review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1146/ANNUREV.PHYSIOL.59.1.171 |
P8608 | Fatcat ID | release_q54m3eflrjecjhsrrzqqoesdq4 |
P698 | PubMed publication ID | 9074760 |
P2093 | author name string | Nichols CG | |
Lopatin AN | |||
P2860 | cites work | Cloning and functional expression of a rat heart KATP channel | Q28245885 |
P304 | page(s) | 171-191 | |
P577 | publication date | 1997-01-01 | |
P1433 | published in | Annual Review of Physiology | Q567364 |
P1476 | title | Inward rectifier potassium channels | |
P478 | volume | 59 |
Q47613034 | A Case of Renal Tubular Acidosis with Sjogren's Syndrome Showing Paradoxical Block of PTH Due to Severe Hypomagnesemia |
Q34735191 | A Kir6.2 pore mutation causes inactivation of ATP-sensitive potassium channels by disrupting PIP2-dependent gating |
Q36436024 | A conserved arginine residue in the pore region of an inward rectifier K channel (IRK1) as an external barrier for cationic blockers |
Q46658287 | A difference in inward rectification and polyamine block and permeation between the Kir2.1 and Kir3.1/Kir3.4 K+ channels |
Q40226766 | A digital atlas of ion channel expression patterns in the two-week-old rat brain |
Q34198516 | A fast BK-type KCa current acts as a postsynaptic modulator of temporal selectivity for communication signals |
Q24544449 | A mechanism for ATP-sensitive potassium channel diversity: Functional coassembly of two pore-forming subunits |
Q56016835 | A mechanism for ATP-sensitive potassium channel diversity: Functional coassembly of two pore-forming subunits |
Q36438667 | A mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) channels in a closed state |
Q24533254 | A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids. |
Q24297875 | A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene |
Q34471139 | A novel inward rectifier K+ channel with unique pore properties |
Q27863888 | A novel mechanism for the suppression of a voltage-gated potassium channel by glucose-dependent insulinotropic polypeptide: protein kinase A-dependent endocytosis |
Q40166773 | A novel type of ATP block on a Ca(2+)-activated K(+) channel from bullfrog erythrocytes |
Q35294146 | A perspective of polyamine metabolism |
Q42020157 | A silk platform that enables electrophysiology and targeted drug delivery in brain astroglial cells |
Q50722459 | A single residue contributes to the difference between Kir4.1 and Kir1.1 channels in pH sensitivity, rectification and single channel conductance. |
Q36574252 | A synergistic blocking effect of Mg²⁺ and spermine on the inward rectifier K⁺ (Kir2.1) channel pore |
Q36137429 | A tandem Di-hydrophobic motif mediates clathrin-dependent endocytosis via direct binding to the AP-2 ασ2 subunits |
Q30469105 | A transcriptomic analysis of type I-III neurons in the bed nucleus of the stria terminalis |
Q35641881 | AMP-activated protein kinase connects cellular energy metabolism to KATP channel function |
Q40027635 | AP-2-dependent internalization of potassium channel Kir2.3 is driven by a novel di-hydrophobic signal |
Q28586584 | Absence of small conductance K+ channel (SK) activity in apical membranes of thick ascending limb and cortical collecting duct in ROMK (Bartter's) knockout mice |
Q48792003 | Activation of inwardly rectifying Kir2.x potassium channels by beta 3-adrenoceptors is mediated via different signaling pathways with a predominant role of PKC for Kir2.1 and of PKA for Kir2.2. |
Q26783129 | Activity-Dependent Plasticity of Astroglial Potassium and Glutamate Clearance |
Q53945077 | Activity-dependent modulation of glutamate receptors by polyamines. |
Q77120311 | Adenosine 5'-triphosphate: an intracellular metabolic messenger |
Q28513769 | Adenosine-triphosphate-sensitive K+ channel (Kir6.1): a novel phosphospecific interaction partner of connexin 43 (Cx43) |
Q40922838 | Amino acid substitutions in the pore of rat glutamate receptors at sites influencing block by polyamines |
Q28348748 | Ammonium ions induce inactivation of Kir2.1 potassium channels expressed in Xenopus oocytes |
Q34460250 | An alternative approach to the identification of respiratory central chemoreceptors in the brainstem |
Q24301003 | An alternatively spliced isoform of PSD-93/chapsyn 110 binds to the inwardly rectifying potassium channel, Kir2.1 |
Q44925277 | An impaired neocortical Ih is associated with enhanced excitability and absence epilepsy. |
Q28345056 | An inward rectifier K(+) channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels |
Q40673383 | An inwardly rectifying K+ channel in bovine parotid acinar cells: possible involvement of Kir2.1. |
Q28141703 | Anion transport in heart |
Q43635172 | Apical membrane of native OMCD(i) cells has nonselective cation channels |
Q64251150 | Aquaporin Channels in the Heart-Physiology and Pathophysiology |
Q34805916 | Arginase and Arginine Decarboxylase - Where Do the Putative Gate Keepers of Polyamine Synthesis Reside in Rat Brain? |
Q34167570 | Assembly of ROMK1 (Kir 1.1a) inward rectifier K+ channel subunits involves multiple interaction sites |
Q62123995 | Basis of Cell Excitability and Cardiac Conduction System |
Q33775096 | Bimodal voltage dependence of TRPA1: mutations of a key pore helix residue reveal strong intrinsic voltage-dependent inactivation |
