Kir6.2
3327 literature references associated to Kir6.2
1
Beurg M
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Development and localization of reverse-polarity mechanotransducer channels in cochlear hair cells.
Proc. Natl. Acad. Sci. U.S.A.,
2016
May
9
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2
Swale DR
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ML418: The First Selective, Sub-Micromolar Pore Blocker of Kir7.1 Potassium Channels.
ACS Chem Neurosci,
2016
May
24
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3
Tosti E
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Ion currents in embryo development.
Birth Defects Res. C Embryo Today,
2016
Mar
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4
Davidson LM
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Molecular mechanisms of membrane interaction at implantation.
Birth Defects Res. C Embryo Today,
2016
Mar
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Lo FS
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Sensory Activity-Dependent and Sensory Activity-Independent Properties of the Developing Rodent Trigeminal Principal Nucleus.
Dev. Neurosci.,
2016
Jun
9
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6
Hawrysh PJ
et al.
Phosphorylation of the mitochondrial ATP-sensitive potassium channel occurs independently of PKCε in turtle brain.
Comp. Biochem. Physiol. B, Biochem. Mol. Biol.,
2016
Jun
6
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7
Izumi G
et al.
Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity?
Pediatr Cardiol,
2016
Jun
, 37 (962-70).
8
Kwon HJ
et al.
Evidence for glucagon-like peptide-1 receptor signaling to activate ATP-sensitive potassium channels in pancreatic beta cells.
Biochem. Biophys. Res. Commun.,
2016
Jan
8
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9
Andrikopoulos S
et al.
Identification of ABCC8 as a contributory gene to impaired early-phase insulin secretion in NZO mice.
J. Endocrinol.,
2016
Jan
, 228 (61-73).
10
Shen XM
et al.
Investigation of Congenital Myasthenia Reveals Functional Asymmetry of Invariant Acetylcholine Receptor (AChR) Cys-loop Aspartates.
J. Biol. Chem.,
2016
Feb
12
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11
Hanukoglu I
et al.
Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases.
Gene,
2016
Apr
1
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12
Pedersen TH
et al.
Role of physiological ClC-1 Cl- ion channel regulation for the excitability and function of working skeletal muscle.
J. Gen. Physiol.,
2016
Apr
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13
McMillan T
et al.
Neonatal diabetes and protein losing enteropathy: a case report.
BMC Med. Genet.,
2016
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14
Behere SP
et al.
Inherited arrhythmias: The cardiac channelopathies.
Ann Pediatr Cardiol,
2015 Sep-Dec
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15
Winterhager E
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Gap junction connexins in female reproductive organs: implications for women's reproductive health.
Hum. Reprod. Update,
2015 May-Jun
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16
Woś H
et al.
Diagnostic problems in cystic fibrosis - specific characteristics of a group of infants and young children diagnosed positive through neonatal screening, in whom cystic fibrosis had not been diagnosed.
Dev Period Med,
2015 Jan-Mar
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17
Boczar M
et al.
Meconium ileus in newborns with cystic fibrosis - results of treatment in the group of patients operated on in the years 2000-2014.
Dev Period Med,
2015 Jan-Mar
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18
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
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19
van der Cruijsen EA
et al.
Biomolecular DNP-Supported NMR Spectroscopy using Site-Directed Spin Labeling.
Chemistry,
2015
Sep
7
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20
Dunham-Snary KJ
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A mitochondrial redox oxygen sensor in the pulmonary vasculature and ductus arteriosus.
Pflugers Arch.,
2015
Sep
23
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21
Grabner CP
et al.
RIM1/2-Mediated Facilitation of Cav1.4 Channel Opening Is Required for Ca2+-Stimulated Release in Mouse Rod Photoreceptors.
J. Neurosci.,
2015
Sep
23
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22
Nessa A
et al.
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8.
Hum. Mol. Genet.,
2015
Sep
15
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23
Waterman M
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Predictors of Outcome in Ulcerative Colitis.
Inflamm. Bowel Dis.,
2015
Sep
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24
Jantzie LL
et al.
Postnatal Erythropoietin Mitigates Impaired Cerebral Cortical Development Following Subplate Loss from Prenatal Hypoxia-Ischemia.
Cereb. Cortex,
2015
Sep
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25
Karstensen HG
et al.
The first mutation in CNGA2 in two brothers with anosmia.
