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James P. Freyer

Researcher at Los Alamos National Laboratory

Publications -  85
Citations -  6822

James P. Freyer is an academic researcher from Los Alamos National Laboratory. The author has contributed to research in topics: Light scattering & Scattering. The author has an hindex of 40, co-authored 85 publications receiving 6569 citations. Previous affiliations of James P. Freyer include University of Rochester & Laval University.

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The use of 3-D cultures for high-throughput screening: the multicellular spheroid model.

TL;DR: 3-D in vitro systems for drug development, with a focus on screening for novel antitumor drugs, are addressed, and the advantages and limitations of these systems of intermediate complexity are discussed.
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Mechanisms of light scattering from biological cells relevant to noninvasive optical-tissue diagnostics

TL;DR: Optical diagnostics are expected to be sensitive to organelle morphology but not directly to the size and shape of the cells, as measured of isolated organelles indicate.
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A Multiscale Model for Avascular Tumor Growth

TL;DR: A new mathematical model for avascular tumor growth and development that spans three distinct scales is presented and predicts the microenvironmental conditions required for tumor cell survival and accurately predicts spheroid growth curves under different external nutrient supply conditions.
Journal Article

Regulation of Growth Saturation and Development of Necrosis in EMT6/Ro Multicellular Spheroids by the Glucose and Oxygen Supply

TL;DR: A model is presented to explain the observed spheroid growth characteristics by proposing a competition between externally supplied growth and viability-promoting factors and internally generated inhibitory factors produced by the process of necrosis, which has critical implications for the use of spheroids as models of cellular growth in tumors.
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Raman Spectroscopy Detects Biochemical Changes Due to Proliferation in Mammalian Cell Cultures

TL;DR: Raman spectra of cells and nuclei from cultures in the plateau (nonproliferating) and exponential phases of growth were measured and show that Raman spectroscopy can monitor changes due to cell proliferation, which will be important for Raman detection of rapidly dividing populations of cancer cells in vivo.