Channelpedia

Kir4.1 Channel

363 automatically matched literature references

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Su XT et al. Disruption of KCNJ10 (Kir4.1) stimulates the expression of ENaC in the collecting duct.
Am. J. Physiol. Renal Physiol., 2016 May 1 , 310 (F985-93).

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Najafi E et al. Inwardly rectifying potassium channel 4.1 expression in post-traumatic syringomyelia.
Neuroscience, 2016 Mar 11 , 317 (23-35).

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Pröbstel AK et al. Multiple Sclerosis and Antibodies against KIR4.1.
N. Engl. J. Med., 2016 Apr 14 , 374 (1496-8).

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Chastre A et al. Evaluation of KIR4.1 as an Immune Target in Multiple Sclerosis.
N. Engl. J. Med., 2016 Apr 14 , 374 (1495-6).

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de Baaij JH et al. P2X6 Knockout Mice Exhibit Normal Electrolyte Homeostasis.
PLoS ONE, 2016 , 11 (e0156803).

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Weller J et al. pH-Sensitive K(+) Currents and Properties of K2P Channels in Murine Hippocampal Astrocytes.
Adv Protein Chem Struct Biol, 2016 , 103 (263-94).

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Olsen ML et al. New Insights on Astrocyte Ion Channels: Critical for Homeostasis and Neuron-Glia Signaling.
J. Neurosci., 2015 Oct 14 , 35 (13827-35).

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Jukkola P et al. Regulation of neurovascular coupling in autoimmunity to water and ion channels.
Autoimmun Rev, 2015 Mar , 14 (258-67).

16

Sibille J et al. The neuroglial potassium cycle during neurotransmission: role of Kir4.1 channels.
PLoS Comput. Biol., 2015 Mar , 11 (e1004137).

17

Dai AI et al. Contribution of KCNJ10 gene polymorphisms in childhood epilepsy.
J. Child Neurol., 2015 Mar , 30 (296-300).

18

Zhang C et al. KCNJ10 (Kir4.1) is expressed in the basolateral membrane of the cortical thick ascending limb.
Am. J. Physiol. Renal Physiol., 2015 Jun 1 , 308 (F1288-96).

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Lunde LK et al. Postnatal development of the molecular complex underlying astrocyte polarization.
Brain Struct Funct, 2015 Jul , 220 (2087-101).

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Chen J et al. [EAST/SeSAME syndrome and functional expression of inward rectifier potassium channel Kir4.1 in the inner ear].
Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi, 2015 Jul , 29 (1318-22).

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Tanemoto M et al. Mislocalization of K+ channels causes the renal salt wasting in EAST/SeSAME syndrome.
FEBS Lett., 2014 Mar 18 , 588 (899-905).

43

Schirmer L et al. Differential loss of KIR4.1 immunoreactivity in multiple sclerosis lesions.
Ann. Neurol., 2014 Jun , 75 (810-28).

44

Khakh BS et al. Astrocytes and Huntington's disease.
ACS Chem Neurosci, 2014 Jul 16 , 5 (494-6).

46

Chen C et al. Role of interleukin-1β in hypoxia-induced depression of glutamate uptake in retinal Müller cells.
Graefes Arch. Clin. Exp. Ophthalmol., 2014 Jan , 252 (51-8).

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Killock D Multiple sclerosis: KIR4.1 as an autoantigen in MS--new questions raised.
Nat Rev Neurol, 2014 Aug , 10 (426).

53

Filippi M et al. KIR4.1: another misleading expectation in multiple sclerosis?
Lancet Neurol, 2014 Aug , 13 (753-5).

54

Sukigara S et al. Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy.
J. Neuropathol. Exp. Neurol., 2014 Aug , 73 (798-806).

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58

Jeong HK et al. Astrogliosis is a possible player in preventing delayed neuronal death.
Mol. Cells, 2014 Apr , 37 (345-55).

64

Takiguchi Y et al. Long-lasting changes in the cochlear K+ recycling structures after acute energy failure.
Neurosci. Res., 2013 Sep-Oct , 77 (33-41).

67

Cross JH et al. Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome.
Dev Med Child Neurol, 2013 Sep , 55 (846-56).

