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Search results 1 to 100 out of 224 for Kcnq1

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Category: Publication
Type Details Score
Publication
First Author: Schultz BM
Year: 2015
Journal: Nucleic Acids Res
Title: Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain.
Volume: 43
Issue: 2
Pages: 745-59
Publication
First Author: Asahara S
Year: 2015
Journal: Proc Natl Acad Sci U S A
Title: Paternal allelic mutation at the Kcnq1 locus reduces pancreatic β-cell mass by epigenetic modification of Cdkn1c.
Volume: 112
Issue: 27
Pages: 8332-7
Publication
First Author: Zhang H
Year: 2014
Journal: J Cell Biol
Title: Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus.
Volume: 204
Issue: 1
Pages: 61-75
Publication
First Author: Lewis A
Year: 2006
Journal: Development
Title: Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo.
Volume: 133
Issue: 21
Pages: 4203-10
Publication
First Author: Thakur N
Year: 2004
Journal: Mol Cell Biol
Title: An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region.
Volume: 24
Issue: 18
Pages: 7855-62
Publication
First Author: Umlauf D
Year: 2004
Journal: Nat Genet
Title: Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.
Volume: 36
Issue: 12
Pages: 1296-300
Publication
First Author: Than BL
Year: 2014
Journal: Oncogene
Title: The role of KCNQ1 in mouse and human gastrointestinal cancers.
Volume: 33
Issue: 29
Pages: 3861-8
Publication
First Author: Knollmann BC
Year: 2007
Journal: Biochem Biophys Res Commun
Title: Kcnq1 contributes to an adrenergic-sensitive steady-state K+ current in mouse heart.
Volume: 360
Issue: 1
Pages: 212-8
Publication
First Author: Song P
Year: 2009
Journal: J Physiol
Title: KCNQ1 is the luminal K+ recycling channel during stimulation of gastric acid secretion.
Volume: 587
Issue: Pt 15
Pages: 3955-65
Publication
First Author: Casimiro MC
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.
Volume: 98
Issue: 5
Pages: 2526-31
Publication  
First Author: Oh-McGinnis R
Year: 2010
Journal: BMC Dev Biol
Title: Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.
Volume: 10
Pages: 50
Publication
First Author: Mohammad F
Year: 2010
Journal: Development
Title: Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1.
Volume: 137
Issue: 15
Pages: 2493-9
Publication
First Author: Chang Q
Year: 2015
Journal: EMBO Mol Med
Title: Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome.
Volume: 7
Issue: 8
Pages: 1077-86
Publication
First Author: Knollmann BC
Year: 2004
Journal: J Pharmacol Exp Ther
Title: Isoproterenol exacerbates a long QT phenotype in Kcnq1-deficient neonatal mice: possible roles for human-like Kcnq1 isoform 1 and slow delayed rectifier K+ current.
Volume: 310
Issue: 1
Pages: 311-8
Publication
First Author: Salas M
Year: 2004
Journal: Mech Dev
Title: Placental growth retardation due to loss of imprinting of Phlda2.
Volume: 121
Issue: 10
Pages: 1199-210
Publication      
First Author: Kim JH
Year: 2001
Journal: MGI Direct Data Submission
Title: A new spontaneous mutation in the Kcnq1 gene in mice
Publication      
First Author: Gagnon LH
Year: 2006
Journal: MGI Direct Data Submission
Title: Vertigo-4J, a new spontaneous mouse mutation in the Kcnq1 gene
Publication
First Author: Singh VB
Year: 2017
Journal: Development
Title: Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.
Volume: 144
Issue: 10
Pages: 1820-1830
Publication
First Author: Shin JY
Year: 2008
Journal: EMBO J
Title: Two distinct mechanisms of silencing by the KvDMR1 imprinting control region.
Volume: 27
Issue: 1
Pages: 168-78
Publication
First Author: Fedoriw AM
Year: 2012
Journal: G3 (Bethesda)
Title: Differentiation-driven nucleolar association of the mouse imprinted Kcnq1 locus.
Volume: 2
Issue: 12
Pages: 1521-8
Publication
First Author: Takagi T
Year: 2007
Journal: Exp Anim
Title: Phenotypic analysis of vertigo 2 Jackson mice with a Kcnq1 potassium channel mutation.