Q36436721 | Biophysical and molecular mechanisms underlying the modulation of heteromeric Kir4.1-Kir5.1 channels by CO2 and pH. |
Q34184957 | Block by extracellular divalent cations of Drosophila big brain channels expressed in Xenopus oocytes |
Q36436070 | Block of the Kir2.1 channel pore by alkylamine analogues of endogenous polyamines |
Q28345895 | Blockade of chloride channels reveals relaxations of rat small mesenteric arteries to raised potassium |
Q36908420 | Blocker protection by short spermine analogs: refined mapping of the spermine binding site in a Kir channel |
Q38819091 | Boosting the signal: Endothelial inward rectifier K+ channels |
Q37071006 | Caveolin-1 regulates corneal wound healing by modulating Kir4.1 activity |
Q30485783 | Cells of adult brain germinal zone have properties akin to hair cells and can be used to replace inner ear sensory cells after damage |
Q35938786 | Cellular mechanisms involved in CO(2) and acid signaling in chemosensitive neurons |
Q42056064 | Changes in inward rectifier K+ channels in hepatic stellate cells during primary culture. |
Q34375784 | Channelopathies: Kir2.1 mutations jeopardize many cell functions |
Q35187683 | Channels as taste receptors in vertebrates |
Q58212469 | Chapter 12 Potassium Channels with Two P Domains |
Q61178563 | Chapter 9 The Assembly of Inwardly Rectifying Potassium Channels |
Q33673386 | Characterization and functional restoration of a potassium channel Kir6.2 pore mutation identified in congenital hyperinsulinism |
Q77893179 | Characterization of the K+ channel opening effect of the anticonvulsant retigabine in PC12 cells |
Q92852955 | Characterization of the relaxin family peptide receptor 3 system in the mouse bed nucleus of the stria terminalis |
Q30837681 | Charged residues in the M2 region of alpha-hENaC play a role in channel conductance |
Q77609667 | Chemical basis for alkali cation selectivity in potassium-channel proteins |
Q37528283 | Cholesterol and Kir channels |
Q37705156 | Cholesterol and ion channels |
Q34494367 | Cholesterol sensitivity of KIR2.1 is controlled by a belt of residues around the cytosolic pore |
Q46973834 | Cholinergic modulation of Kir2 channels selectively elevates dendritic excitability in striatopallidal neurons. |
Q34502033 | Cigarette smoking impairs Na+-K+-ATPase activity in the human coronary microcirculation |
Q22007986 | Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney |
Q28577845 | Cloning, expression, and localization of a rat hepatocyte inwardly rectifying potassium channel |
Q28361734 | Comparison of cloned Kir2 channels with native inward rectifier K+ channels from guinea-pig cardiomyocytes |
Q39323368 | Complex rectification of Müller cell Kir currents. |
Q42236584 | Compound heterozygous mutations in the SUR1 (ABCC 8) subunit of pancreatic K(ATP) channels cause neonatal diabetes by perturbing the coupling between Kir6.2 and SUR1 subunits. |
Q90131372 | Computer simulations of protein-membrane systems |
Q92931649 | Conformational changes upon gating of KirBac1.1 into an open-activated state revealed by solid-state NMR and functional assays |
Q40328981 | Conformational dynamics of the ligand-binding domain of inward rectifier K channels as revealed by molecular dynamics simulations: toward an understanding of Kir channel gating. |
Q46437140 | Constitutively active G-protein-gated inwardly rectifying K+ channels in dendrites of hippocampal CA1 pyramidal neurons. |
Q34134124 | Contributions of intrinsic motor neuron properties to the production of rhythmic motor output in the mammalian spinal cord |
Q42580433 | Control of Kir channel gating by cytoplasmic domain interface interactions |
Q35715226 | Control of aldosterone secretion: a model for convergence in cellular signaling pathways |
Q36445028 | Control of rectification and gating of cloned KATP channels by the Kir6.2 subunit |
Q28360309 | Control of rectification and permeation by two distinct sites after the second transmembrane region in Kir2.1 K+ channel |
Q39866309 | Control of voltage-gated K+ channel permeability to NMDG+ by a residue at the outer pore. |
Q27646617 | Crystal Structure of the Eukaryotic Strong Inward-Rectifier K+ Channel Kir2.2 at 3.1 A Resolution |
Q40267294 | Cytoplasmic accumulation of long-chain coenzyme A esters activates KATP and inhibits Kir2.1 channels |
Q46536039 | Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification |
Q28353602 | Cytoplasmic polyamines as permeant blockers and modulators of the voltage-gated sodium channel |
Q43854347 | Cytoplasmic vestibule of the weak inward rectifier Kir6.2 potassium channel |
Q37872360 | Deciphering the mechanism(s) of action of natural products: analgesic peroxide oil as example |
Q37095382 | Decomposition of slide helix contributions to ATP-dependent inhibition of Kir6.2 channels |
Q40629496 | Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome |
Q42291160 | Dendritic GIRK Channels Gate the Integration Window, Plateau Potentials, and Induction of Synaptic Plasticity in Dorsal But Not Ventral CA1 Neurons. |
Q44859237 | Density-dependent changes of the pore properties of the P2X2 receptor channel |
Q39261263 | Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinism |
