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Allelic distribution of the glycoprotein Ia (alpha2-integrin) C807T/G873A dimorphisms among caucasian venous thrombosis patients and six racial groups.

作者信息

Dinauer D M, Friedman K D, Hessner M J

机构信息

The Diagnostic Laboratories, The Blood Center, Milwaukee, Wisconsin, USA.

出版信息

Br J Haematol. 1999 Dec;107(3):563-5. doi: 10.1046/j.1365-2141.1999.01753.x.

DOI:10.1046/j.1365-2141.1999.01753.x
PMID:10583259
Abstract

Two linked silent dimorphisms, 807 C --> T (Phe224) and 873 G --> A (Thr246) within the glycoprotein Ia (GPIa) gene have been correlated with low and high platelet receptor density, respectively, and associated with vascular disease. A multiplexed allele-specific PCR assay was used to determine the GPIa 807T/873A allele frequency among 331 Caucasian venous thrombosis patients and 3571 unrelated individuals belonging to six different racial groups. The 807T/873A allele frequencies were 54%, 51%, 39%, 39%, 38%, 34% and 30% among Native Americans, Hispanics, Caucasians, Caucasian venous thrombosis patients, Asian Indians, African-Americans, and Koreans, respectively. Significant differences in the GPIa allele frequency among racial groups were revealed which emphasized the need for appropriate controls in studies evaluating the association of GPIa genotype to vascular disease.

摘要

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Genetic regulation of platelet receptor expression and function: application in clinical practice and drug development.血小板受体表达和功能的遗传调控:在临床实践和药物开发中的应用。
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Enzymes that hydrolyze adenine nucleotides in platelets and polymorphisms in the alpha2 gene of integrin alpha2beta1 in patients with von Willebrand disease.
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Thrombophilia, polymorphisms, and vascular disease.血栓形成倾向、基因多态性与血管疾病。
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