Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.
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GPR99, a new G protein-coupled receptor with homology to a new subgroup of nucleotide receptorsPhyla- and Subtype-Selectivity of CgNa, a Na Channel Toxin from the Venom of the Giant Caribbean Sea Anemone Condylactis GiganteaMolecular cloning and functional expression of a human peptide methionine sulfoxide reductase (hMsrA)Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene familyInhibition of human ether à go-go potassium channels by Ca(2+)/calmodulinSpire-type actin nucleators cooperate with Formin-2 to drive asymmetric oocyte divisionCloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsLight modulation of cellular cAMP by a small bacterial photoactivated adenylyl cyclase, bPAC, of the soil bacterium BeggiatoaOpen structure of the Ca2+ gating ring in the high-conductance Ca2+-activated K+ channel.Voltage-sensing domain of voltage-gated proton channel Hv1 shares mechanism of block with pore domainsTMEM16A(a)/anoctamin-1 shares a homodimeric architecture with CLC chloride channelsA recombinant inwardly rectifying potassium channel coupled to GTP-binding proteinsMolecular cloning and characterization of a novel splicing variant of the Kir3.2 subunit predominantly expressed in mouse testisMechanism of inhibition of cyclic nucleotide-gated ion channels by diacylglycerolIdentification and characterization of a monocarboxylate transporter (MCT1) in pig and human colon: its potential to transport L-lactate as well as butyrateFour Ca2+ ions activate TRPM2 channels by binding in deep crevices near the pore but intracellularly of the gateUsing concatenated subunits to investigate the functional consequences of heterotetrameric inositol 1,4,5-trisphosphate receptorsCaenorhabditis elegans paraoxonase-like proteins control the functional expression of DEG/ENaC mechanosensory proteins.kappa-Hefutoxin1, a novel toxin from the scorpion Heterometrus fulvipes with unique structure and function. Importance of the functional diad in potassium channel selectivityTuning activation of the AMPA-sensitive GluR2 ion channel by genetic adjustment of agonist-induced conformational changesFunction and solution structure of hainantoxin-I, a novel insect sodium channel inhibitor from the Chinese bird spider Selenocosmia hainanaSolution structure and alanine scan of a spider toxin that affects the activation of mammalian voltage-gated sodium channelsC-terminal Movement during Gating in Cyclic Nucleotide-modulated ChannelsPhysical determinants of strong voltage sensitivity of K+ channel blockPrinciples of activation and permeation in an anion-selective Cys-loop receptorMolecular mechanism for 3:1 subunit stoichiometry of rod cyclic nucleotide-gated ion channelsEvolutionary Diversification of Mesobuthus -Scorpion Toxins Affecting Sodium ChannelsFunctional and structural analysis of the human SLO3 pH- and voltage-gated K+ channelMultisite Binding of a General Anesthetic to the Prokaryotic Pentameric Erwinia chrysanthemi Ligand-gated Ion Channel (ELIC)A novel µ-conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptorsStructure and stoichiometry of an accessory subunit TRIP8b interaction with hyperpolarization-activated cyclic nucleotide-gated channelsStructural Similarity between Defense Peptide from Wheat and Scorpion Neurotoxin Permits Rational Functional DesignStructural and Functional Elucidation of Peptide Ts11 Shows Evidence of a Novel Subfamily of Scorpion Venom ToxinsScOPT1 and AtOPT4 function as proton-coupled oligopeptide transporters with broad but distinct substrate specificities.Impaired surface membrane insertion of homo- and heterodimeric human muscle chloride channels carrying amino-terminal myotonia-causing mutationsThe functional unit of the renal type IIa Na+/Pi cotransporter is a monomerIdentification of a tyrosine in the agonist binding site of the homomeric rho1 gamma-aminobutyric acid (GABA) receptor that, when mutated, produces spontaneous openingIdentification of critical residues controlling G protein-gated inwardly rectifying K(+) channel activity through interactions with the beta gamma subunits of G proteinsFunctional and molecular characterization of nucleobase transport by recombinant human and rat equilibrative nucleoside transporters 1 and 2. Chimeric constructs reveal a role for the ENT2 helix 5-6 region in nucleobase translocationFunctional consequences of progressive cone dystrophy-associated mutations in the human cone photoreceptor cyclic nucleotide-gated channel CNGA3 subunit
P2860
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P2860
Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@en
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@nl
type
label
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@en
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@nl
prefLabel
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@en
Subunit stoichiometry of a mam ...... struction of multimeric cDNAs.
@nl
P1433
P1476
Subunit stoichiometry of a mam ...... nstruction of multimeric cDNAs
@en
P304
P356
10.1016/0896-6273(92)90239-A
P407
P577
1992-11-01T00:00:00Z