Channelpedia

Kir1.1

1054 literature references associated to Kir1.1

used / unused
Pubmed id

1

364897

2

365564

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).

4

362197

5

367270

Kuhn M et al. Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients.
J. Neurol. Neurosurg. Psychiatr., 2016 Jan , 87 (49-52).

6

365107

McMillan T et al. Neonatal diabetes and protein losing enteropathy: a case report.
BMC Med. Genet., 2016 , 17 (32).

8

364750

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

9

357647

Nikitin AG et al. [Association of the polymorphisms of the FTO, KCNJ11, SLC30A8 and CDKN2B genes with type 2 diabetes].
Mol. Biol. (Mosk.), 2015 Jan-Feb , 49 (119-28).

10

356219

Sitprija V et al. Animal toxins and renal ion transport: Another dimension in tropical nephrology.
Nephrology (Carlton), 2015 Sep 30 , ().

11

366884

Furukawa F et al. In vivo and in vitro effects of high-K(+) stress on branchial expression of ROMKa in seawater-acclimated Mozambique tilapia.
Comp. Biochem. Physiol., Part A Mol. Integr. Physiol., 2015 Sep , 187 (111-8).

14

363711

Bonfanti DH et al. ATP-dependent potassium channels and type 2 diabetes mellitus.
Clin. Biochem., 2015 May , 48 (476-82).

15

348562

Swale DR et al. Computational and Functional Analyses of a Small-Molecule Binding Site in ROMK.
Biophys. J., 2015 Mar 10 , 108 (1094-103).

17

358786

19

364400

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

20

357871

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).

22

366137

Khawash P et al. Nifedipine in Congenital Hyperinsulinism - A Case Report.
J Clin Res Pediatr Endocrinol, 2015 Jun , 7 (151-4).

25

367485

Zhang M et al. Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds.
J. Pediatr. Endocrinol. Metab., 2015 Jul , 28 (877-84).

29

368113

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).

30

349509

Gleason CE et al. mTORC2 regulates renal tubule sodium uptake by promoting ENaC activity.
J. Clin. Invest., 2015 Jan , 125 (117-28).

31

359184

35

361876

36

362081

38

365980

Rozenkova K et al. High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.
J. Clin. Endocrinol. Metab., 2015 Dec , 100 (E1540-9).

39

362673

Yuan J et al. Potassium channel KCNJ15 is required for histamine-stimulated gastric acid secretion.
Am. J. Physiol., Cell Physiol., 2015 Aug 15 , 309 (C264-70).

41

357919

Lin DH et al. Src-family protein tyrosine kinase phosphorylates WNK4 and modulates its inhibitory effect on KCNJ1 (ROMK).
Proc. Natl. Acad. Sci. U.S.A., 2015 Apr 7 , 112 (4495-500).

42

355722

48

348673

50

356151

Haghvirdizadeh P et al. KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus.
J Diabetes Res, 2015 , 2015 (908152).

54

366937

Martelli A et al. Inhibitors of the renal outer medullary potassium channel: a patent review.
Expert Opin Ther Pat, 2015 , 25 (1035-51).

55

367131

Kharade SV et al. ROMK (Kir1.1) pharmacology comes of age.
Channels (Austin), 2015 , 9 (119-20).

56

366218

64

352399

Jindal R et al. Novel mutation c.597_598dup in exon 5 of ABCC8 gene causing congenital hyperinsulinism.
Diabetes Metab Syndr, 2014 Jan-Mar , 8 (45-7).

65

360578

Abujbara MA et al. Permanent neonatal diabetes mellitus in Jordan.
J. Pediatr. Endocrinol. Metab., 2014 Sep , 27 (879-83).

66

355887

67

364410

68

364402

Lee CH et al. Pregabalin activates ROMK1 channels via cAMP-dependent protein kinase and protein kinase C.
Eur. J. Pharmacol., 2014 Oct 5 , 740 (35-44).