73

Zaika OL et al. Direct inhibition of basolateral Kir4.1/5.1 and Kir4.1 channels in the cortical collecting duct by dopamine.
Am. J. Physiol. Renal Physiol., 2013 Nov 1 , 305 (F1277-87).

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Kara B et al. KCNJ10 gene mutation in an 8-year-old boy with seizures.
Acta Neurol Belg, 2013 Mar , 113 (75-7).

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Denton JS et al. Invited Review - Novel Diuretic Targets.
Am. J. Physiol. Renal Physiol., 2013 Jul 17 , ().

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Maldonado PP et al. Oligodendrocyte precursor cells are accurate sensors of local K+ in mature gray matter.
J. Neurosci., 2013 Feb 6 , 33 (2432-42).

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Methner A et al. Multiple sclerosis in 2012: Novel therapeutic options and drug targets in MS.
Nat Rev Neurol, 2013 Feb , 9 (72-3).

87

Parrock S et al. KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16.
Nephron Physiol, 2013 , 123 (7-14).

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Srivastava R et al. Potassium channel KIR4.1 as an immune target in multiple sclerosis.
N. Engl. J. Med., 2012 Jul 12 , 367 (115-23).

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108

Cirello V et al. Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss.
Mol. Cell. Endocrinol., 2012 Apr 4 , 351 (342-50).

113

Olsen M Examining potassium channel function in astrocytes.
Methods Mol. Biol., 2012 , 814 (265-81).

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Morris LM et al. Mouse middle ear ion homeostasis channels and intercellular junctions.
PLoS ONE, 2012 , 7 (e39004).

117

Zhang X et al. The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome.
Am. J. Physiol., Cell Physiol., 2011 Sep , 301 (C729-38).

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Edvinsson JM et al. Kir4.1 K (+) channels are regulated by external cations.
, 2011 May 1 , 5 ().

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Prüss H et al. Potassium channel expression in adult murine neural progenitor cells.
Neuroscience, 2011 Apr 28 , 180 (19-29).

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Thompson DA et al. Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome.
J. Physiol. (Lond.), 2011 Apr 1 , 589 (1681-9).

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Freudenthal B et al. KCNJ10 mutations disrupt function in patients with EAST syndrome.
Nephron Physiol, 2011 , 119 (p40-8).

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Wagner CA New roles for renal potassium channels.
J. Nephrol., 2010 Jan-Feb , 23 (5-8).

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Tang X et al. Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
Biochem. Biophys. Res. Commun., 2010 Sep 3 , 399 (537-41).

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San-Cristobal P et al. Novel molecular pathways in renal Mg2+ transport: a guided tour along the nephron.
Curr. Opin. Nephrol. Hypertens., 2010 Sep , 19 (456-62).

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Wang WH et al. Regulation and function of potassium channels in aldosterone-sensitive distal nephron.
Curr. Opin. Nephrol. Hypertens., 2010 Sep , 19 (463-70).

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Sala-Rabanal M et al. Molecular mechanisms of EAST/SeSAME syndrome mutations in Kir4.1 (KCNJ10).
J. Biol. Chem., 2010 Nov 12 , 285 (36040-8).

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Rosenhouse-Dantsker A et al. Comparative analysis of cholesterol sensitivity of Kir channels: Role of the CD loop.
Channels (Austin), 2010 Jan 20 , 4 ().

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McCoy E et al. MAPK induces AQP1 expression in astrocytes following injury.
Glia, 2010 Jan 15 , 58 (209-17).

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Huang C et al. Novel Ca receptor signaling pathways for control of renal ion transport.
Curr. Opin. Nephrol. Hypertens., 2010 Jan , 19 (106-12).

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Williams DM et al. Molecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome.
J. Am. Soc. Nephrol., 2010 Dec , 21 (2117-29).

166

Ren H et al. Müller cells upregulate the expression of SAP97 in light-injured rat retina.
Neuroreport, 2010 Aug 23 , 21 (832-6).

170

Dibas A et al. Changes in ocular aquaporin expression following optic nerve crush.
Mol. Vis., 2010 , 16 (330-40).

