Kir3.4

1

Sertedaki A et al. Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without Primary Aldosteronism but with ACTH-dependent aldosterone hypersecretion.
Clin. Endocrinol. (Oxf), 2016 Jun 13 , ().

2

Nishimoto K et al. Case Report: Nodule Development From Subcapsular Aldosterone-Producing Cell Clusters Causes Hyperaldosteronism.
J. Clin. Endocrinol. Metab., 2016 Jan , 101 (6-9).

3

Williams TA et al. Genotype-Specific Steroid Profiles Associated With Aldosterone-Producing Adenomas.
Hypertension, 2016 Jan , 67 (139-45).

4

Zhao Y et al. Regulation of SCN3B/scn3b by Interleukin 2 (IL-2): IL-2 modulates SCN3B/scn3b transcript expression and increases sodium current in myocardial cells.
BMC Cardiovasc Disord, 2016 , 16 (1).

5

Holmes AP et al. A Regional Reduction in Ito and IKACh in the Murine Posterior Left Atrial Myocardium Is Associated with Action Potential Prolongation and Increased Ectopic Activity.
PLoS ONE, 2016 , 11 (e0154077).

6

Touhara KK et al. The GIRK1 subunit potentiates G protein activation of cardiac GIRK1/4 hetero-tetramers.
Elife, 2016 , 5 ().

7

Bragança B et al. Ion Fluxes through KCa2 (SK) and Cav1 (L-type) Channels Contribute to Chronoselectivity of Adenosine A1 Receptor-Mediated Actions in Spontaneously Beating Rat Atria.
Front Pharmacol, 2016 , 7 (45).

8

He F et al. Effect of small interference RNA on the acetylcholine-sensitive potassium channel in H9c2 cells.
Ann. Clin. Lab. Sci., 2015 Winter , 45 (58-63).

9

Kienitz MC et al. NCI-H295R cell line as in vitro model of hyperaldosteronism lacks functional KCNJ5 (GIRK4; Kir3.4) channels.
Mol. Cell. Endocrinol., 2015 Sep 5 , 412 (272-80).

10

Bukiya AN et al. Cholesterol increases the open probability of cardiac KACh currents.
Biochim. Biophys. Acta, 2015 Oct , 1848 (2406-13).

11

Åkerström T et al. Novel somatic mutations and distinct molecular signature in aldosterone-producing adenomas.
Endocr. Relat. Cancer, 2015 Oct , 22 (735-44).

12

Fernandes-Rosa FL et al. Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing Adenoma.
Hypertension, 2015 Nov , 66 (1014-22).

13

Felizola SJ et al. Pre-B Lymphocyte Protein 3 (VPREB3) Expression in the Adrenal Cortex: Precedent for non-Immunological Roles in Normal and Neoplastic Human Tissues.
Endocr. Pathol., 2015 May , 26 (119-28).

14

Zheng FF et al. Clinical characteristics of somatic mutations in Chinese patients with aldosterone-producing adenoma.
Hypertension, 2015 Mar , 65 (622-8).

15

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

16

Fernandes-Rosa FL et al. Functional histopathological markers of aldosterone producing adenoma and somatic KCNJ5 mutations.
Mol. Cell. Endocrinol., 2015 Jun 15 , 408 (220-6).

17

Monticone S et al. 6C.03: A CASE OF SEVERE HYPERALDOSTERONISM CAUSED BY A DE NOVO KCNJ5 MUTATION.
J. Hypertens., 2015 Jun , 33 Suppl 1 (e79-80).

18

Duan K et al. Clinicopathologic Correlates of Primary Aldosteronism.
Arch. Pathol. Lab. Med., 2015 Jul , 139 (948-54).

19

Monticone S et al. A case of severe hyperaldosteronism caused by a de novo mutation affecting a critical salt bridge Kir3.4 residue.
J. Clin. Endocrinol. Metab., 2015 Jan , 100 (E114-8).

20

Cheng CJ et al. Novel KCNJ5 mutations in sporadic aldosterone-producing adenoma reduce Kir3.4 membrane abundance.
J. Clin. Endocrinol. Metab., 2015 Jan , 100 (E155-63).

