dai Yuwen, Liu Aimin, Xia Yonghui, Mao Jianh |
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NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Genetics in medicine : official journal of the American College of Medical Genetics 2006 Feb 8 (2): 63-75. Franceschini Nora, North Kari E, Kopp Jeffrey B, McKenzie Louise, Winkler Cher |
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Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.
Gene expression 2006 13 (1): 59-66. Oleggini Roberta, Bertelli Roberta, Di Donato Armando, Di Duca Marco, Caridi Gianluca, Sanna-Cherchi Simone, Scolari Francesco, Murer Luisa, Allegri Landino, Coppo Rosanna, Emma Francesco, Camussi Giovanni, Perfumo Francesco, Ghiggeri Gian Mar |
- Page last reviewed:Jul 30, 2019
- Page last updated:Aug 15, 2019
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