Volume: 56
Issue: 4
Pages: 295-300
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: Mancini-Dinardo D
Year: 2006
Journal: Genes Dev
Title: Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes.
Volume: 20
Issue: 10
Pages: 1268-82
Publication
First Author: Goldman AM
Year: 2009
Journal: Sci Transl Med
Title: Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.
Volume: 1
Issue: 2
Pages: 2ra6
Publication
First Author: Elso CM
Year: 2004
Journal: Hum Mol Genet
Title: Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice.
Volume: 13
Issue: 22
Pages: 2813-21
Publication
First Author: Rivas A
Year: 2005
Journal: Otol Neurotol
Title: Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome.
Volume: 26
Issue: 3
Pages: 415-24
Publication
First Author: Zheng W
Year: 2007
Journal: Am J Physiol Renal Physiol
Title: Cellular distribution of the potassium channel KCNQ1 in normal mouse kidney.
Volume: 292
Issue: 1
Pages: F456-66
Publication
First Author: Nguyen N
Year: 2013
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Independent trafficking of the KCNQ1 K+ channel and H+-K+-ATPase in gastric parietal cells from mice.
Volume: 304
Issue: 2
Pages: G157-66
Publication
First Author: Agsten M
Year: 2015
Journal: J Mol Cell Cardiol
Title: BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (IKs).
Volume: 89
Issue: Pt B
Pages: 335-48
Publication
First Author: Roepke TK
Year: 2011
Journal: FASEB J
Title: KCNE2 forms potassium channels with KCNA3 and KCNQ1 in the choroid plexus epithelium.
Volume: 25
Issue: 12
Pages: 4264-73
Publication
First Author: Fitzpatrick GV
Year: 2002
Journal: Nat Genet
Title: Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1.
Volume: 32
Issue: 3
Pages: 426-31
Publication
First Author: Koppes E
Year: 2015
Journal: PLoS One
Title: Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development.
Volume: 10
Issue: 8
Pages: e0135202
Publication
First Author: Korostowski L
Year: 2012
Journal: PLoS Genet
Title: The Kcnq1ot1 long non-coding RNA affects chromatin conformation and expression of Kcnq1, but does not regulate its imprinting in the developing heart.
Volume: 8
Issue: 9
Pages: e1002956
Publication
First Author: Green K
Year: 2007
Journal: Mamm Genome
Title: A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA.
Volume: 18
Issue: 1
Pages: 32-42
Publication
First Author: Redrup L
Year: 2009
Journal: Development
Title: The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing.
Volume: 136
Issue: 4
Pages: 525-30
Publication
First Author: Kanduri C
Year: 2006
Journal: EMBO J
Title: The length of the transcript encoded from the Kcnq1ot1 antisense promoter determines the degree of silencing.
Volume: 25
Issue: 10
Pages: 2096-106
Publication
First Author: Yatsuki H
Year: 2000
Journal: DNA Res
Title: Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.
Volume: 7
Issue: 3
Pages: 195-206
Publication
First Author: Cerrato F
Year: 2005
Journal: Hum Mol Genet
Title: The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
Volume: 14
Issue: 4
Pages: 503-11
Publication
First Author: Bastian H
Year: 1990
Journal: EMBO J
Title: A murine even-skipped homologue, Evx 1, is expressed during early embryogenesis and neurogenesis in a biphasic manner.
Volume: 9
Issue: 6
Pages: 1839-52
Publication
First Author: Lewis A
Year: 2004
Journal: Nat Genet
Title: Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.
Volume: 36
Issue: 12
Pages: 1291-5
Publication
First Author: Vallon V
Year: 2005
Journal: Proc Natl Acad Sci U S A
Title: KCNQ1-dependent transport in renal and gastrointestinal epithelia.
Volume: 102
Issue: 49
Pages: 17864-9
Publication
First Author: Boini KM
Year: 2009
Journal: Am J Physiol Regul Integr Comp Physiol
Title: Enhanced insulin sensitivity of gene-targeted mice lacking functional KCNQ1.
