A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor.
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A. Bertomoro | R. Padrini | V. Daidone | A. Casonato | E. Pontara | M. Cattini | F. Sartorello | L. Gallinaro | A. Pagnan | M. Sztukowska
[1] P. Collins,et al. von Willebrand factor: evidence for variable clearance in vivo according to Y/C1584 phenotype and ABO blood group , 2007, Journal of thrombosis and haemostasis : JTH.
[2] P. D. de Groot,et al. Variations in glycosylation of von Willebrand factor with O-linked sialylated T antigen are associated with its plasma levels. , 2007, Blood.
[3] D. Bellissimo,et al. Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival. , 2006, Blood.
[4] J. O’Donnell,et al. ABO blood group determines plasma von Willebrand factor levels: a biologic function after all? , 2006, Transfusion.
[5] M. Laffan,et al. Bombay phenotype is associated with reduced plasma-VWF levels and an increased susceptibility to ADAMTS13 proteolysis. , 2005, Blood.
[6] D. Bowen,et al. An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13 , 2003, Journal of thrombosis and haemostasis : JTH.
[7] A. Varki,et al. Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[8] M. Laffan,et al. Amount of H Antigen Expressed on Circulating von Willebrand Factor Is Modified by ABO Blood Group Genotype and Is a Major Determinant of Plasma von Willebrand Factor Antigen Levels , 2002, Arteriosclerosis, thrombosis, and vascular biology.
[9] S. Yip. Sequence variation at the human ABO locus , 2002, Annals of human genetics.
[10] M. Laffan,et al. Human Umbilical Vein Endothelial Cells Differ from Other Endothelial Cells in Failing to Express ABO Blood Group Antigens , 2000, Journal of Vascular Research.
[11] L. Almasy,et al. Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time. , 2000, Arteriosclerosis, thrombosis, and vascular biology.
[12] A. Rumley,et al. Factor VIII, von Willebrand factor and the risk of major ischaemic heart disease in the Caerphilly Heart Study , 1999, British journal of haematology.
[13] K. Mohlke,et al. Mvwf, a Dominant Modifier of Murine von Willebrand Factor, Results from Altered Lineage-Specific Expression of a Glycosyltransferase , 1999, Cell.
[14] Chediak,et al. Pharmacokinetics, efficacy and safety of Humate‐P® in von Willebrand disease , 1998 .
[15] M. Shen,et al. A longitudinal study of immunological status in Chinese Haemophiliacs: importance of the heat viral inactivation of factor concentrates. II. Improvements of CD4/CD8 ratio after treatments with heat‐inactivated factor concentrates , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.
[16] A. Bertomoro,et al. Abnormal collagen binding activity of 2A von Willebrand factor: evidence that the defect depends only on the lack of large multimers. , 1997, The Journal of laboratory and clinical medicine.
[17] C. Kessler,et al. Pharmacokinetics of von Willebrand factor and factor VIIIC in patients with severe von Willebrand disease (type 3 VWD): estimation of the rate of factor VIIIC synthesis , 1996, British journal of haematology.
[18] K. Titani,et al. ABO Blood Group Genotype and Plasma von Willebrand Factor in Normal Individuals , 1995, Vox sanguinis.
[19] J. Vandenbroucke,et al. Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis , 1995, The Lancet.
[20] J. Sadler,et al. A Revised Classification of von Willebrand Disease , 1994, Thrombosis and Haemostasis.
[21] J. Sweeney,et al. Intraplatelet von Willebrand factor and ABO blood group. , 1992, Thrombosis research.
[22] K. Titani,et al. Structures of the asparagine-linked oligosaccharide chains of human von Willebrand factor. Occurrence of blood group A, B, and H(O) structures. , 1992, The Journal of biological chemistry.
[23] A. Girolami,et al. Impaired release of tissue plasminogen activator (t‐PA) following DDAVP infusion in von Willebrand's disease with low platelet von Willebrand factor content , 1992, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[24] J. Sixma,et al. Structure-function relationship of human von Willebrand factor. , 1987, Blood.
[25] K. Titani,et al. Amino acid sequence of the von Willebrand factor-binding domain of platelet membrane glycoprotein Ib. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[26] W. Marks,et al. The effect of ABO blood group on the diagnosis of von Willebrand disease. , 1987, Blood.
[27] T. Mayadas,et al. Initial glycosylation and acidic pH in the Golgi apparatus are required for multimerization of von Willebrand factor , 1986, The Journal of cell biology.
[28] I. Sussman,et al. Factor VIII/von Willebrand factor in subendothelium mediates platelet adhesion. , 1985, Blood.
[29] D. Morisato,et al. Effect of multimeric structure of the factor VIII/von Willebrand factor protein on binding to platelets , 1981 .
[30] Z. Ruggeri,et al. The complex multimeric composition of factor VIII/von Willebrand factor , 1981 .
[31] S. Pizzo,et al. Relationship of sialic acid to function and in vivo survival of human factor VIII/von Willebrand factor protein. , 1977, The Journal of biological chemistry.
[32] E. Jaffe,et al. Synthesis of von Willebrand factor by cultured human endothelial cells. , 1974, Proceedings of the National Academy of Sciences of the United States of America.
[33] J. Medalie,et al. Blood groups, myocardial infarction and angina pectoris among 10,000 adult males. , 1971, The New England journal of medicine.
[34] R. Scarpa,et al. A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred , 1970, British journal of haematology.
[35] A. Girolami,et al. Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. , 2002, Blood.
[36] J. Sixma,et al. The Half-life of Infused Factor VIII Is Shorter in Hemophiliac Patients with Blood Group 0 than in those with Blood Group A , 2000, Thrombosis and Haemostasis.
[37] P. Mannucci,et al. Von Willebrand Disease Type 2M “Vicenza” in Italian and German Patients: Identification of the First Candidate Mutation (G3864A; R1205H) in 8 Families , 2000, Thrombosis and Haemostasis.
[38] F. Yamamoto,et al. Molecular genetics of ABO. , 2000, Vox sanguinis.
[39] F. Cohen,et al. Biochemistry and genetics of von Willebrand factor. , 1998, Annual review of biochemistry.
[40] P. Magnus,et al. Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level. , 1985, American journal of human genetics.
[41] G. Ashwell,et al. Carbohydrate-specific receptors of the liver. , 1982, Annual review of biochemistry.
[42] Z. Ruggeri,et al. The complex multimeric composition of factor VIII/von Willebrand factor. , 1981, Blood.
[43] H. Gralnick,et al. Effect of multimeric structure of the factor VIII/von Willebrand factor protein on binding to platelets. , 1981, Blood.