Q46593101 | Determinant role of membrane helices in K ATP channel gating |
Q45236615 | Different intracellular polyamine concentrations underlie the difference in the inward rectifier K(+) currents in atria and ventricles of the guinea-pig heart |
Q48151711 | Differential expression of intrinsic membrane currents in defined cell types of the anterolateral bed nucleus of the stria terminalis |
Q42503017 | Differential expression of potassium channels in placentas from normal and pathological pregnancies: targeting of the K(ir) 2.1 channel to lipid rafts |
Q24647286 | Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1 |
Q43192675 | Differential roles of blocking ions in KirBac1.1 tetramer stability |
Q37532733 | Differential subunit composition of the G protein-activated inward-rectifier potassium channel during cardiac development |
Q43559592 | Direct activation of cloned K(atp) channels by intracellular acidosis |
Q47153504 | Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins. |
Q58063090 | Divalent cation gating of an ammonium permeable channel in the symbiotic membrane from soybean nodules |
Q44814728 | Dopamine modulates inwardly rectifying potassium currents in medial prefrontal cortex pyramidal neurons. |
Q40019050 | Dual regulation of the ATP-sensitive potassium channel by activation of cGMP-dependent protein kinase |
Q40170511 | Dual regulation of the ATP-sensitive potassium channel by caffeine |
Q48272998 | Effect of catecholamines on the hyperpolarization-activated cationic Ih and the inwardly rectifying potassium I(Kir) currents in the rat substantia nigra pars compacta |
Q42121553 | Effect of spermine synthase deficiency on polyamine biosynthesis and content in mice and embryonic fibroblasts, and the sensitivity of fibroblasts to 1,3-bis-(2-chloroethyl)-N-nitrosourea |
Q87345457 | Effects of Ca2+-activated potassium and inward rectifier potassium channel on the differentiation of endothelial progenitor cells from human peripheral blood |
Q44049308 | Effects of chloride transport on bistable behaviour of the membrane potential in mouse skeletal muscle |
Q48921011 | Effects of intra- and extracellular acidifications on single channel Kir2.3 currents |
Q48568485 | Effects of leucine-enkephalin on potassium currents in neurons in the rat respiratory center in vitro |
Q90220566 | Electrocardiographic manifestations in severe hypokalemia |
Q42623732 | Electrokinetics of miniature K+ channel: open-state V sensitivity and inhibition by K+ driving force. |
Q45918890 | Electrophysiological properties of the microstome and macrostome morph of the polymorphic ciliate Tetrahymena vorax. |
Q54969469 | Electrophysiology of Hypokalemia and Hyperkalemia. |
Q38669157 | Endoplasmic reticulum-associated degradation of the renal potassium channel, ROMK, leads to type II Bartter syndrome |
Q54382820 | Endothelial progenitor cells functionally express inward rectifier potassium channels. |
Q48222364 | Enhanced ornithine decarboxylase activity is associated with attenuated rate of damage evolution and reduction of infarct volume in transient middle cerebral artery occlusion in the rat. |
Q61937212 | Estimulación vagal y remodelado eléctrico auricular |
Q28510686 | Evidence for direct physical association between a K+ channel (Kir6.2) and an ATP-binding cassette protein (SUR1) which affects cellular distribution and kinetic behavior of an ATP-sensitive K+ channel |
Q47888530 | Expression and coexpression of CO2-sensitive Kir channels in brainstem neurons of rats |
Q28355578 | Expression and permeation properties of the K(+) channel Kir7.1 in the retinal pigment epithelium |
Q28512133 | Expression of ATP-sensitive K+ channel subunits during perinatal maturation in the mouse heart |
Q24651542 | Expression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liver |
Q43215797 | Expression of inwardly rectifying potassium channel subunits in native human retinal pigment epithelium |
Q40287714 | Filter flexibility and distortion in a bacterial inward rectifier K+ channel: simulation studies of KirBac1.1. |
Q35061235 | Flexibility of the Kir6.2 inward rectifier K(+) channel pore |
Q30448604 | Fragile X syndrome: mechanistic insights and therapeutic avenues regarding the role of potassium channels. |
Q34718408 | Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: a battle between K(ATP) gain of channel activity and loss of channel expression. |
Q28284685 | Functional characterization of a prokaryotic Kir channel |
Q44688125 | Functional consequences of polyamine synthesis inhibition by L-alpha-difluoromethylornithine (DFMO): cellular mechanisms for DFMO-mediated ototoxicity |
Q43968153 | Functional expression of Kir 6.1/SUR1-K(ATP) channels in frog retinal Müller glial cells |
Q28256776 | Functional expression of Kir2.x in human aortic endothelial cells: the dominant role of Kir2.2 |
Q36908536 | Functional expression of Kir4.1 channels in spinal cord astrocytes |
Q24685031 | Functional expression of inward rectifier potassium channels in cultured human pulmonary smooth muscle cells: evidence for a major role of Kir2.4 subunits |
Q36968600 | Functional implications for Kir4.1 channels in glial biology: from K+ buffering to cell differentiation |
