Kir4.1

1

Swale DR et al. ML418: The First Selective, Sub-Micromolar Pore Blocker of Kir7.1 Potassium Channels.
ACS Chem Neurosci, 2016 May 24 , ().

2

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).

3

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

4

Brasko C et al. Expression of Kir4.1 and Kir5.1 inwardly rectifying potassium channels in oligodendrocytes, the myelinating cells of the CNS.
Brain Struct Funct, 2016 Feb 15 , ().

5

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

6

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).

7

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

8

Zaragoza MV et al. Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.
PLoS ONE, 2016 , 11 (e0155421).

9

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).

10

Jo AO et al. TRPV4 and AQP4 Channels Synergistically Regulate Cell Volume and Calcium Homeostasis in Retinal Müller Glia.
J. Neurosci., 2015 Sep 30 , 35 (13525-37).

11

Rajasekhar P et al. P2Y1 receptor activation of the TRPV4 ion channel enhances purinergic signaling in satellite glial cells.
J. Biol. Chem., 2015 Oct 16 , ().

12

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).

13

Wang L et al. Caveolin-1 Deficiency Inhibits the Basolateral K+ Channels in the Distal Convoluted Tubule and Impairs Renal K+ and Mg2+ Transport.
J. Am. Soc. Nephrol., 2015 Nov , 26 (2678-90).

14

Takeda M et al. Activation of GABA(B) receptors potentiates inward rectifying potassium currents in satellite glial cells from rat trigeminal ganglia: in vivo patch-clamp analysis.
Neuroscience, 2015 Mar 12 , 288 (51-8).

15

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).

19

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

20

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).

21

Hertz L et al. Role of the Astrocytic Na(+), K (+)-ATPase in K (+) Homeostasis in Brain: K (+) Uptake, Signaling Pathways and Substrate Utilization.
Neurochem. Res., 2015 Jan 3 , ().

22

Wu SN et al. Investigations on contribution of glial inwardly-rectifying K(+) current to membrane potential and ion flux: an experimental and theoretical study.
Kaohsiung J. Med. Sci., 2015 Jan , 31 (9-17).

23

Gao F et al. Group I metabotropic glutamate receptor agonist DHPG modulates Kir4.1 protein and mRNA in cultured rat retinal Müller cells.
Neurosci. Lett., 2015 Feb 19 , 588 (12-7).

24

Fujita A et al. Clustering of Kir4.1 at specialized compartments of the lateral membrane in ependymal cells of rat brain.
Cell Tissue Res., 2015 Feb , 359 (627-34).

25

Slaats GG et al. Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis.
J. Cell. Sci., 2015 Dec 15 , 128 (4550-9).

26

Brill L et al. Increased anti-KIR4.1 antibodies in multiple sclerosis: could it be a marker of disease relapse?
Mult. Scler., 2015 Apr , 21 (572-9).

27

Arai E et al. Ablation of Kcnj10 expression in retinal explants revealed pivotal roles for Kcnj10 in the proliferation and development of Müller glia.
Mol. Vis., 2015 , 21 (148-59).

28

Cazals Y et al. KCNK5 channels mostly expressed in cochlear outer sulcus cells are indispensable for hearing.
Nat Commun, 2015 , 6 (8780).

29

Rohdin C et al. A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds.
Acta Vet. Scand., 2015 , 57 (26).

30

Ramos HE et al. Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesis.
Horm Res Paediatr, 2015 , 83 (141-7).

31

Malyavantham K et al. Humoral Responses to Diverse Autoimmune Disease-Associated Antigens in Multiple Sclerosis.
PLoS ONE, 2015 , 10 (e0129503).

32

Yang Z et al. Effect of adenosine and adenosine receptor antagonist on Müller cell potassium channel in Rat chronic ocular hypertension models.
Sci Rep, 2015 , 5 (11294).

33

Guo Y et al. Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsies.
PLoS ONE, 2015 , 10 (e0124896).

34

Gilliam D et al. A homozygous KCNJ10 mutation in Jack Russell Terriers and related breeds with spinocerebellar ataxia with myokymia, seizures, or both.
J. Vet. Intern. Med., 2014 May-Jun , 28 (871-7).

35

Obara-Michlewska M et al. Astroglial NMDA receptors inhibit expression of Kir4.1 channels in glutamate-overexposed astrocytes in vitro and in the brain of rats with acute liver failure.
Neurochem. Int., 2014 Oct 23 , ().

36

Wang L et al. Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling.
Am. J. Physiol., Cell Physiol., 2014 Oct 15 , 307 (C710-7).

37

Nerrant E et al. Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis.
Mult. Scler., 2014 Nov , 20 (1699-703).

38

Tong X et al. Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice.
Nat. Neurosci., 2014 May , 17 (694-703).

39

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).

40

Nwaobi SE et al. DNA methylation functions as a critical regulator of Kir4.1 expression during CNS development.
Glia, 2014 Mar , 62 (411-27).

41

Cheung So E et al. High effectiveness of triptolide, an active diterpenoid triepoxide, in suppressing Kir-channel currents from human glioma cells.
Eur. J. Pharmacol., 2014 Jun 11 , ().

42

Eckhard A et al. [Water regulation in the cochlea : Do molecular water channels facilitate potassium-dependent sound transduction?].
HNO, 2014 Jun , 62 (423-31).

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).

45

Sibille J et al. Astroglial potassium clearance contributes to short-term plasticity of synaptically evoked currents at the tripartite synapse.
J. Physiol. (Lond.), 2014 Jan 1 , 592 (87-102).

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).

47

Phani NM et al. Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.
Gene, 2014 Feb 25 , 536 (247-53).

48

Kraus V et al. Potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease.
Neurology, 2014 Feb 11 , 82 (470-3).

49

Köferl P et al. Effects of arteriolar constriction on retinal gene expression and Müller cell responses in a rat model of branch retinal vein occlusion.
Graefes Arch. Clin. Exp. Ophthalmol., 2014 Feb , 252 (257-65).

