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• W2556784225 endingPage "346" @default.
• W2556784225 startingPage "323" @default.
• W2556784225 abstract "Cells are highly dynamic biological systems that are comprised of a vast number of molecular processes that interact both spatially and temporally. For mesenchymal stromal cell (MSC) cultures, which are heterogeneous and may only contain a small population of stem cells, single cell analyses are even more critical. Live cell imaging is a multidisciplinary area of research that has evolved through input from engineers, physicists, chemists, biologists, computer scientists, and mathematicians. Image acquisition parameters must be defined for each live cell imaging experiment. Image restoration and enhancement methods are required to improve the accuracy of cellular tracking and fluorescent quantification. Live cell imaging experiments, particularly long-term imaging experiments, have the potential to generate a large volume of image data. Time-lapse imaging experiments generate image stacks for individual field of views (FOV) over a period of hours, days, or weeks." @default.
• W2556784225 created "2016-11-30" @default.
• W2556784225 creator A5018044486 @default.
• W2556784225 creator A5048628682 @default.
• W2556784225 creator A5061874736 @default.
• W2556784225 creator A5080807147 @default.
• W2556784225 date "2016-11-26" @default.
• W2556784225 modified "2023-10-14" @default.
• W2556784225 title "Live cell imaging and single cell tracking of mesenchymal stromal cellsin vitro" @default.
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