69

350694

72

359985

74

359349

Thewjitcharoen Y et al. Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosis.
Diabetes Res. Clin. Pract., 2014 Nov , 106 (e22-4).

75

351592

Kalaivanan P et al. Chromosome 6q24 transient neonatal diabetes mellitus and protein sensitive hyperinsulinaemic hypoglycaemia.
J. Pediatr. Endocrinol. Metab., 2014 Nov , 27 (1065-9).

79

352258

80

354358

Doneray H et al. Permanent neonatal diabetes mellitus caused by a novel mutation in the KCNJ11 gene.
J. Pediatr. Endocrinol. Metab., 2014 Mar , 27 (367-71).

83

344409

Bollepalli MK et al. State-Dependent Network Connectivity Determines Gating in a K(+) Channel.
Structure, 2014 Jun 24 , ().

85

345500

Li HX et al. GATA-4 induces changes in electrophysiological properties of rat mesenchymal stem cells.
Biochim. Biophys. Acta, 2014 Jun , 1840 (2060-9).

88

353725

89

352248

Cooper PE et al. Cantú syndrome resulting from activating mutation in the KCNJ8 gene.
Hum. Mutat., 2014 Jul , 35 (809-13).

91

346387

Lin DH et al. MicroRNA-194 (miR-194) regulates ROMK channel activity by targeting intersectin 1.
Am. J. Physiol. Renal Physiol., 2014 Jan 1 , 306 (F53-60).

93

354061

Welling PA Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function.
Curr. Opin. Nephrol. Hypertens., 2014 Jan , 23 (1-8).

94

364524

Xia XH et al. [Effects of E23K polymorphism in KCNJ11 gene on membrane current].
Zhongguo Ying Yong Sheng Li Xue Za Zhi, 2014 Jan , 30 (23-6).

97

356008

Huang L et al. Nephrocalcinosis as adult presentation of Bartter syndrome type II.
Neth J Med, 2014 Feb , 72 (91-3).

98

349939

101

359569

Carmody D et al. Sulfonylurea treatment before genetic testing in neonatal diabetes: pros and cons.
J. Clin. Endocrinol. Metab., 2014 Dec , 99 (E2709-14).

102

350797

103

352706

Lahmann C et al. A mutation causing increased KATP channel activity leads to reduced anxiety in mice.
Physiol. Behav., 2014 Apr 22 , 129 (79-84).

104

353089

105

360930

Chang WL et al. A novel mutation of KCNJ11 gene in a patient with permanent neonatal diabetes mellitus.
Diabetes Res. Clin. Pract., 2014 Apr , 104 (e29-32).

106

353318

107

353250

108

352139

Wen D et al. Interacting influence of diuretics and diet on BK channel-regulated K homeostasis.
Curr Opin Pharmacol, 2014 Apr , 15 (28-32).

115

358752

116

358466

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

120

351333

Durmaz E et al. A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant.
J Clin Res Pediatr Endocrinol, 2014 , 6 (119-21).

121

359308

Elvira B et al. SPAK and OSR1 dependent down-regulation of murine renal outer medullary K channel ROMK1.
Kidney Blood Press. Res., 2014 , 39 (353-60).

123

353288

126

334883

[To the mechanisms of antiarrhythmic action of Allapinine].
Bioorg. Khim., 2013 Jan-Feb , 39 (105-16).

127

341293

Lang F et al. Serum and glucocorticoid inducible kinase, metabolic syndrome, inflammation, and tumor growth.
Hormones (Athens), 2013 Apr-Jun , 12 (160-71).

128

339524

Duan X Ion Channels, Channelopathies, and Tooth Formation.
J. Dent. Res., 2013 Sep 27 , ().

130

342412

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

131

339450

Pathare G et al. A molecular update on Pseudohypoaldosteronism type II.
Am. J. Physiol. Renal Physiol., 2013 Oct 9 , ().

