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Search results 101 to 200 out of 212 for Scn5a

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Category: Publication
Type Details Score
Publication
First Author: Shimizu A
Year: 2020
Journal: FASEB J
Title: Identification of transmembrane protein 168 mutation in familial Brugada syndrome.
Volume: 34
Issue: 5
Pages: 6399-6417
Publication
First Author: Schleef M
Year: 1993
Journal: Genomics
Title: Chromosomal localization and genomic cloning of the mouse alpha-tropomyosin gene Tpm-1.
Volume: 17
Issue: 2
Pages: 519-21
Publication
First Author: Hund TJ
Year: 2010
Journal: J Clin Invest
Title: A β(IV)-spectrin/CaMKII signaling complex is essential for membrane excitability in mice.
Volume: 120
Issue: 10
Pages: 3508-19
Publication
First Author: Tran PV
Year: 2014
Journal: J Am Soc Nephrol
Title: Downregulating hedgehog signaling reduces renal cystogenic potential of mouse models.
Volume: 25
Issue: 10
Pages: 2201-12
Publication
First Author: van den Boogaard M
Year: 2012
Journal: J Clin Invest
Title: Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer.
Volume: 122
Issue: 7
Pages: 2519-30
Publication
First Author: Misra C
Year: 2020
Journal: Dev Cell
Title: Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy.
Volume: 52
Issue: 6
Pages: 748-763.e6
Publication
First Author: Lodder EM
Year: 2014
Journal: Circ Cardiovasc Genet
Title: Integrative genomic approach identifies multiple genes involved in cardiac collagen deposition.
Volume: 7
Issue: 6
Pages: 790-8
Publication
First Author: Zhang MM
Year: 2007
Journal: J Biol Chem
Title: Structure/function characterization of micro-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels.
Volume: 282
Issue: 42
Pages: 30699-706
Publication
First Author: Hao MM
Year: 2012
Journal: J Neurosci
Title: Early development of electrical excitability in the mouse enteric nervous system.
Volume: 32
Issue: 32
Pages: 10949-60
Publication
First Author: Haufe V
Year: 2005
Journal: J Physiol
Title: Expression pattern of neuronal and skeletal muscle voltage-gated Na+ channels in the developing mouse heart.
Volume: 564
Issue: Pt 3
Pages: 683-96
Publication  
First Author: Li H
Year: 2019
Journal: Development
Title: Nkx2-5 defines a subpopulation of pacemaker cells and is essential for the physiological function of the sinoatrial node in mice.
Volume: 146
Issue: 14
Publication
First Author: Malhotra JD
Year: 2004
Journal: J Biol Chem
Title: Tyrosine-phosphorylated and nonphosphorylated sodium channel beta1 subunits are differentially localized in cardiac myocytes.
Volume: 279
Issue: 39
Pages: 40748-54
Publication
First Author: Fotia AB
Year: 2004
Journal: J Biol Chem
Title: Regulation of neuronal voltage-gated sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2.
Volume: 279
Issue: 28
Pages: 28930-5
Publication
First Author: Furtado MB
Year: 2016
Journal: Differentiation
Title: A novel conditional mouse model for Nkx2-5 reveals transcriptional regulation of cardiac ion channels.
Volume: 91
Issue: 1-3
Pages: 29-41
Publication    
First Author: Ogiwara I
Year: 2018
Journal: Commun Biol
Title: Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.
Volume: 1
Publication
First Author: Gaborit N
Year: 2012
Journal: Development
Title: Cooperative and antagonistic roles for Irx3 and Irx5 in cardiac morphogenesis and postnatal physiology.
Volume: 139
Issue: 21
Pages: 4007-19
Publication
First Author: Shawer H
Year: 2020
Journal: PLoS One
Title: A missense mutation of ErbB2 produces a novel mouse model of stillbirth associated with a cardiac abnormality but lacking abnormalities of placental structure.
Volume: 15
Issue: 6
Pages: e0233007
Publication
First Author: Lopez-Santiago LF
Year: 2007
Journal: J Mol Cell Cardiol
Title: Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals.
Volume: 43
Issue: 5
Pages: 636-47
Publication  
First Author: Samal E
Year: 2019
Journal: Front Physiol
Title: Premature MicroRNA-1 Expression Causes Hypoplasia of the Cardiac Ventricular Conduction System.