Volume: 296
Issue: 6
Pages: R1695-701
Publication
First Author: Tosaka T
Year: 2003
Journal: J Pharmacol Exp Ther
Title: Nicotine induces a long QT phenotype in Kcnq1-deficient mouse hearts.
Volume: 306
Issue: 3
Pages: 980-7
Publication  
First Author: Aubin Vega M
Year: 2024
Journal: Front Physiol
Title: Function of KvLQT1 potassium channels in a mouse model of bleomycin-induced acute lung injury.
Volume: 15
Pages: 1345488
Publication
First Author: Sharma A
Year: 2019
Journal: Dev Biol
Title: miR-126 regulates glycogen trophoblast proliferation and DNA methylation in the murine placenta.
Volume: 449
Issue: 1
Pages: 21-34
Publication  
First Author: Du C
Year: 2019
Journal: Biol Open
Title: Different functional roles for K+ channel subtypes in regulating small intestinal glucose and ion transport.
Volume: 8
Issue: 7
Publication
First Author: Onyango P
Year: 2000
Journal: Genome Res
Title: Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain.
Volume: 10
Issue: 11
Pages: 1697-710
Publication
First Author: Hudson QJ
Year: 2011
Journal: Dev Biol
Title: Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.
Volume: 353
Issue: 2
Pages: 420-31
Publication
First Author: Mager J
Year: 2003
Journal: Nat Genet
Title: Genome imprinting regulated by the mouse Polycomb group protein Eed.
Volume: 33
Issue: 4
Pages: 502-7
Publication
First Author: Mahy NL
Year: 2002
Journal: J Cell Biol
Title: Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH.
Volume: 159
Issue: 5
Pages: 753-63
Publication
First Author: Engemann S
Year: 2000
Journal: Hum Mol Genet
Title: Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
Volume: 9
Issue: 18
Pages: 2691-706
Publication
First Author: Xie R
Year: 2014
Journal: J Biol Chem
Title: Molecular mechanisms of calcium-sensing receptor-mediated calcium signaling in the modulation of epithelial ion transport and bicarbonate secretion.
Volume: 289
Issue: 50
Pages: 34642-53
Publication
First Author: Choi JD
Year: 2001
Journal: Mamm Genome
Title: Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes.
Volume: 12
Issue: 10
Pages: 758-64
Publication
First Author: Kim JD
Year: 2011
Journal: Hum Mol Genet
Title: Rex1/Zfp42 as an epigenetic regulator for genomic imprinting.
Volume: 20
Issue: 7
Pages: 1353-62
Publication
First Author: Casimiro MC
Year: 2004
Journal: Genomics
Title: Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.
Volume: 84
Issue: 3
Pages: 555-64
Publication
First Author: Dilly KW
Year: 2004
Journal: J Biol Chem
Title: Overexpression of beta2-adrenergic receptors cAMP-dependent protein kinase phosphorylates and modulates slow delayed rectifier potassium channels expressed in murine heart: evidence for receptor/channel co-localization.
Volume: 279
Issue: 39
Pages: 40778-87
Publication
First Author: Lubberding AF
Year: 2021
Journal: Sci Rep
Title: Age-dependent transition from islet insulin hypersecretion to hyposecretion in mice with the long QT-syndrome loss-of-function mutation Kcnq1-A340V.
Volume: 11
Issue: 1
Pages: 12253
Publication
First Author: Rannals MD
Year: 2016
Journal: Neuron
Title: Psychiatric Risk Gene Transcription Factor 4 Regulates Intrinsic Excitability of Prefrontal Neurons via Repression of SCN10a and KCNQ1.
Volume: 90
Issue: 1
Pages: 43-55
Publication
First Author: Guseva N
Year: 2012
Journal: Dev Biol
Title: Antisense noncoding RNA promoter regulates the timing of de novo methylation of an imprinting control region.
Volume: 361
Issue: 2
Pages: 403-11
Publication
First Author: Cleary MA
Year: 2001
Journal: Nat Genet
Title: Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice.
Volume: 29
Issue: 1
Pages: 78-82
Publication
First Author: Warth R
Year: 2002
Journal: Pflugers Arch
Title: The role of KCNQ1/KCNE1 K(+) channels in intestine and pancreas: lessons from the KCNE1 knockout mouse.
