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Journal Abstract Search

196 related items for PubMed ID: 31924668

  • 21. The formin INF2 in disease: progress from 10 years of research.
    Labat-de-Hoz L, Alonso MA.
    Cell Mol Life Sci; 2020 Nov; 77(22):4581-4600. PubMed ID: 32451589
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  • 22. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.
    Büscher AK, Celebi N, Hoyer PF, Klein HG, Weber S, Hoefele J.
    Pediatr Nephrol; 2018 Mar; 33(3):433-437. PubMed ID: 29038887
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  • 23. A cryptic splicing mutation in the INF2 gene causing Charcot-Marie-Tooth disease with minimal glomerular dysfunction.
    Echaniz-Laguna A, Latour P.
    J Peripher Nerv Syst; 2019 Mar; 24(1):120-124. PubMed ID: 30680856
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  • 28. Actin monomers activate inverted formin 2 by competing with its autoinhibitory interaction.
    Ramabhadran V, Hatch AL, Higgs HN.
    J Biol Chem; 2013 Sep 13; 288(37):26847-55. PubMed ID: 23921379
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  • 30. Splice variant-specific cellular function of the formin INF2 in maintenance of Golgi architecture.
    Ramabhadran V, Korobova F, Rahme GJ, Higgs HN.
    Mol Biol Cell; 2011 Dec 13; 22(24):4822-33. PubMed ID: 21998196
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  • 31. INF2 is an endoplasmic reticulum-associated formin protein.
    Chhabra ES, Ramabhadran V, Gerber SA, Higgs HN.
    J Cell Sci; 2009 May 01; 122(Pt 9):1430-40. PubMed ID: 19366733
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  • 35. FSGS-associated alpha-actinin-4 (K256E) impairs cytoskeletal dynamics in podocytes.
    Michaud JL, Chaisson KM, Parks RJ, Kennedy CR.
    Kidney Int; 2006 Sep 01; 70(6):1054-61. PubMed ID: 16837921
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  • 36. Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.
    Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM.
    Nephrol Dial Transplant; 2014 Sep 01; 29 Suppl 4():iv80-6. PubMed ID: 25165188
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  • 38. Human Kidney Disease-causing INF2 Mutations Perturb Rho/Dia Signaling in the Glomerulus.
    Sun H, Al-Romaih KI, MacRae CA, Pollak MR.
    EBioMedicine; 2014 Dec 01; 1(2-3):107-15. PubMed ID: 26086034
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  • 39. Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.
    Rood IM, Bongers EM, Lugtenberg D, Klein IH, Steenbergen EJ, Wetzels JF, Deegens JK.
    Neth J Med; 2016 Feb 01; 74(2):82-5. PubMed ID: 26951353
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  • 40. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
    Büscher AK, Konrad M, Nagel M, Witzke O, Kribben A, Hoyer PF, Weber S.
    Clin Nephrol; 2012 Jul 01; 78(1):47-53. PubMed ID: 22732337
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