Search Results - "Vishwasrao, H D"

Evidence against dopamine D1/D2 receptor heteromers by Frederick, A L, Yano, H, Trifilieff, P, Vishwasrao, H D, Biezonski, D, Mészáros, J, Urizar, E, Sibley, D R, Kellendonk, C, Sonntag, K C, Graham, D L, Colbran, R J, Stanwood, G D, Javitch, J A

“…Hetero-oligomers of G-protein-coupled receptors have become the subject of intense investigation, because their purported potential to manifest signaling and…”
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Uniform Polarity Microtubule Assemblies Imaged in Native Brain Tissue by Second-Harmonic Generation Microscopy by Dombeck, Daniel A., Kasischke, Karl A., Vishwasrao, Harshad D., Ingelsson, Martin, Hyman, Bradley T., Webb, Watt W.

“…Microtubule (MT) ensemble polarity is a diagnostic determinant of the structure and function of neuronal processes. Here, polarized MT structures are…”
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Neural Activity Triggers Neuronal Oxidative Metabolism Followed by Astrocytic Glycolysis by Kasischke, Karl A., Vishwasrao, Harshad D., Fisher, Patricia J., Zipfel, Warren R., Webb, Watt W.

“…We have found that two-photon fluorescence imaging of nicotinamide adenine dinucleotide (NADH) provides the sensitivity and spatial three-dimensional…”
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Conformational Dependence of Intracellular NADH on Metabolic State Revealed by Associated Fluorescence Anisotropy by Vishwasrao, Harshad D., Heikal, Ahmed A., Kasischke, Karl A., Webb, Watt W.

“…Global analysis of fluorescence and associated anisotropy decays of intrinsic tissue fluorescence offers a sensitive and non-invasive probe of the…”
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Blinking and Nonradiant Dark Fraction of Water-Soluble Quantum Dots in Aqueous Solution by Yao, Jie, Larson, Daniel R., Vishwasrao, Harshad D., Zipfel, Warren R., Webb, Watt W.

“…Water-soluble quantum dots (qdots) are now being used in life sciences research to take advantage of their bright, easily excited fluorescence and high…”
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Imaging enzyme activity with polarization‐sensitive confocal fluorescence microscopy by BIGELOW, CHAD E., VISHWASRAO, HARSHAD D., FRELINGER, JOHN G., FOSTER, THOMAS H.

“…Summary We describe a technique for imaging enzyme activity through steady‐state fluorescence anisotropy measurements on a per‐pixel basis with a confocal…”
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