Volume: 443
Issue: 5-6
Pages: 822-8
Publication
First Author: Nicolas M
Year: 2001
Journal: Hear Res
Title: KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells.
Volume: 153
Issue: 1-2
Pages: 132-45
Publication
First Author: Purtell K
Year: 2012
Journal: FASEB J
Title: The KCNQ1-KCNE2 K⁺ channel is required for adequate thyroid I⁻ uptake.
Volume: 26
Issue: 8
Pages: 3252-9
Publication
First Author: Preston P
Year: 2010
Journal: J Biol Chem
Title: Disruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transport.
Volume: 285
Issue: 10
Pages: 7165-75
Publication
First Author: Zhou L
Year: 2019
Journal: FASEB J
Title: The KCNE2 potassium channel β subunit is required for normal lung function and resilience to ischemia and reperfusion injury.
Volume: 33
Issue: 9
Pages: 9762-9774
Publication
First Author: Vanhoof-Villalba SL
Year: 2018
Journal: Epilepsia
Title: Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy.
Volume: 59
Issue: 2
Pages: 358-368
Publication
First Author: Singh AK
Year: 2013
Journal: J Physiol
Title: Molecular transport machinery involved in orchestrating luminal acid-induced duodenal bicarbonate secretion in vivo.
Volume: 591
Issue: 21
Pages: 5377-91
Publication  
First Author: Liu X
Year: 2011
Journal: J Biomed Biotechnol
Title: ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice.
Volume: 2011
Pages: 130947
Publication
First Author: Grahammer F
Year: 2001
Journal: J Biol Chem
Title: The small conductance K+ channel, KCNQ1: expression, function, and subunit composition in murine trachea.
Volume: 276
Issue: 45
Pages: 42268-75
Publication
First Author: Knipper M
Year: 2006
Journal: J Physiol
Title: Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis.
Volume: 576
Issue: Pt 1
Pages: 73-86
Publication
First Author: Slaats GG
Year: 2015
Journal: J Cell Sci
Title: Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis.
Volume: 128
Issue: 24
Pages: 4550-9
Publication
First Author: de Castro MP
Year: 2006
Journal: Anat Rec A Discov Mol Cell Evol Biol
Title: Protein distribution of Kcnq1, Kcnh2, and Kcne3 potassium channel subunits during mouse embryonic development.
Volume: 288
Issue: 3
Pages: 304-15
Publication
First Author: Enklaar T
Year: 2000
Journal: Genomics
Title: Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family.
Volume: 67
Issue: 2
Pages: 179-87
Publication
First Author: Abbott GW
Year: 2014
Journal: Sci Signal
Title: KCNQ1, KCNE2, and Na+-coupled solute transporters form reciprocally regulating complexes that affect neuronal excitability.
Volume: 7
Issue: 315
Pages: ra22
Publication
First Author: Franco D
Year: 2001
Journal: Cardiovasc Res
Title: Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development.
Volume: 52
Issue: 1
Pages: 65-75
Publication
First Author: Paulsen M
Year: 1998
Journal: Hum Mol Genet
Title: Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
Volume: 7
Issue: 7
Pages: 1149-59
Publication
First Author: Demolombe S
Year: 2001
Journal: Am J Physiol Cell Physiol
Title: Differential expression of KvLQT1 and its regulator IsK in mouse epithelia.
Volume: 280
Issue: 2
Pages: C359-72
Publication
First Author: Dvir M
Year: 2014
Journal: J Cell Sci
Title: Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP₂.
Volume: 127
Issue: Pt 18
Pages: 3943-55
Publication
First Author: Li X
Year: 2013
Journal: PLoS One
Title: Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin.
Volume: 8
Issue: 5
Pages: e65977
Publication
First Author: Julio-Kalajzić F
Year: 2018
Journal: J Physiol
Title: K2P TASK-2 and KCNQ1-KCNE3 K+ channels are major players contributing to intestinal anion and fluid secretion.
Volume: 596
Issue: 3
Pages: 393-407
Publication
First Author: Lee MP
Year: 2000
Journal: J Clin Invest
Title: Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice.