Volume: 10
Pages: 235
Publication  
First Author: Moumne O
Year: 2018
Journal: Front Cardiovasc Med
Title: Mechanism Sharing Between Genetic and Gestational Hypoxia-Induced Cardiac Anomalies.
Volume: 5
Pages: 100
Publication    
First Author: van Weerd JH
Year: 2020
Journal: Elife
Title: Trait-associated noncoding variant regions affect TBX3 regulation and cardiac conduction.
Volume: 9
Publication
First Author: Shekhar A
Year: 2016
Journal: J Clin Invest
Title: Transcription factor ETV1 is essential for rapid conduction in the heart.
Volume: 126
Issue: 12
Pages: 4444-4459
Publication
First Author: Gillers BS
Year: 2015
Journal: Circ Res
Title: Canonical wnt signaling regulates atrioventricular junction programming and electrophysiological properties.
Volume: 116
Issue: 3
Pages: 398-406
Publication  
First Author: Semmler J
Year: 2018
Journal: Pharmacol Res
Title: Pacsin 2 is required for the maintenance of a normal cardiac function in the developing mouse heart.
Volume: 128
Pages: 200-210
Publication
First Author: Chinchilla A
Year: 2011
Journal: Circ Cardiovasc Genet
Title: PITX2 insufficiency leads to atrial electrical and structural remodeling linked to arrhythmogenesis.
Volume: 4
Issue: 3
Pages: 269-79
Publication  
First Author: Greulich F
Year: 2016
Journal: J Mol Cell Cardiol
Title: Misexpression of Tbx18 in cardiac chambers of fetal mice interferes with chamber-specific developmental programs but does not induce a pacemaker-like gene signature.
Volume: 97
Pages: 140-9
Publication
First Author: Aanhaanen WT
Year: 2011
Journal: J Clin Invest
Title: Defective Tbx2-dependent patterning of the atrioventricular canal myocardium causes accessory pathway formation in mice.
Volume: 121
Issue: 2
Pages: 534-44
Publication
First Author: de la Rosa AJ
Year: 2013
Journal: Cardiovasc Res
Title: Functional suppression of Kcnq1 leads to early sodium channel remodelling and cardiac conduction system dysmorphogenesis.
Volume: 98
Issue: 3
Pages: 504-14
Publication
First Author: Hoogaars WM
Year: 2007
Journal: Genes Dev
Title: Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria.
Volume: 21
Issue: 9
Pages: 1098-112
Publication  
First Author: Zakariyah AF
Year: 2017
Journal: J Mol Cell Cardiol
Title: Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit.
Volume: 105
Pages: 89-98
Publication  
First Author: Gharibeh L
Year: 2021
Journal: Proc Natl Acad Sci U S A
Title: GATA6 is a regulator of sinus node development and heart rhythm.
Volume: 118
Issue: 1
Publication  
First Author: Moreau JLM
Year: 2019
Journal: Development
Title: Gene-environment interaction impacts on heart development and embryo survival.
Volume: 146
Issue: 4
Publication
First Author: Gómez-Del Arco P
Year: 2024
Journal: Nat Commun
Title: The G4 resolvase Dhx36 modulates cardiomyocyte differentiation and ventricular conduction system development.
Volume: 15
Issue: 1
Pages: 8602
Publication
First Author: Ferguson DA
Year: 2005
Journal: Gene Expr Patterns
Title: eXPRESSION: an in silico tool to predict patterns of gene expression.
Volume: 5
Issue: 5
Pages: 619-28
Publication
First Author: Kim GE
Year: 2015
Journal: Cardiovasc Res
Title: LKB1 deletion causes early changes in atrial channel expression and electrophysiology prior to atrial fibrillation.
Volume: 108
Issue: 1
Pages: 197-208
Publication
First Author: Li C
Year: 2024
Journal: Adv Sci (Weinh)
Title: Cfp1 Controls Cardiomyocyte Maturation by Modifying Histone H3K4me3 of Structural, Metabolic, and Contractile Related Genes.