21

Zennaro MC et al. An update on novel mechanisms of primary aldosteronism.
J. Endocrinol., 2015 Feb , 224 (R63-77).

22

Xiong WH et al. Voriconazole, an antifungal triazol that causes visual side effects, is an inhibitor of TRPM1 and TRPM3 channels.
Invest. Ophthalmol. Vis. Sci., 2015 Feb , 56 (1367-73).

23

Zhang J et al. [Sequence analysis of coding regions of KCNJ5 gene in unilateral adrenal hyperplasia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2015 Feb , 32 (21-5).

24

Monticone S et al. Immunohistochemical, genetic and clinical characterization of sporadic aldosterone-producing adenomas.
Mol. Cell. Endocrinol., 2015 Aug 15 , 411 (146-54).

25

Henn MC et al. Adenosine Triphosphate-Sensitive Potassium Channel Kir Subunits Implicated in Cardioprotection by Diazoxide.
J Am Heart Assoc, 2015 Aug , 4 (e002016).

26

Lenzini L et al. A Meta-Analysis of Somatic KCNJ5 K(+) Channel Mutations In 1636 Patients With an Aldosterone-Producing Adenoma.
J. Clin. Endocrinol. Metab., 2015 Aug , 100 (E1089-95).

27

Markou A et al. Stress-induced Aldosterone Hyper-Secretion in a Substantial Subset of Patients With Essential Hypertension.
J. Clin. Endocrinol. Metab., 2015 Aug , 100 (2857-64).

28

Wang B et al. Prevalence and characterization of somatic mutations in Chinese aldosterone-producing adenoma patients.
Medicine (Baltimore), 2015 Apr , 94 (e708).

29

Cannon SC Channelopathies of skeletal muscle excitability.
Compr Physiol, 2015 Apr , 5 (761-90).

30

Lenzini L et al. The molecular basis of primary aldosteronism: from chimeric gene to channelopathy.
Curr Opin Pharmacol, 2015 Apr , 21 (35-42).

31

Ip JC et al. Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism.
ANZ J Surg, 2015 Apr , 85 (279-83).

32

Boulkroun S et al. Molecular and Cellular Mechanisms of Aldosterone Producing Adenoma Development.
Front Endocrinol (Lausanne), 2015 , 6 (95).

33

Kitamoto T et al. Comparison of cardiovascular complications in patients with and without KCNJ5 gene mutations harboring aldosterone-producing adenomas.
J. Atheroscler. Thromb., 2015 , 22 (191-200).

34

Allegue C et al. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PLoS ONE, 2015 , 10 (e0133037).

35

Wu VC et al. Prevalence and clinical correlates of somatic mutation in aldosterone producing adenoma-Taiwanese population.
Sci Rep, 2015 , 5 (11396).

36

Zhang H et al. [Progress on genetic basis of primary aldosteronism].
Zhejiang Da Xue Xue Bao Yi Xue Ban, 2014 Sep , 43 (612-8).

37

Kuppusamy M et al. A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassium.
J. Clin. Endocrinol. Metab., 2014 Sep , 99 (E1765-73).

38

Felizola SJ et al. Voltage-gated calcium channels in the human adrenal and primary aldosteronism.
J. Steroid Biochem. Mol. Biol., 2014 Oct , 144 Pt B (410-6).

39

Ye G et al. Effects of Ca2+-activated potassium and inward rectifier potassium channel on the differentiation of endothelial progenitor cells from human peripheral blood.
Mol. Biol. Rep., 2014 May , 41 (3413-23).

40

Kokunai Y et al. A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.
Neurology, 2014 Mar 25 , 82 (1058-64).

41

Zhang H et al. Enhanced excitability of primary sensory neurons and altered gene expression of neuronal ion channels in dorsal root ganglion in paclitaxel-induced peripheral neuropathy.
Anesthesiology, 2014 Jun , 120 (1463-75).

42

Fischer E et al. Novel genes in primary aldosteronism.
Curr Opin Endocrinol Diabetes Obes, 2014 Jun , 21 (154-8).

