|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0014279,
umls-concept:C0030306,
umls-concept:C0030685,
umls-concept:C0042449,
umls-concept:C0391871,
umls-concept:C0439851,
umls-concept:C0600210,
umls-concept:C0680255,
umls-concept:C1135918,
umls-concept:C1283071,
umls-concept:C1514485,
umls-concept:C1515655,
umls-concept:C1527362,
umls-concept:C1549649,
umls-concept:C1552596,
umls-concept:C1801960,
umls-concept:C1947931,
umls-concept:C1963578,
umls-concept:C2349209
|
|
pubmed:issue |
7
|
|
pubmed:dateCreated |
2002-7-16
|
|
pubmed:abstractText |
Saphenous vein bypass grafting for coronary revascularization procedures remains limited by accelerated neointima formation. It was hypothesized that creation of a modified chemotactic gradient in vivo could guide migration of smooth muscle cells (SMCs) peripherally instead of in a luminal direction and reduce intimal hyperplasia during vein graft arterialization.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
1051-0443
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
13
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
709-15
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:12119330-Analysis of Variance,
pubmed-meshheading:12119330-Angioplasty, Balloon,
pubmed-meshheading:12119330-Animals,
pubmed-meshheading:12119330-Cell Division,
pubmed-meshheading:12119330-Cell Movement,
pubmed-meshheading:12119330-Femoral Vein,
pubmed-meshheading:12119330-Male,
pubmed-meshheading:12119330-Microspheres,
pubmed-meshheading:12119330-Muscle, Smooth, Vascular,
pubmed-meshheading:12119330-Pancreatic Elastase,
pubmed-meshheading:12119330-Photomicrography,
pubmed-meshheading:12119330-Rabbits,
pubmed-meshheading:12119330-Time Factors,
pubmed-meshheading:12119330-Tunica Intima,
pubmed-meshheading:12119330-Vascular Surgical Procedures
|
|
pubmed:year |
2002
|
|
pubmed:articleTitle |
In vivo vascular engineering of vein grafts: directed migration of smooth muscle cells by perivascular release of elastase limits neointimal proliferation.
|
|
pubmed:affiliation |
Department of Cardiovascular and Interventional Radiology, Stanford University, 300 Pasteur Drive, H3648, Stanford, California 94305, USA.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
