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1 ly operates in a low resistance or impedance arterial system.
2 ile apparatus in SMCs located throughout the arterial system.
3 yonic development to govern formation of the arterial system.
4 factory studies clearly defining the hepatic arterial system.
5 ental insertion of venous catheters into the arterial system.
6 rpretations of the aorta and lower-extremity arterial system.
7 ic plaque located in the aorto-iliac-femoral arterial system.
8 tation by the vein to its insertion into the arterial system.
9 at may avoid embolization of debris from the arterial system.
10 diovascular, cerebrovascular, and peripheral arterial systems.
11 he small and large vessels of the venous and arterial systems.
12 circulation consisted of separate venous and arterial systems.
13 HSPG damage, autophagy and apoptosis in the arterial system, an ex vivo model of swirling flow was d
14 ion of the blood flow as spiral in the whole arterial system and is believed to improve the graft lon
15 line could be erroneously inserted into the arterial system and the radiologic findings can give the
17 ction for the brain stem and vertebrobasilar arterial system and was associated with high mortality f
18 ver, the size and caliber of the iliofemoral arterial system are influenced by patient size, sex, and
21 nvolve multiple organs, including the heart, arterial system, brain, skeletal muscle, adipose tissue,
26 nch points and flexures in the high pressure arterial system have long been recognized as sites of un
31 esis of atherosclerotic lesions in the human arterial system is critically influenced by the fluid me
33 tion, as well as after implantation into the arterial system, leading to the development of intimal h
34 gest that placement of a venous graft in the arterial system leads to expression of TN-C, which may i
35 nical applications include assessment of the arterial system, lung perfusion, neoplasm, bowel disease
36 th factor (VEGF) could be implanted into the arterial system of a pre-clinical ovine animal model, wh
38 of latex and black ink was injected into the arterial system of rodents, resulting in high contrast d
39 cation or extent of involvement of the renal arterial system precludes surgical revascularization.
40 ovel mechanism by which swirling flow in the arterial system protects arterial wall from atherogenesi
41 ng lineage-restricted gene expression in the arterial system, the bladder, and the embryonic lung.
42 ble to that seen in the straight part of the arterial system, the intracellular and junction tensions
45 cate that blood flows from the high-pressure arterial system to the lower-pressure venous system duri
47 whether transplanting islets into the gut's arterial system would more safely and as effectively sup