Q36295651 | Functional roles of charged amino acid residues on the wall of the cytoplasmic pore of Kir2.1. |
Q28294120 | GIRK4 confers appropriate processing and cell surface localization to G-protein-gated potassium channels |
Q31882890 | GTP-binding protein Gq mediates muscarinic-receptor-induced inhibition of the inwardly rectifying potassium channel IRK1 (Kir 2.1). |
Q35918682 | Gating currents associated with intramembrane charge displacement in HERG potassium channels |
Q40659405 | Gating dependence of inner pore access in inward rectifier K(+) channels |
Q48886814 | Gating of inward rectifier K+ channels by proton-mediated interactions of N- and C-terminal domains |
Q53815690 | Gating of the kir2.1 channel at the bundle crossing region by intracellular spermine and other cations. |
Q41732513 | General principles of the structure of ion channels |
Q28592574 | Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina |
Q52121482 | Genome-wide detection and family clustering of ion channels. |
Q28505249 | Golgi export of the Kir2.1 channel is driven by a trafficking signal located within its tertiary structure |
Q48485531 | Guanosine promotes the up-regulation of inward rectifier potassium current mediated by Kir4.1 in cultured rat cortical astrocytes |
Q35102994 | Heartburn: cardiac potassium channels involved in parietal cell acid secretion |
Q40077162 | Heterogeneity of IK1 in the mouse heart |
Q24530714 | Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome |
Q43656762 | Homeostatic control of presynaptic release is triggered by postsynaptic membrane depolarization |
Q37710852 | Homeostatic regulation of neuronal excitability by K(+) channels in normal and diseased brains |
Q36366011 | Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channels |
Q33283815 | Hypercholesterolemia suppresses Kir channels in porcine bone marrow progenitor cells in vivo |
Q73473089 | Hyperpolarization-activated cation currents in stellate and pyramidal neurons of rat entorhinal cortex |
Q42436719 | Hyperpolarization-activated cyclic nucleotide-gated channels in mouse vomeronasal sensory neurons. |
Q52572742 | Hyperpolarization-activated inward potassium and calcium-sensitive chloride currents in beating pacemaker insect neurosecretory cells (dorsal unpaired median neurons). |
Q51386641 | Hyperpolarization-activated, mixed-cation current (I(h)) in octopus cells of the mammalian cochlear nucleus. |
Q48464508 | Hypoxia activates ATP-dependent potassium channels in inspiratory neurones of neonatal mice |
Q42557038 | IK1 and cardiac hypoxia: after the long and short QT syndromes, what else can go wrong with the inward rectifier K+ currents? |
Q28202136 | Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels |
Q48847047 | Identification of a site involved in the block by extracellular Mg(2+) and Ba(2+) as well as permeation of K(+) in the Kir2.1 K(+) channel |
Q35716412 | Identification of the Conformational transition pathway in PIP2 Opening Kir Channels |
Q33412138 | Identification of thyroid hormone receptor binding sites and target genes using ChIP-on-chip in developing mouse cerebellum. |
Q40900685 | Immunolocalization of the arachidonic acid and mechanosensitive baseline traak potassium channel in the nervous system. |
Q35596819 | Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome |
Q44675448 | In skeletal muscle the relaxation of the resting membrane potential induced by K(+) permeability changes depends on Cl(-) transport |
Q34378622 | In vivo expression of a light-activatable potassium channel using unnatural amino acids |
Q28359677 | Increased inwardly rectifying potassium currents in HEK-293 cells expressing murine transient receptor potential 4 |
Q35490916 | Integrin α9β1-mediated cell migration in glioblastoma via SSAT and Kir4.2 potassium channel pathway |
Q36734643 | Integrins step up the pace of cell migration through polyamines and potassium channels |
Q97522071 | Intellectual Disability and Potassium Channelopathies: A Systematic Review |
Q38472529 | Interactions of natural polyamines with mammalian proteins |
Q37340622 | Intracellular ATP binding is required to activate the slowly activating K+ channel I(Ks) |
Q36842363 | Intracellular Mg2+ is a voltage-dependent pore blocker of HCN channels |
Q73490722 | Intracellular pH in mammalian stages of Trypanosoma cruzi is K+-dependent and regulated by H+-ATPases |
Q73337659 | Intracellular signalling pathways modulate K(ATP) channels in inspiratory brainstem neurones and their hypoxic activation: involvement of metabotropic receptors, G-proteins and cytoskeleton |
Q37377592 | Intrinsic voltage dependence of the epithelial Na+ channel is masked by a conserved transmembrane domain tryptophan. |
Q57178143 | Investigating Potassium Channels in Budding Yeast: A Genetic Sandbox |
Q42754613 | Involvement of inward rectifier and M-type currents in carbachol-induced epileptiform synchronization |
Q28551706 | Inward Rectifier K+ Currents Are Regulated by CaMKII in Endothelial Cells of Primarily Cultured Bovine Pulmonary Arteries |
Q33852328 | Inward rectification in KATP channels: a pH switch in the pore. |
Q42629234 | Inward rectifier K(+) channel Kir2.3 (IRK3) in reactive astrocytes from adult rat brain |
