Legendre P - Search Results

1

Two clusters of charged residues located in the electropositive face of the von Willebrand factor A1 domain are essential for heparin binding.

Rastegar-Lari G, Villoutreix BO, Ribba AS, Legendre P, Meyer D, Baruch D. Rastegar-Lari G, et al. Among authors: legendre p. Biochemistry. 2002 May 28;41(21):6668-78. doi: 10.1021/bi020044f. Biochemistry. 2002. PMID: 12022870

2

Modulation by heparin of the interaction of the A1 domain of Von Willebrand factor with glycoprotein Ib.

Perrault C, Ajzenberg N, Legendre P, Rastegar-Lari G, Meyer D, Lopez JA, Baruch D. Perrault C, et al. Among authors: legendre p. Blood. 1999 Dec 15;94(12):4186-94. Blood. 1999. PMID: 10590063 Free article.

3

Defect of heparin binding in plasma and recombinant von Willebrand factor with type 2 von Willebrand disease mutations.

Rastegar-Lari G, Ajzenberg N, Ribba AS, Vereycken-Holler V, Legendre P, Villoutreix B, Meyer D, Baruch D. Rastegar-Lari G, et al. Among authors: legendre p. Thromb Haemost. 2001 Dec;86(6):1459-65. Thromb Haemost. 2001. PMID: 11776314

4

von Willebrand factor binding to heparin in various types of von Willebrand disease.

Rastegar-Lari G, Legendre P, Ajzenberg N, Warszawski J, Meyer D, Baruch D. Rastegar-Lari G, et al. Among authors: legendre p. Hematol J. 2000;1(3):190-8. doi: 10.1038/sj.thj.6200026. Hematol J. 2000. PMID: 11920189

5

Activation of integrin alphaIIbbeta3 expressed in Chinese hamster ovary cells is required for interaction with solid-phase von Willebrand factor.

Mekrache M, Legendre P, Kieffer N, Baruch D. Mekrache M, et al. Among authors: legendre p. Br J Haematol. 2002 Dec;119(4):1024-32. doi: 10.1046/j.1365-2141.2002.03960.x. Br J Haematol. 2002. PMID: 12472584 Free article.

6

Activation of pp125FAK by type 2B recombinant von Willebrand factor binding to platelet GPIb at a high shear rate occurs independently of alpha IIb beta 3 engagement.

Mekrache M, Bachelot-Loza C, Ajzenberg N, Saci A, Legendre P, Baruch D. Mekrache M, et al. Among authors: legendre p. Blood. 2003 Jun 1;101(11):4363-71. doi: 10.1182/blood-2002-06-1879. Epub 2003 Jan 23. Blood. 2003. PMID: 12543870 Free article.

7

Binding of heparin fractions to von Willebrand factor: effect of molecular weight and affinity for antithrombin III.

Baruch D, Ajzenberg N, Denis C, Legendre P, Lormeau JC, Meyer D. Baruch D, et al. Among authors: legendre p. Thromb Haemost. 1994 Jan;71(1):141-6. Thromb Haemost. 1994. PMID: 8165633

8

Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Hommais A, Rayes J, Houllier A, Obert B, Legendre P, Veyradier A, Girma JP, Ribba AS. Hommais A, et al. Among authors: legendre p. Thromb Haemost. 2007 Sep;98(3):593-9. Thromb Haemost. 2007. PMID: 17849048

9

CHO cells expressing the high affinity alpha(IIb)beta3 T562N integrin demonstrate enhanced adhesion under shear.

Legendre P, Salsmann A, Rayes J, Trassard O, Kieffer N, Baruch D. Legendre P, et al. J Thromb Haemost. 2006 Jan;4(1):236-46. doi: 10.1111/j.1538-7836.2005.01653.x. J Thromb Haemost. 2006. PMID: 16409474 Free article.

10

Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13.

Rayes J, Hommais A, Legendre P, Tout H, Veyradier A, Obert B, Ribba AS, Girma JP. Rayes J, et al. Among authors: legendre p. J Thromb Haemost. 2007 Feb;5(2):321-8. doi: 10.1111/j.1538-7836.2007.02296.x. Epub 2006 Nov 1. J Thromb Haemost. 2007. PMID: 17087728 Free article.

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