By Richard A. Walsh M.D. (auth.), Brian D. Hoit, Richard A. Walsh (eds.)
The huge, immense advances in molecular biology and genetics coupled with the growth in instrumentation and surgical ideas have produced a voluminous and sometimes bewildering volume of knowledge. the necessity for a moment variation of Cardiovascular body structure within the Genetically Engineered Mouse is underscored not just by means of those swift advances, yet by way of the expanding numbers of scientists who've focussed their learn on genetically engineered mice. it's the fundamental goal of this moment version to interpret significantly the literature and to supply a framework for the large volume of data during this burgeoning box. As within the first version, the monograph serves as a pragmatic consultant for the investigator attracted to the sensible equipment used to symbolize the murine cardiovascular phenotype. notwithstanding, this guidebook is a extra entire textual content than its predecessor; even if the main pursuits enumerated within the first version haven't considerably replaced, they've been subtle based on the elevated sophistication of the molecular biologist, geneticist, and physiologist in each one other's self-discipline. every one bankruptcy has been accelerated and up-to-date, richly stronger with unique tables and figures, and in lots of instances, broadly rewritten. 8 chapters written by way of the world over famous specialists were further; this represents a forty three % bring up from the 1st edition.
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Additional resources for Cardiovascular Physiology in the Genetically Engineered Mouse
11. Chien KR. Genes and physiology: molecular physiology in genetically engineered animals. J Clin Invest. 1996;97:901-9. Christensen G, Wang Y, Chien KR. Physiological assessment of complex cardiac phenotypes in genetically engineered mice. Am J Physiol. 1997;272:H2513-24. 13. Kadambi VJ, Ponniah S, Harrer JM, Hoit BD, Dorn GW, 2nd, Walsh RA, Kranias EG. Cardiac-specific overexpression of phospholamban alters calcium kinetics and resultant cardiomyocyte mechanics in transgenic mice. J Clin Invest.
3) Implantation of injected eggs: DNA that is microinjected into eggs is incorporated into the genome in a random location within the chromosomal DNA (usually on autosomes - only occasionally on X- or Y-chromosomes). Typically, more than one copy (1 to 200) is incorporated at a single random site (usually as a tandem, head-to-tail-orientation) in the mouse genome. The eggs are transferred either immediately after microinjection to the oviduct of day 1 pseudopregnant female mice (recipients), or cultured overnight to the two-cell stage and then transferred.
1998;249:786-90. Cross HR, Lu L, Steenbergen C, Philipson KD, Murphy E. Overexpression of the cardiac Na+/Ca2+ exchanger increases susceptibility to ischemiaireperfusion injury in male, but not female, transgenic mice. eire Res. 1998;83:1215-23. 3 CONDITIONAL TRANS GENESIS Tetsuo Minamino, MD, PhD and Michael D. Schneider, MD Center for Cardiovascular Development Baylor College of Medicine Houston, TX INTRODUCTION Gain- and loss-of-function mutations allow a direct assessment of gene function in vivo and the creation of useful animal models of human disease.