@article {252,
	title = {Ultrafast optical encoding of magnetic resonance},
	journal = {Chemical Physics Letters},
	volume = {503},
	year = {2011},
	note = {Chem Phys Lett719FWTimes Cited:0Cited References Count:19},
	month = {Feb 17},
	pages = {187-190},
	abstract = {<p>Temporal resolution in magnetic resonance imaging (MRI) is limited by the time required to encode the position of spins using time-varying (10-100 ms) magnetic field gradients. Here, we demonstrate spatial encoding of MRI images in a time that is three orders of magnitude shorter than what is possible by conventional gradient encoding techniques. Our method exploits the chemically induced dynamic nuclear polarization (CIDNP) effect and is an initial example of a set of approaches that seek to combine the favorable properties of optical spectroscopy with those of NMR for polarization, encoding, and detection. (C) 2010 Elsevier B.V. All rights reserved.</p>
},
	keywords = {state},
	isbn = {0009-2614},
	doi = {Doi 10.1016/J.Cplett.2010.12.063},
	url = {<Go to ISI>://WOS:000287187800001},
	author = {Trease, D. and Bajaj, V. S. and Paulsen, J. and Pines, A.}
}
@article {266,
	title = {Zooming In on Microscopic Flow by Remotely Detected MRI},
	journal = {Science},
	volume = {330},
	year = {2010},
	note = {Science682BUTimes Cited:12Cited References Count:27},
	month = {Nov 19},
	pages = {1078-1081},
	abstract = {<p>Magnetic resonance imaging (MRI) can elucidate the interior structure of an optically opaque object in unparalleled detail but is ultimately limited by the need to enclose the object within a detection coil; acquiring the image with increasingly smaller pixels reduces the sensitivity, because each pixel occupies a proportionately smaller fraction of the detector\&$\#$39;s volume. We developed a technique that overcomes this limitation by means of remotely detected MRI. Images of fluids flowing in channel assemblies are encoded into the phase and intensity of the constituent molecules\&$\#$39; nuclear magnetic resonance signals and then decoded by a volume-matched detector after the fluids flow out of the sample. In combination with compressive sampling, we thus obtain microscopic images of flow and velocity distributions similar to 10(6) times faster than is possible with conventional MRI on this hardware. Our results illustrate the facile integration of MRI with microfluidic assays and suggest generalizations to other systems involving microscopic flow.</p>
},
	keywords = {biosensor},
	isbn = {0036-8075},
	doi = {Doi 10.1126/Science.1192313},
	url = {<Go to ISI>://WOS:000284374700036},
	author = {Bajaj, V. S. and Paulsen, J. and Harel, E. and Pines, A.}
}