50

Zhang C et al. KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1).
Proc. Natl. Acad. Sci. U.S.A., 2014 Aug 12 , 111 (11864-9).

51

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

52

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

53

Brickshawana A et al. Investigation of the KIR4.1 potassium channel as a putative antigen in patients with multiple sclerosis: a comparative study.
Lancet Neurol, 2014 Aug , 13 (795-806).

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).

55

Chen J et al. The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.
Neuroscience, 2014 Apr 18 , 265 (137-46).

56

Swale DR et al. Cardiac and renal inward rectifier potassium channel pharmacology: emerging tools for integrative physiology and therapeutics.
Curr Opin Pharmacol, 2014 Apr , 15 (7-15).

57

Larsen BR et al. Contributions of the Na⁺/K⁺-ATPase, NKCC1, and Kir4.1 to hippocampal K⁺ clearance and volume responses.
Glia, 2014 Apr , 62 (608-22).

58

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

59

Zayas-Santiago A et al. Unidirectional photoreceptor-to-Müller glia coupling and unique K+ channel expression in Caiman retina.
PLoS ONE, 2014 , 9 (e97155).

60

Larsen BR et al. Kir4.1-mediated spatial buffering of K(+): experimental challenges in determination of its temporal and quantitative contribution to K(+) clearance in the brain.
Channels (Austin), 2014 , 8 (544-50).

61

Pannicke T et al. Differential effects of P2Y1 deletion on glial activation and survival of photoreceptors and amacrine cells in the ischemic mouse retina.
Cell Death Dis, 2014 , 5 (e1353).

62

Vogler S et al. Müller cell reactivity in response to photoreceptor degeneration in rats with defective polycystin-2.
PLoS ONE, 2014 , 8 (e61631).

63

Zhao J et al. KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects.
PLoS ONE, 2014 , 9 (e108134).

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).

65

Raphemot R et al. Development and validation of fluorescence-based and automated patch clamp-based functional assays for the inward rectifier potassium channel Kir4.1.
Assay Drug Dev Technol, 2013 Nov-Dec , 11 (532-43).

66

Kim HJ et al. Precise toxigenic ablation of intermediate cells abolishes the "battery" of the cochlear duct.
J. Neurosci., 2013 Sep 4 , 33 (14601-6).

67

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

68

Chai Y et al. Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.
Am. J. Med. Genet. A, 2013 Sep , 161 (2226-33).

69

Yang H et al. Compromised potassium recycling in the cochlea contributes to conservation of endocochlear potential in a mouse model of age-related hearing loss.
Neurosci. Lett., 2013 Oct 25 , 555 (97-101).

70

Gupta RK et al. Early down regulation of the glial Kir4.1 and GLT-1 expression in pericontusional cortex of the old male mice subjected to traumatic brain injury.
Biogerontology, 2013 Oct , 14 (531-41).

71

Arjona FJ et al. Tissue-specific expression and in vivo regulation of zebrafish orthologues of mammalian genes related to symptomatic hypomagnesemia.
Pflugers Arch., 2013 Oct , 465 (1409-21).

72

Nakajima M et al. Enhanced accumulation of Kir4.1 protein, but not mRNA, in a murine model of cuprizone-induced demyelination.
Brain Res., 2013 Nov 6 , 1537 (340-9).

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).

74

Mahmood F et al. Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome.
Dis Model Mech, 2013 May , 6 (652-60).

75

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

76

Lorente-Cánovas B et al. Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear.
Dis Model Mech, 2013 Mar , 6 (434-42).

77

Harada Y et al. Expressional analysis of inwardly rectifying Kir4.1 channels in Noda epileptic rat (NER).
Brain Res., 2013 Jun 23 , 1517 (141-9).

78

Zhang C et al. Src-family protein tyrosine kinase regulates the basolateral K channel in the distal convoluted tubule (DCT) by phosphorylation of KCNJ10.
J. Biol. Chem., 2013 Jul 19 , ().

79

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

80

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).

81

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

82

Gupta RK et al. Glial molecular alterations with mouse brain development and aging: up-regulation of the Kir4.1 and aquaporin-4.
Age (Dordr), 2013 Feb , 35 (59-67).

83

Hertz L et al. Astrocytic and neuronal accumulation of elevated extracellular K(+) with a 2/3 K(+)/Na(+) flux ratio-consequences for energy metabolism, osmolarity and higher brain function.
Front Comput Neurosci, 2013 , 7 (114).

84

Landa P et al. Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts.
BMC Med. Genet., 2013 , 14 (85).

85

Zschüntzsch J et al. Heterologous expression of a glial Kir channel (KCNJ10) in a neuroblastoma spinal cord (NSC-34) cell line.
Physiol Res, 2013 , 62 (95-105).

86

Lin D et al. Inhibition of miR-205 impairs the wound-healing process in human corneal epithelial cells by targeting KIR4.1 (KCNJ10).
Invest. Ophthalmol. Vis. Sci., 2013 , 54 (6167-78).

87

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

88

Zdebik AA et al. Epilepsy in kcnj10 morphant zebrafish assessed with a novel method for long-term EEG recordings.
PLoS ONE, 2013 , 8 (e79765).

89

Ji M et al. Group I mGluR-mediated inhibition of Kir channels contributes to retinal Müller cell gliosis in a rat chronic ocular hypertension model.
J. Neurosci., 2012 Sep 12 , 32 (12744-55).

90

Heuser K et al. Loss of perivascular Kir4.1 potassium channels in the sclerotic hippocampus of patients with mesial temporal lobe epilepsy.
J. Neuropathol. Exp. Neurol., 2012 Sep , 71 (814-25).

91

Racke MK Disease mechanisms in MS: the potassium channel KIR4.1--a potential autoantigen in MS.
Nat Rev Neurol, 2012 Nov 5 , 8 (595-6).

