Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
A mechano- and heat-gated two-pore domain K+ channel controls excitability in adult zebrafish skeletal muscle.
Proc Natl Acad Sci U S A. 2023 Nov 7;120(45):e2305959120. doi: 10.1073/pnas.2305959120. Epub 2023 Oct 30.
Proc Natl Acad Sci U S A. 2023.
PMID: 37903280
Free PMC article.
Mammalian skeletal muscle does not express functional voltage-gated H+ channels.
Fuster C, Idoux R, Berthier C, Jacquemond V, Allard B.
Fuster C, et al. Among authors: idoux r.
Am J Physiol Cell Physiol. 2018 Nov 1;315(5):C776-C779. doi: 10.1152/ajpcell.00357.2018. Epub 2018 Oct 3.
Am J Physiol Cell Physiol. 2018.
PMID: 30281323
Free article.
Item in Clipboard
Superfast excitation-contraction coupling in adult zebrafish skeletal muscle fibers.
Idoux R, Bretaud S, Berthier C, Ruggiero F, Jacquemond V, Allard B.
Idoux R, et al.
J Gen Physiol. 2022 Sep 5;154(9):e202213158. doi: 10.1085/jgp.202213158. Epub 2022 Jun 29.
J Gen Physiol. 2022.
PMID: 35767225
Free PMC article.
Item in Clipboard
[Unraveling the pathophysiology of Bethlem Myopathy using a unique zebrafish model for the disease].
Idoux R, Bretaud S, Berthier C, Jacquemond V, Ruggiero F, Allard B.
Idoux R, et al.
Med Sci (Paris). 2019 Nov;35 Hors série n° 2:39-42. doi: 10.1051/medsci/2019182. Epub 2019 Dec 20.
Med Sci (Paris). 2019.
PMID: 31859630
Free article.
Review.
French.
Item in Clipboard
Divalent cations permeation in a Ca2+ non-conducting skeletal muscle dihydropyridine receptor mouse model.
Idoux R, Fuster C, Jacquemond V, Dayal A, Grabner M, Charnet P, Allard B.
Idoux R, et al.
Cell Calcium. 2020 Nov;91:102256. doi: 10.1016/j.ceca.2020.102256. Epub 2020 Aug 20.
Cell Calcium. 2020.
PMID: 32866694
Item in Clipboard
Item in Clipboard
A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.
Stringer RN, Jurkovicova-Tarabova B, Huang S, Haji-Ghassemi O, Idoux R, Liashenko A, Souza IA, Rzhepetskyy Y, Lacinova L, Van Petegem F, Zamponi GW, Pamphlett R, Weiss N.
Stringer RN, et al. Among authors: idoux r.
Mol Brain. 2020 Mar 6;13(1):33. doi: 10.1186/s13041-020-00577-6.
Mol Brain. 2020.
PMID: 32143681
Free PMC article.
Item in Clipboard
Cite
Cite