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Journal Abstract Search

195 related items for PubMed ID: 15208719

  • 1. Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein.
    Yao J, Le TC, Kos CH, Henderson JM, Allen PG, Denker BM, Pollak MR.
    PLoS Biol; 2004 Jun; 2(6):e167. PubMed ID: 15208719
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  • 2. 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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  • 3. Ubiquitin C-terminal hydrolase L1 deletion ameliorates glomerular injury in mice with ACTN4-associated focal segmental glomerulosclerosis.
    Read NC, Gutsol A, Holterman CE, Carter A, Coulombe J, Gray DA, Kennedy CR.
    Biochim Biophys Acta; 2014 Jul; 1842(7):1028-40. PubMed ID: 24662305
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  • 4. 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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  • 7. 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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  • 8. Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury.
    Henderson JM, Alexander MP, Pollak MR.
    J Am Soc Nephrol; 2009 May; 20(5):961-8. PubMed ID: 19357256
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  • 9. Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS.
    Bartram MP, Habbig S, Pahmeyer C, Höhne M, Weber LT, Thiele H, Altmüller J, Kottoor N, Wenzel A, Krueger M, Schermer B, Benzing T, Rinschen MM, Beck BB.
    Hum Mol Genet; 2016 Mar 15; 25(6):1152-64. PubMed ID: 26740551
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  • 10. 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 15; 25(1):87-93. PubMed ID: 12617336
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  • 13. Familial focal segmental glomerulosclerosis (FSGS)-linked α-actinin 4 (ACTN4) protein mutants lose ability to activate transcription by nuclear hormone receptors.
    Khurana S, Chakraborty S, Lam M, Liu Y, Su YT, Zhao X, Saleem MA, Mathieson PW, Bruggeman LA, Kao HY.
    J Biol Chem; 2012 Apr 06; 287(15):12027-35. PubMed ID: 22351778
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  • 14. Disease-causing mutation in α-actinin-4 promotes podocyte detachment through maladaptation to periodic stretch.
    Feng D, Notbohm J, Benjamin A, He S, Wang M, Ang LH, Bantawa M, Bouzid M, Del Gado E, Krishnan R, Pollak MR.
    Proc Natl Acad Sci U S A; 2018 Feb 13; 115(7):1517-1522. PubMed ID: 29378953
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  • 15. Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations.
    Shao H, Wingert B, Weins A, Pollak MR, Camacho C, Wells A.
    Sci Rep; 2019 Oct 29; 9(1):15517. PubMed ID: 31664084
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  • 16. Disease-associated mutant alpha-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity.
    Weins A, Schlondorff JS, Nakamura F, Denker BM, Hartwig JH, Stossel TP, Pollak MR.
    Proc Natl Acad Sci U S A; 2007 Oct 09; 104(41):16080-5. PubMed ID: 17901210
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  • 17. Mice deficient in alpha-actinin-4 have severe glomerular disease.
    Kos CH, Le TC, Sinha S, Henderson JM, Kim SH, Sugimoto H, Kalluri R, Gerszten RE, Pollak MR.
    J Clin Invest; 2003 Jun 09; 111(11):1683-90. PubMed ID: 12782671
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  • 18. 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 Jun 09; 181():91-100. PubMed ID: 23689571
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  • 19. 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 Jun 09; 111(2):c87-94. PubMed ID: 19142020
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  • 20. 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 Jun 09; 99(2):c31-6. PubMed ID: 15627790
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