92

Lien CF et al. Absence of glial α-dystrobrevin causes abnormalities of the blood-brain barrier and progressive brain edema.
J. Biol. Chem., 2012 Nov 30 , 287 (41374-85).

93

Jin X et al. S-Glutathionylation underscores the modulation of the heteromeric Kir4.1-Kir5.1 channel in oxidative stress.
J. Physiol. (Lond.), 2012 Nov 1 , 590 (5335-48).

94

Braganza O et al. Albumin is taken up by hippocampal NG2 cells and astrocytes and decreases gap junction coupling.
Epilepsia, 2012 Nov , 53 (1898-906).

95

Scholl UI et al. SeSAME/EAST syndrome--phenotypic variability and delayed activity of the distal convoluted tubule.
Pediatr. Nephrol., 2012 Nov , 27 (2081-90).

96

Steiner E et al. Loss of astrocyte polarization upon transient focal brain ischemia as a possible mechanism to counteract early edema formation.
Glia, 2012 Nov , 60 (1646-59).

97

Stephan J et al. Kir4.1 channels mediate a depolarization of hippocampal astrocytes under hyperammonemic conditions in situ.
Glia, 2012 May , 60 (965-78).

98

Berner AK et al. Protection against methylglyoxal-derived AGEs by regulation of glyoxalase 1 prevents retinal neuroglial and vasodegenerative pathology.
Diabetologia, 2012 Mar , 55 (845-54).

99

Chen K et al. Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation.
Otolaryngol Head Neck Surg, 2012 Jun , 146 (972-8).

100

Udagawa T et al. Inwardly rectifying potassium channel Kir4.1 is localized at the calyx endings of vestibular afferents.
Neuroscience, 2012 Jul 26 , 215 (209-16).

101

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).

102

Zhao T et al. The changes of potassium currents in RCS rat Müller cell during retinal degeneration.
Brain Res., 2012 Jan 3 , 1427 (78-87).

103

Lanciotti A et al. Megalencephalic leukoencephalopathy with subcortical cysts protein 1 functionally cooperates with the TRPV4 cation channel to activate the response of astrocytes to osmotic stress: dysregulation by pathological mutations.
, 2012 Feb 9 , ().

104

Steinhäuser C et al. Astrocyte dysfunction in temporal lobe epilepsy: K(+) channels and gap junction coupling.
, 2012 Feb 10 , ().

105

Xie B et al. Effect of pigment epithelium-derived factor on glutamate uptake in retinal Muller cells under high-glucose conditions.
Invest. Ophthalmol. Vis. Sci., 2012 Feb , 53 (1023-32).

106

Tajada S et al. High blood pressure associates with the remodelling of inward rectifier K+ channels in mice mesenteric vascular smooth muscle cells.
J. Physiol. (Lond.), 2012 Dec 1 , 590 (6075-91).

107

Bataveljic D et al. Changes in the astrocytic aquaporin-4 and inwardly rectifying potassium channel expression in the brain of the amyotrophic lateral sclerosis SOD1(G93A) rat model.
Glia, 2012 Dec , 60 (1991-2003).

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).

109

Bay V et al. Relationship between glial potassium regulation and axon excitability: a role for glial Kir4.1 channels.
Glia, 2012 Apr , 60 (651-60).

110

Fang Q et al. Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.
J. Assoc. Res. Otolaryngol., 2012 Apr , 13 (173-84).

111

Yan JH et al. p53-induced uncoupling expression of aquaporin-4 and inwardly rectifying K+ 4.1 channels in cytotoxic edema after subarachnoid hemorrhage.
CNS Neurosci Ther, 2012 Apr , 18 (334-42).

112

Benesova J et al. Distinct Expression/Function of Potassium and Chloride Channels Contributes to the Diverse Volume Regulation in Cortical Astrocytes of GFAP/EGFP Mice.
PLoS ONE, 2012 , 7 (e29725).

113

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

114

Drechsler F et al. Effect of intravitreal anti-vascular endothelial growth factor treatment on the retinal gene expression in acute experimental central retinal vein occlusion.
Ophthalmic Res., 2012 , 47 (157-62).

115

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

116

Zurolo E et al. Regulation of Kir4.1 expression in astrocytes and astrocytic tumors: a role for interleukin-1 β.
J Neuroinflammation, 2012 , 9 (280).

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).

118

Takeda M et al. Peripheral inflammation suppresses inward rectifying potassium currents of satellite glial cells in the trigeminal ganglia.
Pain, 2011 Sep , 152 (2147-56).

119

Haj-Yasein NN et al. Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human Kir4.1 gene (KCNJ10).
Glia, 2011 Nov , 59 (1635-42).

120

Tham DK et al. REGULATION OF KIR4.1 AND AQP4 EXPRESSION AND STABILITY AT THE BASOLATERAL DOMAIN OF EPITHELIAL MDCK CELLS BY THE EXTRACELLULAR MATRIX.
, 2011 May 4 , ().

121

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

122

Mercer S et al. Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysis.
Genet Test Mol Biomarkers, 2011 May , 15 (365-8).

123

Hsu MS et al. Laminar-specific and developmental expression of aquaporin-4 in the mouse hippocampus.
Neuroscience, 2011 Mar 31 , 178 (21-32).

124

Song P et al. Kir4.1 channel expression is essential for parietal cell control of acid secretion.
, 2011 Mar 2 , ().

125

Paulais M et al. Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.
Proc. Natl. Acad. Sci. U.S.A., 2011 Jun 21 , 108 (10361-6).

126

Strohschein S et al. Impact of aquaporin-4 channels on K+ buffering and gap junction coupling in the hippocampus.
Glia, 2011 Jun , 59 (973-80).

127

Sicca F et al. Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
Neurobiol. Dis., 2011 Jul , 43 (239-47).

128

Shen Q et al. No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population.
Neurosci. Lett., 2011 Jan 3 , 487 (61-5).

