CHELATOR: an improved method for computing metal ion concentrations in physiological solutions.
about
Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homologA neuronal beta subunit (KCNMB4) makes the large conductance, voltage- and Ca2+-activated K+ channel resistant to charybdotoxin and iberiotoxinA forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporterMICU1 and MICU2 finely tune the mitochondrial Ca2+ uniporter by exerting opposite effects on MCU activityCyclic nucleotide-gated channel subunit glycosylation regulates matrix metalloproteinase-dependent changes in channel gatingA novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degenerationLentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindnessNew insights on the mechanism of the K(+-) independent activity of crenarchaeota pyruvate kinasesInsights into the Regulatory Landscape of the Lysine RiboswitchStructural Basis for Gating and Activation of RyR1.Soluble fusion proteins between single transmembrane photoreceptor guanylyl cyclases and their activators.Two domains in dihydropyridine receptor activate the skeletal muscle Ca(2+) release channel.Calcium-sensitive regions of GCAP1 as observed by chemical modifications, fluorescence, and EPR spectroscopiesInternal aluminum block of plant inward K(+) channelsEarly cardiac hypertrophy in mice with impaired calmodulin regulation of cardiac muscle Ca release channel.Maturation and secretion of rat hepatic lipase is inhibited by alpha1B-adrenergic stimulation through changes in Ca2+ homoeostasis: thapsigargin and EGTA both mimic the effect of adrenalineThe mitochondrial calcium uniporter is a multimer that can include a dominant-negative pore-forming subunitDefining a key receptor-CheA kinase contact and elucidating its function in the membrane-bound bacterial chemosensory array: a disulfide mapping and TAM-IDS Study.Biophysical and functional characterization of hippocalcin mutants responsible for human dystonia.Sodium selectivity of Reissner's membrane epithelial cellsPathophysiologically relevant levels of hydrogen peroxide induce glutamate-independent neurodegeneration that involves activation of transient receptor potential melastatin 7 channelsInward-rectifier chloride currents in Reissner's membrane epithelial cellsThe mitochondrial permeability transition pore is a dispensable element for mitochondrial calcium efflux.Molecular determinants of a Ca2+-binding site in the pore of cyclic nucleotide-gated channels: S5/S6 segments control affinity of intrapore glutamates.Sarcoplasmic reticulum lumenal Ca2+ has access to cytosolic activation and inactivation sites of skeletal muscle Ca2+ release channelCalmodulin activation and inhibition of skeletal muscle Ca2+ release channel (ryanodine receptor)Single-molecule force spectroscopy reveals force-enhanced binding of calcium ions by gelsolinCalcium-dependent inactivation of L-type calcium channels in planar lipid bilayers.Regulation of cardiac muscle Ca2+ release channel by sarcoplasmic reticulum lumenal Ca2+Mechanism of calmodulin inhibition of cardiac sarcoplasmic reticulum Ca2+ release channel (ryanodine receptor)Calcium-dependent assembly of centrin-G-protein complex in photoreceptor cellsCharacterization of retinal guanylate cyclase-activating protein 3 (GCAP3) from zebrafish to man.Probing the role of negatively charged amino acid residues in ion permeation of skeletal muscle ryanodine receptorTwo rings of negative charges in the cytosolic vestibule of type-1 ryanodine receptor modulate ion fluxes.Apamin-sensitive calcium-activated potassium currents in rabbit ventricles with chronic myocardial infarction.Membrane-induced allosteric control of phospholipase C-β isozymes.Activation of methanogenesis by cadmium in the marine archaeon Methanosarcina acetivorans.Stabilization of the skeletal muscle ryanodine receptor ion channel-FKBP12 complex by the 1,4-benzothiazepine derivative S107Modulation of sarcoplasmic reticulum Ca2+ release in skeletal muscle expressing ryanodine receptor impaired in regulation by calmodulin and S100A1.
P2860
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P2860
CHELATOR: an improved method for computing metal ion concentrations in physiological solutions.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh-hant
name
CHELATOR: an improved method f ...... ns in physiological solutions.
@en
CHELATOR: an improved method f ...... ns in physiological solutions.
@nl
type
label
CHELATOR: an improved method f ...... ns in physiological solutions.
@en
CHELATOR: an improved method f ...... ns in physiological solutions.
@nl
prefLabel
CHELATOR: an improved method f ...... ns in physiological solutions.
@en
CHELATOR: an improved method f ...... ns in physiological solutions.
@nl
P2093
P1433
P1476
CHELATOR: an improved method f ...... ons in physiological solutions
@en
P2093
Schoenmakers TJ
Theuvenet AP
P304
870-4, 876-9
P577
1992-06-01T00:00:00Z