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Biochimica Et Biophysica Acta|March 21, 2006
Cell penetration properties of maurocalcine, a natural venom peptide active on the intracellular ryanodine receptorSylvie Boisseau, Kamel Mabrouk, Narendra Ram, et al.
The Journal of Biological Chemistry|July 16, 2008
Design of a disulfide-less, pharmacologically inert, and chemically competent analog of maurocalcine for the efficient transport of impermeant compounds into cellsNarendra Ram, Norbert Weiss, Isabelle Texier-Nogues, et al.
The Journal of Biological Chemistry|April 6, 2017
C-terminal splice variants of P/Q-type Ca2+ channel CaV2.1 α1 subunits are differentially regulated by Rab3-interacting molecule proteinsMitsuru Hirano, Yoshinori Takada, Chee Fah Wong, et al.
Biophysical Journal|July 16, 2008
Charged surface area of maurocalcine determines its interaction with the skeletal ryanodine receptorBalázs Lukács, Mónika Sztretye, János Almássy, et al.
International Journal of Molecular Sciences|October 1, 2020
Functional Impact of BeKm-1, a High-Affinity hERG Blocker, on Cardiomyocytes Derived from Human-Induced Pluripotent Stem CellsStephan De Waard, Jérôme Montnach, Barbara Ribeiro, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2016
In cellulo phosphorylation induces pharmacological reprogramming of maurocalcin, a cell-penetrating venom peptideMichel Ronjat, Wei Feng, Lucie Dardevet, et al.
The Journal of Biological Chemistry|January 18, 2005
Transduction of the scorpion toxin maurocalcine into cells. Evidence that the toxin crosses the plasma membraneEric Estève, Kamel Mabrouk, Alain Dupuis, et al.
The Journal of Cell Biology|August 11, 2004
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletionSusan Treves, Clara Franzini-Armstrong, Luca Moccagatta, et al.
The Biochemical Journal|October 9, 2020
Maurocalcin and its analog MCaE12A facilitate Ca2+ mobilization in cardiomyocytesStephan De Waard, Jérome Montnach, Charly Cortinovis, et al.
Scientific Reports|June 20, 2020
Inhibition of G protein-gated K+ channels by tertiapin-Q rescues sinus node dysfunction and atrioventricular conduction in mouse models of primary bradycardiaIsabelle Bidaud, Antony Chung You Chong, Agnes Carcouet, et al.
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