172

Søe R et al. Modulation of Kir4.1 and Kir4.1-Kir5.1 channels by extracellular cations.
Biochim. Biophys. Acta, 2009 Sep , 1788 (1706-13).

173

Shang L et al. Kir5.1 underlies long-lived subconductance levels in heteromeric Kir4.1/Kir5.1 channels from Xenopus tropicalis.
Biochem. Biophys. Res. Commun., 2009 Oct 23 , 388 (501-5).

174

Satz JS et al. Visual impairment in the absence of dystroglycan.
J. Neurosci., 2009 Oct 21 , 29 (13136-46).

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Bockenhauer D et al. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
N. Engl. J. Med., 2009 May 7 , 360 (1960-70).

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Rehak M et al. Retinal gene expression and Müller cell responses after branch retinal vein occlusion in the rat.
Invest. Ophthalmol. Vis. Sci., 2009 May , 50 (2359-67).

180

Pegg AE et al. Mouse models to investigate the function of spermine.
Commun Integr Biol, 2009 May , 2 (271-4).

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Zou SB et al. Role of potassium channel gene Kcnj10 in ethanol preference in C57bl/6J and DBA/2J mice.
Alcohol. Clin. Exp. Res., 2009 Mar , 33 (394-9).

183

Soe R et al. Modulation of Kir4.1 and Kir4.1-Kir5.1 channels by small changes in cell volume.
Neurosci. Lett., 2009 Jun 26 , 457 (80-4).

184

Yuan S et al. Increased sensitivity to retinal light damage in aquaporin-4 knockout mice.
Exp. Eye Res., 2009 Jun 15 , 89 (119-22).

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Shi M et al. The EAST syndrome and KCNJ10 mutations.
N. Engl. J. Med., 2009 Aug 6 , 361 (630; author reply 630-1).

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Tanemoto M et al. MAGI-1a functions as a scaffolding protein for the distal renal tubular basolateral K+ channels.
J. Biol. Chem., 2008 May 2 , 283 (12241-7).

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Kucheryavykh YV et al. Complex rectification of Müller cell Kir currents.
Glia, 2008 May , 56 (775-90).

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Yamamoto Y et al. Expression of inwardly rectifying K+ channels in the carotid body of rat.
Histol. Histopathol., 2008 Jul , 23 (799-806).

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Zhang H et al. Aquaporin-4 independent Kir4.1 K+ channel function in brain glial cells.
Mol. Cell. Neurosci., 2008 Jan , 37 (1-10).

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Machida S et al. Photopic ERG negative response from amacrine cell signaling in RCS rat retinal degeneration.
Invest. Ophthalmol. Vis. Sci., 2008 Jan , 49 (442-52).

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Iandiev I et al. Müller cell response to blue light injury of the rat retina.
Invest. Ophthalmol. Vis. Sci., 2008 Aug , 49 (3559-67).

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Iandiev I et al. Localization of glial aquaporin-4 and Kir4.1 in the light-injured murine retina.
Neurosci. Lett., 2008 Apr 4 , 434 (317-21).

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Zou J et al. Progressive hearing loss in mice with a mutated vitamin D receptor gene.
Audiol. Neurootol., 2008 , 13 (219-30).

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Kucheryavykh YV et al. Polyamine permeation and rectification of Kir4.1 channels.
Channels (Austin), 2007 May-Jun , 1 (172-8).

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Rojas A et al. Protein kinase C dependent inhibition of the heteromeric Kir4.1-Kir5.1 channel.
Biochim. Biophys. Acta, 2007 Sep , 1768 (2030-42).

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Lucarini N et al. Genetic polymorphisms and idiopathic generalized epilepsies.
Pediatr. Neurol., 2007 Sep , 37 (157-64).

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Ohno Y et al. Inhibition of astroglial Kir4.1 channels by selective serotonin reuptake inhibitors.
Brain Res., 2007 Oct 31 , 1178 (44-51).

227

Boor I et al. MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeet.
Acta Neuropathol., 2007 Oct , 114 (403-10).

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Lang F et al. Functional significance of channels and transporters expressed in the inner ear and kidney.
Am. J. Physiol., Cell Physiol., 2007 Oct , 293 (C1187-208).

