共 15 条
[1]
Isolation and characterization of two domain of human von Willebrand factor that interact with fibrillar collegen type Ⅰand Ⅲ. Pareti FI,Niiya K,Mcpherson JM,et al. Journal of Biological Chemistry . 1987
[2]
Commentary: A new classification for von Willebrand disease. Sadler JE,Gralnick HR. Blood . 1994
[3]
On behalf of the RCPA Quality Assurance Program ( QAP ) in Haematology Haemostasis Scientific Advisory Panel.Laboratory testing for von Willebrand′s disease: An assessment of current diagnostic practice And efficacy by means of a multi-laboratory survey. Favaloro EJ,Smith J,Petinos P,et al. Thrombosis and Haemostasis . 1999
[4]
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Furlan M,Roble R,Solenthaler M,et al. Blood . 1997
[5]
A methA for assaying von Willebrand′s factor (ristocetin cofactor). MacFarlane DE,Stibbe J,Kirby EP,et al. Thrombosis et Diathesis Haemorrhagica . 1975
[6]
Isolation of the von Willebrand factor domain interaction with platelet glycoprotein Ⅰb,heparin, and collagen, and characterization of its three distinct functional sites. Mohri H,Yoshioka A,Zimmerman TS,et al. Journal of Biological Chemistry . 1989
[7]
Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments prAuced by in vivo proteolysis. Furlan M,Roble R,Lammle B. Blood . 1996
[8]
von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co-factor activity. Casonato A,Pontara E,Bertomoro A,et al. British Journal of Haematology . 2001
[9]
LaboratoryassessmentofvonWillebrandfactor:alteredinterpretationoflaboratorydata.AndaltereddiagnosisofvonWillebrand′sdisease.AsinfluencedbytheuseofdifferentVwfassayandassaycondition. FavaloroEJ,MehrabaniPA,KouttsJ. ClinApplThrombHaemost . 1997
[10]
von Willebrand factor bind to native collagen Ⅵprimarily via its A1domain. Hoylaerts MF,Yamamoto H,Nuyts K,et al. Biochemical Journal . 1997