Clin. Genet.,
2015
Sep
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26
Alfonso J
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Downregulation of Sphingosine 1-Phosphate Receptor 1 Promotes the Switch from Tangential to Radial Migration in the OB.
J. Neurosci.,
2015
Oct
7
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27
Halmos KC
et al.
Molecular and functional changes in glucokinase expression in the brainstem dorsal vagal complex in a murine model of type 1 diabetes.
Neuroscience,
2015
Oct
15
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28
Jang H
et al.
The Effects of a Single Developmentally Entrained Pulse of Testosterone in Female Neonatal Mice on Reproductive and Metabolic Functions in Adult Life.
Endocrinology,
2015
Oct
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29
Wang W
et al.
Effect of electronic stimulation at Neiguan (PC 6) acupoint on gene expression of adenosine triphosphate-sensitive potassium channel and protein kinases in rats with myocardial ischemia.
J Tradit Chin Med,
2015
Oct
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30
Goychuk I
Modeling magnetosensitive ion channels in the viscoelastic environment of living cells.
Phys Rev E Stat Nonlin Soft Matter Phys,
2015
Oct
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31
Murillo A
et al.
Identification of Host Cell Factors Associated with Astrovirus Replication in Caco-2 Cells.
J. Virol.,
2015
Oct
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32
Wang C
et al.
Simvastatin prevents β-amyloid(25-35)-impaired neurogenesis in hippocampal dentate gyrus through α7nAChR-dependent cascading PI3K-Akt and increasing BDNF via reduction of farnesyl pyrophosphate.
Neuropharmacology,
2015
Oct
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33
Fusco C
et al.
New phenotype and neonatal onset of sodium channel myotonia in a child with a novel mutation of SCN4A gene.
Brain Dev.,
2015
Oct
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34
De Luca A
et al.
Expression and Localization of Aquaporin-1 Along the Intestine of Colostrum Suckling Buffalo Calves.
Anat Histol Embryol,
2015
Oct
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35
Benton R
Multigene Family Evolution: Perspectives from Insect Chemoreceptors.
Trends Ecol. Evol. (Amst.),
2015
Oct
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36
Santella L
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Assisted yes, but where do we draw the line?
Reprod. Biomed. Online,
2015
Oct
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37
Parker-McGill K
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Changing incidence of cystic fibrosis in Wisconsin, USA.
Pediatr. Pulmonol.,
2015
Nov
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38
Wenke JL
et al.
MALDI Imaging Mass Spectrometry Spatially Maps Age-Related Deamidation and Truncation of Human Lens Aquaporin-0.
Invest. Ophthalmol. Vis. Sci.,
2015
Nov
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39
Kayser V
et al.
Altered nociception in mice with genetically induced hypoglutamatergic tone.
Neuroscience,
2015
May
7
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40
Foong JP
et al.
Changes in Nicotinic Neurotransmission during Enteric Nervous System Development.
J. Neurosci.,
2015
May
6
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41
Shen S
et al.
Effect of adenosine triphosphate-sensitive potassium activation on peripheral and central pain sensitization.
J. Surg. Res.,
2015
May
15
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42
Qian Y
et al.
Joint effect of CENTD2 and KCNQ1 polymorphisms on the risk of type 2 diabetes mellitus among Chinese Han population.
Mol. Cell. Endocrinol.,
2015
May
15
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43
Sasaki-Hamada S
et al.
Changes in hippocampal synaptic functions and protein expression in monosodium glutamate-treated obese mice during development of glucose intolerance.
Eur. J. Neurosci.,
2015
May
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44
Zhang Q
et al.
Effect of sulfur dioxide inhalation on the expression of KATP and L-Ca(2+) channels in rat hearts.
Environ. Toxicol. Pharmacol.,
2015
May
, 39 (1132-8).
45
Gasparino E
et al.
Thermal stress induces changes in gene expression and blood parameters in high and low feed efficiency meat quail.
J. Appl. Genet.,
2015
May
, 56 (253-60).
46
Bonfanti DH
et al.
ATP-dependent potassium channels and type 2 diabetes mellitus.
Clin. Biochem.,
2015
May
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47
Zhao YT
et al.
Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function.
Proc. Natl. Acad. Sci. U.S.A.,
2015
Mar
31
, 112 (E1669-77).
48
Devaraneni PK
et al.
Structurally distinct ligands rescue biogenesis defects of the KATP channel complex via a converging mechanism.
J. Biol. Chem.,
2015
Mar
20
, 290 (7980-91).
