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Lawrence Lifshitz, Ph.D.
Academic Role: Associate Professor
Faculty Appointment(s) In:
Program in Molecular Medicine
Other Affiliation(s):
Program in Neuroscience
Computer Vision and Image Processing
Research in this lab involves developing and appying new computer vision algorithms to aid in the identification and quantification of structures of interest in medical images of various types. The research is directed towards solving certain "driving problems" of interest to medical researchers and physicians at UMW.
Some driving problems to date have been: the automatic identification and tracking of microtubules in a time series of microscopic images of moving cells; the determination of cell membrane location in 3D fluorescently labelled fixed cells (to aid in quantification); the alignment of nuclear medicine and CT images to aid in the interpretation of nuclear medicine images; and the visualization and quantification of atherosclerosis in blood vessels.
For more information, see my lab page .
Figure

This figure shows a computer generated deformable surface which
has deformed to match the true position of the cell membrane of a 3D
image of a florescently labelled cell. Several slices from the 3D data
set are also shown. The interactive visualization software and the
deformable model software were developed by Dr. Lifshitz (in
collaboration with others).
Recent Publications
ZhuGe, R., K.E. Fogarty, R.A. Tuft, L.M. Lifshitz, K. Sayer, and J.V. Walsh, Jr. Dynamics of Signaling between Ca2+ Sparks and Ca2+ activated K+ Channels Studied with a Novel Image-based Method for Direct Intracellular Measurement of Ryanodine receptor Ca2+ Current. J. Gen. Physiol., 116:845-864, 2000.
Kirber, M.T., E.F. Etter, K.A. Bellvé, L.M. Lifshitz, R.A. Tuft, F.S. Fay, J.V. Walsh, Jr., and K.E. Fogarty. The Relationship of Ca2+ Sparks to STOCs Studied with 2D and 3D Imaging in Feline Oesophageal Smooth Muscle Cells. J. Physiol., 531(2):315-327, 2001.
Patki, V., J. Buxton, A. Chawla, L. Lifshitz, K. Fogarty, W. Carrington, R. Tuft, and S. Corvera. Insulin action on GLUT4 traffic visualized in single 3T3-L1 adipocytes using ultra-fast microscopy. Molec. Biol. Cell, 12(1):129-141, 2001.
Stachelek, S., R. Tuft, L. Lifshitz, D. Leonard, A. Farwell, J. Leonard. Real-time Visualization of Processive, Myosin 5a mediated Vesicle Movement in Living Astrocytes. J. Biol. Chem., 276(38):35652-35659, 2001.
Miyazaki, K., Yano, T., Schmidt, D.J., Tokui, T., Shibata, M., Lifshitz, L.M., Kimura, S., Tuft, R.A., and Ikebe, M. Rho dependent agonist induced spatio-temporal change in myosin phosphorylation in smooth muscle cells. J. Biol. Chem., 277(1) :725-734, 2002.
Zou, H., Lifshitz, L.M., Tuft, R.A., Fogarty, K.E., and Singer, J.J. Visualization of Ca2+ entry through single stretch-activated cation channels. Proc. Natl. Acad. Sci. U.S.A., 99(9) :6404-6409, 2002.
Lawe, D., A. Chawla, E. Merithew, J. Dumas, W. Carrington, K. Fogarty, L. Lifshitz, R. Tuft, D.Lambright, and S. Corvera. Sequential roles for phosphatidylinositol 3-phosphate and Rab5 in tethering and fusion of early endosomes via their interaction with EEA1. J. Biol. Chem., 277(10) :8611-8617, 2002.
Lawe, D.C., Sitouah, N., Hayes, S., Chawla, A., Virbasius, J.V., Tuft, R., Fogarty, K., Lifshitz, L., Lambright, D., and Corvera, S. Essential role of Ca2+/calmodulin in Early Endosome Antigen-1 localization. Mol. Biol. Cell, 14(7):2935-45, 2003.
Femino, A.M., Fogarty, K., Lifshitz, L.M., Carrington, W., and Singer, R.H. Visualization of single molecules of mRNA in situ. Methods Enzymol., 361:245-304, 2003.
Zou, H., Lifshitz, L.M., Tuft, R.A., Fogarty, K.E., and Singer, J.J. Using total fluorescence increase (signal mass) to determine the Ca2+ current underlying localized Ca2+ events. J. Gen. Physiol., 124 :259-272, 2004.
Huang, S., Lifshitz, L., Patki-Kamath, V., Tuft, R., Fogarty, K., and Czech, M.P. Phosphatidylinositol-4,5-bisphosphate-rich plasma membrane patches organize active zones of endocytosis and ruffling in cultured adipocytes. Mol. Cell. Biol., 24(20) :9102-23, 2004.
ZhuGe, R., Fogarty, K.E., Baker, S.P., McCarron, J.G., Tuft, R.A., Lifshitz, L.M., and Walsh, Jr., J.V. Ca2+ spark sites in smooth muscle cells are numerous and differ in number of ryanodine recepors, BK channels and coupling ratio between them. Am. J. Physiol., Cell Physiol., 287(6) :C1577-88, 2004.
DeCrescenzo, V., ZhuGe, R., Velazquez-Marrero, C., Lifshitz, L.M., Custer, E., Carmichael, J., Lai, F.A., Tuft, R.A., Fogarty, K.E., Lemos, J.R., Walsh, Jr., J.V. Ca2+ syntillas, miniature Ca2+ release events in terminals of hypothalamic neurons, are increased in frequency by depolarization in the absence of Ca2+ influx. J. Neurosci. 24(5) :1226-35, 2004.
Academic Background
1980, B.A., Harvard University
1983, M.S., University of North Carolina
1987, Ph.D., University of North Carolina
My Personal Home Page
The Biomedical Imaging Group Home Page
Office: Biotech 2 Suite 114
Phone: 508 856 3392
E-mail: Lawrence.Lifshitz@umassmed.edu
Keywords:
Biophysics,
Intracellular Trafficking,
Cell Dynamics,
Bioinformatics,
Imaging and Microscopy
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