Regular ArticleChanges in Magnesium Content and Subcellular Distribution during Retinoic Acid-Induced Differentiation of HL60 Cells☆
References (38)
- et al.
J. Nutr.
(1977) - et al.
Arch. Biochem. Biophys.
(1996) - et al.
Ultramicroscopy
(1976) Blood
(1987)- et al.
Blood
(1981) - et al.
J. Biol. Chem.
(1992) - et al.
J. Biol. Chem.
(1987) - et al.
Arch. Biochem. Biophys.
(1994) - et al.
Biomed. Pharmacother.
(1991) - et al.
Arch. Bioch. Biophys.
(1992)
J. Theor. Biol.
FEBS Lett.
Mg
Metal Ions Biol.
Mg: Its Biological Significance
Proc. Acad. Natl. Acad. Sci. USA
J. Cell. Physiol.
Proc. Natl. Acad. Sci. USA
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2016, Biosensors and BioelectronicsCitation Excerpt :Therefore, it is urgent to develop efficient analytical methods for detecting and monitoring Mg2+ at the level of cells and tissues in animals and plants. Over the last few decades, many conventional analytical techniques have been reported for detecting Mg2+, which include atomic absorbance, Mg2+-selective electrodes, null-point titration techniques and NMR (Di Francesco et al., 1998; Rink et al., 1982; Stewart et al., 2016; Flatman and Lew, 1977; Parlak and Turner, 2016). These methods require troublesome sample pretreatment, reagent preparation, time-consuming, and complicated instruments.
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2008, Annals of Vascular SurgeryCitation Excerpt :On the other hand, we found that the intracellular content of magnesium increased from the second to the third passage in cultured ECs. According to previous work by Buja et al.26 and Di Francesco et al.,49 one possible explanation for this ionic increase could be a variation in the intracellular concentration of adenosine triphosphate (ATP). In addition, in this work we found a marginally significant increase of intracellular concentration of phosphorus in the third EC subculture.
Chapter 2 Electron Probe X-ray Microanalysis for the Study of Cell Physiology
2008, Methods in Cell BiologyCitation Excerpt :Thin frozen sections are not analyzed in the TEM in their fully hydrated form since, at the probe currents that are required to elicit X-ray formation, interaction of incident electrons with ice in the specimens leads to the generation of free radicals that destroy the specimen (Zierold, 1988). Instead they are either transferred to a proprietary cryoworkstation to allow placement in a cryoholder and transfer to the EM column where they are freeze-dried by raising the temperature of the holder to −110 °C for a period of 20–30 min (Scott et al., 1997), or freeze-dried externally using either a carbon coating unit (Di Francesco et al., 1998; LeFurgey et al., 2001) or a specially designed freeze-drier with temperature controlled stage (Warley and Skepper, 2000). The grids are transferred to the freeze-drying apparatus in a covered cryotransfer device under liquid nitrogen.
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Aikawa, J. K.
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To whom correspondence should be addressed at Department of Molecular Cardiology, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH 44195. Fax: (216) 445-6062. E-mail:[email protected].