49
Zhang Q
et al.
Effects of sodium metabisulfite on the expression of BK(Ca), K(ATP), and L-Ca(2+) channels in rat aortas in vivo and in vitro.
J. Hazard. Mater.,
2015
Mar
2
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50
Ramdya P
et al.
Mechanosensory interactions drive collective behaviour in Drosophila.
Nature,
2015
Mar
12
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51
Pai VP
et al.
Endogenous Gradients of Resting Potential Instructively Pattern Embryonic Neural Tissue via Notch Signaling and Regulation of Proliferation.
J. Neurosci.,
2015
Mar
11
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52
Lemaire LA
et al.
Bicaudal C1 promotes pancreatic NEUROG3+ endocrine progenitor differentiation and ductal morphogenesis.
Development,
2015
Mar
1
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53
Zhang L
et al.
Lipopolysaccharides upregulate calcium concentration in mouse uterine smooth muscle cells through the T-type calcium channels.
Int. J. Mol. Med.,
2015
Mar
, 35 (784-90).
54
Khan AO
et al.
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutations.
Ophthalmic Genet.,
2015
Mar
, 36 (79-84).
55
Chan KH
et al.
Genetic Variations in Magnesium-Related Ion Channels May Affect Diabetes Risk among African American and Hispanic American Women.
J. Nutr.,
2015
Mar
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56
Back SJ
et al.
Imaging features of tuberous sclerosis complex with autosomal-dominant polycystic kidney disease: a contiguous gene syndrome.
Pediatr Radiol,
2015
Mar
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57
Harel S
et al.
Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture.
J. Pediatr. Endocrinol. Metab.,
2015
Mar
, 28 (345-51).
58
Pai VP
et al.
Local and long-range endogenous resting potential gradients antagonistically regulate apoptosis and proliferation in the embryonic CNS.
Int. J. Dev. Biol.,
2015
Jun
26
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59
Zhang Q
et al.
The molecular mechanism of the effect of sulfur dioxide inhalation on the potassium and calcium ion channels in rat aortas.
Hum Exp Toxicol,
2015
Jun
24
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60
Zhang RS
et al.
A Conserved Residue Cluster That Governs Kinetics of ATP-dependent Gating of Kir6.2 Potassium Channels.
J. Biol. Chem.,
2015
Jun
19
, 290 (15450-61).
61
Keiser NW
et al.
Defective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungs.
Am. J. Respir. Cell Mol. Biol.,
2015
Jun
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62
Ohba C
et al.
GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.
Epilepsia,
2015
Jun
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63
Shaw JC
et al.
Preterm birth affects GABAA receptor subunit mRNA levels during the foetal-to-neonatal transition in guinea pigs.
J Dev Orig Health Dis,
2015
Jun
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64
Fu Y
et al.
Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring.
Birth Defects Res. Part A Clin. Mol. Teratol.,
2015
Jun
, 103 (471-8).
65
Zhuang L
et al.
The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population.
Mol. Cell. Biochem.,
2015
Jun
, 404 (133-41).
66
Khawash P
et al.
Nifedipine in Congenital Hyperinsulinism - A Case Report.
J Clin Res Pediatr Endocrinol,
2015
Jun
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67
Nozari M
et al.
Sex-specific restoration of MK-801-induced sensorimotor gating deficit by environmental enrichment.
Neuroscience,
2015
Jul
23
, 299 (28-34).
68
Thurber BW
et al.
Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes.
Diabetologia,
2015
Jul
, 58 (1430-5).
69
Claycombe KJ
et al.
Maternal low-protein diet causes body weight loss in male, neonate Sprague-Dawley rats involving UCP-1-mediated thermogenesis.
J. Nutr. Biochem.,
2015
Jul
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70
Zhang M
et al.
Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds.
J. Pediatr. Endocrinol. Metab.,
2015
Jul
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71
Parolin Schnekenberg R
et al.
De novo point mutations in patients diagnosed with ataxic cerebral palsy.
Brain,
2015
Jul
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72
Bryant AS
et al.
Cholinergic control of gamma power in the midbrain spatial attention network.
J. Neurosci.,
2015
Jan
14
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73
Sharma AA
et al.
Impaired NLRP3 inflammasome activity during fetal development regulates IL-1β production in human monocytes.
Eur. J. Immunol.,
2015
Jan
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74
Yazaki-Sugiyama Y
et al.
