Volume 279, July 2000 Volume 48, July 2000

Pages H429-H436: Y.-Y. Zhou, S.-Q. Wang, W.-Z. Zhu, A. Chruscinski, B. K. Kobilka, B. Ziman, S. Wang, E. G. Lakatta, H. Cheng, and R.-P. Xiao. "Culture and adenoviral infection of adult mouse cardiac myocytes: methods for cellular genetic physiology." On page H433, Fig. 4A should have been printed in a color version. It should appear as shown below.

View larger version (24K): [in this window] [in a new window]   Fig. 4.   Ca2+ transients and cell contraction in cardiomyocytes cultured for 1 day. A: space-time plot of the fluo 3 fluorescence signal (top) and the spatially averaged Ca2+ transients as indexed by one- to fivefold increases in fluorescence signal (F/F0, middle) and change in cell length (bottom). [Ca2+]i, intracellular Ca2+ concentration. B: peak amplitude of Ca2+ transients (F/F0) and half-relaxation time (Ca50) in freshly isolated (day 0, n = 6) and 1-day cultured myocytes (day 1, n = 22). **P < 0.01 vs. day 0. C: peak amplitude of cell contraction and half-relaxation time of contraction (TA50) in freshly isolated (day 0, n = 16) and 1-day cultured myocytes (day 1, n = 31). *P < 0.05 vs. day 0.