Published in BMC Neurosci on November 23, 2005
Cerebrovascular responses in mice deficient in the potassium channel, TREK-1. Am J Physiol Regul Integr Comp Physiol (2010) 1.54
Structural consequences of Kcna1 gene deletion and transfer in the mouse hippocampus. Epilepsia (2007) 1.19
Shaker and Shal mediate transient calcium-independent potassium current in a Drosophila flight motoneuron. J Neurophysiol (2009) 0.99
Kv1.1 null mice have enlarged hippocampus and ventral cortex. BMC Neurosci (2007) 0.84
Kv1.1-dependent control of hippocampal neuron number as revealed by mosaic analysis with double markers. J Physiol (2012) 0.80
Evidence for presence and functional effects of Kv1.1 channels in β-cells: general survey and results from mceph/mceph mice. PLoS One (2011) 0.76
Quality control in the endoplasmic reticulum. Nat Rev Mol Cell Biol (2003) 9.85
A perfect message: RNA surveillance and nonsense-mediated decay. Cell (1999) 7.08
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet (1994) 3.90
Evidence for the formation of heteromultimeric potassium channels in Xenopus oocytes. Nature (1990) 3.88
Deletion of the K(V)1.1 potassium channel causes epilepsy in mice. Neuron (1998) 3.18
The VGL-chanome: a protein superfamily specialized for electrical signaling and ionic homeostasis. Sci STKE (2004) 3.09
Heteromultimeric channels formed by rat brain potassium-channel proteins. Nature (1990) 2.83
Kv beta 1 subunit binding specific for shaker-related potassium channel alpha subunits. Neuron (1996) 1.80
A conserved domain in axonal targeting of Kv1 (Shaker) voltage-gated potassium channels. Science (2003) 1.76
Subunit composition determines Kv1 potassium channel surface expression. J Biol Chem (2000) 1.75
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability. Ann Neurol (2000) 1.64
Generation and characterization of subtype-specific monoclonal antibodies to K+ channel alpha- and beta-subunit polypeptides. Neuropharmacology (1996) 1.61
NAB domain is essential for the subunit assembly of both alpha-alpha and alpha-beta complexes of shaker-like potassium channels. Neuron (1996) 1.29
Determinants of voltage-gated potassium channel surface expression and localization in Mammalian neurons. Crit Rev Biochem Mol Biol (2004) 1.28
Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvbeta2, and Caspr. J Neurocytol (2000) 1.26
Identification of a trafficking determinant localized to the Kv1 potassium channel pore. Proc Natl Acad Sci U S A (2001) 1.25
Differential asparagine-linked glycosylation of voltage-gated K+ channels in mammalian brain and in transfected cells. J Membr Biol (1999) 1.25
Use of a bicistronic GFP-expression vector to characterise ion channels after transfection in mammalian cells. Pflugers Arch (1997) 1.24
Subunit composition of Kv1 channels in human CNS. J Neurochem (1999) 1.22
The human intronless melanocortin 4-receptor gene is NMD insensitive. Hum Mol Genet (2002) 1.19
Assembly of mammalian voltage-gated potassium channels: evidence for an important role of the first transmembrane segment. Neuron (1994) 1.18
Subunit composition of brain voltage-gated potassium channels determined by hongotoxin-1, a novel peptide derived from Centruroides limbatus venom. J Biol Chem (1998) 1.15
alpha subunit compositions of Kv1.1-containing K+ channel subtypes fractionated from rat brain using dendrotoxins. Eur J Biochem (1999) 1.11
Molecular diversity and function of voltage-gated (Kv) potassium channels in epithelial cells. Int J Biochem Cell Biol (2005) 1.05
Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2). J Biol Chem (2002) 1.04
Episodic ataxia type-1 mutations in the Kv1.1 potassium channel display distinct folding and intracellular trafficking properties. J Biol Chem (2001) 1.01
Truncation of the Shaker-like voltage-gated potassium channel, Kv1.1, causes megencephaly. Eur J Neurosci (2003) 1.00
A cellular model for long QT syndrome. Trapping of heteromultimeric complexes consisting of truncated Kv1.1 potassium channel polypeptides and native Kv1.4 and Kv1.5 channels in the endoplasmic reticulum. J Biol Chem (1997) 0.96
MRI and in situ hybridization reveal early disturbances in brain size and gene expression in the megencephalic (mceph/mceph) mouse. Eur J Neurosci (2003) 0.95
Cell-free expression of functional Shaker potassium channels. Nature (1992) 0.94
Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1. J Physiol (2002) 0.93
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain. Mamm Genome (1996) 0.90
Somatic mutations of calreticulin in myeloproliferative neoplasms. N Engl J Med (2013) 9.65
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Genetic loci influencing kidney function and chronic kidney disease. Nat Genet (2010) 3.75
