| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1042983436 |
| P356 | DOI | 10.1186/1471-2148-9-188 |
| P932 | PMC publication ID | 2743666 |
| P698 | PubMed publication ID | 19660109 |
| P5875 | ResearchGate publication ID | 26722152 |
| P2093 | author name string | Hans Zischler | |
| Thomas Haaf | |||
| Arne Pfeufer | |||
| Franz Oswald | |||
| Holger Herlyn | |||
| Ulrich Zechner | |||
| P2860 | cites work | Retroposed elements as archives for the evolutionary history of placental mammals | Q21092781 |
| Adenosine deaminases acting on RNA (ADARs): RNA-editing enzymes | Q21999772 | ||
| Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel | Q24318271 | ||
| Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences | Q24336098 | ||
| Aneuploid neurons are functionally active and integrated into brain circuitry | Q24523693 | ||
| Underediting of glutamate receptor GluR-B mRNA in malignant gliomas | Q24555062 | ||
| Computational and experimental identification of novel human imprinted genes | Q24684684 | ||
| Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel † ‡ | Q27651069 | ||
| PAML: a program package for phylogenetic analysis by maximum likelihood | Q27861096 | ||
| Mitochondrial genome variation and the origin of modern humans | Q28141023 | ||
| Nervous system targets of RNA editing identified by comparative genomics | Q28156219 | ||
| Resolution of the early placental mammal radiation using Bayesian phylogenetics | Q28211064 | ||
| Altered editing of serotonin 2C receptor pre-mRNA in the prefrontal cortex of depressed suicide victims | Q28216417 | ||
| Control of kinetic properties of AMPA receptor channels by nuclear RNA editing | Q28242756 | ||
| Glutamate receptors: RNA editing and death of motor neurons | Q28247026 | ||
| Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome | Q28250352 | ||
| Control of human potassium channel inactivation by editing of a small mRNA hairpin | Q28281627 | ||
| Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition | Q28286712 | ||
| K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current | Q28295470 | ||
| Bayes empirical bayes inference of amino acid sites under positive selection | Q29547692 | ||
| Evaluation of an improved branch-site likelihood method for detecting positive selection at the molecular level | Q29547731 | ||
| The PredictProtein server. | Q30333040 | ||
| N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome | Q33154865 | ||
| Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1. | Q33175720 | ||
| Functional interactions between KCNE1 C-terminus and the KCNQ1 channel | Q33425857 | ||
| Epigenetic reprogramming and imprinting in origins of disease | Q33751081 | ||
| Genome-wide prediction of imprinted murine genes | Q33841575 | ||
| Constitutional aneuploidy in the normal human brain. | Q34399858 | ||
| The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss | Q34545156 | ||
| RNA editing of the Drosophila para Na(+) channel transcript. Evolutionary conservation and developmental regulation | Q34609810 | ||
| Genomic imprinting and dermatological disease | Q36562187 | ||
| Alteration of gene expression by chromosome loss in the postnatal mouse brain. | Q38352877 | ||
| RNA editing generates a diverse array of transcripts encoding squid Kv2 K+ channels with altered functional properties | Q38555786 | ||
| KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity | Q40543524 | ||
| Extensive editing of mRNAs for the squid delayed rectifier K+ channel regulates subunit tetramerization | Q44025648 | ||
| Characterization of a novel Long QT syndrome mutation G52R-KCNE1 in a Chinese family | Q44590292 | ||
| Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization. | Q51815243 | ||
| Protein sequence alignments: a strategy for the hierarchical analysis of residue conservation. | Q52387510 | ||
| Single nucleotide polymorphism map of five long-QT genes. | Q52941187 | ||
| Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human | Q56982001 | ||
| The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study | Q57251851 | ||
| Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population | Q57251865 | ||
| Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study | Q57417521 | ||
| Maternal uniparental disomy of chromosome 21 in a normal child | Q62712498 | ||
| A routine method for the establishment of permanent growing lymphoblastoid cell lines | Q70146139 | ||
| Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice | Q71593532 | ||
| Recurrent trisomy 21 and uniparental disomy 21 in a family | Q79176826 | ||
| Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population | Q81138718 | ||
| Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families | Q81433592 | ||
| P304 | page(s) | 188 | |
| P577 | publication date | 2009-08-06 | |
| P1433 | published in | BMC Evolutionary Biology | Q13418959 |
| P1476 | title | Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes | |
| P478 | volume | 9 |
| Q37651406 | An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus. |
| Q33691283 | Association of a common KCNE1 variant with heart failure |
| Q33166303 | Probing Structural Dynamics and Topology of the KCNE1 Membrane Protein in Lipid Bilayers via Site-Directed Spin Labeling and Electron Paramagnetic Resonance Spectroscopy |
| Q34337330 | Structural investigation of the transmembrane domain of KCNE1 in proteoliposomes |
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