Physical characterization of hematopoietic stem cells using multidirectional label-free light scatterings
Optics Express, ISSN: 1094-4087, Vol: 24, Issue: 25, Page: 28877-28888
2016
- 23Citations
- 13Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations23
- Citation Indexes23
- 23
- CrossRef17
- Captures13
- Readers13
- 13
Article Description
An experimental setup capable of measuring simultaneous 2D scattered light angular distribution from two directions to study cell morphology without the use of biolabels was developed. Experiments with hematopoietic stem cells (CD34 cells) show good agreement with detailed numerical simulations of light scattering. Numerical simulations and computer models of cells are used to identify physical features of cells with the largest scattering cross sections. This allows for determination of size, geometry of the nucleus and distribution of mitochondria in hematopoietic stem cells by means of our label-free method.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85006086337&origin=inward; http://dx.doi.org/10.1364/oe.24.028877; http://www.ncbi.nlm.nih.gov/pubmed/27958553; https://www.osapublishing.org/abstract.cfm?URI=oe-24-25-28877; https://www.osapublishing.org/viewmedia.cfm?URI=oe-24-25-28877&seq=0; https://opg.optica.org/abstract.cfm?URI=oe-24-25-28877; https://dx.doi.org/10.1364/oe.24.028877; https://opg.optica.org/oe/fulltext.cfm?uri=oe-24-25-28877&id=355809
The Optical Society
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