Acute inhibition of a cortical motor area impairs vocal control in singing zebra finches.
Eur. J. Neurosci.,
2015
Jan
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75
Viart V
et al.
Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosis.
Eur. Respir. J.,
2015
Jan
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76
Sun HS
et al.
Neuronal K(ATP) channels mediate hypoxic preconditioning and reduce subsequent neonatal hypoxic-ischemic brain injury.
Exp. Neurol.,
2015
Jan
, 263 (161-71).
77
Fleischmann R
et al.
Severe cognitive impairment associated with intrathecal antibodies to the NR1 subunit of the N-methyl-D-aspartate receptor in a patient with multiple sclerosis.
JAMA Neurol,
2015
Jan
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78
Larsen J
et al.
The phenotypic spectrum of SCN8A encephalopathy.
Neurology,
2015
Feb
3
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79
Baronas VA
et al.
Use-dependent activation of neuronal kv1.2 channel complexes.
J. Neurosci.,
2015
Feb
25
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80
Lim JH
et al.
Ion-channel-coupled receptor-based platform for a real-time measurement of g-protein-coupled receptor activities.
ACS Nano,
2015
Feb
24
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81
Gong C
et al.
Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.
Pediatr Diabetes,
2015
Feb
2
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82
Catalán MA
et al.
A fluid secretion pathway unmasked by acinar-specific Tmem16A gene ablation in the adult mouse salivary gland.
Proc. Natl. Acad. Sci. U.S.A.,
2015
Feb
17
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83
Audrezet MP
et al.
Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy.
Genet. Med.,
2015
Feb
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84
Zaharieva IT
et al.
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.
Brain,
2015
Dec
22
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85
Matalon S
et al.
Role of epithelial sodium channels in the regulation of lung fluid homeostasis.
Am. J. Physiol. Lung Cell Mol. Physiol.,
2015
Dec
1
, 309 (L1229-38).
86
Vimaleswaran KS
et al.
Interactions between uncoupling protein 2 gene polymorphisms, obesity and alcohol intake on liver function: a large meta-analysed population-based study.
Eur. J. Endocrinol.,
2015
Dec
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87
Kharrazi M
et al.
Newborn Screening for Cystic Fibrosis in California.
Pediatrics,
2015
Dec
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88
Rozenkova K
et al.
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.
J. Clin. Endocrinol. Metab.,
2015
Dec
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89
Baier LJ
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ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes.
Diabetes,
2015
Dec
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90
Alotaibi M
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Hypoxia-induced force increase (HIFI) is a novel mechanism underlying the strengthening of labor contractions, produced by hypoxic stresses.
Proc. Natl. Acad. Sci. U.S.A.,
2015
Aug
4
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91
Chen T
et al.
[Effect of curcumin on oligomer formation and mitochondrial ATP-sensitive potassium channels induced by overexpression or mutation of α-synuclein].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi,
2015
Aug
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92
Kay DM
et al.
Utility of a very high IRT/No mutation referral category in cystic fibrosis newborn screening.
Pediatr. Pulmonol.,
2015
Aug
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93
Zhang Q
et al.
The molecular mechanisms of sodium metabisulfite on the expression of K ATP and L-Ca2+ channels in rat hearts.
Regul. Toxicol. Pharmacol.,
2015
Aug
, 72 (440-6).
94
Henn MC
et al.
Diazoxide Cardioprotection Is Independent of Adenosine Triphosphate-Sensitive Potassium Channel Kir6.1 Subunit in Response to Stress.
J. Am. Coll. Surg.,
2015
Aug
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95
Oh EH
et al.
Coupling of olfactory receptor and ion channel for rapid and sensitive visualization of odorant response.
Acta Biomater,
2015
Aug
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96
Datta D
et al.
Developmental Expression Patterns of GABAA Receptor Subunits in Layer 3 and 5 Pyramidal Cells of Monkey Prefrontal Cortex.
Cereb. Cortex,
2015
Aug
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97
Zúñiga-García V
et al.
Differential Expression of Ion Channels and Transporters During Hepatocellular Carcinoma Development.
Dig. Dis. Sci.,
2015
Apr
5
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98
Agné AM
et al.
Hydrogen sulfide decreases β-adrenergic agonist-stimulated lung liquid clearance by inhibiting ENaC-mediated transepithelial sodium absorption.
Am. J. Physiol. Regul. Integr. Comp. Physiol.,
2015
Apr
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99
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The role of K⁺ conductances in regulating membrane excitability in human gastric corpus smooth muscle.
