CARDIAC-MUSCLE DISEASES IN GENETICALLY-ENGINEERED MICE - EVOLUTION OF MOLECULAR PHYSIOLOGY
被引:27
作者:
CHIEN, KR
论文数: 0引用数: 0
h-index: 0
机构:
UNIV CALIF SAN DIEGO, AMER HEART ASSOC, BUGHER FDN, CTR MOLEC BIOL, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, AMER HEART ASSOC, BUGHER FDN, CTR MOLEC BIOL, LA JOLLA, CA 92093 USA
CHIEN, KR
[1
]
机构:
[1] UNIV CALIF SAN DIEGO, AMER HEART ASSOC, BUGHER FDN, CTR MOLEC BIOL, LA JOLLA, CA 92093 USA
来源:
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
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1995年
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269卷
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03期
Recent advances in molecular, cellular, and genetically based technologies now offer the possibility of generating genetically engineered mice that display physiological phenotypes with direct relevance to human pathophysiological states. The ability to create gene ablations, gene duplications, and gene modifications should allow the use of genetic approaches to map in vivo pathways responsible for complex physiological phenotypes. Recent work from our laboratory utilizing this approach to study cardiac muscle diseases in both the adult context (cardiac hypertrophy) and in the embryonic context (congenital ventricular defects) will be discussed, as well as the steps that led to the generation and characterization of these novel mouse model systems. A large body of work from independent laboratories now points to the inception of a new field of molecular physiology that will fuse mouse genetics and in vivo physiology using appropriate miniaturized physiological technology. Recent advances and prospects for future directions are summarized.