129

Cha SK et al. Calcium-sensing receptor decreases cell surface expression of the inwardly rectifying K+ channel Kir4.1.
J. Biol. Chem., 2011 Jan 21 , 286 (1828-35).

130

Sone M et al. Morphological observation of the stria vascularis in midkine and pleiotrophin knockout mice.
Auris Nasus Larynx, 2011 Feb , 38 (41-5).

131

Obara-Michlewska M et al. Down-regulation of Kir4.1 in the cerebral cortex of rats with liver failure and in cultured astrocytes treated with glutamine: Implications for astrocytic dysfunction in hepatic encephalopathy.
J. Neurosci. Res., 2011 Dec , 89 (2018-27).

132

Zhao M et al. Differential regulations of AQP4 and Kir4.1 by triamcinolone acetonide and dexamethasone in the healthy and inflamed retina.
Invest. Ophthalmol. Vis. Sci., 2011 Aug , 52 (6340-7).

133

Rehak M et al. Effects of intravitreal triamcinolone acetonide on retinal gene expression in a rat model of central retinal vein occlusion.
Graefes Arch. Clin. Exp. Ophthalmol., 2011 Aug , 249 (1175-83).

134

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

135

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

136

Bandulik S et al. The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.
Pflugers Arch., 2011 Apr , 461 (423-35).

137

Trapp S et al. Respiratory responses to hypercapnia and hypoxia in mice with genetic ablation of Kir5.1 (Kcnj16).
Exp. Physiol., 2011 Apr , 96 (451-9).

138

Mulkey DK et al. Astrocyte chemoreceptors: mechanisms of H+ sensing by astrocytes in the retrotrapezoid nucleus and their possible contribution to respiratory drive.
Exp. Physiol., 2011 Apr , 96 (400-6).

139

Hirrlinger PG et al. Genetic Deletion of Laminin Isoforms β2 and γ3 Induces a Reduction in Kir4.1 and Aquaporin-4 Expression and Function in the Retina.
PLoS ONE, 2011 , 6 (e16106).

140

Zhang Y et al. Expression of aquaporin 4 and Kir4.1 in diabetic rat retina: treatment with minocycline.
J. Int. Med. Res., 2011 , 39 (464-79).

141

Chen CP et al. Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.
Genet. Couns., 2011 , 22 (273-80).

142

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

143

Paynter JJ et al. Random mutagenesis screening indicates the absence of a separate H(+)-sensor in the pH-sensitive Kir channels.
Channels (Austin), 2010 Sep-Oct , 4 (390-7).

144

Obara-Michlewska M et al. Gain of function of Kir4.1 channel increases cell resistance to changes of potassium fluxes and cell volume evoked by ammonia and hypoosmotic stress.
Pharmacol Rep, 2010 Nov-Dec , 62 (1237-42).

145

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

146

Pivonkova H et al. Impact of Global Cerebral Ischemia on K(+) Channel Expression and Membrane Properties of Glial Cells in the Rat Hippocampus.
, 2010 Sep 9 , ().

147

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).

148

Inyushin M et al. Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice.
Epilepsia, 2010 Sep , 51 (1707-13).

149

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).

150

Jonard L et al. Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.
Int. J. Pediatr. Otorhinolaryngol., 2010 Sep , 74 (1049-53).

151

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

152

D'Adamo MC et al. Genetic inactivation of KCNJ16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.
, 2010 Nov 3 , ().

153

Chever O et al. Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice.
J. Neurosci., 2010 Nov 24 , 30 (15769-77).

154

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).

155

Zhao M et al. The neuroretina is a novel mineralocorticoid target: aldosterone up-regulates ion and water channels in Muller glial cells.
, 2010 May 13 , ().

156

Parvas M et al. The embryonic blood-CSF barrier has molecular elements to control E-CSF osmolarity during early CNS development.
J. Neurosci. Res., 2010 May 1 , 88 (1205-12).

157

Tang X et al. Inwardly rectifying potassium channel Kir4.1 is responsible for the native inward potassium conductance of satellite glial cells in sensory ganglia.
Neuroscience, 2010 Mar 17 , 166 (397-407).

158

Raz-Prag D et al. Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration.
Proc. Natl. Acad. Sci. U.S.A., 2010 Jul 13 , 107 (12710-5).

159

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

160

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

161

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

162

Heuser K et al. Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.
Epilepsy Res., 2010 Jan , 88 (55-64).

163

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

164

Wenker IC et al. Astrocytes in the retrotrapezoid nucleus sense H+ by inhibition of a Kir4.1-Kir5.1-like current and may contribute to chemoreception by a purinergic mechanism.
J. Neurophysiol., 2010 Dec , 104 (3042-52).

165

Stewart TH et al. Chronic dysfunction of astrocytic inwardly rectifying K+ channels specific to the neocortical epileptic focus after fluid percussion injury in the rat.
J. Neurophysiol., 2010 Dec , 104 (3345-60).

166

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

167

Reichold M et al. KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function.
Proc. Natl. Acad. Sci. U.S.A., 2010 Aug 10 , 107 (14490-5).

168

Durham PL et al. Development of functional units within trigeminal ganglia correlates with increased expression of proteins involved in neuron-glia interactions.
Neuron Glia Biol., 2010 Aug , 6 (171-81).

169

Olsen ML et al. Spinal cord injury causes a wide-spread, persistent loss of Kir4.1 and glutamate transporter 1: benefit of 17 beta-oestradiol treatment.
Brain, 2010 Apr , 133 (1013-25).

170

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

171

Goodyear MJ et al. Spatial and temporal dissociation of AQP4 and Kir4.1 expression during induction of refractive errors.
Mol. Vis., 2010 , 16 (1610-9).

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).

175

Rash JE Molecular disruptions of the panglial syncytium block potassium siphoning and axonal saltatory conduction: pertinence to neuromyelitis optica and other demyelinating diseases of the central nervous system.
, 2009 Oct 20 , ().

