review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | H Robert Guy | |
Steffen Hering | |||
Annette Hohaus | |||
Eugen Timin | |||
Michaela Kudrnac | |||
Anna Stary | |||
Stansilav Beyl | |||
P2860 | cites work | The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity | Q22337058 |
X-ray structure of a voltage-dependent K+ channel | Q22337257 | ||
Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolution | Q22337277 | ||
A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation. | Q24302179 | ||
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons | Q24538702 | ||
Activation of Shaker potassium channels. III. An activation gating model for wild-type and V2 mutant channels | Q24642407 | ||
Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment | Q27649044 | ||
The role of distal S6 hydrophobic residues in the voltage-dependent gating of CaV2.3 channels | Q27865194 | ||
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism | Q28117072 | ||
Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine | Q28137616 | ||
Molecular physiology of low-voltage-activated t-type calcium channels | Q28200827 | ||
Currents related to movement of the gating particles of the sodium channels | Q28244673 | ||
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel | Q28260421 | ||
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics | Q28263620 | ||
Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects | Q28284668 | ||
International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels | Q28289138 | ||
Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels | Q28301295 | ||
The Ca2+ channel alpha2delta-1 subunit determines Ca2+ current kinetics in skeletal muscle but not targeting of alpha1S or excitation-contraction coupling | Q28593153 | ||
Biodiversity of voltage sensor domain proteins. | Q30360268 | ||
Familial hemiplegic migraine | Q33280531 | ||
Voltage-dependent calcium channels: from structure to function | Q33715812 | ||
Voltage-gated ion channels and hereditary disease | Q33744648 | ||
Isoform-specific regulation of mood behavior and pancreatic beta cell and cardiovascular function by L-type Ca 2+ channels | Q33784992 | ||
The voltage sensor in voltage-dependent ion channels | Q33881262 | ||
Role of S4 segments and the leucine heptad motif in the activation of an L-type calcium channel | Q33915557 | ||
Critical role of conserved proline residues in the transmembrane segment 4 voltage sensor function and in the gating of L-type calcium channels | Q34990517 | ||
Voltage-gated K channels | Q35161667 | ||
Auxiliary subunits: essential components of the voltage-gated calcium channel complex. | Q35172799 | ||
Cardiac calcium signalling | Q35541340 | ||
L-type Ca2+ channels in Ca2+ channelopathies | Q35874336 | ||
Shaker potassium channel gating. III: Evaluation of kinetic models for activation | Q36411441 | ||
Functional architecture of the inner pore of a voltage-gated Ca2+ channel | Q36493546 | ||
The Timothy syndrome mutation differentially affects voltage- and calcium-dependent inactivation of CaV1.2 L-type calcium channels | Q36883128 | ||
Critical roles of the S3 segment and S3-S4 linker of repeat I in activation of L-type calcium channels | Q37558500 | ||
Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder | Q38660530 | ||
Determinants of the differential gating properties of Cav3.1 and Cav3.3 T-type channels: a role of domain IV? | Q40228543 | ||
Evidence for common structural determinants of activation and inactivation in T-type Ca2+ channels | Q40235133 | ||
Voltage gating of ion channels | Q40391780 | ||
Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia | Q40763673 | ||
Influence of L-type Ca channel alpha 2/delta-subunit on ionic and gating current in transiently transfected HEK 293 cells | Q41200281 | ||
Modulation of human neuronal alpha 1E-type calcium channel by alpha 2 delta-subunit. | Q43977150 | ||
beta-Subunits: fine tuning of Ca(2+) channel block | Q44203164 | ||
Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina | Q44743341 | ||
A gating hinge in Na+ channels; a molecular switch for electrical signaling | Q44815981 | ||
Structures and functions of calcium channel beta subunits | Q46459475 | ||
Voltage sensor of Kv1.2: structural basis of electromechanical coupling | Q46588794 | ||
Roles of molecular regions in determining differences between voltage dependence of activation of CaV3.1 and CaV1.2 calcium channels | Q47726373 | ||
Potentiation by the beta subunit of the ratio of the ionic current to the charge movement in the cardiac calcium channel | Q49130329 | ||
Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. | Q54075376 | ||
Energetics of pore opening in a voltage-gated K(+) channel | Q78454007 | ||
P433 | issue | 2 | |
P304 | page(s) | 61-69 | |
P577 | publication date | 2008-03-14 | |
P1433 | published in | Channels | Q15764469 |
P1476 | title | Pore stability and gating in voltage-activated calcium channels | |
P478 | volume | 2 |