Q63246497 | Inward rectifier potassium (Kir) channels mediate salivary gland function and blood feeding in the lone star tick, Amblyomma americanum |
Q26865121 | Inward rectifiers and their regulation by endogenous polyamines |
Q48337808 | Inward-rectifying membrane currents activated by hyperpolarization in immature rat olfactory cortex neurones in vitro |
Q28506559 | Inwardly rectifying potassium channel Kir4.1 is responsible for the native inward potassium conductance of satellite glial cells in sensory ganglia |
Q36430849 | Inwardly rectifying potassium channels (Kir) in central nervous system glia: a special role for Kir4.1 in glial functions |
Q28575801 | Inwardly rectifying potassium channels in rat retinal ganglion cells |
Q33712453 | Inwardly rectifying potassium channels. |
Q26829681 | Ion Channels in the Heart |
Q57176937 | Ion Channels in the Paraventricular Hypothalamic Nucleus (PVN); Emerging Diversity and Functional Roles |
Q28087459 | Ion channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac death |
Q36681454 | Ion channels and calcium signaling in cerebral arteries following subarachnoid hemorrhage |
Q53287029 | Ion channels and transporters in cancer. 3. Ion channels in the tumor cell-microenvironment cross talk. |
Q33821521 | Ion channels and vascular tone |
Q73666122 | Ion channels in glial cells |
Q34469912 | Ion conduction through the hERG potassium channel |
Q36422478 | KATP Channels in the Cardiovascular System |
Q36758886 | Kainate receptor pore-forming and auxiliary subunits regulate channel block by a novel mechanism |
Q34354013 | Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling |
Q40959711 | Kir 4.1 channel expression in neuroblastomaxglioma hybrid NG108-15 cell line |
Q44180875 | Kir2.4 and Kir2.1 K(+) channel subunits co-assemble: a potential new contributor to inward rectifier current heterogeneity |
Q37124248 | KirBac1.1: it's an inward rectifying potassium channel |
Q34414845 | Lack of negatively charged residues at the external mouth of Kir2.2 channels enable the voltage-dependent block by external Mg2+. |
Q57458238 | Linkage analysis reveals allosteric coupling in Kir2.1 channels |
Q92646547 | Lipopolysaccharides increase Kir2.1 expression in lung endothelial cells |
Q40404510 | Long chain CoA esters as competitive antagonists of phosphatidylinositol 4,5-bisphosphate activation in Kir channels |
Q44619532 | Long-chain acyl-CoA esters and phosphatidylinositol phosphates modulate ATP inhibition of KATP channels by the same mechanism |
Q36980037 | Long-pore electrostatics in inward-rectifier potassium channels |
Q34372355 | Lysophosphatidic acid-operated K+ channels. |
Q44654343 | Mammalian retinal bipolar cells express inwardly rectifying K+ currents (IKir) with a different distribution than that of Ih. |
Q37685010 | Mapping the function of neuronal ion channels in model and experiment |
Q44238745 | Mechanisms of dopamine activation of fast-spiking interneurons that exert inhibition in rat prefrontal cortex |
Q26749114 | Mechanisms of lipid regulation and lipid gating in TRPC channels |
Q27024176 | Mechanisms of sudden cardiac death: oxidants and metabolism |
Q43701707 | Membrane properties of principal neurons of the lateral superior olive |
Q36412396 | Mg2+-dependent gating and strong inward rectification of the cation channel TRPV6. |
Q36901703 | Mislocalization of Kir channels in malignant glia |
Q33896746 | Mitochondria and arrhythmias. |
Q38201407 | Mitochondrial channels: ion fluxes and more |
Q35542470 | Mitochondrial potassium transport: the K(+) cycle. |
Q34044898 | Modulation of the heteromeric Kir4.1-Kir5.1 channel by multiple neurotransmitters via Galphaq-coupled receptors |
Q43765118 | Modulation of the heteromeric Kir4.1-Kir5.1 channels by P(CO(2)) at physiological levels |
Q43640015 | Modulation of the hyperpolarisation-activated current, Ih, in rat facial motoneurones in vitro by ZD-7288. |
Q34285417 | Molecular Mechanisms of EAST/SeSAME Syndrome Mutations in Kir4.1 (KCNJ10) |
Q34800154 | Molecular aspects of structure, gating, and physiology of pH-sensitive background K2P and Kir K+-transport channels |
Q34457174 | Molecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome |
Q36445674 | Molecular basis of inward rectification: polyamine interaction sites located by combined channel and ligand mutagenesis |
Q44592821 | Molecular basis of ion selectivity, block, and rectification of the inward rectifier Kir3.1/Kir3.4 K(+) channel |
Q31817227 | Molecular biology of K(+) channels and their role in cardiac arrhythmias |
Q40524509 | Molecular characterization of an inward rectifier channel (IKir) found in avian vestibular hair cells: cloning and expression of pKir2.1. |
Q47822765 | Molecular determinants for the distinct pH sensitivity of Kir1.1 and Kir4.1 channels. |
Q33888944 | Molecular determinants of KATP channel inhibition by ATP. |
Q47287191 | Molecular determinants responsible for differential cellular distribution of G protein-gated inwardly rectifying K+ channels |
Q34534301 | Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2. |
Q33728388 | Molecular diversity and regulation of renal potassium channels |
Q48848783 | Molecular mechanism of a COOH-terminal gating determinant in the ROMK channel revealed by a Bartter's disease mutation |
