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Journal Abstract Search

169 related items for PubMed ID: 19142020

  • 1. ACTN4 gene mutations and single nucleotide polymorphisms in idiopathic focal segmental glomerulosclerosis.
    Dai S, Wang Z, Pan X, Chen X, Wang W, Ren H, Feng Q, He JC, Han B, Chen N.
    Nephron Clin Pract; 2009; 111(2):c87-94. PubMed ID: 19142020
    [Abstract] [Full Text] [Related]

  • 2. Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis.
    Dai S, Wang Z, Pan X, Wang W, Chen X, Ren H, Hao C, Han B, Chen N.
    Nephrol Dial Transplant; 2010 Mar; 25(3):824-35. PubMed ID: 19666657
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  • 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 Mar; 181():91-100. PubMed ID: 23689571
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  • 4. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
    Aucella F, De Bonis P, Gatta G, Muscarella LA, Vigilante M, di Giorgio G, D'Errico M, Zelante L, Stallone C, Bisceglia L.
    Nephron Clin Pract; 2005 Mar; 99(2):c31-6. PubMed ID: 15627790
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  • 5. Characterization of the transcriptional regulation of the human MT1-MMP gene and association of risk reduction for focal-segmental glomerulosclerosis with two functional promoter SNPs.
    Munkert A, Helmchen U, Kemper MJ, Bubenheim M, Stahl RA, Harendza S.
    Nephrol Dial Transplant; 2009 Mar; 24(3):735-42. PubMed ID: 18927121
    [Abstract] [Full Text] [Related]

  • 6. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.
    Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR.
    Nat Genet; 2000 Mar; 24(3):251-6. PubMed ID: 10700177
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  • 7. Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.
    Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI.
    Am J Kidney Dis; 2008 May; 51(5):834-8. PubMed ID: 18436095
    [Abstract] [Full Text] [Related]

  • 8. 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; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 9. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
    Komatsuda A, Wakui H, Maki N, Kigawa A, Goto H, Ohtani H, Hamai K, Oyama Y, Makoto H, Sawada K, Imai H.
    Ren Fail; 2003 Jan; 25(1):87-93. PubMed ID: 12617336
    [Abstract] [Full Text] [Related]

  • 10. CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).
    Gigante M, Pontrelli P, Montemurno E, Roca L, Aucella F, Penza R, Caridi G, Ranieri E, Ghiggeri GM, Gesualdo L.
    Nephrol Dial Transplant; 2009 Jun; 24(6):1858-64. PubMed ID: 19131354
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  • 13. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Jun; 107(1):5-16. PubMed ID: 16752799
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  • 15. Focal and segmental glomerulosclerosis in mice with podocyte-specific expression of mutant alpha-actinin-4.
    Michaud JL, Lemieux LI, Dubé M, Vanderhyden BC, Robertson SJ, Kennedy CR.
    J Am Soc Nephrol; 2003 May; 14(5):1200-11. PubMed ID: 12707390
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  • 18. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
    Aucella F, Bisceglia L, Stallone C.
    G Ital Nefrol; 2003 May; 20(4):356-67. PubMed ID: 14523896
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