Voorberg J - Search Results

1

Storage of factor VIII variants with impaired von Willebrand factor binding in Weibel-Palade bodies in endothelial cells.

van den Biggelaar M, Bouwens EA, Voorberg J, Mertens K. van den Biggelaar M, et al. Among authors: voorberg j. PLoS One. 2011;6(8):e24163. doi: 10.1371/journal.pone.0024163. Epub 2011 Aug 31. PLoS One. 2011. PMID: 21909383 Free PMC article.

2

The pro-polypeptide of von Willebrand factor is required for the formation of a functional factor VIII-binding site on mature von Willebrand factor.

Leyte A, Voorberg J, Van Schijndel HB, Duim B, Pannekoek H, Van Mourik JA. Leyte A, et al. Among authors: voorberg j. Biochem J. 1991 Feb 15;274 ( Pt 1)(Pt 1):257-61. doi: 10.1042/bj2740257. Biochem J. 1991. PMID: 1900418 Free PMC article.

3

Characterization of des-(741-1668)-factor VIII, a single-chain factor VIII variant with a fusion site susceptible to proteolysis by thrombin and factor Xa.

Donath MJ, de Laaf RT, Biessels PT, Lenting PJ, van de Loo JW, van Mourik JA, Voorberg J, Mertens K. Donath MJ, et al. Among authors: voorberg j. Biochem J. 1995 Nov 15;312 ( Pt 1)(Pt 1):49-55. doi: 10.1042/bj3120049. Biochem J. 1995. PMID: 7492334 Free PMC article.

4

Association of idiopathic venous thromboembolism with single point-mutation at Arg506 of factor V.

Voorberg J, Roelse J, Koopman R, Büller H, Berends F, ten Cate JW, Mertens K, van Mourik JA. Voorberg J, et al. Lancet. 1994 Jun 18;343(8912):1535-6. doi: 10.1016/s0140-6736(94)92939-4. Lancet. 1994. PMID: 7911872

5

Enhanced thrombin sensitivity of a factor VIII-heparin cofactor II hybrid.

Voorberg J, van Stempvoort G, Bos JM, Mertens K, van Mourik JA, Donath MJ. Voorberg J, et al. J Biol Chem. 1996 Aug 30;271(35):20985-8. doi: 10.1074/jbc.271.35.20985. J Biol Chem. 1996. PMID: 8702860 Free article.

6

A human alloantibody interferes with binding of factor IXa to the factor VIII light chain.

Fijnvandraat K, Celie PH, Turenhout EA, ten Cate JW, van Mourik JA, Mertens K, Peters M, Voorberg J. Fijnvandraat K, et al. Among authors: voorberg j. Blood. 1998 Apr 1;91(7):2347-52. Blood. 1998. PMID: 9516133 Free article.

7

Small GTP-binding protein RalA associates with Weibel-Palade bodies in endothelial cells.

de Leeuw HP, Wijers-Koster PM, van Mourik JA, Voorberg J. de Leeuw HP, et al. Among authors: voorberg j. Thromb Haemost. 1999 Sep;82(3):1177-81. Thromb Haemost. 1999. PMID: 10494784

8

Multiple VH genes are used to assemble human antibodies directed toward the A3-C1 domains of factor VIII.

van den Brink EN, Turenhout EA, Bovenschen N, Heijnen BG, Mertens K, Peters M, Voorberg J. van den Brink EN, et al. Among authors: voorberg j. Blood. 2001 Feb 15;97(4):966-72. doi: 10.1182/blood.v97.4.966. Blood. 2001. PMID: 11159524 Free article.

9

Small GTP-binding protein Ral modulates regulated exocytosis of von Willebrand factor by endothelial cells.

de Leeuw HP, Fernandez-Borja M, Reits EA, Romani de Wit T, Wijers-Koster PM, Hordijk PL, Neefjes J, van Mourik JA, Voorberg J. de Leeuw HP, et al. Among authors: voorberg j. Arterioscler Thromb Vasc Biol. 2001 Jun;21(6):899-904. doi: 10.1161/01.atv.21.6.899. Arterioscler Thromb Vasc Biol. 2001. PMID: 11397694

10

Two classes of germline genes both derived from the V(H)1 family direct the formation of human antibodies that recognize distinct antigenic sites in the C2 domain of factor VIII.

van den Brink EN, Bril WS, Turenhout EA, Zuurveld M, Bovenschen N, Peters M, Yee TT, Mertens K, Lewis DA, Ortel TL, Lollar P, Scandella D, Voorberg J. van den Brink EN, et al. Among authors: voorberg j. Blood. 2002 Apr 15;99(8):2828-34. doi: 10.1182/blood.v99.8.2828. Blood. 2002. PMID: 11929772 Free article.

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