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Relationship of von Willebrand factor gene single-nucleotide polymorphism with thrombosis diseases / 中国实验血液学杂志
Article en Zh | WPRIM | ID: wpr-243315
Biblioteca responsable: WPRO
ABSTRACT
Recently it has been discovered that not only von Willebrand factor (vWF) decrease results in von Willebrand disease, but also vWF increase can lead to several thrombosis diseases. Plasma vWF level is affected by genetic factors. Individuals with different single nucleotide polymorphism (SNP) genotype in vWF have different susceptibility to disease; individuals with different blood group have different plasma vWF level. Environment factors also affect plasma vWF level. Understanding relationship of polymorphisms in promoter, exon and intron with thrombosis diseases contribute to prevent and cure these diseases. In this review, the relationship of SNP in promoter, exon and intron of vWF gene with thrombosis diseases is summarized.
Asunto(s)
Texto completo: 1 Índice: WPRIM Asunto principal: Trombosis / Factor de von Willebrand / Intrones / Exones / Regiones Promotoras Genéticas / Polimorfismo de Nucleótido Simple / Genética / Genotipo Límite: Humans Idioma: Zh Revista: Journal of Experimental Hematology Año: 2010 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Trombosis / Factor de von Willebrand / Intrones / Exones / Regiones Promotoras Genéticas / Polimorfismo de Nucleótido Simple / Genética / Genotipo Límite: Humans Idioma: Zh Revista: Journal of Experimental Hematology Año: 2010 Tipo del documento: Article