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Journal Abstract Search

205 related items for PubMed ID: 35328514

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  • 24. Storage and secretion of naturally occurring von Willebrand factor A domain variants.
    Groeneveld DJ, Wang JW, Mourik MJ, Dirven RJ, Valentijn KM, Voorberg J, Reitsma PH, Eikenboom J.
    Br J Haematol; 2014 Nov; 167(4):529-40. PubMed ID: 25103891
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  • 27. Factor VIII Is Synthesized in Human Endothelial Cells, Packaged in Weibel-Palade Bodies and Secreted Bound to ULVWF Strings.
    Turner NA, Moake JL.
    PLoS One; 2015 Nov; 10(10):e0140740. PubMed ID: 26473492
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  • 29. Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms.
    Cartwright A, Webster SJ, de Jong A, Dirven RJ, Bloomer LDS, Al-Buhairan AM, Budde U, Halldén C, Habart D, Goudemand J, Peake IR, Eikenboom JCJ, Goodeve AC, Hampshire DJ.
    Blood Adv; 2020 Jul 14; 4(13):2979-2990. PubMed ID: 32609846
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  • 32. The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients.
    Pagliari MT, Baronciani L, Cordiglieri C, Colpani P, Cozzi G, Siboni SM, Peyvandi F.
    Haemophilia; 2022 Mar 14; 28(2):292-300. PubMed ID: 35064738
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  • 38. Requirements for cellular co-trafficking of factor VIII and von Willebrand factor to Weibel-Palade bodies.
    van den Biggelaar M, Bierings R, Storm G, Voorberg J, Mertens K.
    J Thromb Haemost; 2007 Nov 14; 5(11):2235-42. PubMed ID: 17958741
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