133

342497

Wang Z et al. Regulation of large-conductance Ca2+-activated K+ channels by WNK4 kinase.
Am. J. Physiol., Cell Physiol., 2013 Oct 15 , 305 (C846-53).

138

348396

144

335618

Shibata S et al. Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4.
Proc. Natl. Acad. Sci. U.S.A., 2013 May 7 , 110 (7838-43).

145

335910

146

347040

Welling PA Regulation of renal potassium secretion: molecular mechanisms.
Semin. Nephrol., 2013 May , 33 (215-28).

147

343951

150

335751

Nichols CG et al. KATP channels and cardiovascular disease: suddenly a syndrome.
Circ. Res., 2013 Mar 29 , 112 (1059-72).

153

341246

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

156

343698

Hussain S et al. Permanent neonatal diabetes due to a novel insulin signal peptide mutation.
Pediatr Diabetes, 2013 Jun , 14 (299-303).

158

344069

Sanda S et al. A SNP in G6PC2 predicts insulin secretion in type 1 diabetes.
Acta Diabetol, 2013 Jun , 50 (459-62).

159

344072

160

347631

Fretzayas A et al. Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II.
Pediatr Int, 2013 Jun , 55 (371-3).

161

335911

Lang F et al. Therapeutic potential of serum and glucocorticoid inducible kinase inhibition.
Expert Opin Investig Drugs, 2013 Jun , 22 (701-14).

162

334913

Angsanakul J et al. Scorpion venoms, kidney and potassium.
Toxicon, 2013 Jul 5 , ().

164

334833

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

165

340169

Frindt G et al. Inhibition of ROMK channels by low extracellular K+ and oxidative stress.
Am. J. Physiol. Renal Physiol., 2013 Jul 15 , 305 (F208-15).

166

340718

Arya VB et al. Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age.
Arch. Dis. Child. Fetal Neonatal Ed., 2013 Jul , 98 (F356-8).

167

343103

169

337245

van der Lubbe N et al. Effects of angiotensin II on kinase-mediated sodium and potassium transport in the distal nephron.
Curr. Opin. Nephrol. Hypertens., 2013 Jan , 22 (120-6).

171

331114

172

336607

173

337141

Cheng CJ et al. Kidney-specific WNK1 regulates sodium reabsorption and potassium secretion in mouse cortical collecting duct.
Am. J. Physiol. Renal Physiol., 2013 Feb 15 , 304 (F397-402).

174

336522

Ronzaud C et al. Renal tubular NEDD4-2 deficiency causes NCC-mediated salt-dependent hypertension.
J. Clin. Invest., 2013 Feb 1 , 123 (657-65).

175

336804

Snider KE et al. Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.
J. Clin. Endocrinol. Metab., 2013 Feb , 98 (E355-63).

176

337187

177

354352

Tizioto PC et al. Identification of KCNJ11 as a functional candidate gene for bovine meat tenderness.
Physiol. Genomics, 2013 Dec 15 , 45 (1215-21).

180

348003

Üstün NU et al. A novel mutation in ABCC8 gene in a newborn with congenital hyperinsulinism -a case report.
Fetal Pediatr Pathol, 2013 Dec , 32 (412-7).

183

339969

Szuts V et al. Altered expression of genes for Kir ion channels in dilated cardiomyopathy.
Can. J. Physiol. Pharmacol., 2013 Aug , 91 (648-56).

184

340082

Cabral PD et al. Less potassium coming out, less sodium going in: phenotyping ROMK knockout rats.
Hypertension, 2013 Aug , 62 (240-1).

188

344225

Xu ZD et al. [ABCC8, KCNJ11 and GLUD1 gene mutation analysis in congenital hyperinsulinism pedigree].
Zhonghua Yi Xue Za Zhi, 2013 Apr 9 , 93 (1089-92).

189

336528

Kapoor RR et al. Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
Eur. J. Endocrinol., 2013 Apr , 168 (557-64).

