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1 yonic development to govern formation of the arterial system.
2 factory studies clearly defining the hepatic arterial system.
3 ental insertion of venous catheters into the arterial system.
4 rpretations of the aorta and lower-extremity arterial system.
5 ic plaque located in the aorto-iliac-femoral arterial system.
6 tation by the vein to its insertion into the arterial system.
7 ly operates in a low resistance or impedance arterial system.
8 ile apparatus in SMCs located throughout the arterial system.
9 diovascular, cerebrovascular, and peripheral arterial systems.
10 HSPG damage, autophagy and apoptosis in the arterial system, an ex vivo model of swirling flow was d
11 ion of the blood flow as spiral in the whole arterial system and is believed to improve the graft lon
12 line could be erroneously inserted into the arterial system and the radiologic findings can give the
19 nch points and flexures in the high pressure arterial system have long been recognized as sites of un
25 gest that placement of a venous graft in the arterial system leads to expression of TN-C, which may i
26 of latex and black ink was injected into the arterial system of rodents, resulting in high contrast d
27 cation or extent of involvement of the renal arterial system precludes surgical revascularization.
28 ovel mechanism by which swirling flow in the arterial system protects arterial wall from atherogenesi
29 ng lineage-restricted gene expression in the arterial system, the bladder, and the embryonic lung.
30 ble to that seen in the straight part of the arterial system, the intracellular and junction tensions
33 cate that blood flows from the high-pressure arterial system to the lower-pressure venous system duri
35 whether transplanting islets into the gut's arterial system would more safely and as effectively sup
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