Channelpedia

Kir1.1 Channel

1054 automatically matched literature references

1

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).

5

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

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

8

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

9

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

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

11

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

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

15

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

18

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

20

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

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

27

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

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

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

37

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

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

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).

46

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

58

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

59

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

64

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).

66

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

68

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

75

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

76

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).

78

82

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

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

85

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

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

91

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

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

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

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

99

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

103

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

105

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

107

108

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).

113

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).

118

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

121

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).

126

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

127

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

128

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

129

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

131

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

133

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).

144

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).

149

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

150

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

154

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

155

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

157

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

159

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

161

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

162

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

164

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

165

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

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).

170

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).

173

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

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

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

177

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

179

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

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

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

188

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

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

190

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

192

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).

193

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

204

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

206

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

216

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

219

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

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).

224

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).

225

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

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

231

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

233

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).

235

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

242

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

244

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

245

246

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

248

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

249

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

251

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

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

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

255

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

258

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).

260

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

264

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

267

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

269

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

274

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

276

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).

279

282

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

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

286

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

291

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

292

296

301

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

304

305

308

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

313

314

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).

315

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

319

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

320

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

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

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

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

331

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

332

334

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

337

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).

342

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

345

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

348

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

349

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

352

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

353

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).

354

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

355

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

359

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

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

361

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

363

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).

365

366

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).

370

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

374

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

377

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

381

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).

384

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).

385

386

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

389

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

390

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

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

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

394

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

395

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

396

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

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

399

Gupta V et al. Population structure of Aggarwals of north India as revealed by molecular markers.
Genet Test Mol Biomarkers, 2010 Dec , 14 (781-5).

405

Flanagan SE et al. Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations.
Genet Test Mol Biomarkers, 2010 Aug , 14 (533-7).

406

Kochar IP et al. Transient Neonatal Diabetes due to Kcnj11 Mutation.
Indian Pediatr, 2010 Apr 7 , 47 (359-60).

408

Noczynska A et al. [Three-year observation of permanent neonatal diabetes]
Pediatr Endocrinol Diabetes Metab, 2010 , 16 (50-4).

409

413

Yue P et al. Src family protein tyrosine kinase (PTK) modulates the effect of SGK1 and WNK4 on ROMK channels.
Proc. Natl. Acad. Sci. U.S.A., 2009 Sep 1 , 106 (15061-6).

415

418

Welling PA et al. A comprehensive guide to the ROMK potassium channel: form and function in health and disease.
Am. J. Physiol. Renal Physiol., 2009 Oct , 297 (F849-63).

419

Reyes S et al. Targeted disruption of K(ATP) channels aggravates cardiac toxicity in cocaine abuse.
Clin Transl Sci, 2009 Oct , 2 (361-5).

420

421

422

424

Lang F et al. Targeting SGK1 in diabetes.
Expert Opin. Ther. Targets, 2009 Nov , 13 (1303-11).

426

Batra CM et al. Transient neonatal diabetes due to activating mutation in the ABCC8 gene encoding SUR1.
Indian J Pediatr, 2009 Nov , 76 (1169-72).

427

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

428

Liu Z et al. Regulation of ROMK channel and K+ homeostasis by kidney-specific WNK1 kinase.
J. Biol. Chem., 2009 May 1 , 284 (12198-206).

429

Wang WH et al. Regulation of potassium (K) handling in the renal collecting duct.
Pflugers Arch., 2009 May , 458 (157-68).

430

Brochard K et al. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Nephrol. Dial. Transplant., 2009 May , 24 (1455-64).

432

James C et al. The genetic basis of congenital hyperinsulinism.
J. Med. Genet., 2009 May , 46 (289-99).

440

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).

441

Cheng WW et al. KirBac1.1: it's an inward rectifying potassium channel.
J. Gen. Physiol., 2009 Mar , 133 (295-305).

443

Zaks-Makhina E et al. Specific and slow inhibition of the kir2.1 K+ channel by gambogic acid.
J. Biol. Chem., 2009 Jun 5 , 284 (15432-8).

444

Lauridsen MH et al. [Diabetes in infants may be treated with sulfonylurea as a replacement for insulin]
Ugeskr. Laeg., 2009 Jun 1 , 171 (1923-4).

446

Hartemann-Heurtier A et al. Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes.
Diabetes Metab., 2009 Jun , 35 (233-5).

450

453

Rodan AR et al. Distal potassium handling based on flow modulation of maxi-K channel activity.
Curr. Opin. Nephrol. Hypertens., 2009 Jul , 18 (350-5).

459

Nelson TJ et al. KCNJ11 knockout morula re-engineered by stem cell diploid aggregation.
Philos. Trans. R. Soc. Lond., B, Biol. Sci., 2009 Jan 27 , 364 (269-76).

464

Frindt G et al. Dietary K regulates ROMK channels in connecting tubule and cortical collecting duct of rat kidney.
Am. J. Physiol. Renal Physiol., 2009 Feb , 296 (F347-54).

466

Stechman MJ et al. Genetic causes of hypercalciuric nephrolithiasis.
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