190

343781

Cameron JS et al. Cardiac K(ATP) channel alterations associated with acclimation to hypoxia in goldfish (Carassius auratus L.).
Comp. Biochem. Physiol., Part A Mol. Integr. Physiol., 2013 Apr , 164 (554-64).

191

341210

Falhammar H et al. Thyrotoxic periodic paralysis: clinical and molecular aspects.
Endocrine, 2013 Apr , 43 (274-84).

193

346690

194

346396

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

196

340226

201

336431

Itoh S et al. DEND syndrome due to V59A mutation in KCNJ11 gene: unresponsive to sulfonylureas.
J. Pediatr. Endocrinol. Metab., 2013 , 26 (143-6).

205

341752

207

343034

Sogno Valin P et al. Genetic analysis of Italian patients with congenital hyperinsulinism of infancy.
Horm Res Paediatr, 2013 , 79 (236-42).

210

338005

213

332558

215

338962

216

337526

Yang L et al. Interactions of external K+ and internal blockers in a weak inward-rectifier K+ channel.
J. Gen. Physiol., 2012 Nov , 140 (529-40).

217

338397

219

348430

Tang H et al. Discovery of Selective Small Molecule ROMK Inhibitors as Potential New Mechanism Diuretics.
ACS Med Chem Lett, 2012 May 10 , 3 (367-72).

220

328631

Frindt G et al. Effects of insulin on Na and K transporters in the rat CCD.
Am. J. Physiol. Renal Physiol., 2012 May , 302 (F1227-33).

222

332851

Ko JM et al. E23K polymorphism of the KCNJ11 gene in Korean children with type 1 diabetes.
World J Pediatr, 2012 May , 8 (169-72).

223

330182

225

326727

Troncoso Brindeiro CM et al. Tempol prevents altered K(+) channel regulation of afferent arteriolar tone in diabetic rat kidney.
Hypertension, 2012 Mar , 59 (657-64).

229

332175

Sackin H et al. Residues at the outer mouth of Kir1.1 determine K-dependent gating.
Biophys. J., 2012 Jun 20 , 102 (2742-50).

230

331904

Jain V et al. Permanent neonatal diabetes caused by a novel mutation.
Indian Pediatr, 2012 Jun , 49 (486-8).

232

329896

233

333949

Rubio-Cabezas O et al. KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life.
Pediatr Diabetes, 2012 Jun , 13 (322-5).

234

332975

235

333105

Lin DH et al. Protein phosphatase 1 modulates the inhibitory effect of With-no-Lysine kinase 4 on ROMK channels.
Am. J. Physiol. Renal Physiol., 2012 Jul 1 , 303 (F110-9).

236

331834

238

333192

240

327423

Wang SY et al. [Neonatal diabetes mellitus caused by KCNJ11 mutation: a case report].
Zhongguo Dang Dai Er Ke Za Zhi, 2012 Jan , 14 (73-5).

243

325150

244

324435

Yang L et al. Ion selectivity and current saturation in inward-rectifier K+ channels.
J. Gen. Physiol., 2012 Feb , 139 (145-57).

245

333982

246

330457

Zhang W et al. Characterization of the R162W Kir7.1 mutation associated with Snowflake vitreoretinopathy.
Am. J. Physiol., Cell Physiol., 2012 Dec 19 , ().

247

334510

248

337917

Mohamed Z et al. Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.
J Clin Res Pediatr Endocrinol, 2012 Dec , 4 (169-81).

249

338070

Klupa T et al. Monogenic models: what have the single gene disorders taught us?
Curr. Diab. Rep., 2012 Dec , 12 (659-66).

251

331368

Robertson JL et al. Multi-ion distributions in the cytoplasmic domain of inward rectifier potassium channels.
Biophys. J., 2012 Aug 8 , 103 (434-43).

252

331674

Rines AK et al. A new pROM king for the mitoK(ATP) dance: ROMK takes the lead.
Circ. Res., 2012 Aug 3 , 111 (392-3).