Q34337751 | Molecular properties and physiological roles of ion channels in the immune system |
Q35566998 | Molecular substrates of potassium spatial buffering in glial cells. |
Q36411979 | Monovalent permeability, rectification, and ionic block of store-operated calcium channels in Jurkat T lymphocytes |
Q28216225 | Mouse model of Prinzmetal angina by disruption of the inward rectifier Kir6.1 |
Q43565372 | Mouse taste cells with glialike membrane properties |
Q33726168 | Multi-ion versus single-ion conduction mechanisms can yield current rectification in biological ion channels |
Q42953307 | Multiple Firing Patterns in Deep Dorsal Horn Neurons of the Spinal Cord: Computational Analysis of Mechanisms and Functional Implications |
Q41014688 | Multiple promoter elements interact to control the transcription of the potassium channel gene, KCNJ2. |
Q41679311 | Muscarinic receptor activity has multiple effects on the resting membrane potentials of CA1 hippocampal interneurons. |
Q36477647 | Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degeneration |
Q24291252 | Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome |
Q24295040 | Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis |
Q51824425 | Na(+)-induced inward rectification in the two-pore domain K(+) channel, TASK-2. |
Q59113089 | Nanomaterials-Based Approaches for the Modulation of Sodium Bicarbonate Cotransporters |
Q35089876 | Naringin directly activates inwardly rectifying potassium channels at an overlapping binding site to tertiapin-Q. |
Q48939796 | Neuronal nicotinic acetylcholine receptors are blocked by intracellular spermine in a voltage-dependent manner. |
Q32014780 | Neuroprotective role of ornithine decarboxylase activation in transient focal cerebral ischaemia: a study using ornithine decarboxylase-overexpressing transgenic rats |
Q37783442 | New Insights into the Regulation of Ion Channels by Integrins |
Q42520063 | Nitric oxide activates leak K+ currents in the presumed cholinergic neuron of basal forebrain |
Q36755104 | Novel KCNJ10 Gene Variations Compromise Function of Inwardly Rectifying Potassium Channel 4.1. |
Q73704038 | Novel inhibition of gbetagamma-activated potassium currents induced by M(2) muscarinic receptors via a pertussis toxin-insensitive pathway |
Q28564824 | Novel nucleotide-binding sites in ATP-sensitive potassium channels formed at gating interfaces |
Q36436003 | Octameric stoichiometry of the KATP channel complex |
Q53928937 | Odorants suppress a voltage-activated K+ conductance in rat olfactory neurons. |
Q35091057 | Oep23 forms an ion channel in the chloroplast outer envelope |
Q48906675 | Opposite effects of pH on open-state probability and single channel conductance of kir4.1 channels |
Q41821808 | Overexpression of antizyme in the hearts of transgenic mice prevents the isoprenaline-induced increase in cardiac ornithine decarboxylase activity and polyamines, but does not prevent cardiac hypertrophy. |
Q41875615 | Overproduction of cardiac S-adenosylmethionine decarboxylase in transgenic mice. |
Q33925775 | Oxidation of polyamines and brain injury |
Q42031021 | PIP(2)-binding site in Kir channels: definition by multiscale biomolecular simulations. |
Q47322426 | Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men. |
Q36956861 | Parvalbumin-positive basket interneurons in monkey and rat prefrontal cortex |
Q36445212 | Permeant ion-dependent changes in gating of Kir2.1 inward rectifier potassium channels |
Q36436110 | Permeation and gating of an inwardly rectifying potassium channel. Evidence for a variable energy well |
Q36444965 | Permeation properties of inward-rectifier potassium channels and their molecular determinants |
Q36339192 | Pharmacogenetics and cardiac ion channels |
Q28533988 | Pharmacologic Approach to Defective Protein Trafficking in the E637K-hERG Mutant with PD-118057 and Thapsigargin |
Q38849787 | Pharmacological Conversion of a Cardiac Inward Rectifier into an Outward Rectifier Potassium Channel |
Q37409971 | Pharmacological rescue of trafficking-impaired ATP-sensitive potassium channels |
Q44270128 | Phosphatidylinositol 4,5-bisphosphate (PIP2) modulation of ATP and pH sensitivity in Kir channels. A tale of an active and a silent PIP2 site in the N terminus |
Q48893530 | Phosphatidylinositol 4,5-bisphosphate and intracellular pH regulate the ROMK1 potassium channel via separate but interrelated mechanisms |
Q36829579 | Phosphoinositide-mediated gating of inwardly rectifying K(+) channels |
Q52642500 | Phylogenomic analysis and evolution of the potassium channel gene family. |
Q28211116 | Plasticity of KIR channels in human smooth muscle cells from internal thoracic artery |
Q39985852 | Polyamine block of inwardly rectifying potassium channels |
Q44578383 | Polyamine flux in Xenopus oocytes through hemi-gap junctional channels |
Q36784291 | Polyamine transport by the polyspecific organic cation transporters OCT1, OCT2, and OCT3 |
Q44297173 | Polyamine transport, accumulation, and release in brain. |
Q58544820 | Polyamine-mediated channel block of ionotropic glutamate receptors and its regulation by auxiliary proteins |
Q58544829 | Polyamines and potassium channels: A twenty five year romance |
Q34039970 | Polyamines as gating molecules of inward-rectifier K+ channels |