43

Kienitz MC et al. Differential effects of genetically-encoded Gβγ scavengers on receptor-activated and basal Kir3.1/Kir3.4 channel current in rat atrial myocytes.
Cell. Signal., 2014 Jun , 26 (1182-92).

44

Tanwar V et al. Gremlin 2 promotes differentiation of embryonic stem cells to atrial fate by activation of the signaling pathway.
Stem Cells, 2014 Jul , 32 (1774-88).

45

Gómez L et al. Association of the KCNJ5 gene with Tourette Syndrome and Attention-Deficit/Hyperactivity Disorder.
Genes Brain Behav., 2014 Jul , 13 (535-42).

46

Rossi GP et al. KCNJ5 gene somatic mutations affect cardiac remodelling but do not preclude cure of high blood pressure and regression of left ventricular hypertrophy in primary aldosteronism.
J. Hypertens., 2014 Jul , 32 (1514-21; discussion 1522).

47

Zhang Y et al. Glycogen Synthase Kinase-3β Inhibition Ameliorates Cardiac Parasympathetic Dysfunction in Type 1 Diabetic Akita Mice.
Diabetes, 2014 Jan 23 , ().

48

Liang B et al. G-protein-coupled inward rectifier potassium current contributes to ventricular repolarization.
Cardiovasc. Res., 2014 Jan 1 , 101 (175-84).

49

Feldman RD Aldosterone and blood pressure regulation: recent milestones on the long and winding road from electrocortin to KCNJ5, GPER, and beyond.
Hypertension, 2014 Jan , 63 (19-21).

50

Gomez-Sanchez CE et al. Minireview: potassium channels and aldosterone dysregulation: is primary aldosteronism a potassium channelopathy?
Endocrinology, 2014 Jan , 155 (47-55).

51

Dutta RK et al. Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.
Endocr. Relat. Cancer, 2014 Feb , 21 (L1-4).

52

Li N et al. [Association of GIRK4 gene polymorphisms with essential hypertension in obese ethnics Uygur from southern Xinjiang].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2014 Feb , 31 (88-92).

53

Gomez-Sanchez CE et al. Somatic mutations of the ATP1A1 gene and aldosterone-producing adenomas.
Mol. Cell. Endocrinol., 2014 Dec 10 , ().

54

Fernandes-Rosa FL et al. Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma.
Hypertension, 2014 Aug , 64 (354-61).

55

Weeke P et al. Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
J. Am. Coll. Cardiol., 2014 Apr 15 , 63 (1430-7).

56

Li N et al. [Association of KCNJ5 gene rs3740835(C/A) and rs2604204(A/C) polymorphism with unilateral and bilateral primary aldosteronism].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2014 Apr , 31 (233-7).

57

Tauber P et al. Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.
Endocrinology, 2014 Apr , 155 (1353-62).

58

Murthy M et al. Role for germline mutations and a rare coding single nucleotide polymorphism within the KCNJ5 potassium channel in a large cohort of sporadic cases of primary aldosteronism.
Hypertension, 2014 Apr , 63 (783-9).

59

Sivagangabalan G et al. Regional ion channel gene expression heterogeneity and ventricular fibrillation dynamics in human hearts.
PLoS ONE, 2014 , 9 (e82179).

60

Al-Salameh A et al. Overview of the genetic determinants of primary aldosteronism.
Appl Clin Genet, 2014 , 7 (67-79).

61

Funder JW Genetics of primary aldosteronism.
Front Horm Res, 2014 , 43 (70-8).

62

Kumar M et al. Focus on Kir7.1: physiology and channelopathy.
Channels (Austin), 2014 , 8 (488-95).

63

Adachi M et al. Discordant genotype-phenotype correlation in familial hyperaldosteronism type III with KCNJ5 gene mutation: a patient report and review of the literature.
Horm Res Paediatr, 2014 , 82 (138-42).

64

Mesirca P et al. Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivation.
Nat Commun, 2014 , 5 (4664).

65

Williams TA et al. Somatic ATP1A1, ATP2B3, and KCNJ5 Mutations in Aldosterone-Producing Adenomas.
Hypertension, 2013 Sep 30 , ().

