Pages that link to "Q48971899"

The following pages link to Two amino acid residues in the IIIS5 segment of L-type calcium channels differentially contribute to 1,4-dihydropyridine sensitivity (Q48971899):

Displaying 34 items.

• Inhibition of Recombinant L-Type Voltage-Gated Calcium Channels by Positive Allosteric Modulators of GABAA Receptors (Q24632514) (← links)
• Structural Basis for Pharmacology of Voltage-Gated Sodium and Calcium Channels (Q28082803) (← links)
• Identification and functional characterization of voltage-dependent calcium channels in T lymphocytes (Q28204919) (← links)
• Ca2 channel sensitivity towards the blocker isradipine is affected by alternative splicing of the human alpha1C subunit gene (Q28272430) (← links)
• A genetic screen for dihydropyridine (DHP)-resistant worms reveals new residues required for DHP-blockage of mammalian calcium channels (Q28472680) (← links)
• Calcium channel blockers: current controversies and basic mechanisms of action (Q33637659) (← links)
• Functional expression of transgenic α1sDHPR channels in adult mammalian skeletal muscle fibres (Q33801924) (← links)
• Potentiation of the cardiac L-type Ca(2 ) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms (Q36445185) (← links)
• Construction of a high-affinity receptor site for dihydropyridine agonists and antagonists by single amino acid substitutions in a non- l -type Ca 2 channel (Q36833695) (← links)
• Calcicludine binding to the outer pore of L-type calcium channels is allosterically coupled to dihydropyridine binding (Q36853494) (← links)
• Manipulating L-type calcium channels in cardiomyocytes using split-intein protein transsplicing (Q37192045) (← links)
• Reverse engineering the L-type Ca2 channel alpha1c subunit in adult cardiac myocytes using novel adenoviral vectors (Q37362283) (← links)
• Slow deactivation and U-shaped inactivation properties in cloned Cav1.2b channels in Chinese hamster ovary cells (Q40228063) (← links)
• Nine L-type amino acid residues confer full 1,4-dihydropyridine sensitivity to the neuronal calcium channel alpha1A subunit. Role of L-type Met1188. (Q40879522) (← links)
• Conserved Ca2 -antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain. (Q40886220) (← links)
• Alternatively Spliced IS6 Segments of the α 1C Gene Determine the Tissue-Specific Dihydropyridine Sensitivity of Cardiac and Vascular Smooth Muscle L-Type Ca 2 Channels (Q41088823) (← links)
• Analysis of the Dihydropyridine Receptor Site ofl-type Calcium Channels by Alanine-scanning Mutagenesis (Q41098698) (← links)
• Structural model for dihydropyridine binding to L-type calcium channels (Q42092107) (← links)
• Serine residue in the IIIS5-S6 linker of the L-type Ca2 channel alpha 1C subunit is the critical determinant of the action of dihydropyridine Ca2 channel agonists (Q42635265) (← links)
• Mechanism of dihydropyridine interaction with critical binding residues of L-type Ca2 channel alpha 1 subunits. (Q43559720) (← links)
• Dissociation of charge movement from calcium release and calcium current in skeletal myotubes by gabapentin (Q44101904) (← links)
• DHP-insensitive L-type-like Ca channel of ascidian acquires sensitivity to DHP with single amino acid change in domain III P-region (Q44546916) (← links)
• Reconstitution of local Ca2 signaling between cardiac L-type Ca2 channels and ryanodine receptors: insights into regulation by FKBP12.6. (Q46622472) (← links)
• In vitro characterization of L-type calcium channels and their contribution to firing behavior in invertebrate respiratory neurons (Q46703326) (← links)
• Molecular mimicking of C-terminal phosphorylation tunes the surface dynamics of CaV1.2 calcium channels in hippocampal neurons. (Q46799360) (← links)
• Cloning and functional expression of a voltage-gated calcium channel alpha1 subunit from jellyfish (Q48029276) (← links)
• A region in IVS5 of the human cardiac L-type calcium channel is required for the use-dependent block by phenylalkylamines and benzothiazepines (Q48254892) (← links)
• Molecular studies on the voltage dependence of dihydropyridine action on L-type Ca2 channels. Critical involvement of tyrosine residues in motif IIIS6 and IVS6. (Q48952010) (← links)
• Sequence Differences between α1Cand α1SCa2 Channel Subunits Reveal Structural Determinants of a Guarded and Modulated Benzothiazepine Receptor (Q61918639) (← links)
• Structural basis of drug binding to L Ca2 channels (Q61918643) (← links)
• Molecular Determinants of High Affinity Phenylalkylamine Block of l-type Calcium Channels in Transmembrane Segment IIIS6 and the Pore Region of the α1Subunit (Q64980401) (← links)
• Photochemical identification of transmembrane segment IVS6 as the binding region of semotiadil, a new modulator for the L-type voltage-dependent Ca2 channel (Q74192512) (← links)
• Molecular basis of drug interaction with L-type Ca2 channels (Q77363488) (← links)
• Photochemical localization of the semotiadil binding region within the cardiac Ca2 channel alpha1 subunit. Comparison with the skeletal muscle counterpart (Q77758379) (← links)