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Journal Abstract Search

205 related items for PubMed ID: 35328514

  • 61.
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  • 63. [Weibel-Palade bodies: unique secretory organelles within endothelial cells].
    Romani de Wit T, Rondaij MG, van Mourik JA.
    Ned Tijdschr Geneeskd; 2004 Aug 07; 148(32):1572-7. PubMed ID: 15382555
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  • 64.
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  • 65. Investigating von Willebrand Factor Pathophysiology Using a Flow Chamber Model of von Willebrand Factor-platelet String Formation.
    Michels A, Swystun LL, Mewburn J, Albánez S, Lillicrap D.
    J Vis Exp; 2017 Aug 14; (126):. PubMed ID: 28829426
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  • 66. Regulated von Willebrand factor (vWf) secretion is restored by pro-vWf expression in a transfectable endothelial cell line.
    Rosnoblet C, Ribba AS, Wollheim CB, Kruithof EK, Vischer UM.
    Biochim Biophys Acta; 2000 Jan 10; 1495(1):112-9. PubMed ID: 10634936
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  • 70. Basal secretion of von Willebrand factor from human endothelial cells.
    Giblin JP, Hewlett LJ, Hannah MJ.
    Blood; 2008 Aug 15; 112(4):957-64. PubMed ID: 18344423
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  • 71. von-Willebrand factor influences blood brain barrier permeability and brain inflammation in experimental allergic encephalomyelitis.
    Noubade R, del Rio R, McElvany B, Zachary JF, Millward JM, Wagner DD, Offner H, Blankenhorn EP, Teuscher C.
    Am J Pathol; 2008 Sep 15; 173(3):892-900. PubMed ID: 18688020
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  • 72.
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  • 74. Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.
    Yadegari H, Driesen J, Pavlova A, Biswas A, Hertfelder HJ, Oldenburg J.
    Thromb Haemost; 2012 Oct 15; 108(4):662-71. PubMed ID: 22871923
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  • 75.
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  • 77. Structural basis of von Willebrand factor multimerization and tubular storage.
    Zeng J, Shu Z, Liang Q, Zhang J, Wu W, Wang X, Zhou A.
    Blood; 2022 Jun 02; 139(22):3314-3324. PubMed ID: 35148377
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  • 78. Regulatory components of the alternative complement pathway in endothelial cell cytoplasm, factor H and factor I, are not packaged in Weibel-Palade bodies.
    Turner NA, Sartain SE, Hui SK, Moake JL.
    PLoS One; 2015 Jun 02; 10(3):e0121994. PubMed ID: 25803806
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  • 79.
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  • 80. Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site.
    Yadegari H, Biswas A, Akhter MS, Driesen J, Ivaskevicius V, Marquardt N, Oldenburg J.
    Blood; 2016 Oct 27; 128(17):2144-2152. PubMed ID: 27543438
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