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151 related items for PubMed ID: 26086034

  • 1. 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; 1(2-3):107-15. PubMed ID: 26086034
    [Abstract] [Full Text] [Related]

  • 2. Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury.
    Subramanian B, Sun H, Yan P, Charoonratana VT, Higgs HN, Wang F, Lai KV, Valenzuela DM, Brown EJ, Schlöndorff JS, Pollak MR.
    Kidney Int; 2016 Aug; 90(2):363-372. PubMed ID: 27350175
    [Abstract] [Full Text] [Related]

  • 3. Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling.
    Sun H, Schlondorff J, Higgs HN, Pollak MR.
    J Am Soc Nephrol; 2013 May; 24(6):917-29. PubMed ID: 23620398
    [Abstract] [Full Text] [Related]

  • 4. INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
    Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G.
    N Engl J Med; 2011 Dec 22; 365(25):2377-88. PubMed ID: 22187985
    [Abstract] [Full Text] [Related]

  • 5. Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2).
    Sun H, Schlondorff JS, Brown EJ, Higgs HN, Pollak MR.
    Proc Natl Acad Sci U S A; 2011 Feb 15; 108(7):2933-8. PubMed ID: 21278336
    [Abstract] [Full Text] [Related]

  • 6. FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes.
    Subramanian B, Chun J, Perez-Gill C, Yan P, Stillman IE, Higgs HN, Alper SL, Schlöndorff JS, Pollak MR.
    J Am Soc Nephrol; 2020 Feb 15; 31(2):374-391. PubMed ID: 31924668
    [Abstract] [Full Text] [Related]

  • 7. Missense Mutant Gain-of-Function Causes Inverted Formin 2 (INF2)-Related Focal Segmental Glomerulosclerosis (FSGS).
    Subramanian B, Williams S, Karp S, Hennino MF, Jacas S, Lee M, Riella CV, Alper SL, Higgs HN, Pollak MR.
    bioRxiv; 2024 Jun 10. PubMed ID: 38915495
    [Abstract] [Full Text] [Related]

  • 8. A complex containing lysine-acetylated actin inhibits the formin INF2.
    A M, Fung TS, Kettenbach AN, Chakrabarti R, Higgs HN.
    Nat Cell Biol; 2019 May 10; 21(5):592-602. PubMed ID: 30962575
    [Abstract] [Full Text] [Related]

  • 9. Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.
    Roos A, Weis J, Korinthenberg R, Fehrenbach H, Häusler M, Züchner S, Mache C, Hubmann H, Auer-Grumbach M, Senderek J.
    J Peripher Nerv Syst; 2015 Mar 10; 20(1):52-9. PubMed ID: 25676889
    [Abstract] [Full Text] [Related]

  • 10. Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.
    Safarikova M, Stekrova J, Honsova E, Horinova V, Tesar V, Reiterova J.
    BMC Med Genet; 2018 Aug 20; 19(1):147. PubMed ID: 30126379
    [Abstract] [Full Text] [Related]

  • 11. A Deregulated Stress Response Underlies Distinct INF2-Associated Disease Profiles.
    Bayraktar S, Nehrig J, Menis E, Karli K, Janning A, Struk T, Halbritter J, Michgehl U, Krahn MP, Schuberth CE, Pavenstädt H, Wedlich-Söldner R.
    J Am Soc Nephrol; 2020 Jun 20; 31(6):1296-1313. PubMed ID: 32444357
    [Abstract] [Full Text] [Related]

  • 12. INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.
    Park JH, Kwon HM, Nam DE, Kim HJ, Nam SH, Kim SB, Choi BO, Chung KW.
    J Peripher Nerv Syst; 2023 Mar 20; 28(1):108-118. PubMed ID: 36637069
    [Abstract] [Full Text] [Related]

  • 13. 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 20; 24(1):120-124. PubMed ID: 30680856
    [Abstract] [Full Text] [Related]

  • 14. Novel INF2 mutation p. L77P in a family with glomerulopathy and Charcot-Marie-Tooth neuropathy.
    Rodriguez PQ, Lohkamp B, Celsi G, Mache CJ, Auer-Grumbach M, Wernerson A, Hamajima N, Tryggvason K, Patrakka J.
    Pediatr Nephrol; 2013 Feb 20; 28(2):339-43. PubMed ID: 22961558
    [Abstract] [Full Text] [Related]

  • 15. The formin INF2 in disease: progress from 10 years of research.
    Labat-de-Hoz L, Alonso MA.
    Cell Mol Life Sci; 2020 Nov 20; 77(22):4581-4600. PubMed ID: 32451589
    [Abstract] [Full Text] [Related]

  • 16. De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy.
    Mademan I, Deconinck T, Dinopoulos A, Voit T, Schara U, Devriendt K, Meijers B, Lerut E, De Jonghe P, Baets J.
    Neurology; 2013 Nov 26; 81(22):1953-8. PubMed ID: 24174593
    [Abstract] [Full Text] [Related]

  • 17. Disease causing mutations in inverted formin 2 regulate its binding to G-actin, F-actin capping protein (CapZ α-1) and profilin 2.
    Rollason R, Wherlock M, Heath JA, Heesom KJ, Saleem MA, Welsh GI.
    Biosci Rep; 2016 Jan 13; 36(1):e00302. PubMed ID: 26764407
    [Abstract] [Full Text] [Related]

  • 18. Characterization of cytoskeletal and structural effects of INF2 variants causing glomerulopathy and neuropathy.
    Ueda H, Tran QTH, Tran LNT, Higasa K, Ikeda Y, Kondo N, Hashiyada M, Sato C, Sato Y, Ashida A, Nishio S, Iwata Y, Iida H, Matsuoka D, Hidaka Y, Fukui K, Itami S, Kawashita N, Sugimoto K, Nozu K, Hattori M, Tsukaguchi H.
    Sci Rep; 2023 Jul 25; 13(1):12003. PubMed ID: 37491439
    [Abstract] [Full Text] [Related]

  • 19. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.
    Boyer O, Benoit G, Gribouval O, Nevo F, Tête MJ, Dantal J, Gilbert-Dussardier B, Touchard G, Karras A, Presne C, Grunfeld JP, Legendre C, Joly D, Rieu P, Mohsin N, Hannedouche T, Moal V, Gubler MC, Broutin I, Mollet G, Antignac C.
    J Am Soc Nephrol; 2011 Feb 25; 22(2):239-45. PubMed ID: 21258034
    [Abstract] [Full Text] [Related]

  • 20. INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death.
    Labat-de-Hoz L, Fernández-Martín L, Correas I, Alonso MA.
    Cell Mol Life Sci; 2024 Jun 25; 81(1):279. PubMed ID: 38916773
    [Abstract] [Full Text] [Related]

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