Light Microscopy Techniques for Live Cell Imaging

By D. Stephens, V. Allan. Science, 2003

1,189 citations recorded by the source corpus.

Subfields: Biophysics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/557a57d3f7b8ff0962365ac697e2c1ef61d08a92

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Citations in the corpus

Fluorescent proteins and their applications in imaging living cells and tissues. (2010, background): “15), along with the tendency of living cells to autofluoresce in the violet part of the visible spectrum and general toxicity of violet and UV light (412), will likely limit applicability of Sirius in its present form.”
Tracking in cell and developmental biology. (2009, background): “Going beyond ensemble averages of motion parameters, measured by fluorescence recovery after (or loss in) photobleaching (FRAP or FLIP) experiments [5, 58], these offer the possibility to study dynamic processes at the highest possible level of detail (individual particles), and are often collective”
Toward fluorescence nanoscopy (2003, background): “Future research on its spectroscopy conditions and on practical aspect”
Live-cell photoactivated localization microscopy of nanoscale adhesion dynamics (2008, background): “Although these markers are targeted to specific proteins with molecular precision, most of this information is lost when conventional, diffraction-limited live-cell imaging method”
Advanced Level-Set-Based Cell Tracking in Time-Lapse Fluorescence Microscopy (2010, background): “Third, since cells are sensitive to photodamage, the (laser) light intensity needed to excite the fluorescent proteins is often reduced to a minimum, leading to very low SNRs [ 8 ], [20].”
Lattice Light Sheet Microscopy: Imaging Molecules to Embryos at High Spatiotemporal Resolution (2014, neutral): “Fortunately, the most common tools used for in vivomolecular and organelle-specific imaging, widefield and confocal fluorescence microscopy (1, 2), leave substantial room for improvement, because they each illuminate the entire thickness of the specimen, even though high-resolution information is ob”
Fluorescence molecular imaging. (2006, neutral): “φsc(r, rs , ω) = ∫ g(r, r ′, ω)O(r ′)φ(r ′, rs , ω)dr ′, (2)”
Hot‐spring Systems Geobiology: abiotic and biotic influences on travertine formation at Mammoth Hot Springs, Yellowstone National Park, USA (2011, background): “…being developed for optical, mineralogical, structural, chemical, hydrological and sedimentological analyses at, or below, the 1 lm average diameter of single microbial cells (Stephens & Allan, 2003; Sweedlow et al., 2003; Lipfert & Doniach, 2007; Garcia, 2008; Stock, 2008; U.S. DOE, 2008).”