摘要
Hypertrophic cardiomyopathy is an autosomal-dominant disease.Disease-causing mutations have been found in genes encoding structural components of the thick and thin filament systems of cardiac myocyte;it has therefore been named as a disease of sarcomere.Many approaches have been used to characterize the pathogenesis of the desease.Transgenic animal models have been created to gain further insight into the pathogenesis of this disease.Most of these models has been made in mice;however,recently a transgenic rabbit model has been created.In addition,there are several natural-occurring forms of HCM in animals.The discovery of responsible genes and the elucidation of the molecular mechanisms of pathogenesis through the use of animal models promise improved and early diagnosis and the potential for mechanism-based therapeutics.
SUMMARY Hypertrophic have been found in genes e cardiomyopathy is an autosomal-dominant disease. Disease-causing mutations ncoding structural components of the thick and thin filament systems of cardiac myoeyte ; it has therefore been named as a disease of sareomere. Many approaches have been used to characterize the pathogenesis of the desease. Transgenic animal models have been created to gain further insight into the pathogenesis of this disease. Most of these models has been made in mice ; however, recently a transgenic rabbit model has been created. In addition,there are several natural-occurring forms of HCM in animals. The discovery of responsible genes and the elucidation of the molecular mechanisms of pathogenesis through the use of animal models promise improved and early diagnosis and the potential for mechanism-based therapeutics.
出处
《北京大学学报(医学版)》
CAS
CSCD
北大核心
2007年第6期666-669,共4页
Journal of Peking University:Health Sciences
基金
国家自然科学基金(30540038)资助~~
关键词
心肌病
肥厚性
动物
基因修饰
突变
Cardiomyopathy, hypertrophic
Animals, genetically modified
Mutation