@article{2dbb7aa2baa74388927bd971fe347d7b,
title = "Synthesis and evaluation of MR probes for targeted-reporter imaging",
abstract = "Visualizing disease heterogeneity remains a challenging task since most imaging agents are targeted to a single receptor. We describe the development of an MR platform able to report on multiple molecular events. Enzyme activation and enhanced cellular uptake of this modular probe make it suitable for subsequent targeted-reporter imaging applications.",
author = "Verma, {Kirti Dhingra} and Massing, {Justin O.} and Kamper, {Sarah G.} and Carney, {Christiane E.} and Macrenaris, {Keith W.} and Basilion, {James P.} and Meade, {Thomas J.}",
note = "Funding Information: This work was supported by the NIH (R01EB005866 and P01HL108795), a CBC Postdoctoral Award (J.O.M.), NSF GRFP and a Biophysics Training Grant (T32GM008382) from the NIGMS (S. G. K.), and NFCR (J. P. B.). Imaging was performed at the Center for Advanced Molecular Imaging (NU) generously supported by NCI CCSG P30 CA060553 awarded to the Robert H. Lurie Comprehensive Cancer Center. ICP-MS was performed at the Quantitative Bioelemental Imaging Center (NU) generously supported by the NASA Ames Research Center NNA06CB93G. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2017.",
year = "2017",
doi = "10.1039/c7sc02217d",
language = "English (US)",
volume = "8",
pages = "5764--5768",
journal = "Chemical Science",
issn = "2041-6520",
publisher = "Royal Society of Chemistry",
number = "8",
}