Cedric Viero, Ph.D.
Affiliations: | 2013-2015 | Institute of Pharmacology and Toxicology | Saarland University, Saarbrücken, Saarland, Germany |
Area:
Calcium signalling, Intracellular ion channels, Cardiovascular research, NeuroendocrinologyWebsite:
http://www.uni-saarland.de/fachrichtung/pharmakologietoxikologie/cavalie/cavalie-mitarbeiter/dr-cedric-viero.htmlGoogle:
"Cedric Viero"Bio:
Born in France, Cedric Viero holds a PhD in Molecular Cell Biology from Saarland University, Germany. After a postdoctoral research position at the Wales Heart Research Institute (Cardiff, UK), he currently works as a Senior Research Associate at the Department of Experimental and Clinical Pharmacology and Toxicology, Saarland University Medical Faculty, Germany. His scientific interests focus on the structure-function relationship of ion channels and the role of calcium signalling in pathophysiological states. He currently serves as an Editorial Board Member of Journal of Cardiovascular Disease Research and The IIOAB Journal.
With a background in endocrinology and calcium imaging, Cedric Viero studies now the molecular physiology of intracellular calcium ion channels localised in the membranes of the sarcoplasmic and endoplasmic reticulum.
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Publications
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| Stanczyk PJ, Seidel M, White J, et al. (2018) Association of cardiac myosin binding protein-C with the ryanodine receptor channel: putative retrograde regulation? Journal of Cell Science |
| Stanczyk P, Seidel M, White J, et al. (2018) Association of Cardiac Myosin Binding Protein-C with the Ryanodine Receptor-Ca2+ Release Channel: Putative Retrograde Regulation? Biophysical Journal. 114: 621a |
| Viero C, Wegener S, Scholz A, et al. (2016) Endothelin-1-induced remodelling of murine adult ventricular myocytes. Cell Calcium |
| Viero C. (2015) Clueless with fewer cues from endothelin. Commentary: Venous endothelin guides sympathetic innervation of the developing mouse heart. Frontiers in Cell and Developmental Biology. 3: 54 |
| Viero C, Euden J, Mason S, et al. (2014) P373Two key regions of the human cardiac ryanodine receptor calcium release channel modulate its gating properties in a dual manner Cardiovascular Research. 103 |
| Zissimopoulos S, Viero C, Seidel M, et al. (2013) N-terminus oligomerization regulates the function of cardiac ryanodine receptors. Journal of Cell Science. 126: 5042-51 |
| Euden J, Mason SA, Viero C, et al. (2013) Investigations of the contribution of a putative glycine hinge to ryanodine receptor channel gating. The Journal of Biological Chemistry. 288: 16671-9 |
| Euden J, Mason SA, Viero C, et al. (2013) Gating of the Pore of the Human Ryanodine Receptor Type 2 does not require Glycine Hinges Biophysical Journal. 104 |
| Moriya T, Kayano T, Kitamura N, et al. (2012) Vasopressin-induced intracellular Ca²⺠concentration responses in non-neuronal cells of the rat dorsal root ganglion. Brain Research. 1483: 1-12 |
| Mason SA, Viero C, Euden J, et al. (2012) The contribution of hydrophobic residues in the pore-forming region of the ryanodine receptor channel to block by large tetraalkylammonium cations and Shaker B inactivation peptides. The Journal of General Physiology. 140: 325-39 |