66

Azizan EA et al. Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
Nat. Genet., 2013 Sep , 45 (1055-60).

67

Scholl UI et al. Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism.
Nat. Genet., 2013 Sep , 45 (1050-4).

68

Wang F et al. The phenotype characteristics of type 13 long QT syndrome with mutation in KCNJ5 (Kir3.4-G387R).
Heart Rhythm, 2013 Oct , 10 (1500-6).

69

Monticone S et al. a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.
J. Clin. Endocrinol. Metab., 2013 Nov , 98 (E1861-5).

70

Oßwald A et al. Lack of influence of somatic mutations on steroid gradients during adrenal vein sampling in aldosterone-producing adenoma patients.
Eur. J. Endocrinol., 2013 Nov , 169 (657-63).

71

Boulkroun S et al. KCNJ5 mutations in aldosterone producing adenoma and relationship with adrenal cortex remodeling.
Mol. Cell. Endocrinol., 2013 May 22 , 371 (221-7).

72

Scholl UI et al. New insights into aldosterone-producing adenomas and hereditary aldosteronism: mutations in the K+ channel KCNJ5.
Curr. Opin. Nephrol. Hypertens., 2013 Mar , 22 (141-7).

73

Kaufmann K et al. ML297 (VU0456810), the First Potent and Selective Activator of the GIRK Potassium Channel, Displays Antiepileptic Properties in Mice.
ACS Chem Neurosci, 2013 Jun 13 , ().

74

Stowasser M Primary aldosteronism and potassium channel mutations.
Curr Opin Endocrinol Diabetes Obes, 2013 Jun , 20 (170-9).

75

Kiss T et al. Identification of diterpene alkaloids from Aconitum napellus subsp. firmum and GIRK channel activities of some Aconitum alkaloids.
Fitoterapia, 2013 Jul 19 , ().

76

Ravens U et al. Atrial selectivity of antiarrhythmic drugs.
J. Physiol. (Lond.), 2013 Jul 16 , ().

77

Mesirca P et al. The G-protein-gated K+ channel, IKACh, is required for regulation of pacemaker activity and recovery of resting heart rate after sympathetic stimulation.
J. Gen. Physiol., 2013 Jul 15 , ().

78

Zennaro MC et al. Genetics of mineralocorticoid excess: an update for clinicians.
Eur. J. Endocrinol., 2013 Jul , 169 (R15-25).

79

Mulatero P et al. Role of KCNJ5 in familial and sporadic primary aldosteronism.
Nat Rev Endocrinol, 2013 Feb , 9 (104-12).

80

Kang YA et al. [Expression of GIRK4 gene in kidney tissues of obese rat].
Zhongguo Yi Xue Ke Xue Yuan Xue Bao, 2013 Feb , 35 (36-9).

81

Bingen BO et al. Atrium-specific Kir3.x determines inducibility, dynamics, and termination of fibrillation by regulating restitution-driven alternans.
Circulation, 2013 Dec 24 , 128 (2732-44).

82

Velarde-Miranda C et al. Regulation of aldosterone biosynthesis by the Kir3.4 (KCNJ5) potassium channel.
Clin. Exp. Pharmacol. Physiol., 2013 Dec , 40 (895-901).

83

Shao D et al. [Relationship between the G protein gated inward rectifier potassium channel 4 gene polymorphism and dyslipidemia of Uyghur residents].
Zhongguo Yi Xue Ke Xue Yuan Xue Bao, 2013 Dec , 35 (611-7).

84

Mahajan R et al. A computational model predicts that Gβγ acts at a cleft between channel subunits to activate GIRK1 channels.
Sci Signal, 2013 Aug 13 , 6 (ra69).

85

Arnesen T et al. Outcome after surgery for primary hyperaldosteronism may depend on KCNJ5 tumor mutation status: a population-based study from Western Norway.
Langenbecks Arch Surg, 2013 Aug , 398 (869-74).

86

Treiber F et al. Molecular basis of the facilitation of the heterooligomeric GIRK1/GIRK4 complex by cAMP dependent protein kinase.
Biochim. Biophys. Acta, 2013 Apr , 1828 (1214-21).

