These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

196 related items for PubMed ID: 31924668

  • 1. 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; 31(2):374-391. PubMed ID: 31924668
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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 15; 22(2):239-45. PubMed ID: 21258034
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 24(6):917-29. PubMed ID: 23620398
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 15; 88(3):593-604. PubMed ID: 26039629
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. New Paradigm for Cytoskeletal Organization in Podocytes: Proteolytic Fragments of INF2 Formin Function Independently of INF2 Actin Regulatory Activity.
    Krendel M, Pruyne D.
    J Am Soc Nephrol; 2020 Feb 13; 31(2):235-236. PubMed ID: 31924669
    [No Abstract] [Full Text] [Related]

  • 10. 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]

  • 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 25; 31(6):1296-1313. PubMed ID: 32444357
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
    Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR.
    Nat Genet; 2010 Jan 10; 42(1):72-6. PubMed ID: 20023659
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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]

  • 16. Role of formin INF2 in human diseases.
    Zhao Y, Zhang H, Wang H, Ye M, Jin X.
    Mol Biol Rep; 2022 Jan 22; 49(1):735-746. PubMed ID: 34698992
    [Abstract] [Full Text] [Related]

  • 17. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
    Gbadegesin RA, Lavin PJ, Hall G, Bartkowiak B, Homstad A, Jiang R, Wu G, Byrd A, Lynn K, Wolfish N, Ottati C, Stevens P, Howell D, Conlon P, Winn MP.
    Kidney Int; 2012 Jan 22; 81(1):94-9. PubMed ID: 21866090
    [Abstract] [Full Text] [Related]

  • 18. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
    Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR.
    Kidney Int; 2013 Feb 22; 83(2):316-22. PubMed ID: 23014460
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. 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 22; 28(1):108-118. PubMed ID: 36637069
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.