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Journal Abstract Search

211 related items for PubMed ID: 38916773

  • 1. 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]

  • 2. 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 25; 31(2):374-391. PubMed ID: 31924668
    [Abstract] [Full Text] [Related]

  • 3. Altered Endoplasmic Reticulum Integrity and Organelle Interactions in Living Cells Expressing INF2 Variants.
    Tran QTH, Kondo N, Ueda H, Matsuo Y, Tsukaguchi H.
    Int J Mol Sci; 2024 Sep 10; 25(18):. PubMed ID: 39337270
    [Abstract] [Full Text] [Related]

  • 4. 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 10; 31(6):1296-1313. PubMed ID: 32444357
    [Abstract] [Full Text] [Related]

  • 5. Novel mutations in the inverted formin 2 gene of Chinese families contribute to focal segmental glomerulosclerosis.
    Xie J, Hao X, Azeloglu EU, Ren H, Wang Z, Ma J, Liu J, Ma X, Wang W, Pan X, Zhang W, Zhong F, Li Y, Meng G, Kiryluk K, He JC, Gharavi AG, Chen N.
    Kidney Int; 2015 Sep 10; 88(3):593-604. PubMed ID: 26039629
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. 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 15; 28(1):108-118. PubMed ID: 36637069
    [Abstract] [Full Text] [Related]

  • 9. Role of formin INF2 in human diseases.
    Zhao Y, Zhang H, Wang H, Ye M, Jin X.
    Mol Biol Rep; 2022 Jan 15; 49(1):735-746. PubMed ID: 34698992
    [Abstract] [Full Text] [Related]

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

  • 11. 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 15; 90(2):363-372. PubMed ID: 27350175
    [Abstract] [Full Text] [Related]

  • 12. Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related Podocytopathy.
    Sun H, Perez-Gill C, Schlöndorff JS, Subramanian B, Pollak MR.
    J Am Soc Nephrol; 2021 Feb 15; 32(2):307-322. PubMed ID: 33443052
    [Abstract] [Full Text] [Related]

  • 13. 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
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  • 17. 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 22; 24(6):917-29. PubMed ID: 23620398
    [Abstract] [Full Text] [Related]

  • 18. Variable renal phenotype in a family with an INF2 mutation.
    Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2011 Jan 22; 26(1):73-6. PubMed ID: 20803156
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. 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]

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