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199 related items for PubMed ID: 12177068

  • 21. Role of lipid microdomains in P/Q-type calcium channel (Cav2.1) clustering and function in presynaptic membranes.
    Taverna E, Saba E, Rowe J, Francolini M, Clementi F, Rosa P.
    J Biol Chem; 2004 Feb 13; 279(7):5127-34. PubMed ID: 14660672
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  • 22. Cellular vacuolation induced by Clostridium perfringens epsilon-toxin.
    Nagahama M, Itohayashi Y, Hara H, Higashihara M, Fukatani Y, Takagishi T, Oda M, Kobayashi K, Nakagawa I, Sakurai J.
    FEBS J; 2011 Sep 13; 278(18):3395-407. PubMed ID: 21781280
    [Abstract] [Full Text] [Related]

  • 23. The C-terminal domain of perfringolysin O is an essential cholesterol-binding unit targeting to cholesterol-rich microdomains.
    Shimada Y, Maruya M, Iwashita S, Ohno-Iwashita Y.
    Eur J Biochem; 2002 Dec 13; 269(24):6195-203. PubMed ID: 12473115
    [Abstract] [Full Text] [Related]

  • 24. Interaction of Clostridium perfringens Epsilon Toxin with the Plasma Membrane: The Role of Amino Acids Y42, Y43 and H162.
    Marshall S, McGill B, Morcrette H, Winlove CP, Chimerel C, Petrov PG, Bokori-Brown M.
    Toxins (Basel); 2022 Nov 03; 14(11):. PubMed ID: 36356007
    [Abstract] [Full Text] [Related]

  • 25. Assembly of Clostridium perfringens epsilon-toxin on MDCK cell membrane.
    Nagahama M, Ochi S, Sakurai J.
    J Nat Toxins; 1998 Oct 03; 7(3):291-302. PubMed ID: 9783265
    [Abstract] [Full Text] [Related]

  • 26. Cholesterol depletion alters detergent-specific solubility profiles of selected tight junction proteins and the phosphorylation of occludin.
    Lynch RD, Francis SA, McCarthy KM, Casas E, Thiele C, Schneeberger EE.
    Exp Cell Res; 2007 Jul 15; 313(12):2597-610. PubMed ID: 17574235
    [Abstract] [Full Text] [Related]

  • 27. Identification of tyrosine 71 as a critical residue for the cytotoxic activity of Clostridium perfringens epsilon toxin towards MDCK cells.
    Jiang Z, Chang J, Wang F, Yu L.
    J Microbiol; 2015 Feb 15; 53(2):141-6. PubMed ID: 25626370
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  • 28. Heliothis virescens and Manduca sexta lipid rafts are involved in Cry1A toxin binding to the midgut epithelium and subsequent pore formation.
    Zhuang M, Oltean DI, Gómez I, Pullikuth AK, Soberón M, Bravo A, Gill SS.
    J Biol Chem; 2002 Apr 19; 277(16):13863-72. PubMed ID: 11836242
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  • 29. Synaptic proteins and SNARE complexes are localized in lipid rafts from rat brain synaptosomes.
    Gil C, Soler-Jover A, Blasi J, Aguilera J.
    Biochem Biophys Res Commun; 2005 Apr 01; 329(1):117-24. PubMed ID: 15721282
    [Abstract] [Full Text] [Related]

  • 30. Recoverin and rhodopsin kinase activity in detergent-resistant membrane rafts from rod outer segments.
    Senin II, Höppner-Heitmann D, Polkovnikova OO, Churumova VA, Tikhomirova NK, Philippov PP, Koch KW.
    J Biol Chem; 2004 Nov 19; 279(47):48647-53. PubMed ID: 15355976
    [Abstract] [Full Text] [Related]

  • 31. Plasma membrane microdomains act as concentration platforms to facilitate intoxication by aerolysin.
    Abrami L, van Der Goot FG.
    J Cell Biol; 1999 Oct 04; 147(1):175-84. PubMed ID: 10508864
    [Abstract] [Full Text] [Related]

  • 32. Clostridium perfringens epsilon-toxin shows structural similarity to the pore-forming toxin aerolysin.
    Cole AR, Gibert M, Popoff M, Moss DS, Titball RW, Basak AK.
    Nat Struct Mol Biol; 2004 Aug 04; 11(8):797-8. PubMed ID: 15258571
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  • 33. Biological activities and pore formation of Clostridium perfringens beta toxin in HL 60 cells.
    Nagahama M, Hayashi S, Morimitsu S, Sakurai J.
    J Biol Chem; 2003 Sep 19; 278(38):36934-41. PubMed ID: 12851396
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  • 34. Glycosphingolipids are not essential for formation of detergent-resistant membrane rafts in melanoma cells. methyl-beta-cyclodextrin does not affect cell surface transport of a GPI-anchored protein.
    Ostermeyer AG, Beckrich BT, Ivarson KA, Grove KE, Brown DA.
    J Biol Chem; 1999 Nov 26; 274(48):34459-66. PubMed ID: 10567427
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  • 35. Channel formation by the glycosylphosphatidylinositol-anchored protein binding toxin aerolysin is not promoted by lipid rafts.
    Nelson KL, Buckley JT.
    J Biol Chem; 2000 Jun 30; 275(26):19839-43. PubMed ID: 10770947
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  • 36. Resistance of human erythrocyte membranes to Triton X-100 and C12E8.
    Crepaldi Domingues C, Ciana A, Buttafava A, Balduini C, de Paula E, Minetti G.
    J Membr Biol; 2009 Jan 30; 227(1):39-48. PubMed ID: 19067023
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  • 37. Pore-forming epsilon toxin causes membrane permeabilization and rapid ATP depletion-mediated cell death in renal collecting duct cells.
    Chassin C, Bens M, de Barry J, Courjaret R, Bossu JL, Cluzeaud F, Ben Mkaddem S, Gibert M, Poulain B, Popoff MR, Vandewalle A.
    Am J Physiol Renal Physiol; 2007 Sep 30; 293(3):F927-37. PubMed ID: 17567938
    [Abstract] [Full Text] [Related]

  • 38. Cellular vacuolation and mitochondrial-associated factors induced by Clostridium perfringens epsilon toxin detected using acoustic flow cytometry.
    Ferrarezi MC, Curci VC, Cardoso TC.
    Anaerobe; 2013 Dec 30; 24():55-9. PubMed ID: 24076036
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  • 39. Calcium enhances binding of Clostridium perfringens epsilon toxin to sulfatide.
    Gil C, Dorca-Arévalo J, Blasi J.
    Biochim Biophys Acta Biomembr; 2019 Jan 30; 1861(1):161-169. PubMed ID: 30463699
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  • 40. The pore structure of Clostridium perfringens epsilon toxin.
    Savva CG, Clark AR, Naylor CE, Popoff MR, Moss DS, Basak AK, Titball RW, Bokori-Brown M.
    Nat Commun; 2019 Jun 14; 10(1):2641. PubMed ID: 31201325
    [Abstract] [Full Text] [Related]

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