253

331845

Foster DB et al. Mitochondrial ROMK channel is a molecular component of mitoK(ATP).
Circ. Res., 2012 Aug 3 , 111 (446-54).

256

331676

Habeb AM et al. Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans.
Arch. Dis. Child., 2012 Aug , 97 (721-3).

258

333690

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).

263

330218

Lee BH et al. Genetic basis of Bartter syndrome in Korea.
Nephrol. Dial. Transplant., 2012 Apr , 27 (1516-21).

265

328557

Javorsky M et al. KCNJ11 gene E23K variant and therapeutic response to sulfonylureas.
Eur. J. Intern. Med., 2012 Apr , 23 (245-9).

266

325621

Huang CL Regulation of ion channels by secreted klotho.
Adv. Exp. Med. Biol., 2012 , 728 (100-6).

271

328122

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

272

336826

273

337717

274

322999

Winkler G et al. [Pharmacogenetics of insulin secretagogue antidiabetics].
Orv Hetil, 2011 Oct 9 , 152 (1651-60).

276

327134

278

323356

He W et al. Acid secretion-associated translocation of KCNJ15 in gastric parietal cells.
Am. J. Physiol. Gastrointest. Liver Physiol., 2011 Oct , 301 (G591-600).

283

323189

Liu W et al. Role of NKCC in BK channel-mediated net K⁺ secretion in the CCD.
Am. J. Physiol. Renal Physiol., 2011 Nov , 301 (F1088-97).

284

325516

Joshi R et al. Neonatal diabetes mellitus due to L233F mutation in the KCNJ11 gene.
World J Pediatr, 2011 Nov , 7 (371-2).

286

317070

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

289

316414

290

316318

291

318188

Sackin H et al. Modulation of Kir1.1 inactivation by extracellular Ca and Mg.
Biophys. J., 2011 Mar 2 , 100 (1207-15).

292

316771

295

318186

296

317878

298

321313

299

321701

Lin DH et al. MicroRNA 802 stimulates ROMK channels by suppressing caveolin-1.
J. Am. Soc. Nephrol., 2011 Jun , 22 (1087-98).

303

326622

304

321068

306

321792

308

314157

Winther SA et al. [The effect of aldosterone A on renal potassium excretion].
Ugeskr. Laeg., 2011 Jan 10 , 173 (126-9).

309

317494

314

317153

Saint-Martin C et al. KATP channel mutations in congenital hyperinsulinism.
Semin. Pediatr. Surg., 2011 Feb , 20 (18-22).

317

316277

Alper SL et al. Native and recombinant Slc26a3 (downregulated in adenoma, Dra) do not exhibit properties of 2Cl-/1HCO3- exchange.
Am. J. Physiol., Cell Physiol., 2011 Feb , 300 (C276-86).

319

327700

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

320

327326

Boodram LG et al. Association of the KCNJ11 variant E23K with type 2 diabetes in Indo-Trinidadians.
West Indian Med J, 2011 Dec , 60 (604-7).

321

327717

Greeley SA et al. Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
Curr. Diab. Rep., 2011 Dec , 11 (519-32).

323

321555

Zhuang J et al. WNK4 kinase inhibits Maxi K channel activity by a kinase-dependent mechanism.
Am. J. Physiol. Renal Physiol., 2011 Aug , 301 (F410-9).

326

316757

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

329

319489

332

321198

Wang Y et al. Association of KCNJ11 with impaired glucose regulation in essential hypertension.
Genet. Mol. Res., 2011 , 10 (1111-9).

339

323844

Sang Y et al. AV59M KCNJ11 gene mutation leading to intermediate DEND syndrome in a Chinese child.
J. Pediatr. Endocrinol. Metab., 2011 , 24 (763-6).

340

316276

Jeck N et al. Loop disorders: insights derived from defined genotypes.
Nephron Physiol, 2011 , 118 (p7-14).

