Zobrazeno 1 - 10
of 75
pro vyhledávání: '"V. Brechler"'
Autor:
Miura, Daimei1,2 (AUTHOR), Hayashi, Wakana1 (AUTHOR), Hirano, Kensuke3 (AUTHOR), Sasaki, Ikkei1 (AUTHOR), Tsukakoshi, Kaori1 (AUTHOR), Kakizoe, Hidehumi4 (AUTHOR), Asai, Satomi4,5 (AUTHOR), Vavricka, Christopher J.1,2 (AUTHOR), Takemae, Hitoshi6 (AUTHOR), Mizutani, Tetsuya6,7 (AUTHOR), Tsugawa, Wakako1 (AUTHOR), Sode, Koji8 (AUTHOR), Ikebukuro, Kazunori1 (AUTHOR) ikebu@cc.tuat.ac.jp, Asano, Ryutaro1,2 (AUTHOR) ryutaroa@cc.tuat.ac.jp
Publikováno v:
Advanced Science. 11/20/2024, Vol. 11 Issue 43, p1-12. 12p.
Autor:
Alain Kervran, Philippe Blache, V. Brechler, Dominique Bataille, Catherine Pavoine, Françoise Pecker, Dung Le-Nguyen, S. Laurent
Publikováno v:
American Journal of Physiology-Cell Physiology. 260:C993-C999
Glucagon is well known for its cardiotonic effect, but its mechanism of action remains undetermined. In the present study, we showed that glucagon, under minimal degradation conditions, had no effect on the amplitude of contractility of beating chick
Publikováno v:
Regulatory peptides. 77(1-3)
Angiotensin II (Ang II) increases the level of tyrosine phosphorylation of several proteins in nondifferentiated NG108-15 cells, a hybrid derived from the fusion of mouse neuroblastoma and rat glioma cells. Conversely, incubation of NG108-15 cells wi
Publikováno v:
Advances in experimental medicine and biology. 436
Publikováno v:
Receptorschannels. 2(2)
Most of angiotensin II's (Ang II) documented effects have been attributed to the interaction of this peptide with a G-protein coupled receptor termed AT1. The role and the signalling mechanisms of the more recently characterized AT2 receptor, which d
Publikováno v:
Receptorschannels. 2(2)
Ever since the identification of two distinct Ang II receptor subtypes, the function of the AT2 receptor has been a subject of debate. As opposed to the AT1 subtype, this receptor does not interact with G-proteins in most cell lines and tissues. We s
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 1992, 267 (22), pp.15496-501
ResearcherID
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 1992, 267 (22), pp.15496-501
ResearcherID
International audience; We have recently reported that glucagon activated the L-type Ca2+ channel current in frog ventricular myocytes and showed that this was linked to the inhibition of a membrane-bound low-Km cAMP phosphodiesterase (PDE) (Méry, P
Autor:
B. Roche, Françoise Pecker, Catherine Pavoine, M. Dufour, Sophie Lotersztajn, Dominique Bataille, Dung Le-Nguyen, V. Brechler
Publikováno v:
The Journal of biological chemistry. 265(17)
We have recently shown that nanomolar concentrations of glucagon-(19-29), which can derive from native glucagon by proteolytic cleavage of the dibasic doublet Arg17-Arg18, inhibit the Ca2+ pump in liver plasma membrane vesicles independently of adeny
Autor:
Catherine Pavoine, Françoise Pecker, Pierre-François Méry, Rodolphe Fischmeister, V. Brechler
Publikováno v:
Nature. 345(6271)
Glucagon exerts positive inotropic and chronotropic effects in the heart. Like its glycogenolytic effect in liver cells, the cardiac effects of glucagon are often correlated with adenylyl cyclase stimulation. Therefore, cyclic AMP-dependent phosphory
Autor:
Rodolphe Fischmeister, Françoise Pecker, V. Brechler, Alvin Shrier, Pierre-François Méry, Catherine Pavoine
Publikováno v:
Developments in Cardiovascular Medicine ISBN: 9781461288138
The influx of Ca2+ ions through transmembrane Ca2+ channels is fundamental in many aspects of cardiac function. Regulation of the heart beat by noradrenaline and acetylcholine (ACh) is in part mediated by the effects of these neurotransmitters on cal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::852b4c1676272c45144ee85bb9928131
https://doi.org/10.1007/978-1-4613-1513-1_3
https://doi.org/10.1007/978-1-4613-1513-1_3