176

Lewis LM et al. High-throughput screening reveals a small-molecule inhibitor of the renal outer medullary potassium channel and Kir7.1.
Mol. Pharmacol., 2009 Nov , 76 (1094-103).

177

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

178

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).

179

Yang T et al. Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.
Am. J. Hum. Genet., 2009 May , 84 (651-7).

180

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

181

Wilcock DM et al. Vascular amyloid alters astrocytic water and potassium channels in mouse models and humans with Alzheimer's disease.
Neuroscience, 2009 Mar 31 , 159 (1055-69).

182

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).

185

Seifert G et al. Analysis of astroglial K+ channel expression in the developing hippocampus reveals a predominant role of the Kir4.1 subunit.
J. Neurosci., 2009 Jun 10 , 29 (7474-88).

186

Furutani K et al. Mutational and in silico analyses for antidepressant block of astroglial inward-rectifier Kir4.1 channel.
Mol. Pharmacol., 2009 Jun , 75 (1287-95).

187

Pawelczyk M et al. Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss.
Ann. Hum. Genet., 2009 Jul , 73 (411-21).

188

Mustapha M et al. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.
J. Neurosci., 2009 Jan 28 , 29 (1212-23).

189

Benesova J et al. Quantification of astrocyte volume changes during ischemia in situ reveals two populations of astrocytes in the cortex of GFAP/EGFP mice.
J. Neurosci. Res., 2009 Jan , 87 (96-111).

190

Zou J et al. Mitochondrial dysfunction disrupts trafficking of Kir4.1 in spiral ganglion satellite cells.
J. Neurosci. Res., 2009 Jan , 87 (141-9).

191

Hibino H et al. How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus.
, 2009 Dec 11 , ().

192

Tang X et al. Heterogeneity of Kir4.1 channel expression in glia revealed by mouse transgenesis.
Glia, 2009 Dec , 57 (1706-15).

193

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

194

Scholl UI et al. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.
Proc. Natl. Acad. Sci. U.S.A., 2009 Apr 7 , 106 (5842-7).

195

Sene A et al. Functional implication of Dp71 in osmoregulation and vascular permeability of the retina.
PLoS ONE, 2009 , 4 (e7329).

196

Wurm A et al. Involvement of A(1) adenosine receptors in osmotic volume regulation of retinal glial cells in mice.
Mol. Vis., 2009 , 15 (1858-67).

197

Aw S et al. H,K-ATPase protein localization and Kir4.1 function reveal concordance of three axes during early determination of left-right asymmetry.
Mech. Dev., 2008 Mar-Apr , 125 (353-72).

198

Olsen ML et al. Functional implications for Kir4.1 channels in glial biology: from K+ buffering to cell differentiation.
J. Neurochem., 2008 Nov , 107 (589-601).

199

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).

200

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

201

Lichter-Konecki U et al. Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivo.
Glia, 2008 Mar , 56 (365-77).

202

Smith SB et al. Quantitative trait locus and computational mapping identifies Kcnj9 (GIRK3) as a candidate gene affecting analgesia from multiple drug classes.
Pharmacogenet. Genomics, 2008 Mar , 18 (231-41).

203

Yamamoto Y et al. Immunohistochemical distribution of inwardly rectifying K+ channels in the medulla oblongata of the rat.
J. Vet. Med. Sci., 2008 Mar , 70 (265-71).

204

Lachheb S et al. Kir4.1/Kir5.1 channel forms the major K+ channel in the basolateral membrane of mouse renal collecting duct principal cells.
Am. J. Physiol. Renal Physiol., 2008 Jun , 294 (F1398-407).

205

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

206

Rojas A et al. Modulation of the heteromeric Kir4.1-Kir5.1 channel by multiple neurotransmitters via Galphaq-coupled receptors.
J. Cell. Physiol., 2008 Jan , 214 (84-95).

207

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

208

Singh R et al. Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.
Am. J. Physiol. Renal Physiol., 2008 Jan , 294 (F139-48).

209

Jin Z et al. Spatiotemporal loss of K+ transport proteins in the developing cochlear lateral wall of guinea pigs with hereditary deafness.
Eur. J. Neurosci., 2008 Jan , 27 (145-54).

210

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).

211

Shang L et al. Non-equivalent role of TM2 gating hinges in heteromeric Kir4.1/Kir5.1 potassium channels.
Eur. Biophys. J., 2008 Feb , 37 (165-71).

212

Ulbricht E et al. Proliferative gliosis causes mislocation and inactivation of inwardly rectifying K(+) (Kir) channels in rabbit retinal glial cells.
Exp. Eye Res., 2008 Feb , 86 (305-13).

213

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

214

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).

215

Vit JP et al. Silencing the Kir4.1 potassium channel subunit in satellite glial cells of the rat trigeminal ganglion results in pain-like behavior in the absence of nerve injury.
J. Neurosci., 2008 Apr 16 , 28 (4161-71).

216

Fort PE et al. Kir4.1 and AQP4 associate with Dp71- and utrophin-DAPs complexes in specific and defined microdomains of Müller retinal glial cell membrane.
Glia, 2008 Apr 15 , 56 (597-610).

217

Kaufhold MA et al. Localization, trafficking, and significance for acid secretion of parietal cell Kir4.1 and KCNQ1 K+ channels.
Gastroenterology, 2008 Apr , 134 (1058-69).

218

Papadopoulos N et al. Possible roles of the weakly inward rectifying k+ channel Kir4.1 (KCNJ10) in the pre-Bötzinger complex.
Adv. Exp. Med. Biol., 2008 , 605 (109-13).

219

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

220

Rapedius M et al. Control of pH and PIP2 gating in heteromeric Kir4.1/Kir5.1 channels by H-Bonding at the helix-bundle crossing.
Channels (Austin), 2007 Sep-Oct , 1 (327-30).

