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232 related items for PubMed ID: 23291369

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 3. 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 Jul; 181():91-100. PubMed ID: 23689571
    [Abstract] [Full Text] [Related]

  • 4. 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 12; 664(1-2):84-90. PubMed ID: 19124028
    [Abstract] [Full Text] [Related]

  • 5. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
    Mir S, Yavascan O, Berdeli A, Sozeri B.
    Nephrol Dial Transplant; 2012 Jan 12; 27(1):205-9. PubMed ID: 21511817
    [Abstract] [Full Text] [Related]

  • 6. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N, Damodaran TV, Winn MP.
    Biochim Biophys Acta; 2007 Aug 12; 1772(8):859-68. PubMed ID: 17459670
    [Abstract] [Full Text] [Related]

  • 7. 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 12; 15(12):3229-38. PubMed ID: 26147534
    [Abstract] [Full Text] [Related]

  • 8. 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, FSGS Study Group, 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 12; 24(10):3089-96. PubMed ID: 19458060
    [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 12; 102(3):241-51. PubMed ID: 26551740
    [Abstract] [Full Text] [Related]

  • 10. A novel TRPC6 mutation that causes childhood FSGS.
    Heeringa SF, Möller CC, Du J, Yue L, Hinkes B, Chernin G, Vlangos CN, Hoyer PF, Reiser J, Hildebrandt F.
    PLoS One; 2009 Nov 10; 4(11):e7771. PubMed ID: 19936226
    [Abstract] [Full Text] [Related]

  • 11. TRPC6 - a new podocyte gene involved in focal segmental glomerulosclerosis.
    Kriz W.
    Trends Mol Med; 2005 Dec 10; 11(12):527-30. PubMed ID: 16290061
    [Abstract] [Full Text] [Related]

  • 12. 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 10; 26(12):1018-1025. PubMed ID: 34387384
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 29(8):2099-2109. PubMed ID: 29954830
    [Abstract] [Full Text] [Related]

  • 14. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
    Löwik M, Levtchenko E, Westra D, Groenen P, Steenbergen E, Weening J, Lilien M, Monnens L, van den Heuvel L.
    Nephrol Dial Transplant; 2008 Oct 10; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 37(7):739-44. PubMed ID: 15924139
    [Abstract] [Full Text] [Related]

  • 16. A mutation in TRPC6 channels abolishes their activation by hypoosmotic stretch but does not affect activation by diacylglycerol or G protein signaling cascades.
    Wilson C, Dryer SE.
    Am J Physiol Renal Physiol; 2014 May 01; 306(9):F1018-25. PubMed ID: 24598806
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 27(9):2771-83. PubMed ID: 26892346
    [Abstract] [Full Text] [Related]

  • 18. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.
    Winn MP, Conlon PJ, Lynn KL, Farrington MK, Creazzo T, Hawkins AF, Daskalakis N, Kwan SY, Ebersviller S, Burchette JL, Pericak-Vance MA, Howell DN, Vance JM, Rosenberg PB.
    Science; 2005 Jun 17; 308(5729):1801-4. PubMed ID: 15879175
    [Abstract] [Full Text] [Related]

  • 19. 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 17; 83(2):316-22. PubMed ID: 23014460
    [Abstract] [Full Text] [Related]

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