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Reichenbach A et al. Müller cells as players in retinal degeneration and edema.
Graefes Arch. Clin. Exp. Ophthalmol., 2007 May , 245 (627-36).

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Metea MR et al. Neurovascular coupling is not mediated by potassium siphoning from glial cells.
J. Neurosci., 2007 Mar 7 , 27 (2468-71).

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Higashimori H et al. Role of Kir4.1 channels in growth control of glia.
Glia, 2007 Dec , 55 (1668-79).

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Iandiev I et al. Glial cell reactivity in a porcine model of retinal detachment.
Invest. Ophthalmol. Vis. Sci., 2006 May , 47 (2161-71).

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Iandiev I et al. Differential regulation of Kir4.1 and Kir2.1 expression in the ischemic rat retina.
Neurosci. Lett., 2006 Mar 27 , 396 (97-101).

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Iandiev I et al. Atypical gliosis in Müller cells of the slowly degenerating rds mutant mouse retina.
Exp. Eye Res., 2006 Mar , 82 (449-57).

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Mao X et al. Aquaporin 4 changes in rat brain with severe hydrocephalus.
Eur. J. Neurosci., 2006 Jun , 23 (2929-36).

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Connors NC et al. Potassium channel Kir4.1 macromolecular complex in retinal glial cells.
Glia, 2006 Jan 15 , 53 (124-31).

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Olsen ML et al. Functional expression of Kir4.1 channels in spinal cord astrocytes.
Glia, 2006 Apr 1 , 53 (516-28).

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Tanemoto M et al. PDZ-binding and di-hydrophobic motifs regulate distribution of Kir4.1 channels in renal cells.
J. Am. Soc. Nephrol., 2005 Sep , 16 (2608-14).

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Tenckhoff S et al. Diversity of aquaporin mRNA expressed by rat and human retinas.
Neuroreport, 2005 Jan 19 , 16 (53-6).

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Pannicke T et al. Ocular inflammation alters swelling and membrane characteristics of rat Müller glial cells.
J. Neuroimmunol., 2005 Apr , 161 (145-54).

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Wu J et al. Contribution of Kir4.1 to the mouse electroretinogram.
Mol. Vis., 2004 Sep 1 , 10 (650-4).

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Nishijima K et al. Taste buds and nerve fibers in the rat larynx: an ultrastructural and immunohistochemical study.
Arch. Histol. Cytol., 2004 Sep , 67 (195-209).

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Wu JV et al. An inwardly rectifying potassium channel in apical membrane of Calu-3 cells.
J. Biol. Chem., 2004 Nov 5 , 279 (46558-65).

273

Malinowska DH et al. Gastric parietal cell secretory membrane contains PKA- and acid-activated Kir2.1 K+ channels.
Am. J. Physiol., Cell Physiol., 2004 Mar , 286 (C495-506).

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Wu J et al. Expression and coexpression of CO2-sensitive Kir channels in brainstem neurons of rats.
J. Membr. Biol., 2004 Feb 1 , 197 (179-91).

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Tanemoto M et al. PDZ binding motif-dependent localization of K+ channel on the basolateral side in distal tubules.
Am. J. Physiol. Renal Physiol., 2004 Dec , 287 (F1148-53).

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Pannicke T et al. A potassium channel-linked mechanism of glial cell swelling in the postischemic retina.
Mol. Cell. Neurosci., 2004 Aug , 26 (493-502).

284

Chen L et al. Inwardly rectifying potassium channels in rat retinal ganglion cells.
Eur. J. Neurosci., 2004 Aug , 20 (956-64).

288

Amiry-Moghaddam M et al. Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice.
Proc. Natl. Acad. Sci. U.S.A., 2003 Nov 11 , 100 (13615-20).

289

Stockklausner C et al. Surface expression of inward rectifier potassium channels is controlled by selective Golgi export.
J. Biol. Chem., 2003 May 9 , 278 (17000-5).

293

Tian M et al. Expression patterns of inwardly rectifying potassium channel subunits in rat retina.
Neurosci. Lett., 2003 Jul 10 , 345 (9-12).

294

Dalloz C et al. Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.
Hum. Mol. Genet., 2003 Jul 1 , 12 (1543-54).