Am. J. Physiol. Gastrointest. Liver Physiol.,
2015
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100
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The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.
Epilepsia,
2015
Apr
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101
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Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations.
J. Hum. Genet.,
2015
Apr
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102
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Premyelinated central axons express neurotoxic NMDA receptors: relevance to early developing white-matter injury.
J. Cereb. Blood Flow Metab.,
2015
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103
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Clinical and genetic investigation of 17 Japanese patients with hyperekplexia.
Dev Med Child Neurol,
2015
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104
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Dyad content is reduced in cardiac myocytes of mice with impaired calmodulin regulation of RyR2.
J. Muscle Res. Cell. Motil.,
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Apr
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105
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Successful transition to sulfonylurea in neonatal diabetes, developmental delay, and seizures (DEND syndrome) due to R50P KCNJ11 mutation.
Diabetes Res. Clin. Pract.,
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106
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Visual Stimuli Evoked Action Potentials Trigger Rapidly Propagating Dendritic Calcium Transients in the Frog Optic Tectum Layer 6 Neurons.
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[The study of the association of polymorphism rs5219 gene KCNJ11 with obesity and the risk of type 2 diabetes among residents of the Moscow Region].
Vopr Pitan,
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108
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Control of Phasic Firing by a Background Leak Current in Avian Forebrain Auditory Neurons.
Front Cell Neurosci,
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109
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Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities.
PLoS ONE,
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110
Gunewardena SS
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Deciphering the Developmental Dynamics of the Mouse Liver Transcriptome.
PLoS ONE,
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111
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Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) Association in Russian Diabetes Mellitus 2 Type Cohort and Meta-Analysis.
PLoS ONE,
2015
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112
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Evidence for a KATP Channel in Rough Endoplasmic Reticulum (rerKATP Channel) of Rat Hepatocytes.
PLoS ONE,
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113
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Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling.
BMC Genomics,
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114
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Olmsted syndrome: clinical, molecular and therapeutic aspects.
Orphanet J Rare Dis,
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115
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Deletion of PDK1 causes cardiac sodium current reduction in mice.
PLoS ONE,
2015
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116
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Three novel pathogenic mutations in KATP channel genes and somatic imprinting alterations of the 11p15 region in pancreatic tissue in patients with congenital hyperinsulinism.
Horm Res Paediatr,
2015
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117
Harvey TJ
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Maternal Nutrient Restriction Alters Ca2+ Handling Properties and Contractile Function of Isolated Left Ventricle Bundles in Male But Not Female Juvenile Rats.
PLoS ONE,
2015
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118
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Cleft Palate, Moderate Lung Developmental Retardation and Early Postnatal Lethality in Mice Deficient in the Kir7.1 Inwardly Rectifying K+ Channel.
PLoS ONE,
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119
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Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia.
BMC Res Notes,
2015
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120
Caffes N
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Glibenclamide for the treatment of ischemic and hemorrhagic stroke.
Int J Mol Sci,
2015
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121
Liu WJ
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Developmental expression of inositol 1, 4, 5-trisphosphate receptor in the post-natal rat cochlea.
Eur J Histochem,
2015
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122
Duan Z
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Polymorphisms in Ion Transport Genes Are Associated with Eggshell Mechanical Property.
PLoS ONE,
2015
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123
Maejima Y
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Water intake disorder in a DEND syndrome afflicted patient with R50P mutation.
Endocr. J.,
2015
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124
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Differential mRNA expression and glucocorticoid-mediated regulation of TRPM6 and TRPM7 in the heart and kidney throughout murine pregnancy and development.
PLoS ONE,
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125
Chabwine JN
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NKCC1 downregulation induces hyperpolarizing shift of GABA responsiveness at near term fetal stages in rat cultured dorsal root ganglion neurons.
BMC Neurosci,
2015
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126
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Ion channel regulation by phosphoinositides analyzed with VSPs-PI(4,5)P2 affinity, phosphoinositide selectivity, and PI(4,5)P2 pool accessibility.
Front Pharmacol,
2015
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127
Haghvirdizadeh P
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KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus.
J Diabetes Res,
2015
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128
Yamanushi TT
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Comparison of formaldehyde and methanol fixatives used in the detection of ion channel proteins in isolated rat ventricular myocytes by immunofluorescence labelling and confocal microscopy.
Folia Morphol. (Warsz),
2015
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