Volume: 11
Issue: 11
Pages: e2305992
Publication
First Author: Menendez-Montes I
Year: 2016
Journal: Dev Cell
Title: Myocardial VHL-HIF Signaling Controls an Embryonic Metabolic Switch Essential for Cardiac Maturation.
Volume: 39
Issue: 6
Pages: 724-739
Publication
First Author: Harrell MD
Year: 2007
Journal: Physiol Genomics
Title: Large-scale analysis of ion channel gene expression in the mouse heart during perinatal development.
Volume: 28
Issue: 3
Pages: 273-83
Publication      
First Author: European Mouse Mutant Archive
Year: 2003
Journal: Unpublished
Title: Information obtained from the European Mouse Mutant Archive (EMMA)
Publication      
First Author: NIH Mouse Knockout Inventory
Year: 2004
Journal: MGI Direct Data Submission
Title: Information obtained from the NIH Mouse Knockout Inventory
Publication        
First Author: The Gene Ontology Consortium
Year: 2016
Title: Automatic assignment of GO terms using logical inference, based on on inter-ontology links
Publication
First Author: Thompson CL
Year: 2014
Journal: Neuron
Title: A high-resolution spatiotemporal atlas of gene expression of the developing mouse brain.
Volume: 83
Issue: 2
Pages: 309-323
Publication  
First Author: Bedogni F
Year: 2021
Journal: Front Mol Neurosci
Title: Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.
Volume: 14
Pages: 686034
Publication
First Author: Hansen GM
Year: 2008
Journal: Genome Res
Title: Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.
Volume: 18
Issue: 10
Pages: 1670-9
Publication      
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
Publication        
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
Publication        
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Publication
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
Publication
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication      
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
Publication        
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
Publication        
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Publication        
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication      
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication
First Author: Zaklyazminskaya E
Year: 2016
Journal: Biochim Biophys Acta
Title: The role of mutations in the SCN5A gene in cardiomyopathies.
Volume: 1863
Issue: 7 Pt B
Pages: 1799-805
Publication
First Author: Remme CA
Year: 2013
Journal: J Physiol
Title: Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.
Volume: 591
Issue: 17
Pages: 4099-116
Publication
First Author: Wang Q
Year: 1995
Journal: Cell
Title: SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.
Volume: 80
Issue: 5
Pages: 805-11
Publication  
First Author: Doisne N
Year: 2021
Journal: Front Physiol
Title: In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant.
Volume: 12
Pages: 661413
Publication
First Author: Milam AAV
Year: 2018
Journal: J Immunol
Title: Tuning T Cell Signaling Sensitivity Alters the Behavior of CD4+ T Cells during an Immune Response.
Volume: 200
Issue: 10
Pages: 3429-3437
Publication  
First Author: Abrams J
Year: 2020
Journal: JCI Insight
Title: Fibroblast growth factor homologous factors tune arrhythmogenic late NaV1.5 current in calmodulin binding-deficient channels.
Volume: 5
Issue: 19
Publication
First Author: Chakouri N
Year: 2022
Journal: Nat Cardiovasc Res
Title: Fibroblast growth factor homologous factors serve as a molecular rheostat in tuning arrhythmogenic cardiac late sodium current.
Volume: 1
Issue: 5
Pages: 1-13
Publication
First Author: Antzelevitch C
Year: 1999
Journal: Curr Opin Cardiol
Title: Ion channels and ventricular arrhythmias: cellular and ionic mechanisms underlying the Brugada syndrome.
Volume: 14
Issue: 3
Pages: 274-9
Publication
First Author: Schott JJ
Year: 1999
Journal: Nat Genet
Title: Cardiac conduction defects associate with mutations in SCN5A.
Volume: 23
Issue: 1
Pages: 20-1
Publication
First Author: Hesse M
Year: 2007
Journal: Cardiovasc Res
Title: Dilated cardiomyopathy is associated with reduced expression of the cardiac sodium channel Scn5a.
Volume: 75
Issue: 3
Pages: 498-509
Publication
First Author: Wu L
Year: 2007
Journal: Biochem Biophys Res Commun
Title: Induction of high STAT1 expression in transgenic mice with LQTS and heart failure.
Volume: 358
Issue: 2
Pages: 449-54
Publication  
First Author: Avula UMR
Year: 2021
Journal: JCI Insight
Title: Attenuating persistent sodium current-induced atrial myopathy and fibrillation by preventing mitochondrial oxidative stress.
