共 6 条
[1]
Analysis of platelet glycoprotein Ⅰa(α2 integrin) allele frequencies in three north American populations reveal genetic association between nucleotide 807C T and amino acid 505 Glu Lys (HPA-5) dimorphisms. Reiner AP,Aramaki KM,Teramura G,et al. Thrombosis and Haemostasis . 1998
[2]
Low plateletα2β1 levels in type Ⅰvon Willebrand disease correlate with impaired platelet function in a high shear stress system. Paola JD,Federici AB,Mannucci PM,et al. Blood . 1999
[3]
Association of the platelet glycoprotein Ⅰa C807T gene polymorphism with nonfatal myocardial infarction in younger patients. Santoso S,Kunicki TJ,Kroll H,et al. Blood . 1999
[4]
Hereditary variation in platelet integrinα2β1 density is associated with two silent polymorphisms in theα2 gene coding sequence. Kunicki TJ,Kritzik M,Annis DS,et al. Blood . 1997
[5]
Nucleotide polymorphisms in theα2 gene define multiple alleles that are associated with differences in plateletα2β1 density. Kritzik M,Savage B,Nugent DJ,et al. Blood . 1998
[6]
Variability of integrinα2β1 activity on human platelets. Kunicki TJ,Orchekowski R,Annis DS,et al. Blood . 1993