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Journal of Clinical Medicine|May 14, 2022
Relationships between Plasma Pyrophosphate, Vascular Calcification and Clinical Severity in Patients Affected by Pseudoxanthoma ElasticumGeorges Leftheriotis, Nastassia Navasiolava, Laetitia Clotaire, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2012
TWIK1, a unique background channel with variable ion selectivityFranck C Chatelain, Delphine Bichet, Dominique Douguet, et al.
Annals of Medicine|June 7, 2006
Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patientsHeidi Fodstad, Saïd Bendahhou, Jean-Sébastien Rougier, et al.
Scientific Reports|February 3, 2018
Substitutions of the S4DIV R2 residue (R1451) in Na<sub>V</sub>1.4 lead to complex forms of paramyotonia congenita and periodic paralysesHugo Poulin, Pascal Gosselin-Badaroudine, Savine Vicart, et al.
The Journal of Physiology|April 16, 2005
In vivo and in vitro functional characterization of Andersen's syndrome mutationsSaïd Bendahhou, Emmanuel Fournier, Damien Sternberg, et al.
Human Molecular Genetics|August 25, 2012
Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortexAbeer El Wakil, Sascha Bandulik, Nicolas Guy, et al.
Scientific Reports|May 23, 2020
New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studiesCharline Fagnen, Ludovic Bannwarth, Iman Oubella, et al.
International Journal of Molecular Sciences|January 11, 2022
Integrative Study of the Structural and Dynamical Properties of a KirBac3.1 Mutant: Functional Implication of a Highly Conserved Tryptophan in the Transmembrane DomainCharline Fagnen, Ludovic Bannwarth, Iman Oubella, et al.
Science Advances|September 23, 2022
Cryo-electron microscopy unveils unique structural features of the human Kir2.1 channelCarlos A H Fernandes, Dania Zuniga, Charline Fagnen, et al.
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