Volume: 106
Issue: 12
Pages: 1447-55
Publication      
First Author: Gagnon LH
Year: 2002
Journal: MGI Direct Data Submission
Title: New allele of potassium voltage-gated channel, subfamily Q, member 1 (Kcnq1) named vertigo 2 Jackson. Mouse Mutant Resources Web Site, The Jackson Laboratory, Bar Harbor, Maine
Publication
First Author: Jiang S
Year: 1998
Journal: Genomics
Title: Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.
Volume: 53
Issue: 3
Pages: 395-9
Publication    
First Author: Kim HJ
Year: 2016
Journal: Elife
Title: Protein arginine methylation facilitates KCNQ channel-PIP2 interaction leading to seizure suppression.
Volume: 5
Publication
First Author: Sachyani D
Year: 2014
Journal: Structure
Title: Structural basis of a Kv7.1 potassium channel gating module: studies of the intracellular c-terminal domain in complex with calmodulin.
Volume: 22
Issue: 11
Pages: 1582-94
Publication
First Author: Barhanin J
Year: 1996
Journal: Nature
Title: K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current.
Volume: 384
Issue: 6604
Pages: 78-80
Publication
First Author: Teixeira M
Year: 2006
Journal: J Biol Chem
Title: Functional IsK/KvLQT1 potassium channel in a new corticosteroid-sensitive cell line derived from the inner ear.
Volume: 281
Issue: 15
Pages: 10496-507
Publication
First Author: Croteau S
Year: 2005
Journal: Mamm Genome
Title: Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors.
Volume: 16
Issue: 2
Pages: 127-35
Publication
First Author: Koay G
Year: 2002
Journal: Hear Res
Title: Behavioral audiograms of homozygous med(J) mutant mice with sodium channel deficiency and unaffected controls.
Volume: 171
Issue: 1-2
Pages: 111-118
Publication
First Author: Terrenoire C
Year: 2009
Journal: J Biol Chem
Title: The cardiac IKs potassium channel macromolecular complex includes the phosphodiesterase PDE4D3.
Volume: 284
Issue: 14
Pages: 9140-6
Publication
First Author: Dao D
Year: 1999
Journal: Hum Mol Genet
Title: Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.
Volume: 8
Issue: 7
Pages: 1337-52
Publication
First Author: Sampson KJ
Year: 2008
Journal: J Physiol
Title: Adrenergic regulation of a key cardiac potassium channel can contribute to atrial fibrillation: evidence from an I Ks transgenic mouse.
Volume: 586
Issue: 2
Pages: 627-37
Publication
First Author: Paulsen M
Year: 2000
Journal: Hum Mol Genet
Title: Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse.
Volume: 9
Issue: 12
Pages: 1829-41
Publication
First Author: Miwa T
Year: 2020
Journal: Mol Brain
Title: Tsukushi is essential for the development of the inner ear.
Volume: 13
Issue: 1
Pages: 29
Publication
First Author: Mai W
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: Thyroid hormone receptor alpha is a molecular switch of cardiac function between fetal and postnatal life.
Volume: 101
Issue: 28
Pages: 10332-7
Publication
First Author: Nguyên-Trân VT
Year: 2000
Journal: Cell
Title: A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages.
Volume: 102
Issue: 5
Pages: 671-82
Publication
First Author: Wang J
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification.
Volume: 107
Issue: 21
Pages: 9753-8
Publication
First Author: Gould TD
Year: 1998
Journal: Hum Mol Genet
Title: Imprinting of mouse Kvlqt1 is developmentally regulated.
Volume: 7
Issue: 3
Pages: 483-7
Publication
First Author: Labialle S
Year: 2008
Journal: Hum Mol Genet
Title: Coordinated diurnal regulation of genes from the Dlk1-Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes.
Volume: 17
Issue: 1
Pages: 15-26
Publication  
First Author: Renauld JM
Year: 2022
Journal: Front Cell Dev Biol
Title: Intermediate Cells of Dual Embryonic Origin Follow a Basal to Apical Gradient of Ingression Into the Lateral Wall of the Cochlea.
Volume: 10
Pages: 867153