87

Li NF et al. Genetic variations in the KCNJ5 gene in primary aldosteronism patients from Xinjiang, China.
PLoS ONE, 2013 , 8 (e54051).

88

Atkinson AJ et al. Functional, anatomical, and molecular investigation of the cardiac conduction system and arrhythmogenic atrioventricular ring tissue in the rat heart.
J Am Heart Assoc, 2013 , 2 (e000246).

89

Molina-Navarro MM et al. Differential gene expression of cardiac ion channels in human dilated cardiomyopathy.
PLoS ONE, 2013 , 8 (e79792).

90

Holmegard HN et al. Genetic variation in the parasympathetic signaling pathway in patients with reflex syncope.
Genet. Mol. Res., 2013 , 12 (2601-10).

91

Oki K et al. The potassium channel, Kir3.4 participates in angiotensin II-stimulated aldosterone production by a human adrenocortical cell line.
Endocrinology, 2012 Sep , 153 (4328-35).

92

Charmandari E et al. A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension.
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93

Azizan EA et al. Microarray, qPCR, and KCNJ5 sequencing of aldosterone-producing adenomas reveal differences in genotype and phenotype between zona glomerulosa- and zona fasciculata-like tumors.
J. Clin. Endocrinol. Metab., 2012 May , 97 (E819-29).

94

Kloukina V et al. G-protein-gated inwardly rectifying K+ channel 4 (GIRK4) immunoreactivity in chemically defined neurons of the hypothalamic arcuate nucleus that control body weight.
J. Chem. Neuroanat., 2012 May , 44 (14-23).

95

Boulkroun S et al. Prevalence, clinical, and molecular correlates of KCNJ5 mutations in primary aldosteronism.
Hypertension, 2012 Mar , 59 (592-8).

96

Azizan EA et al. Somatic mutations affecting the selectivity filter of KCNJ5 are frequent in 2 large unselected collections of adrenal aldosteronomas.
Hypertension, 2012 Mar , 59 (587-91).

97

Mussa A et al. Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism.
Endocr. J., 2012 Jun 30 , 59 (497-502).

98

Murthy M et al. Characterization of a novel somatic KCNJ5 mutation delI157 in an aldosterone-producing adenoma.
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99

Bar-Lev A et al. Genetics of adrenocortical disease: an update.
Curr Opin Endocrinol Diabetes Obes, 2012 Jun , 19 (159-67).

100

Xekouki P et al. KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.
Endocr. Relat. Cancer, 2012 Jun , 19 (255-60).

101

Li N et al. Influence of age on the association of GIRK4 with metabolic syndrome.
Ann. Clin. Biochem., 2012 Jul , 49 (369-76).

102

Scholl UI et al. Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5.
Proc. Natl. Acad. Sci. U.S.A., 2012 Feb 14 , 109 (2533-8).

103

Deng W et al. Hypercholesterolemia induces up-regulation of KACh cardiac currents via a mechanism independent of phosphatidylinositol 4,5-bisphosphate and Gβγ.
J. Biol. Chem., 2012 Feb 10 , 287 (4925-35).

104

Gomez-Sanchez CE et al. Mutations of the potassium channel KCNJ5 causing aldosterone-producing adenomas: one or two hits?
Hypertension, 2012 Feb , 59 (196-7).

105

Mulatero P et al. KCNJ5 mutations in European families with nonglucocorticoid remediable familial hyperaldosteronism.
Hypertension, 2012 Feb , 59 (235-40).

106

Li NF et al. [Association between GIRK4 gene polymorphisms and insulin resistance in Xinjiang Uygur population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2012 Dec , 29 (715-9).

107

Seccia TM et al. Somatic mutations in the KCNJ5 gene raise the lateralization index: implications for the diagnosis of primary aldosteronism by adrenal vein sampling.
J. Clin. Endocrinol. Metab., 2012 Dec , 97 (E2307-13).

108

Yamada M et al. KCNJ5 mutations in aldosterone- and cortisol-co-secreting adrenal adenomas.
Endocr. J., 2012 Aug 31 , 59 (735-41).

