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1 e right and left ventricles was performed on Langendorff perfused hearts.
2 bolished atrial T-wave alternans in isolated Langendorff perfused hearts.
3 d in vivo by echocardiography and in ex vivo Langendorff perfused hearts.
4 e evaluated by echocardiography, ECG, and in Langendorff-perfused hearts.
5 electric measurements and optical mapping in Langendorff-perfused hearts.
6 tly using mitochondria rapidly isolated from Langendorff-perfused hearts.
7 y internalized in cardiomyocyte cultures and Langendorff-perfused hearts.
8 cardiac myofibrillar proteins was studied in Langendorff-perfused hearts.
9 tile function in isolated cardiomyocytes and Langendorff-perfused hearts.
10 echocardiography, histology, and ECG and in Langendorff-perfused hearts.
11 al activity from the entire outer surface of Langendorff-perfused hearts.
12 s rhythm was similar to patterns recorded in Langendorff-perfused hearts.
13 the EGSH in isolated cardiac myocytes and in Langendorff-perfused hearts.
14 pped using voltage-sensitive dye in isolated Langendorff-perfused hearts along with single glass-micr
16 ance and calcium transients were measured in Langendorff-perfused hearts and isolated cardiac myocyte
19 l matrix of isolated cardiac myocytes and in Langendorff-perfused hearts based on the use of the redo
21 development and pressure decline in isolated Langendorff-perfused hearts compared with saline-treated
22 Dual voltage- and Ca(2+)-optical mapping of Langendorff-perfused hearts demonstrated that empagliflo
23 ed in situ myocyte Ca(2+) dynamics in intact Langendorff-perfused hearts (ex vivo) from wild-type and
26 ucose uptake using isometrically contracting Langendorff-perfused hearts from normal mice (C57BL/6J),
29 a-reperfusion, but not by ischemia alone, of Langendorff-perfused hearts from wild-type and p53 knock
30 Compared with control hearts, transgenic Langendorff-perfused hearts had a significantly lower in
32 schemia-reperfusion injury was determined in Langendorff-perfused hearts isolated from wild-type mice
33 technique in establishing single-cell SL in Langendorff-perfused hearts loaded with the membrane dye
34 rom the screen were subsequently tested in a Langendorff-perfused heart model of IR injury, revealing
35 simultaneously from 128 ventricular sites in Langendorff-perfused hearts (n = 15) in which propagatio
45 on in vivo and epicardial voltage mapping in Langendorff-perfused hearts, we demonstrated that focal