James Rusling

Prof. James Rusling

Department of Chemistry, U-60 and Department of Surgery and Neag Cancer Center (Health Center) 55 N. Eagleville Rd., University of Connecticut, Storrs, CT 06269-3060, USA
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Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 January 2009 in ACS Nano
Verified
Journal Article
Closed access
ABAshwin A. Bhirde
Ashwin A. Bhirde
VPVyomesh Patel
Vyomesh Patel
JGJulie Gavard
Julie Gavard
GZGuofeng Zhang
Guofeng Zhang
ASAlioscka A. Sousa
Alioscka A. Sousa
James RuslingJames Rusling
James Rusling

1 August 2006 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
XYXin Yu
Xin Yu
BMBernard Munge
Bernard Munge
VPVyomesh Patel
Vyomesh Patel
GJGary Jensen
Gary Jensen
ABAshwin Bhirde
Ashwin Bhirde
James RuslingJames Rusling
James Rusling

8 July 2010 in The Analyst
Verified
Journal Article
Closed access
PDF file
James RuslingJames Rusling
James Rusling
Challa KumarChalla Kumar
Challa Kumar
JGJ.Silvio Gutkind
J.Silvio Gutkind
VPVyomesh Patel
Vyomesh Patel
This critical review evaluates progress toward viable point-of-care protein biomarker measurements for cancer detection and diagnostics. The ability to measure panels of specific, selective cancer biomarker proteins in physicians' surgeries and clinics has the potential to revolutionize cancer detection, monitoring, and therapy. The dream envisions reliable, cheap, automated, technically undemanding devices that can analyze a patient's serum or saliva in a clinical setting, allowing on-the-spot diagnosis. Existing commercial products for protein assays are reliable in laboratory settings, but have limitations for point-of-care applications. A number of ultrasensitive immunosensors and some arrays have been developed, many based on nanotechnology. Multilabel detection coupled with high capture molecule density in immunosensors and arrays seems to be capable of detecting a wide range of protein concentrations with sensitivity ranging into the sub pg mL−1 level. Multilabel arrays can be designed to detect both high and ultralow abundance proteins in the same sample. However, only a few of the newer ultrasensitive methods have been evaluated with real patient samples, which is key to establishing clinical sensitivity and selectivity.

13 February 2009 in ACS Nano
Verified
Journal Article
Closed access
VMVigneshwaran Mani
Vigneshwaran Mani
BCBhaskara V. Chikkaveeraiah
Bhaskara V. Chikkaveeraiah
VPVyomesh Patel
Vyomesh Patel
JGJ.Silvio Gutkind
J.Silvio Gutkind
James RuslingJames Rusling
James Rusling

21 September 2007 in Advanced Materials
Verified
Journal Article
Closed access
PDF file
SKS. N. Kim
S. N. Kim
James RuslingJames Rusling
James Rusling
FPF. Papadimitrakopoulos
F. Papadimitrakopoulos

1 March 2010 in Analytical Chemistry
Verified
Journal Article
Closed access
RMRuchika Malhotra
Ruchika Malhotra
VPVyomesh Patel
Vyomesh Patel
JVJosé Pedro Vaqué
José Pedro Vaqué
JGJ.Silvio Gutkind
J.Silvio Gutkind
James RuslingJames Rusling
James Rusling