The Swedish Twin Registry in the third millennium: an update. Twin Res Hum Genet (2006) 3.58
LUMA (LUminometric Methylation Assay)--a high throughput method to the analysis of genomic DNA methylation. Exp Cell Res (2006) 2.48
Low fetuin-A levels are associated with cardiovascular death: Impact of variations in the gene encoding fetuin. Kidney Int (2005) 2.42
An evaluation of analysis pipelines for DNA methylation profiling using the Illumina HumanMethylation450 BeadChip platform. Epigenetics (2013) 2.28
No evidence for heritability of Parkinson disease in Swedish twins. Neurology (2004) 2.10
CCR5 deletion protects against inflammation-associated mortality in dialysis patients. J Am Soc Nephrol (2009) 1.88
Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference. Neuropsychopharmacology (2002) 1.82
Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Ann Med (2007) 1.77
Genetic gating of human fear learning and extinction: possible implications for gene-environment interaction in anxiety disorder. Psychol Sci (2009) 1.76
A functional variant of the myeloperoxidase gene is associated with cardiovascular disease in end-stage renal disease patients. Kidney Int Suppl (2003) 1.69
Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression. Blood (2011) 1.63
Multigenic control of disease severity after virulent Mycobacterium tuberculosis infection in mice. Infect Immun (2003) 1.48
Genetic polymorphisms in monoamine systems and outcome of cognitive behavior therapy for social anxiety disorder. PLoS One (2013) 1.44
Epigenetic aberrations in leukocytes of patients with schizophrenia: association of global DNA methylation with antipsychotic drug treatment and disease onset. FASEB J (2012) 1.33
Metal ion effects on ion channel gating. Q Rev Biophys (2003) 1.26
CRY2 is associated with depression. PLoS One (2010) 1.23
Adenovirus-36 is associated with obesity in children and adults in Sweden as determined by rapid ELISA. PLoS One (2012) 1.20
Glycogenin-1 deficiency and inactivated priming of glycogen synthesis. N Engl J Med (2010) 1.20
Maturation of the hypothalamic arcuate agouti-related protein system during postnatal development in the mouse. Brain Res Dev Brain Res (2005) 1.18
Nurr1-RXR heterodimers mediate RXR ligand-induced signaling in neuronal cells. Genes Dev (2003) 1.13
Perception of thermal pain and the thermal grill illusion is associated with polymorphisms in the serotonin transporter gene. PLoS One (2011) 1.13
Increased sensitivity to thermal pain following a single opiate dose is influenced by the COMT val(158)met polymorphism. PLoS One (2009) 1.12
Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study. J Med Ethics (2010) 1.11
Genetic and epigenetic associations of MAOA and NR3C1 with depression and childhood adversities. Int J Neuropsychopharmacol (2013) 1.09
Adiponectin in renal disease: relationship to phenotype and genetic variation in the gene encoding adiponectin. Kidney Int (2004) 1.07
Pyrosequencing-based SNP allele frequency estimation in DNA pools. Hum Mutat (2004) 1.05
CRY2 is associated with rapid cycling in bipolar disorder patients. PLoS One (2010) 1.05
Antidepressant treatment is associated with epigenetic alterations in the promoter of P11 in a genetic model of depression. Int J Neuropsychopharmacol (2011) 1.03
A new muscle glycogen storage disease associated with glycogenin-1 deficiency. Ann Neurol (2014) 1.03
Kv1.1 channels act as mechanical brake in the senses of touch and pain. Neuron (2013) 1.01
Genetic variation in the serotonin transporter gene (5-HTTLPR, rs25531) influences the analgesic response to the short acting opioid Remifentanil in humans. Mol Pain (2009) 1.00
Truncation of the Shaker-like voltage-gated potassium channel, Kv1.1, causes megencephaly. Eur J Neurosci (2003) 1.00
Distinct contributions of the dorsolateral prefrontal and orbitofrontal cortex during emotion regulation. PLoS One (2012) 0.98
The functional Val158Met polymorphism in catechol-O-methyltransferase (COMT) is associated with depression and motivation in men from a Swedish population-based study. J Affect Disord (2010) 0.98
The COMTval158met polymorphism is associated with symptom relief during exposure-based cognitive-behavioral treatment in panic disorder. BMC Psychiatry (2010) 0.96
Circulating levels of visfatin/pre-B-cell colony-enhancing factor 1 in relation to genotype, GFR, body composition, and survival in patients with CKD. Am J Kidney Dis (2007) 0.96
Amygdala-dependent fear conditioning in humans is modulated by the BDNFval66met polymorphism. Behav Neurosci (2010) 0.96
MRI and in situ hybridization reveal early disturbances in brain size and gene expression in the megencephalic (mceph/mceph) mouse. Eur J Neurosci (2003) 0.95