221

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

222

Härtel K et al. Calcium influx mediated by the inwardly rectifying K+ channel Kir4.1 (KCNJ10) at low external K+ concentration.
Cell Calcium, 2007 Sep , 42 (271-80).

223

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).

224

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

225

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

226

Djukic B et al. Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation.
J. Neurosci., 2007 Oct 17 , 27 (11354-65).

227

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

228

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).

229

Hibino H et al. Distinct detergent-resistant membrane microdomains (lipid rafts) respectively harvest K(+) and water transport systems in brain astroglia.
Eur. J. Neurosci., 2007 Nov , 26 (2539-55).

230

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

231

Wangemann P et al. Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model.
Am. J. Physiol. Renal Physiol., 2007 May , 292 (F1345-53).

232

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

233

Huang C et al. Interaction of the Ca2+-sensing receptor with the inwardly rectifying potassium channels Kir4.1 and Kir4.2 results in inhibition of channel function.
Am. J. Physiol. Renal Physiol., 2007 Mar , 292 (F1073-81).

234

Ruiz-Ederra J et al. Evidence against functional interaction between aquaporin-4 water channels and Kir4.1 potassium channels in retinal Müller cells.
J. Biol. Chem., 2007 Jul 27 , 282 (21866-72).

235

Su S et al. Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptyline.
J. Pharmacol. Exp. Ther., 2007 Feb , 320 (573-80).

236

Kucheryavykh YV et al. Downregulation of Kir4.1 inward rectifying potassium channel subunits by RNAi impairs potassium transfer and glutamate uptake by cultured cortical astrocytes.
Glia, 2007 Feb , 55 (274-81).

237

Rurak J et al. Distribution of potassium ion and water permeable channels at perivascular glia in brain and retina of the Large(myd) mouse.
J. Neurochem., 2007 Dec , 103 (1940-53).

238

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

239

Dibaj P et al. Kir4.1 channels regulate swelling of astroglial processes in experimental spinal cord edema.
J. Neurochem., 2007 Dec , 103 (2620-8).

240

Olsen ML et al. Differential distribution of Kir4.1 in spinal cord astrocytes suggests regional differences in K+ homeostasis.
J. Neurophysiol., 2007 Aug , 98 (786-93).

241

Liu XQ et al. Differential expression of Kir4.1 and aquaporin 4 in the retina from endotoxin-induced uveitis rat.
Mol. Vis., 2007 , 13 (309-17).

242

Garcia MA et al. Effect of renal ischemia/reperfusion on gene expression of a pH-sensitive K+ channel.
Nephron Physiol, 2007 , 106 (p1-7).

243

Butt AM et al. Inwardly rectifying potassium channels (Kir) in central nervous system glia: a special role for Kir4.1 in glial functions.
J. Cell. Mol. Med., 2006 Jan-Mar , 10 (33-44).

244

Menichella DM et al. Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity.
J. Neurosci., 2006 Oct 25 , 26 (10984-91).

245

Kaiser M et al. Progressive loss of a glial potassium channel (KCNJ10) in the spinal cord of the SOD1 (G93A) transgenic mouse model of amyotrophic lateral sclerosis.
J. Neurochem., 2006 Nov , 99 (900-12).

246

Vit JP et al. Satellite glial cells in the trigeminal ganglion as a determinant of orofacial neuropathic pain.
Neuron Glia Biol., 2006 Nov , 2 (247-257).

247

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

248

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).

249

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).

250

Neusch C et al. Lack of the Kir4.1 channel subunit abolishes K+ buffering properties of astrocytes in the ventral respiratory group: impact on extracellular K+ regulation.
J. Neurophysiol., 2006 Mar , 95 (1843-52).

251

Pannicke T et al. Diabetes alters osmotic swelling characteristics and membrane conductance of glial cells in rat retina.
Diabetes, 2006 Mar , 55 (633-9).

252

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

253

Benfenati V et al. Guanosine promotes the up-regulation of inward rectifier potassium current mediated by Kir4.1 in cultured rat cortical astrocytes.
J. Neurochem., 2006 Jul , 98 (430-45).

254

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

255

Pondugula SR et al. Glucocorticoid regulation of genes in the amiloride-sensitive sodium transport pathway by semicircular canal duct epithelium of neonatal rat.
Physiol. Genomics, 2006 Jan 12 , 24 (114-23).

256

Jin Z et al. Developmental expression and localization of KCNJ10 K+ channels in the guinea pig inner ear.
Neuroreport, 2006 Apr 3 , 17 (475-9).

257

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

258

Puwarawuttipanit W et al. Differential effect of alpha-syntrophin knockout on aquaporin-4 and Kir4.1 expression in retinal macroglial cells in mice.
Neuroscience, 2006 , 137 (165-75).

259

Shang L et al. Functional characterisation of missense variations in the Kir4.1 potassium channel (KCNJ10) associated with seizure susceptibility.
Brain Res. Mol. Brain Res., 2005 Sep 13 , 139 (178-83).

260

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).

261

Bosco A et al. A developmental switch in the expression of aquaporin-4 and Kir4.1 from horizontal to Müller cells in mouse retina.
Invest. Ophthalmol. Vis. Sci., 2005 Oct , 46 (3869-75).

262

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

263

Lenzen KP et al. Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
Epilepsy Res., 2005 Feb , 63 (113-8).

264

Noël G et al. Dystroglycan and Kir4.1 coclustering in retinal Müller glia is regulated by laminin-1 and requires the PDZ-ligand domain of Kir4.1.
J. Neurochem., 2005 Aug , 94 (691-702).

265

Nie L et al. Functional consequences of polyamine synthesis inhibition by L-alpha-difluoromethylornithine (DFMO): cellular mechanisms for DFMO-mediated ototoxicity.
J. Biol. Chem., 2005 Apr 15 , 280 (15097-102).

