The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Cellular magnesium homeostasis
Open accessAbstract
Magnesium, the second most abundant cellular cation after potassium, is essential to regulate numerous cellular functions and enzymes, including ion channels, metabolic cycles, and signaling pathways, as attested by more than 1000 entries in the literature. Despite significant recent progress, however, our understanding of how cells regulate Mg2+ homeostasis and transport still remains incomplete. For example, the occurrence of major fluxes of Mg2+ in either direction across the plasma membrane of mammalian cells following metabolic or hormonal stimuli has been extensively documented. Yet, the mechanisms ultimately responsible for magnesium extrusion across the cell membrane have not been cloned. Even less is known about the regulation in cellular organelles. The present review is aimed at providing the reader with a comprehensive and up-to-date understanding of the mechanisms enacted by eukaryotic cells to regulate cellular Mg2+ homeostasis and how these mechanisms are altered under specific pathological conditions.
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Cunningham, D., Humblet, Y., Siena, S., Khayat, D., Bleiberg, H., Santoro, A., Bets, D., Mueser, M., Harstrick, A., Verslype, C., et al. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa033025 · Cited by 5,035
Role of calcium ions in regulation of mammalian intramitochondrial metabolism
McCormack, J. G., Halestrap, A. P., & Denton, R. M. (1990) · Physiological Reviews · doi:10.1152/physrev.1990.70.2.391 · Cited by 1,398
Magnesium metabolism in type 2 diabetes mellitus, metabolic syndrome and insulin resistance
Barbagallo, M., & Dominguez, L. J. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2006.05.007 · Cited by 379
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)
Rainier, S., Chai, J.-H., Tokarz, D., Nicholls, R. D., & Fink, J. K. (2003) · The American Journal of Human Genetics · doi:10.1086/378817 · Cited by 207
Smith, R. L., Thompson, L. J., & Maguire, M. E. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.5.1233-1238.1995 · Cited by 127
Mechanisms of MAdCAM-1 gene expression in human intestinal microvascular endothelial cells
Ogawa, H., Binion, D. G., Heidemann, J., Theriot, M., Fisher, P. J., Johnson, N. A., Otterson, M. F., & Rafiee, P. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00406.2003 · Cited by 68
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Metadata
- Authors
- Romani, A. M. P.
- Venue
- Archives of Biochemistry and Biophysics
- Publisher
- Elsevier BV
- Published
- 2011-08
- Volume
- 512
- Issue
- 1
- Pages
- 1-23
- ISSN
- 0003-9861 (ISSN-L)
- OpenAlex
- W2021088564
- Cited by
- 531
- References
- 6
- FWCI
- 15.19
- Type
- journal article
- Language
- en
- Open access
- green
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