In vivo magnetic resonance imaging detection of early endothelial activation in mouse atherosclerosis using dual-targeted microparticles of iron oxide

In vivo magnetic resonance imaging detection of early endothelial activation in mouse atherosclerosis using dual-targeted microparticles of iron oxide

Bibliografiska uppgifter
Huvudupphovsmän:	McAteer, M, Mankia, K, Hagen, R, Stork, L, Schneider, J, Choudhury, R
Materialtyp:	Conference item
Publicerad:	2010

Liknande verk

Magnetic resonance imaging of endothelial adhesion molecules in mouse atherosclerosis using dual-targeted microparticles of iron oxide.
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Targeted magnetic resonance imaging of TNF-alpha induced endothelial VCAM-1 expression in vitro using monoclonal antibody conjugated microparticles of iron oxide
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Magnetic resonance imaging of brain inflammation using microparticles of iron oxide.
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An approach to molecular imaging of atherosclerosis, thrombosis, and vascular inflammation using microparticles of iron oxide.
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Magnetic Resonance Imaging Of Renal Ischemia Reperfusion Injury Using Microparticles Of Iron Oxide Targeting VCAM-1
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A leukocyte-mimetic magnetic resonance imaging contrast agent homes rapidly to activated endothelium and tracks with atherosclerotic lesion macrophage content.
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Molecular magnetic resonance imaging of angiogenesis in vivo using polyvalent cyclic RGD-iron oxide microparticle conjugates.
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Plaque remodeling in mouse atherosclerosis identified by high resolution in vivo magnetic resonance imaging (MRM).
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In vivo quantification of VCAM-1 expression in renal ischemia reperfusion injury using non-invasive magnetic resonance molecular imaging.
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EXOGENOUS MICROPARTICLES OF IRON OXIDE BIND TO ACTIVATED ENDOTHELIAL CELLS BUT, UNLIKE MONOCYTES, DO NOT TRIGGER AN ENDOTHELIAL RESPONSE
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Exogenous microparticles of iron oxide bind to activated endothelial cells but, unlike monocytes, do not trigger an endothelial response.
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Molecular imaging with optical coherence tomography using ligand-conjugated microparticles that detect activated endothelial cells: rational design through target quantification.
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Molecular imaging with optical coherence tomography using ligand-conjugated microparticles that detect activated endothelial cells: Rational design through target quantification
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Binding Characteristics of Microparticles Targeted to E-Selectin versus VCAM-1 Under Conditions of Shear Stress: Implications for the Rational Design of Targeted Imaging Agents
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VCAM-1-targeted magnetic resonance imaging reveals subclinical disease in a mouse model of multiple sclerosis.
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Magnetic resonance imaging of coronary atherosclerosis.
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Dual-modal photoacoustic and magnetic resonance tracking of tendon stem cells with PLGA/iron oxide microparticles in vitro.
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Atherosclerosis and thrombosis: identification of targets for magnetic resonance imaging.
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Quantification and 3D reconstruction of atherosclerotic plaque components in apolipoprotein E knockout mice using ex vivo high-resolution MRI.
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ANTI-IL17 TREATMENT REDUCES CLINICAL SCORE AND VCAM-1 EXPRESSION IN EAE-ABH MICE DETECTED BY IN VIVO MAGNETIC RESONANCE IMAGING
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Tetrahydrobiopterin deficiency increases susceptibility to atherosclerosis
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Molecular magnetic resonance imaging of acute vascular cell adhesion molecule-1 expression in a mouse model of cerebral ischemia.
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Targeted molecular imaging of vascular inflammation in cardiovascular disease using nano- and micro-sized agents
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