Gene Therapy and Vascular Disease
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Publisher
Elsevier
Reference230 articles.
1. Suppression of neointimal smooth muscle cell accumulation in vivo by antisense cdc2 and cdk2 oligonucleotides in rat carotid artery;Abe;Biochem. Biophys. Res. Commun,1994
2. In vivo gene transfer into rat arterial walls with novel adeno-associated virus vectors;Arnold;J. Vasc. Surg,1997
3. Molecular and cellular cardiology: Local delivery of vascular endothelial growth factor accelerates reendothelialization and attenuates intimal hyperplasia in balloon-injured rat carotid artery;Asahara;Circulation,1995
4. Molecular and cellular cardiology/gene transfer: Accelerated restitution of endothelial integrity and endothelium-dependent function after ph VEGF sub 165 gene transfer;Asahara;Circulation,1996
5. Antisense oligonucleotides to the p65 subunit of NF-kB inhibit human vascular smooth muscle cell adherence and proliferation and prevent neointima formation in rat carotid arteries;Autieri;Biochem. Biophys. Res. Commun,1995
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1. 12S-Lipoxygenase is necessary for human vascular smooth muscle cell survival;Experimental Cell Research;2013-06
2. Gene therapy via inducible nitric oxide synthase: a tool for the treatment of a diverse range of pathological conditions;Journal of Pharmacy and Pharmacology;2008-08
3. Overexpression of mutated IκBα inhibits vascular smooth muscle cell proliferation and intimal hyperplasia formation;Journal of Vascular Surgery;2003-10
4. Inducible Nitric Oxide Synthase: From Cloning to Therapeutic Applications;World Journal of Surgery;2002-07-01
5. Endovascular Microcoil Gene Delivery Using Immobilized Anti-adenovirus Antibody for Vector Tethering;Stroke;2002-05
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