296

Schultz JH et al. Central sympathetic chemosensitivity and Kir1 potassium channels in the cat.
Brain Res., 2003 Feb 14 , 963 (113-20).

298

Ishii M et al. Differential expression and distribution of Kir5.1 and Kir4.1 inwardly rectifying K+ channels in retina.
Am. J. Physiol., Cell Physiol., 2003 Aug , 285 (C260-7).

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Konstas AA et al. Identification of domains that control the heteromeric assembly of Kir5.1/Kir4.0 potassium channels.
Am. J. Physiol., Cell Physiol., 2003 Apr , 284 (C910-7).

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Wangemann P K(+) cycling and its regulation in the cochlea and the vestibular labyrinth.
Audiol. Neurootol., 2002 Jul-Aug , 7 (199-205).

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Wangemann P K+ cycling and the endocochlear potential.
Hear. Res., 2002 Mar , 165 (1-9).

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Marcus DC et al. KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.
Am. J. Physiol., Cell Physiol., 2002 Feb , 282 (C403-7).

311

Brochiero E et al. Cloning of rabbit Kir6.1, SUR2A, and SUR2B: possible candidates for a renal K(ATP) channel.
Am. J. Physiol. Renal Physiol., 2002 Feb , 282 (F289-300).

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Higashi K et al. An inwardly rectifying K(+) channel, Kir4.1, expressed in astrocytes surrounds synapses and blood vessels in brain.
Am. J. Physiol., Cell Physiol., 2001 Sep , 281 (C922-31).

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Horio Y Potassium channels of glial cells: distribution and function.
Jpn. J. Pharmacol., 2001 Sep , 87 (1-6).

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Proks P et al. Interaction of stilbene disulphonates with cloned K(ATP) channels.
Br. J. Pharmacol., 2001 Mar , 132 (973-82).

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Mikhailov MV et al. Investigation of the molecular assembly of beta-cell K(ATP) channels.
FEBS Lett., 2000 Sep 29 , 482 (59-64).

326

Schulte U et al. Gating of inward-rectifier K+ channels by intracellular pH.
Eur. J. Biochem., 2000 Oct , 267 (5837-41).

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Xu H et al. Molecular determinants for the distinct pH sensitivity of Kir1.1 and Kir4.1 channels.
Am. J. Physiol., Cell Physiol., 2000 Nov , 279 (C1464-71).

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Khaliq S et al. Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.
Invest. Ophthalmol. Vis. Sci., 2000 Nov , 41 (3709-12).

329

Xu H et al. Modulation of kir4.1 and kir5.1 by hypercapnia and intracellular acidosis.
J. Physiol. (Lond.), 2000 May 1 , 524 Pt 3 (725-35).

330

Sgard F et al. Regulation of ATP-sensitive potassium channel mRNA expression in rat kidney following ischemic injury.
Biochem. Biophys. Res. Commun., 2000 Mar 16 , 269 (618-22).

333

Tanemoto M et al. In vivo formation of a proton-sensitive K+ channel by heteromeric subunit assembly of Kir5.1 with Kir4.1.
J. Physiol. (Lond.), 2000 Jun 15 , 525 Pt 3 (587-92).

340

Yang Z et al. Opposite effects of pH on open-state probability and single channel conductance of kir4.1 channels.
J. Physiol. (Lond.), 1999 Nov 1 , 520 Pt 3 (921-7).

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Pearson WL et al. Expression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liver.
J. Physiol. (Lond.), 1999 Feb 1 , 514 ( Pt 3) (639-53).

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Oliver D et al. Interaction of permeant and blocking ions in cloned inward-rectifier K+ channels.
Biophys. J., 1998 May , 74 (2318-26).

355

Isomoto S et al. Inwardly rectifying potassium channels: their molecular heterogeneity and function.
Jpn. J. Physiol., 1997 Feb , 47 (11-39).

360

Doi T et al. Subunit-specific inhibition of inward-rectifier K+ channels by quinidine.
FEBS Lett., 1995 Nov 20 , 375 (193-6).

362

Glowatzki E et al. Subunit-dependent assembly of inward-rectifier K+ channels.
Proc. Biol. Sci., 1995 Aug 22 , 261 (251-61).