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

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).

6

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

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

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

17

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

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

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).

20

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

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

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).

28

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).

29

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

30

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).

31

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

32

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).

33

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).

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

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

43

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

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

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

52

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

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

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

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

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).

57

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).

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

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

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

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).

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

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).

68

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

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

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).

71

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).

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

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).

76

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

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

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).

84

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).

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

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

88

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

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

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).

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

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).

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

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).

110

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).

111

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).

112

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).

113

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).

114

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

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

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).

118

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).

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

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).

133

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).

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

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).

140

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).

141

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).

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.
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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

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).

149

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).

150

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).

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 , ().

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