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Journal Abstract Search

661 related items for PubMed ID: 21734084

  • 41. 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
    [Abstract] [Full Text] [Related]

  • 42. [TRPC6 mutations in children with steroid-resistant nephrotic syndrome].
    Gigante M, Caridi G, Montemurno E, Trunzo R, Schirinzi A, Aucella F, Messina G, Massella L, Ranieri E, Ghiggeri GM, Gesualdo L.
    G Ital Nefrol; 2011 Dec; 28(4):350-2. PubMed ID: 21809298
    [No Abstract] [Full Text] [Related]

  • 43. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
    Zununi Vahed S, Moghaddas Sani H, Haghi M, Mohajel Shoja M, Ardalan M.
    Mol Biol Rep; 2019 Dec; 46(6):6339-6344. PubMed ID: 31529341
    [Abstract] [Full Text] [Related]

  • 44. 254C>G: a TRPC6 promoter variation associated with enhanced transcription and steroid-resistant nephrotic syndrome in Chinese children.
    Kuang XY, Huang WY, Xu H, Shi Y, Zhang XL, Niu XL, Wu Y, Mei CZ, Zha XL, Zhao ZH, Zhang ZG.
    Pediatr Res; 2013 Nov; 74(5):511-6. PubMed ID: 23999069
    [Abstract] [Full Text] [Related]

  • 45. Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformations.
    Li JG, Zhao D, Ding J, Xiao HJ, Guan N, Fan QF, Zhang HW.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 46. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
    Ramanathan AS, Vijayan M, Rajagopal S, Rajendiran P, Senguttuvan P.
    Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

  • 47. TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis.
    Gheissari A, Meamar R, Kheirollahi M, Rouigari M, Dehbashi M, Dehghani L, Abedini A.
    Iran J Kidney Dis; 2018 Nov; 12(6):341-349. PubMed ID: 30595563
    [Abstract] [Full Text] [Related]

  • 48. Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
    Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F, PodoNet Consortium.
    Kidney Int; 2013 Jul; 84(1):206-13. PubMed ID: 23515051
    [Abstract] [Full Text] [Related]

  • 49. 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
    [Abstract] [Full Text] [Related]

  • 50. Spectrum of adolescent-onset nephrotic syndrome in Indian children.
    Gulati S, Sural S, Sharma RK, Gupta A, Gupta RK.
    Pediatr Nephrol; 2001 Dec; 16(12):1045-8. PubMed ID: 11793097
    [Abstract] [Full Text] [Related]

  • 51. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 52. Cyclosporine in steroid dependent and resistant childhood nephrotic syndrome.
    Iyengar A, Karthik S, Kumar A, Biswas S, Phadke K.
    Indian Pediatr; 2006 Jan; 43(1):14-9. PubMed ID: 16465001
    [Abstract] [Full Text] [Related]

  • 53. De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.
    Weng PL, Majmundar AJ, Khan K, Lim TY, Shril S, Jin G, Musgrove J, Wang M, Ahram DF, Aggarwal VS, Bier LE, Heinzen EL, Onuchic-Whitford AC, Mann N, Buerger F, Schneider R, Deutsch K, Kitzler TM, Klämbt V, Kolb A, Mao Y, Moufawad El Achkar C, Mitrotti A, Martino J, Beck BB, Altmüller J, Benz MR, Yano S, Mikati MA, Gunduz T, Cope H, Shashi V, Undiagnosed Diseases Network, Trachtman H, Bodria M, Caridi G, Pisani I, Fiaccadori E, AbuMaziad AS, Martinez-Agosto JA, Yadin O, Zuckerman J, Kim A, UCLA Clinical Genomics Center, John-Kroegel U, Tyndall AV, Parboosingh JS, Innes AM, Bierzynska A, Koziell AB, Muorah M, Saleem MA, Hoefele J, Riedhammer KM, Gharavi AG, Jobanputra V, Pierce-Hoffman E, Seaby EG, O'Donnell-Luria A, Rehm HL, Mane S, D'Agati VD, Pollak MR, Ghiggeri GM, Lifton RP, Goldstein DB, Davis EE, Hildebrandt F, Sanna-Cherchi S.
    Am J Hum Genet; 2021 Feb 04; 108(2):357-367. PubMed ID: 33508234
    [Abstract] [Full Text] [Related]

  • 54. Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.
    Yang YH, Zhao F, Feng DN, Wang JJ, Wang CF, Huang J, Nie XJ, Xia GZ, Chen GM, Yu ZH.
    Genet Mol Res; 2013 Dec 04; 12(4):6184-91. PubMed ID: 24338413
    [Abstract] [Full Text] [Related]

  • 55. Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome.
    Ye J, Yu Z, Ding J, Chen Y, Huang J, Yao Y, Xiao H, Yang J, Shen Y, Meng Q.
    Biochem Biophys Res Commun; 2006 Sep 22; 348(2):507-13. PubMed ID: 16890204
    [Abstract] [Full Text] [Related]

  • 56. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
    Gigante M, Monno F, Roberto R, Laforgia N, Assael MB, Livolti S, Caringella A, La Manna A, Masella L, Iolascon A.
    J Nephrol; 2002 Sep 22; 15(6):696-702. PubMed ID: 12495287
    [Abstract] [Full Text] [Related]

  • 57. Broadening the spectrum of diseases related to podocin mutations.
    Caridi G, Bertelli R, Di Duca M, Dagnino M, Emma F, Onetti Muda A, Scolari F, Miglietti N, Mazzucco G, Murer L, Carrea A, Massella L, Rizzoni G, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2003 May 22; 14(5):1278-86. PubMed ID: 12707396
    [Abstract] [Full Text] [Related]

  • 58. Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated.
    Ehrich JH, Geerlings C, Zivicnjak M, Franke D, Geerlings H, Gellermann J.
    Nephrol Dial Transplant; 2007 Aug 22; 22(8):2183-93. PubMed ID: 17504846
    [Abstract] [Full Text] [Related]

  • 59. TRPC6 - a new podocyte gene involved in focal segmental glomerulosclerosis.
    Kriz W.
    Trends Mol Med; 2005 Dec 22; 11(12):527-30. PubMed ID: 16290061
    [Abstract] [Full Text] [Related]

  • 60. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
    Ruf RG, Schultheiss M, Lichtenberger A, Karle SM, Zalewski I, Mucha B, Everding AS, Neuhaus T, Patzer L, Plank C, Haas JP, Ozaltin F, Imm A, Fuchshuber A, Bakkaloglu A, Hildebrandt F, APN Study Group.
    Kidney Int; 2004 Aug 22; 66(2):564-70. PubMed ID: 15253707
    [Abstract] [Full Text] [Related]

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