Kaser EG: Genotyp-Phänotyp-Korrelation beim leichten hereditären ...

79
6 Literaturverzeichnis
Ahamed J, Ruf W. Protease-activated receptor 2-dependent phosphorylation of the
tissue factor cytoplasmic domain. J Biol Chem 2004; 279: 23038−23044
Banner DW, D'Arcy A, Chène C, Winkler FK, Guha A, Konigsberg WH, Nemerson Y,
Kirchhofer D.The crystal structure of the complex of blood coagulation factor VIIa with
soluble tissue factor. Nature 1996; 380: 41−46
Belting M, Dorrell MI, Sandgren S, Aguilar E, Ahamed J, Dorfleutner A, Carmeliet P,
Mueller BM, Friedlander M, Ruf W. Regulation of angiogenesis by tissue factor
cytoplasmic domain signaling. Nat Med 2004; 10: 502−509
Bernardi F, Castaman G, Redaelli R. Topologically equivalent mutations causing
dysfunctional coagulation factors VII (Ala294Val) and X (Ser334Pro). Hum Mol Genet
1994; 3: 1175−1177
Bernardi F, Marchetti G, Pinotti M, Arcieri P, Baroncini C, Papacchini M, Zepponi E,
Ursicino N, Chiarotti F, Mariani G. Factor VII gene polymorphisms contribute about one
third of the factor VII level variation in plasma. Arterioscler Thromb Vasc Biol 1996; 16:
72−76
Bruhn HD, Schambeck CM, Hach-Wunderle V. Hämostaseologie für die Praxis.
Stuttgart: Schattauer Verlag, 2007
Budde U, Drewke E, Will K, Schneppenheim R. Diagnostic standards of von Willebrand
disease. Hämostaseologie 2004; 24: 12–26
Davie EW, Ratnoff OD. Waterfall sequence for intrinsic blood clotting. Science 1964;
145: 1319−1312