Volume: 6
Issue: 23
Publication
First Author: Baroni D
Year: 2018
Journal: Hum Mutat
Title: A mutation of SCN1B associated with GEFS+ causes functional and maturation defects of the voltage-dependent sodium channel.
Volume: 39
Issue: 10
Pages: 1402-1415
Publication
First Author: Dib-Hajj SD
Year: 1999
Journal: Genomics
Title: Coding sequence, genomic organization, and conserved chromosomal localization of the mouse gene Scn11a encoding the sodium channel NaN.
Volume: 59
Issue: 3
Pages: 309-18
Publication
First Author: Polina I
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Loss of insulin signaling may contribute to atrial fibrillation and atrial electrical remodeling in type 1 diabetes.
Volume: 117
Issue: 14
Pages: 7990-8000
Publication
First Author: Si M
Year: 2019
Journal: Am J Physiol Cell Physiol
Title: Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice.
Volume: 316
Issue: 2
Pages: C154-C161
Publication
First Author: Wang J
Year: 2021
Journal: Sci Rep
Title: Cardiomyocyte-specific deletion of β-catenin protects mouse hearts from ventricular arrhythmias after myocardial infarction.
Volume: 11
Issue: 1
Pages: 17722
Publication
First Author: Vikram A
Year: 2017
Journal: Nat Med
Title: Sirtuin 1 regulates cardiac electrical activity by deacetylating the cardiac sodium channel.
Volume: 23
Issue: 3
Pages: 361-367
Publication
First Author: Jones JM
Year: 2014
Journal: Genesis
Title: Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8a.
Volume: 52
Issue: 2
Pages: 141-8
Publication  
First Author: Bao Y
Year: 2016
Journal: Circ Arrhythm Electrophysiol
Title: Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
Volume: 9
Issue: 12
Publication
First Author: Hakim P
Year: 2008
Journal: Prog Biophys Mol Biol
Title: Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties.
Volume: 98
Issue: 2-3
Pages: 251-66
Publication
First Author: Hakim P
Year: 2010
Journal: Acta Physiol (Oxf)
Title: Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties.
Volume: 198
Issue: 1
Pages: 47-59
Publication  
First Author: Loi M
Year: 2023
Journal: Int J Mol Sci
Title: Cardiac Functional and Structural Abnormalities in a Mouse Model of CDKL5 Deficiency Disorder.
Volume: 24
Issue: 6
Publication
First Author: Hu YF
Year: 2021
Journal: Biochim Biophys Acta Mol Basis Dis
Title: ALDH2 deficiency induces atrial fibrillation through dysregulated cardiac sodium channel and mitochondrial bioenergetics: A multi-omics analysis.
Volume: 1867
Issue: 5
Pages: 166088
Publication
First Author: Koizumi A
Year: 2016
Journal: Eur Heart J
Title: Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.
Volume: 37
Issue: 18
Pages: 1469-75
Publication
First Author: London B
Year: 2007
Journal: Circulation
Title: Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias.
Volume: 116
Issue: 20
Pages: 2260-8
Publication
First Author: Makara MA
Year: 2014
Journal: Circ Res
Title: Ankyrin-G coordinates intercalated disc signaling platform to regulate cardiac excitability in vivo.
Volume: 115
Issue: 11
Pages: 929-38
Publication
First Author: Makita N
Year: 1994
Journal: J Biol Chem
Title: Voltage-gated Na+ channel beta 1 subunit mRNA expressed in adult human skeletal muscle, heart, and brain is encoded by a single gene.
Volume: 269
Issue: 10
Pages: 7571-8
Publication
First Author: Qin N
Year: 2003
Journal: Eur J Biochem
Title: Molecular cloning and functional expression of the human sodium channel beta1B subunit, a novel splicing variant of the beta1 subunit.
Volume: 270
Issue: 23
Pages: 4762-70
Publication
First Author: Patino GA
Year: 2011
Journal: J Neurosci
Title: Voltage-gated Na+ channel β1B: a secreted cell adhesion molecule involved in human epilepsy.
Volume: 31
Issue: 41
Pages: 14577-91