341

317985

342

348451

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

343

317539

344

315045

345

314023

Lang F et al. SGK, renal function and hypertension.
J. Nephrol., 2010 Nov-Dec , 23 Suppl 16 (S124-9).

348

137196

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

349

140027

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).

351

315390

Bennett K et al. Pancreatic β-cell KATP channels: Hypoglycaemia and hyperglycaemia.
Rev Endocr Metab Disord, 2010 Sep , 11 (157-63).

352

315384

Edghill EL et al. Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11.
Rev Endocr Metab Disord, 2010 Sep , 11 (193-8).

353

141811

354

141857

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

355

142577

Puricelli E et al. Long-term follow-up of patients with Bartter syndrome type I and II.
Nephrol. Dial. Transplant., 2010 Sep , 25 (2976-81).

359

314706

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).

360

314804

Cotsapas C et al. Expression analysis of loci associated with type 2 diabetes in human tissues.
Diabetologia, 2010 Nov , 53 (2334-9).

361

315772

363

141390

Furgeson SB et al. Mechanisms of type I and type II pseudohypoaldosteronism.
J. Am. Soc. Nephrol., 2010 Nov , 21 (1842-5).

364

314841

Bogdanović R et al. A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency.
Pediatr. Nephrol., 2010 Nov , 25 (2363-8).

366

319825

Vendramini MF et al. Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene.
Arq Bras Endocrinol Metabol, 2010 Nov , 54 (682-4).

367

136975

369

316116

Khadilkar VV et al. KCNJ11 activating mutation in an Indian family with remitting and relapsing diabetes.
Indian J Pediatr, 2010 May , 77 (551-4).

371

319614

374

136228

Bantel C et al. Noble gas xenon is a novel adenosine triphosphate-sensitive potassium channel opener.
Anesthesiology, 2010 Mar , 112 (623-30).

376

137399

377

137935

Njølstad PR et al. [Progress in diabetes genetics]
Tidsskr. Nor. Laegeforen., 2010 Jun 3 , 130 (1145-9).

381

140114

López-Izquierdo A et al. Thiopental inhibits function of different inward rectifying potassium channel isoforms by a similar mechanism.
Eur. J. Pharmacol., 2010 Jul 25 , 638 (33-41).

382

138355

383

140762

385

138554

Carrisoza-Gaytán R et al. Potassium secretion by voltage-gated potassium channel Kv1.3 in the rat kidney.
Am. J. Physiol. Renal Physiol., 2010 Jul , 299 (F255-64).

386

121214

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

387

124706

388

136785

Glukhov AV et al. Differential K(ATP) channel pharmacology in intact mouse heart.
J. Mol. Cell. Cardiol., 2010 Jan , 48 (152-60).

389

136805

Zhang H et al. Cardiac sarcolemmal K(ATP) channels: Latest twists in a questing tale!
J. Mol. Cell. Cardiol., 2010 Jan , 48 (71-5).

391

315375

Serratrice G et al. [Potassium channelopathies and Morvan's syndromes].
Bull. Acad. Natl. Med., 2010 Feb , 194 (391-406; discussion 406-7).

392

137142

Meyer TE et al. Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study.
Cancer Epidemiol. Biomarkers Prev., 2010 Feb , 19 (558-65).

393

140258

394

314548

van de Bunt M et al. From genetic association to molecular mechanism.
Curr. Diab. Rep., 2010 Dec , 10 (452-66).

396

314496

Fang L et al. Hypertension resistance polymorphisms in ROMK (Kir1.1) alter channel function by different mechanisms.
Am. J. Physiol. Renal Physiol., 2010 Dec , 299 (F1359-64).

397

314385

Yang L et al. Magnesium modulates ROMK channel-mediated potassium secretion.
J. Am. Soc. Nephrol., 2010 Dec , 21 (2109-16).

398

314315

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

399

316288

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