Q52163217 | Postnatal development of electrophysiological properties of nucleus accumbens neurons. |
Q51803978 | Postnatal developmental decline in IK1 in mouse ventricular myocytes isolated by the Langendorff perfusion method: comparison with the chunk method. |
Q34370562 | Potassium buffering in the central nervous system |
Q28710101 | Potassium channels in articular chondrocytes |
Q38151974 | Potassium channels: structures, diseases, and modulators |
Q39332633 | Potentiation of EDHF-mediated relaxation by chloride channel blockers |
Q32063793 | Probing ion permeation and gating in a K+ channel with backbone mutations in the selectivity filter. |
Q77357162 | Probing pore topology and conformational changes of Kir2.1 potassium channels by cysteine scanning mutagenesis |
Q34005054 | Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration |
Q43948742 | Properties of an inwardly rectifying K(+) channel in the basolateral membrane of mouse TAL. |
Q28250776 | Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins |
Q39672793 | Purinergic P2Y1 Receptors Control Rapid Expression of Plasma Membrane Processes in Hippocampal Astrocytes. |
Q37942127 | Reactive oxygen species inactivate neuronal nicotinic acetylcholine receptors through a highly conserved cysteine near the intracellular mouth of the channel: implications for diseases that involve oxidative stress |
Q43683622 | Redox-dependent gating of G protein-coupled inwardly rectifying K+ channels |
Q40387218 | Regulation of ATP-sensitive potassium channel function by protein kinase A-mediated phosphorylation in transfected HEK293 cells |
Q36372211 | Regulation of ROMK1 channel by protein kinase A via a phosphatidylinositol 4,5-bisphosphate-dependent mechanism |
Q38111276 | Regulation of ion channels by membrane lipids |
Q36986504 | Regulation of ion transport proteins by membrane phosphoinositides |
Q37288568 | Regulation of potassium (K) handling in the renal collecting duct |
Q44196779 | Regulation of the inward rectifying properties of G-protein-activated inwardly rectifying K+ (GIRK) channels by Gbeta gamma subunits |
Q51017878 | Relationship between Kir2.1/Kir2.3 activity and their distributions between cholesterol-rich and cholesterol-poor membrane domains. |
Q74007784 | Residues beyond the selectivity filter of the K+ channel kir2.1 regulate permeation and block by external Rb+ and Cs+ |
Q36295697 | Ring of negative charge in BK channels facilitates block by intracellular Mg2+ and polyamines through electrostatics |
Q38821145 | Role and mechanisms of regulation of the basolateral Kir 4.1/Kir 5.1K+ channels in the distal tubules |
Q40079176 | Role of Kir4.1 channels in growth control of glia |
Q36282875 | Role of a Hydrophobic Pocket in Polyamine Interactions with the Polyspecific Organic Cation Transporter OCT3 |
Q48611494 | Role of amino terminus in voltage gating and junctional rectification of Shaking B innexins |
Q47679110 | Role of an inward rectifier K+ current and of hyperpolarization in human myoblast fusion |
Q34539565 | Scanning the topography of polyamine blocker binding in an inwardly rectifying potassium channel. |
Q43743310 | Second transmembrane domains of ENaC subunits contribute to ion permeation and selectivity |
Q88764238 | Select α-arrestins control cell-surface abundance of the mammalian Kir2.1 potassium channel in a yeast model |
Q36436571 | Ser165 in the second transmembrane region of the Kir2.1 channel determines its susceptibility to blockade by intracellular Mg2+. |
Q92404928 | Shear-Stress Sensitive Inwardly-Rectifying K+ Channels Regulate Developmental Retinal Angiogenesis by Vessel Regression |
Q36445134 | Single channel analysis of conductance and rectification in cation-selective, mutant glycine receptor channels |
Q40734306 | Site-directed glycosylation tagging of functional Kir2.1 reveals that the putative pore-forming segment is extracellular |
Q33603023 | Small-molecule modulators of inward rectifier K+ channels: recent advances and future possibilities |
Q39195631 | Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles |
Q77793146 | Spatial attention and latencies of saccadic eye movements |
Q73804989 | Spatial distribution of spermine/spermidine content and K(+)-current rectification in frog retinal glial (Müller) cells |
Q34470673 | Specificity of activation by phosphoinositides determines lipid regulation of Kir channels |
Q45086510 | Spermine synthesis is required for normal viability, growth, and fertility in the mouse |
Q32037131 | Splitting the two pore domains from TOK1 results in two cationic channels with novel functional properties |
Q36436497 | Stabilization of the activity of ATP-sensitive potassium channels by ion pairs formed between adjacent Kir6.2 subunits |
Q26858790 | State-dependent and reflex drives to the upper airway: basic physiology with clinical implications |
Q88801808 | Stem Cells from Human Exfoliated Deciduous Teeth Modulate Early Astrocyte Response after Spinal Cord Contusion |
Q26853670 | Stop the flow: a paradigm for cell signaling mediated by reactive oxygen species in the pulmonary endothelium |
Q54046109 | Store-Operated Calcium Channels. |
Q36445287 | Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels |
Q37216161 | Structural basis of control of inward rectifier Kir2 channel gating by bulk anionic phospholipids |
Q27640256 | Structural basis of inward rectification: cytoplasmic pore of the G protein-gated inward rectifier GIRK1 at 1.8 A resolution |
Q42673793 | Structural determinants and specificities for ROMK1-phosphoinositide interaction |
Q34170208 | Structural determinants of gating in inward-rectifier K+ channels |
Q43082643 | Structural rearrangements underlying ligand-gating in Kir channels |
Q48038633 | Structure, chromosome localization, and tissue distribution of the mouse twik K+ channel gene |
Q45251275 | Subunit stoichiometry of the Kir1.1 channel in proton-dependent gating |
Q28141759 | Suppression of Kir2.3 activity by protein kinase C phosphorylation of the channel protein at threonine 53 |
Q41679325 | Supralinear summation of synaptic inputs by an invertebrate neuron: dendritic gain is mediated by an "inward rectifier" K(+) current |
Q36435882 | Swelling-activated Gd3+-sensitive cation current and cell volume regulation in rabbit ventricular myocytes |
Q30360691 | Synaptic control of motoneuronal excitability. |
Q30442683 | Synergistic activation of G protein-gated inwardly rectifying potassium channels by the betagamma subunits of G proteins and Na(+) and Mg(2+) ions |
Q24338758 | TMEM175 Is an Organelle K(+) Channel Regulating Lysosomal Function |
Q44408343 | Tamoxifen inhibits Na+ and K+ currents in rat ventricular myocytes |
Q46888987 | Tetrameric subunit structure of the native brain inwardly rectifying potassium channel Kir 2.2. |
Q57927442 | The Biology of Glial Cells and Their Complex Roles in Alzheimer's Disease: New Opportunities in Therapy |
Q55137607 | The Effects of Buthotus schach Scorpion Venom on Electrophysiological Properties of Magnocellular Neurons of Rat Supraoptic Nucleus. |
Q39363477 | The Slo(w) path to identifying the mitochondrial channels responsible for ischemic protection |
Q36660603 | The alpha9beta1 integrin enhances cell migration by polyamine-mediated modulation of an inward-rectifier potassium channel |
Q42610159 | The bundle crossing region is responsible for the inwardly rectifying internal spermine block of the Kir2.1 channel. |
Q34476854 | The epithelial inward rectifier channel Kir7.1 displays unusual K+ permeation properties. |
Q28728048 | The function and molecular identity of inward rectifier channels in vestibular hair cells of the mouse inner ear |
Q44041552 | The low conductance K(+) channel in human colonic crypt cells has a voltage-dependent permeability not affected by Mg(++). |
Q36446243 | The molecular basis of chloroquine block of the inward rectifier Kir2.1 channel |
Q36295661 | The polyamine binding site in inward rectifier K+ channels. |
Q37418212 | The role of ATP-sensitive potassium channels in cellular function and protection in the cardiovascular system |
Q30414096 | The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss |
Q38278661 | The role of glia in stress: polyamines and brain disorders |
Q40989149 | The role of hydrophobic interactions in binding of polyamines to non NMDA receptor ion channels |
Q36296035 | The role of the cytoplasmic pore in inward rectification of Kir2.1 channels |
Q36335244 | The short QT syndrome as a paradigm to understand the role of potassium channels in ventricular fibrillation |
Q34744944 | The surprising role of vascular K(ATP) channels in vasospastic angina |
Q38793871 | The therapeutic agents that target ATP-sensitive potassium channels |
Q47823875 | The therapeutic potential of targeting the Kir1.1 (renal outer medullary K+) channel. |
Q39325298 | Three pairs of weak interactions precisely regulate the G-loop gate of Kir2.1 channel |
Q35566056 | Toward an understanding of the molecular mechanisms of ventricular fibrillation |
Q30658648 | Transmembrane structure of an inwardly rectifying potassium channel |
Q40477316 | Two Kir2.1 channel populations with different sensitivities to Mg(2+) and polyamine block: a model for the cardiac strong inward rectifier K(+) channel. |
Q47867509 | Two independent but synchronized Gβγ subunit-controlled pathways are essential for trailing-edge retraction during macrophage migration. |
Q40192067 | Unitary conductance variation in Kir2.1 and in cardiac inward rectifier potassium channels |
Q35816522 | Use of knock-out mouse models for the study of renal ion channels. |
Q84471499 | Vagal stimulation and atrial electrical remodeling |
Q39672661 | Variable loss of Kir4.1 channel function in SeSAME syndrome mutations. |
Q53808682 | WITHDRAWN: Discovery of SHR1977: A highly potent and selective ROMK inhibitor. |
Q35185504 | What are the roles of the many different types of potassium channel expressed in cerebellar granule cells? |
Q34265101 | X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome |
Q75344252 | [Ionic currents and ventricular fibrillation dynamics] |
Q47869205 | pH dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia |
Q36787083 | pH gating of ROMK (K(ir)1.1) channels: control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome |
Q38330465 | pH-dependent gating of ROMK (Kir1.1) channels involves conformational changes in both N and C termini |
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