Kir5.1

1

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 , ().

2

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).

3

Thomson SJ et al. Identification of the Intracellular Na+ Sensor in Slo2.1 Potassium Channels.
J. Biol. Chem., 2015 Jun 5 , 290 (14528-35).

4

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).

5

Zheng JS et al. Expedient total synthesis of small to medium-sized membrane proteins via Fmoc chemistry.
J. Am. Chem. Soc., 2014 Mar 5 , 136 (3695-704).

6

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).

7

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

8

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).

9

Juang JM et al. Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.
Sci Rep, 2014 , 4 (6733).

10

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).

11

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).

12

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 , ().

13

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

14

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).

15

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).

16

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).

17

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).

18

Edvinsson JM et al. Potassium-dependent activation of Kir4.2 K⁺ channels.
J. Physiol. (Lond.), 2011 Dec 15 , 589 (5949-63).

19

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).

20

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).

21

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 , ().

22

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).

23

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

24

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).

25

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).

26

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

27

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).

28

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).

29

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).

30

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).

31

Sindić A et al. MUPP1 complexes renal K+ channels to alter cell surface expression and whole cell currents.
Am. J. Physiol. Renal Physiol., 2009 Jul , 297 (F36-45).

32

Rosenhouse-Dantsker A et al. A sodium-mediated structural switch that controls the sensitivity of Kir channels to PtdIns(4,5)P(2).
Nat. Chem. Biol., 2008 Oct , 4 (624-31).

33

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).

34

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).

35

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).

36

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).

37

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

38

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).

39

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).

40

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).

41

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).

42

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).

43

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).

44

Lam HD et al. Modulation of Kir4.2 rectification properties and pHi-sensitive run-down by association with Kir5.1.
Biochim. Biophys. Acta, 2006 Nov , 1758 (1837-45).

45

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).

46

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).

47

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).

48

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).

49

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).

50

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).

51

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).

52

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).

53

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).

54

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).

55

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

56

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).

57

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).

58

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

59

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).

60

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).

61

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).

62

Tanemoto M et al. PSD-95 mediates formation of a functional homomeric Kir5.1 channel in the brain.
Neuron, 2002 Apr 25 , 34 (387-97).

63

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).

64

Derst C et al. Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits.
FEBS Lett., 2001 Mar 2 , 491 (305-11).

65

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

66

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).

67

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).

68

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).

69

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).

70

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).

71

Liu Y et al. The human inward rectifier K(+) channel subunit kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas.
Cytogenet. Cell Genet., 2000 , 90 (60-3).

72

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).

73

Mouri T et al. Assignment of mouse inwardly rectifying potassium channel Kcnj16 to the distal region of mouse chromosome 11.
Genomics, 1998 Nov 15 , 54 (181-2).

74

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