109

Monticone S et al. Effect of KCNJ5 mutations on gene expression in aldosterone-producing adenomas and adrenocortical cells.
J. Clin. Endocrinol. Metab., 2012 Aug , 97 (E1567-72).

110

Kang YA et al. Advances in research on G protein-coupled inward rectifier K(+) channel gene.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao, 2012 Aug , 34 (426-30).

111

Williams TA et al. Visinin-like 1 is upregulated in aldosterone-producing adenomas with KCNJ5 mutations and protects from calcium-induced apoptosis.
Hypertension, 2012 Apr , 59 (833-9).

112

Wu J et al. Regulatory mechanisms underlying the modulation of GIRK1/GIRK4 heteromeric channels by P2Y receptors.
Pflugers Arch., 2012 Apr , 463 (625-33).

113

Funder JW The genetic basis of primary aldosteronism.
Curr. Hypertens. Rep., 2012 Apr , 14 (120-4).

114

Oki K et al. Potassium channel mutant KCNJ5 T158A expression in HAC-15 cells increases aldosterone synthesis.
Endocrinology, 2012 Apr , 153 (1774-82).

115

Taguchi R et al. Expression and mutations of KCNJ5 mRNA in Japanese patients with aldosterone-producing adenomas.
J. Clin. Endocrinol. Metab., 2012 Apr , 97 (1311-9).

116

Whorton MR et al. Crystal structure of the mammalian GIRK2 K+ channel and gating regulation by G proteins, PIP2, and sodium.
Cell, 2011 Sep 30 , 147 (199-208).

117

Chopra N et al. Genetics of sudden cardiac death syndromes.
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118

Zennaro MC et al. Mutations in KCNJ5 gene cause hyperaldosteronism.
Circ. Res., 2011 Jun 10 , 108 (1417-8).

119

Choi M et al. K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.
Science, 2011 Feb 11 , 331 (768-72).

120

Kobayashi T et al. Inhibition of g protein-activated inwardly rectifying k channels by different classes of antidepressants.
PLoS ONE, 2011 , 6 (e28208).

121

Jabbari J et al. Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.
Cardiology, 2011 , 118 (116-20).

122

Voigt N et al. Left-to-right atrial inward rectifier potassium current gradients in patients with paroxysmal versus chronic atrial fibrillation.
Circ Arrhythm Electrophysiol, 2010 Oct 1 , 3 (472-80).

123

Yang Y et al. Identification of a Kir3.4 mutation in congenital long QT syndrome.
Am. J. Hum. Genet., 2010 Jun 11 , 86 (872-80).

124

Wagner V et al. Cloning and characterisation of GIRK1 variants resulting from alternative RNA editing of the KCNJ3 gene transcript in a human breast cancer cell line.
J. Cell. Biochem., 2010 Jun 1 , 110 (598-608).

125

Kobayashi T et al. Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine.
Neuropsychopharmacology, 2010 Jun , 35 (1560-9).

126

Nobles M et al. HL-1 cells express an inwardly rectifying K+ current activated via muscarinic receptors comparable to that in mouse atrial myocytes.
Pflugers Arch., 2010 Jun , 460 (99-108).

127

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

128

Walsh KB A real-time screening assay for GIRK1/4 channel blockers.
J Biomol Screen, 2010 Dec , 15 (1229-37).

129

Holmegard HN et al. Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunction.
Cardiology, 2010 , 115 (176-81).

130

Balana B et al. Mutagenesis and functional analysis of ion channels heterologously expressed in Mammalian cells.
J Vis Exp, 2010 , ().

131

Ishihara K et al. Heteromeric assembly of inward rectifier channel subunit Kir2.1 with Kir3.1 and with Kir3.4.
Biochem. Biophys. Res. Commun., 2009 Mar 20 , 380 (832-7).

132

Swartz MF et al. Left versus right atrial difference in dominant frequency, K(+) channel transcripts, and fibrosis in patients developing atrial fibrillation after cardiac surgery.
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133

Park HJ et al. Role of SREBP-1 in the development of parasympathetic dysfunction in the hearts of type 1 diabetic Akita mice.
Circ. Res., 2009 Jul 31 , 105 (287-94).

