Catterall W
Channels (Austin). 2023; 17(1):2281714.
PMID: 37983307
PMC: 10761118.
DOI: 10.1080/19336950.2023.2281714.
Hoffmann S, Balthasar S, Friedrichs U, Ehren M, Ryan S, Wiedemann P
Graefes Arch Clin Exp Ophthalmol. 2005; 244(3):376-81.
PMID: 16088412
DOI: 10.1007/s00417-004-1104-7.
Serysheva I, Ludtke S, Baker M, Chiu W, Hamilton S
Proc Natl Acad Sci U S A. 2002; 99(16):10370-5.
PMID: 12149473
PMC: 124921.
DOI: 10.1073/pnas.162363499.
Dakshinamurti K, Lal K, Ganguly P
Mol Cell Biochem. 1998; 188(1-2):137-48.
PMID: 9823019
Mitterdorfer J, Grabner M, Kraus R, Hering S, Prinz H, Glossmann H
J Bioenerg Biomembr. 1998; 30(4):319-34.
PMID: 9758329
DOI: 10.1023/a:1021933504909.
The benzazepine/benzothiazepine binding domain of the cardiac L-type Ca2+ channel is accessible only from the extracellular side.
Seydl K, KIMBALL D, Schindler H, Romanin C
Pflugers Arch. 1993; 424(5-6):552-4.
PMID: 8255741
DOI: 10.1007/BF00374922.
Phosphorylation modulates the function of the calcium release channel of sarcoplasmic reticulum from skeletal muscle.
Hain J, Nath S, Mayrleitner M, Fleischer S, Schindler H
Biophys J. 1994; 67(5):1823-33.
PMID: 7858121
PMC: 1225556.
DOI: 10.1016/S0006-3495(94)80664-2.
Expression of the L-type calcium channel with two different beta subunits and its modulation by Ro 40-5967.
Welling A, Lacinova L, Donatin K, Ludwig A, Bosse E, Flockerzi V
Pflugers Arch. 1995; 429(3):400-11.
PMID: 7761264
DOI: 10.1007/BF00374156.
[3H]HOE166 defines a novel calcium antagonist drug receptor--distinct from the 1,4 dihydropyridine binding domain.
Grassegger A, Striessnig J, Weiler M, Knaus H, Glossmann H
Naunyn Schmiedebergs Arch Pharmacol. 1989; 340(6 Pt 2):752-9.
PMID: 2561307
DOI: 10.1007/BF00169685.
The effect of the phenylalkylamine D888 (devapamil) on force and Ca2+ current in isolated frog skeletal muscle fibres.
Erdmann R, LUTTGAU H
J Physiol. 1989; 413:521-41.
PMID: 2557440
PMC: 1189114.
DOI: 10.1113/jphysiol.1989.sp017667.
The effects of dihydropyridine derivatives on force and Ca2+ current in frog skeletal muscle fibres.
Neuhaus R, Rosenthal R, LUTTGAU H
J Physiol. 1990; 427:187-209.
PMID: 2170635
PMC: 1189926.
DOI: 10.1113/jphysiol.1990.sp018167.
Modulation of calcium current gating in frog skeletal muscle by conditioning depolarization.
Feldmeyer D, Melzer W, Pohl B, Zollner P
J Physiol. 1992; 457:639-53.
PMID: 1338468
PMC: 1175752.
DOI: 10.1113/jphysiol.1992.sp019399.
A method for estimation of drug affinity constants to the open conformational state of calcium channels.
Timin E, Hering S
Biophys J. 1992; 63(3):808-14.
PMID: 1330037
PMC: 1262213.
DOI: 10.1016/S0006-3495(92)81636-3.
In vivo labeling of L-type Ca2+ channels by fluorescent dihydropyridines: evidence for a functional, extracellular heparin-binding site.
Knaus H, Moshammer T, Friedrich K, Kang H, Haugland R, Glossman H
Proc Natl Acad Sci U S A. 1992; 89(8):3586-90.
PMID: 1314393
PMC: 48913.
DOI: 10.1073/pnas.89.8.3586.