5-HTTLPR and COMTval158met genotype gate amygdala reactivity and habituation. Biol Psychol (2011) 0.94
Kynurenine 3-monooxygenase polymorphisms: relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controls. J Psychiatry Neurosci (2012) 0.93
Alterations of arcuate nucleus neuropeptidergic development in contactin-deficient mice: comparison with anorexia and food-deprived mice. Eur J Neurosci (2005) 0.92
Genetics/Genomics in chronic kidney disease--towards personalized medicine? Semin Dial (2009) 0.92
Evidence for oligomerization between GABAB receptors and GIRK channels containing the GIRK1 and GIRK3 subunits. Eur J Neurosci (2010) 0.91
The symptomatic profile of panic disorder is shaped by the 5-HTTLPR polymorphism. Prog Neuropsychopharmacol Biol Psychiatry (2009) 0.91
Lack of potassium channel induces proliferation and survival causing increased neurogenesis and two-fold hippocampus enlargement. Hippocampus (2007) 0.91
Mechanisms of anesthesia: towards integrating network, cellular, and molecular level modeling. Neuropsychopharmacology (2003) 0.91
Serological data analyses show that adenovirus 36 infection is associated with obesity: a meta-analysis involving 5739 subjects. Obesity (Silver Spring) (2013) 0.90
Conditioned pain modulation is associated with common polymorphisms in the serotonin transporter gene. PLoS One (2011) 0.90
A controlled trial of cognitive-behavior therapy combined with vestibular rehabilitation in the treatment of dizziness. Behav Res Ther (2005) 0.89
Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Ann Neurol (2004) 0.89
P2RX7: expression responds to sleep deprivation and associates with rapid cycling in bipolar disorder type 1. PLoS One (2012) 0.89
Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsy. J Child Neurol (2010) 0.88
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One (2013) 0.88
On the opening of voltage-gated ion channels. Physiol Behav (2007) 0.88
Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism. Mutat Res (2005) 0.88
Changes in fat mass after initiation of maintenance dialysis is influenced by the uncoupling protein 2 exon 8 insertion/deletion polymorphism. Nephrol Dial Transplant (2006) 0.87
Voltage-dependence of the human dopamine D2 receptor. Synapse (2008) 0.87
Visfatin is increased in chronic kidney disease patients with poor appetite and correlates negatively with fasting serum amino acids and triglyceride levels. Nephrol Dial Transplant (2009) 0.87
Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencingtrade mark and validation against the 5'nuclease (Taqman((R))) assay. Hum Mutat (2002) 0.87
Ion channel density regulates switches between regular and fast spiking in soma but not in axons. PLoS Comput Biol (2010) 0.87
Expression of inflammatory and insulin signaling genes in adipose tissue in response to elective surgery. J Clin Endocrinol Metab (2010) 0.86
CLOCK is suggested to associate with comorbid alcohol use and depressive disorders. J Circadian Rhythms (2010) 0.85
Localization of cholesterol, amyloid and glia in Alzheimer's disease transgenic mouse brain tissue using time-of-flight secondary ion mass spectrometry (ToF-SIMS) and immunofluorescence imaging. Acta Neuropathol (2012) 0.85
Carbamazepine protects against megencephaly and abnormal expression of BDNF and Nogo signaling components in the mceph/mceph mouse. Neurobiol Dis (2006) 0.85
Voltage-sensitivity at the human dopamine D2S receptor is agonist-specific. Biochem Biophys Res Commun (2008) 0.85
Cognitive manic symptoms associated with the P2RX7 gene in bipolar disorder. Bipolar Disord (2011) 0.84
A tyrosine substitution in the cavity wall of a k channel induces an inverted inactivation. Biophys J (2008) 0.84
Chemical analysis of osmium tetroxide staining in adipose tissue using imaging ToF-SIMS. Histochem Cell Biol (2009) 0.84
PreproNPY Pro7 protects against depression despite exposure to environmental risk factors. J Affect Disord (2009) 0.84
Kv1.1 null mice have enlarged hippocampus and ventral cortex. BMC Neurosci (2007) 0.84
Azithromycin increases chloride efflux from cystic fibrosis airway epithelial cells. Exp Lung Res (2009) 0.84
Genetic approaches in the clinical investigation of complex disorders: malnutrition, inflammation, and atherosclerosis (MIA) as a prototype. Kidney Int Suppl (2003) 0.84
Reduced gene expression of adiponectin in fat tissue from patients with end-stage renal disease. Kidney Int (2004) 0.84
Agonist-specific voltage sensitivity at the dopamine D2S receptor--molecular determinants and relevance to therapeutic ligands. Neuropharmacology (2011) 0.83
Coenzyme Q10 prevents peripheral neuropathy and attenuates neuron loss in the db-/db- mouse, a type 2 diabetes model. Proc Natl Acad Sci U S A (2012) 0.83