134

Liu X et al. Silencing GIRK4 expression in human atrial myocytes by adenovirus-delivered small hairpin RNA.
Mol. Biol. Rep., 2009 Jul , 36 (1345-52).

135

Gaborit N et al. Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases.
Eur. Heart J., 2009 Feb , 30 (487-96).

136

Zhang C et al. The single nucleotide polymorphisms of Kir3.4 gene and their correlation with lone paroxysmal atrial fibrillation in Chinese Han population.
Heart Lung Circ, 2009 Aug , 18 (257-61).

137

Robitaille M et al. Intracellular trafficking and assembly of specific Kir3 channel/G protein complexes.
Cell. Signal., 2009 Apr , 21 (488-501).

138

Geng X et al. Specificity of Gbetagamma signaling depends on Galpha subunit coupling with G-protein-sensitive K(+) channels.
Pharmacology, 2009 , 84 (82-90).

139

Hong CM et al. Effects of autoantibodies against M2 muscarinic acetylcholine receptors on rabbit atria in vivo.
Cardiology, 2009 , 112 (180-7).

140

Jin T et al. Stoichiometry of Kir channels with phosphatidylinositol bisphosphate.
Channels (Austin), 2008 Jan-Feb , 2 (19-33).

141

Yang D et al. Expression of inwardly rectifying potassium channel subunits in native human retinal pigment epithelium.
Exp. Eye Res., 2008 Sep , 87 (176-83).

142

Zhao Z et al. Molecular basis for genistein-induced inhibition of Kir2.3 currents.
Pflugers Arch., 2008 May , 456 (413-23).

143

Grasser E et al. Subunit stoichiometry of heterologously expressed G-protein activated inwardly rectifying potassium channels analysed by fluorescence intensity ratio measurement.
Pflugers Arch., 2008 Mar , 455 (1017-24).

144

Perry CA et al. Predisposition to late-onset obesity in GIRK4 knockout mice.
Proc. Natl. Acad. Sci. U.S.A., 2008 Jun 10 , 105 (8148-53).

145

Voigt N et al. Changes in I K, ACh single-channel activity with atrial tachycardia remodelling in canine atrial cardiomyocytes.
Cardiovasc. Res., 2008 Jan , 77 (35-43).

146

Ehrlich JR Inward rectifier potassium currents as a target for atrial fibrillation therapy.
J. Cardiovasc. Pharmacol., 2008 Aug , 52 (129-35).

147

Aguado C et al. Cell type-specific subunit composition of G protein-gated potassium channels in the cerebellum.
J. Neurochem., 2008 Apr , 105 (497-511).

148

Thomas AM et al. Determination of phosphoinositide binding to K(+) channel subunits using a protein-lipid overlay assay.
Methods Mol. Biol., 2008 , 491 (103-11).

149

Rosenhouse-Dantsker A et al. Potassium channel gating in the absence of the highly conserved glycine of the inner transmembrane helix.
Channels (Austin), 2007 May-Jun , 1 (189-97).

150

Lopes CM et al. Protein kinase A modulates PLC-dependent regulation and PIP2-sensitivity of K+ channels.
Channels (Austin), 2007 Mar-Apr , 1 (124-34).

151

Mintert E et al. Generation of a constitutive Na+-dependent inward-rectifier current in rat adult atrial myocytes by overexpression of Kir3.4.
J. Physiol. (Lond.), 2007 Nov 15 , 585 (3-13).

152

Eulitz D et al. Heterogeneous distribution of kir3 potassium channel proteins within dopaminergic neurons in the mesencephalon of the rat brain.
Cell. Mol. Neurobiol., 2007 May , 27 (285-302).

153

Liu B et al. Selective inhibition of Kir currents by antihistamines.
Eur. J. Pharmacol., 2007 Mar 8 , 558 (21-6).

154

Kobayashi T et al. Inhibition by cocaine of G protein-activated inwardly rectifying K+ channels expressed in Xenopus oocytes.
Toxicol In Vitro, 2007 Jun , 21 (656-64).

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