266

Warth A et al. Redistribution of the water channel protein aquaporin-4 and the K+ channel protein Kir4.1 differs in low- and high-grade human brain tumors.
Acta Neuropathol., 2005 Apr , 109 (418-26).

267

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

268

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

269

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).

270

Hibino H et al. Differential assembly of inwardly rectifying K+ channel subunits, Kir4.1 and Kir5.1, in brain astrocytes.
J. Biol. Chem., 2004 Oct 15 , 279 (44065-73).

271

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).

272

Leonoudakis D et al. Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins.
J. Biol. Chem., 2004 May 21 , 279 (22331-46).

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).

274

Kalsi AS et al. Kir4.1 expression by astrocytes and oligodendrocytes in CNS white matter: a developmental study in the rat optic nerve.
J. Anat., 2004 Jun , 204 (475-85).

275

Connors NC et al. The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia.
J. Biol. Chem., 2004 Jul 2 , 279 (28387-92).

276

Hibino H et al. Expression of an inwardly rectifying K+ channel, Kir5.1, in specific types of fibrocytes in the cochlear lateral wall suggests its functional importance in the establishment of endocochlear potential.
Eur. J. Neurosci., 2004 Jan , 19 (76-84).

277

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).

278

Buono RJ et al. Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.
Epilepsy Res., 2004 Feb , 58 (175-83).

279

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).

280

Da T et al. Aquaporin-4 gene disruption in mice protects against impaired retinal function and cell death after ischemia.
Invest. Ophthalmol. Vis. Sci., 2004 Dec , 45 (4477-83).

281

Wangemann P et al. Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
, 2004 Aug 20 , 2 (30).

282

Guadagno E et al. Laminin-induced aggregation of the inwardly rectifying potassium channel, Kir4.1, and the water-permeable channel, AQP4, via a dystroglycan-containing complex in astrocytes.
Glia, 2004 Aug 1 , 47 (138-49).

283

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).

285

Ferraro TN et al. Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
Mamm. Genome, 2004 Apr , 15 (239-51).

286

Nagelhus EA et al. Aquaporin-4 in the central nervous system: cellular and subcellular distribution and coexpression with KIR4.1.
Neuroscience, 2004 , 129 (905-13).

287

Casamassima M et al. Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels.
J. Biol. Chem., 2003 Oct 31 , 278 (43533-40).

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).

290

Schulze D et al. 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.
J. Biol. Chem., 2003 Mar 21 , 278 (10500-5).

291

Rozengurt N et al. Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit.
Hear. Res., 2003 Mar , 177 (71-80).

292

Kurachi Y et al. [Molecular dynamics of K+ transport and its crucial involvement in signal transduction]
, 2003 Jun , 23 (135-8).

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).

295

Yang D et al. Expression and localization of the inwardly rectifying potassium channel Kir7.1 in native bovine retinal pigment epithelium.
Invest. Ophthalmol. Vis. Sci., 2003 Jul , 44 (3178-85).

296

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

297

Saadoun S et al. Water transport becomes uncoupled from K+ siphoning in brain contusion, bacterial meningitis, and brain tumours: immunohistochemical case review.
J. Clin. Pathol., 2003 Dec , 56 (972-5).

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).

299

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).

300

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

301

Kofuji P et al. Kir potassium channel subunit expression in retinal glial cells: implications for spatial potassium buffering.
Glia, 2002 Sep , 39 (292-303).

302

Farook VS et al. Molecular analysis of KCNJ10 on 1q as a candidate gene for Type 2 diabetes in Pima Indians.
Diabetes, 2002 Nov , 51 (3342-6).

303

Skatchkov SN et al. Functional expression of Kir 6.1/SUR1-K(ATP) channels in frog retinal Müller glial cells.
Glia, 2002 May , 38 (256-67).

304

Schröder W et al. AMPA receptor-mediated modulation of inward rectifier K+ channels in astrocytes of mouse hippocampus.
Mol. Cell. Neurosci., 2002 Mar , 19 (447-58).

305

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

306

Raap M et al. Diversity of Kir channel subunit mRNA expressed by retinal glial cells of the guinea-pig.
Neuroreport, 2002 Jun 12 , 13 (1037-40).

307

Connors NC et al. Dystrophin Dp71 is critical for the clustered localization of potassium channels in retinal glial cells.
J. Neurosci., 2002 Jun 1 , 22 (4321-7).

308

Konstas AA et al. Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel.
J. Biol. Chem., 2002 Jul 12 , 277 (25377-84).

309

Lourdel S et al. An inward rectifier K(+) channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.
J. Physiol. (Lond.), 2002 Jan 15 , 538 (391-404).

310

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).

312

Fujita A et al. Specific localization of an inwardly rectifying K(+) channel, Kir4.1, at the apical membrane of rat gastric parietal cells; its possible involvement in K(+) recycling for the H(+)-K(+)-pump.
J. Physiol. (Lond.), 2002 Apr 1 , 540 (85-92).

313

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).

314

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

315

Sage CL et al. Immunolocalization of ClC-K chloride channel in strial marginal cells and vestibular dark cells.
Hear. Res., 2001 Oct , 160 (1-9).

316

Cui N et al. Modulation of the heteromeric Kir4.1-Kir5.1 channels by P(CO(2)) at physiological levels.
J. Cell. Physiol., 2001 Nov , 189 (229-36).

317

Takeuchi S et al. Three-dimensional and ultrastructural relationships between intermediate cells and capillaries in the gerbil stria vascularis.
Hear. Res., 2001 May , 155 (103-12).

318

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

319

Li L et al. Identification of an inward rectifier potassium channel gene expressed in mouse cortical astrocytes.
Glia, 2001 Jan , 33 (57-71).

320

Kusaka S et al. Functional Kir7.1 channels localized at the root of apical processes in rat retinal pigment epithelium.
J. Physiol. (Lond.), 2001 Feb 15 , 531 (27-36).

321

Jiang C et al. An alternative approach to the identification of respiratory central chemoreceptors in the brainstem.
, 2001 Dec , 129 (141-57).

