These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis. Sun ZJ; Ng KH; Liao P; Zhang Y; Ng JL; Liu ID; Tan PH; Chong SS; Chan YH; Liu J; Davila S; Heng CK; Jordan SC; Soong TW; Yap HK Am J Transplant; 2015 Dec; 15(12):3229-38. PubMed ID: 26147534 [TBL] [Abstract][Full Text] [Related]
6. Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients. Zhu B; Chen N; Wang ZH; Pan XX; Ren H; Zhang W; Wang WM Mutat Res; 2009 May; 664(1-2):84-90. PubMed ID: 19124028 [TBL] [Abstract][Full Text] [Related]
7. New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis. Hofstra JM; Lainez S; van Kuijk WH; Schoots J; Baltissen MP; Hoefsloot LH; Knoers NV; Berden JH; Bindels RJ; van der Vlag J; Hoenderop JG; Wetzels JF; Nijenhuis T Nephrol Dial Transplant; 2013 Jul; 28(7):1830-8. PubMed ID: 23291369 [TBL] [Abstract][Full Text] [Related]
8. Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis. Zhang Q; Ma J; Xie J; Wang Z; Zhu B; Hao X; Yang L; Ren H; Chen N Contrib Nephrol; 2013; 181():91-100. PubMed ID: 23689571 [TBL] [Abstract][Full Text] [Related]
9. Regulation of TRPC6 ion channels in podocytes - Implications for focal segmental glomerulosclerosis and acquired forms of proteinuric diseases. Szabó T; Ambrus L; Zákány N; Balla G; Bíró T Acta Physiol Hung; 2015 Sep; 102(3):241-51. PubMed ID: 26551740 [TBL] [Abstract][Full Text] [Related]
10. In silico analysis of functional nsSNPs in human TRPC6 gene associated with steroid resistant nephrotic syndrome. Joshi BB; Koringa PG; Mistry KN; Patel AK; Gang S; Joshi CG Gene; 2015 Nov; 572(1):8-16. PubMed ID: 26127002 [TBL] [Abstract][Full Text] [Related]
11. Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method. Safaříková M; Reiterová J; Safránková H; Stekrová J; Zidková A; Obeidová L; Kohoutová M; Tesař V Folia Biol (Praha); 2013; 59(3):110-5. PubMed ID: 23890478 [TBL] [Abstract][Full Text] [Related]
12. TRPC6 channels and their binding partners in podocytes: role in glomerular filtration and pathophysiology. Dryer SE; Reiser J Am J Physiol Renal Physiol; 2010 Oct; 299(4):F689-701. PubMed ID: 20685822 [TBL] [Abstract][Full Text] [Related]
13. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Reiser J; Polu KR; Möller CC; Kenlan P; Altintas MM; Wei C; Faul C; Herbert S; Villegas I; Avila-Casado C; McGee M; Sugimoto H; Brown D; Kalluri R; Mundel P; Smith PL; Clapham DE; Pollak MR Nat Genet; 2005 Jul; 37(7):739-44. PubMed ID: 15924139 [TBL] [Abstract][Full Text] [Related]
14. TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis. Santín S; Ars E; Rossetti S; Salido E; Silva I; García-Maset R; Giménez I; Ruíz P; Mendizábal S; Luciano Nieto J; Peña A; Camacho JA; Fraga G; Cobo MA; Bernis C; Ortiz A; de Pablos AL; Sánchez-Moreno A; Pintos G; Mirapeix E; Fernández-Llama P; Ballarín J; Torra R; ; Zamora I; López-Hellin J; Madrid A; Ventura C; Vilalta R; Espinosa L; García C; Melgosa M; Navarro M; Giménez A; Cots JV; Alexandra S; Caramelo C; Egido J; San José MD; de la Cerda F; Sala P; Raspall F; Vila A; Daza AM; Vázquez M; Ecija JL; Espinosa M; Justa ML; Poveda R; Aparicio C; Rosell J; Muley R; Montenegro J; González D; Hidalgo E; de Frutos DB; Trillo E; Gracia S; de los Ríos FJ Nephrol Dial Transplant; 2009 Oct; 24(10):3089-96. PubMed ID: 19458060 [TBL] [Abstract][Full Text] [Related]
15. Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease. Krall P; Canales CP; Kairath P; Carmona-Mora P; Molina J; Carpio JD; Ruiz P; Mezzano SA; Li J; Wei C; Reiser J; Young JI; Walz K PLoS One; 2010 Sep; 5(9):e12859. PubMed ID: 20877463 [TBL] [Abstract][Full Text] [Related]
16. TRPC6 G757D Loss-of-Function Mutation Associates with FSGS. Riehle M; Büscher AK; Gohlke BO; Kaßmann M; Kolatsi-Joannou M; Bräsen JH; Nagel M; Becker JU; Winyard P; Hoyer PF; Preissner R; Krautwurst D; Gollasch M; Weber S; Harteneck C J Am Soc Nephrol; 2016 Sep; 27(9):2771-83. PubMed ID: 26892346 [TBL] [Abstract][Full Text] [Related]
18. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Barua M; Brown EJ; Charoonratana VT; Genovese G; Sun H; Pollak MR Kidney Int; 2013 Feb; 83(2):316-22. PubMed ID: 23014460 [TBL] [Abstract][Full Text] [Related]
19. Novel gain-of-function mutation of TRPC6 Q134P contributes to late onset focal segmental glomerulosclerosis in a Chinese pedigree. Liu Z; Zhang H; Zhao S; Zhang Q; Zhang R; Han Y; Shao L; Zhao X Nephrology (Carlton); 2021 Dec; 26(12):1018-1025. PubMed ID: 34387384 [TBL] [Abstract][Full Text] [Related]
20. The Calcium-Dependent Protease Calpain-1 Links TRPC6 Activity to Podocyte Injury. Verheijden KAT; Sonneveld R; Bakker-van Bebber M; Wetzels JFM; van der Vlag J; Nijenhuis T J Am Soc Nephrol; 2018 Aug; 29(8):2099-2109. PubMed ID: 29954830 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]