322

Neusch C et al. Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.
J. Neurosci., 2001 Aug 1 , 21 (5429-38).

323

Pessia M et al. Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1.
J. Physiol. (Lond.), 2001 Apr 15 , 532 (359-67).

324

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

325

Xu H et al. A single residue contributes to the difference between Kir4.1 and Kir1.1 channels in pH sensitivity, rectification and single channel conductance.
J. Physiol. (Lond.), 2000 Oct 15 , 528 Pt 2 (267-77).

326

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

327

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).

328

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).

331

Wulfsen I et al. Expression of mRNA for voltage-dependent and inward-rectifying K channels in GH3/B6 cells and rat pituitary.
J. Neuroendocrinol., 2000 Mar , 12 (263-72).

332

Tucker SJ et al. pH dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia.
J. Biol. Chem., 2000 Jun 2 , 275 (16404-7).

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).

334

Poopalasundaram S et al. Glial heterogeneity in expression of the inwardly rectifying K(+) channel, Kir4.1, in adult rat CNS.
Glia, 2000 Jun , 30 (362-72).

335

Yang Z et al. Biophysical and molecular mechanisms underlying the modulation of heteromeric Kir4.1-Kir5.1 channels by CO2 and pH.
J. Gen. Physiol., 2000 Jul 1 , 116 (33-45).

336

Kofuji P et al. Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina.
J. Neurosci., 2000 Aug 1 , 20 (5733-40).

337

Kusaka S et al. Expression and polarized distribution of an inwardly rectifying K+ channel, Kir4.1, in rat retinal pigment epithelium.
J. Physiol. (Lond.), 1999 Oct 15 , 520 Pt 2 (373-81).

338

Hibino H et al. Expression of an inwardly rectifying K(+) channel, Kir4.1, in satellite cells of rat cochlear ganglia.
Am. J. Physiol., 1999 Oct , 277 (C638-44).

339

Ando M et al. Immunological identification of an inward rectifier K+ channel (Kir4.1) in the intermediate cell (melanocyte) of the cochlear stria vascularis of gerbils and rats.
Cell Tissue Res., 1999 Oct , 298 (179-83).

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).

341

Nagelhus EA et al. Immunogold evidence suggests that coupling of K+ siphoning and water transport in rat retinal Müller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains.
Glia, 1999 Mar , 26 (47-54).

342

Tanabe K et al. Direct photoaffinity labeling of the Kir6.2 subunit of the ATP-sensitive K+ channel by 8-azido-ATP.
J. Biol. Chem., 1999 Feb 12 , 274 (3931-3).

343

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).

344

Schoots O et al. Co-expression of human Kir3 subunits can yield channels with different functional properties.
Cell. Signal., 1999 Dec , 11 (871-83).

345

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

346

Kurschner C et al. CIPP, a novel multivalent PDZ domain protein, selectively interacts with Kir4.0 family members, NMDA receptor subunits, neurexins, and neuroligins.
Mol. Cell. Neurosci., 1998 Jun , 11 (161-72).

347

Ma W et al. Prenatal expression of inwardly rectifying potassium channel mRNA (Kir4.1) in rat brain.
Neuroreport, 1998 Jan 26 , 9 (223-7).

348

Tada Y et al. Inwardly rectifying K+ channel in retinal Müller cells: comparison with the KAB-2/Kir4.1 channel expressed in HEK293T cells.
Jpn. J. Physiol., 1998 Feb , 48 (71-80).

349

Yakushigawa H et al. A novel junction-like membrane complex in the optic nerve astrocyte of the Japanese macaque with a possible relation to a potassium ion channel.
Anat. Rec., 1998 Apr , 250 (465-74).

350

Ishii M et al. Expression and clustered distribution of an inwardly rectifying potassium channel, KAB-2/Kir4.1, on mammalian retinal Müller cell membrane: their regulation by insulin and laminin signals.
J. Neurosci., 1997 Oct 15 , 17 (7725-35).

351

Tada Y et al. Assignment of the glial inwardly rectifying potassium channel KAB-2/Kir4.1 (Kcnj10) gene to the distal region of mouse chromosome 1.
Genomics, 1997 Nov 1 , 45 (629-30).

352

Horio Y et al. Clustering and enhanced activity of an inwardly rectifying potassium channel, Kir4.1, by an anchoring protein, PSD-95/SAP90.
J. Biol. Chem., 1997 May 16 , 272 (12885-8).

353

Hibino H et al. An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.
J. Neurosci., 1997 Jun 15 , 17 (4711-21).

354

Shuck ME et al. Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3).
J. Biol. Chem., 1997 Jan 3 , 272 (586-93).

355

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

356

Fakler B et al. Heterooligomeric assembly of inward-rectifier K+ channels from subunits of different subfamilies: Kir2.1 (IRK1) and Kir4.1 (BIR10).
Pflugers Arch., 1996 Nov-Dec , 433 (77-83).

357

Lagrutta AA et al. Inward rectifier potassium channels. Cloning, expression and structure-function studies.
, 1996 Sep , 37 (651-60).

358

Kubo Y et al. A weakly inward rectifying potassium channel of the salmon brain. Glutamate 179 in the second transmembrane domain is insufficient for strong rectification.
J. Biol. Chem., 1996 Jun 28 , 271 (15729-35).

359

Ito M et al. Immunolocalization of an inwardly rectifying K+ channel, K(AB)-2 (Kir4.1), in the basolateral membrane of renal distal tubular epithelia.
FEBS Lett., 1996 Jun 10 , 388 (11-5).

360

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

361

Pessia M et al. Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels.
Neuron, 1995 May , 14 (1039-45).

362

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

363

Fakler B et al. A structural determinant of differential sensitivity of cloned inward rectifier K+ channels to intracellular spermine.
FEBS Lett., 1994 Dec 19 , 356 (199-203).