Found: 24
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The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.
- Published in:
- Pilot & Feasibility Studies, 2023, v. 9, n. 1, p. 1, doi. 10.1186/s40814-023-01259-5
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- Publication type:
- Article
Voltage-Gated Potassium Channels: Regulation by Accessory Subunits.
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- Neuroscientist, 2006, v. 12, n. 3, p. 199, doi. 10.1177/1073858406287717
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- Publication type:
- Article
Pharmacological and Genetic Reversal of Age-Dependent Cognitive Deficits Attributable to Decreased presenilin Function.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 28, p. 9510, doi. 10.1523/JNEUROSCI.1017-10.2010
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- Publication type:
- Article
Sequence and structure-specific elements of HERG mRNA determine channel synthesis and trafficking efficiency.
- Published in:
- FASEB Journal, 2013, v. 27, n. 8, p. 3039, doi. 10.1096/fj.12-227009
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- Publication type:
- Article
Phosphatidylinositol 4,5-bisphosphate interactions with the HERG K<sup>+</sup> channel.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2007, v. 455, n. 1, p. 105, doi. 10.1007/s00424-007-0292-5
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- Publication type:
- Article
A function for tyrosine phosphorylation of type 1 inositol 1,4,5-trisphosphate receptor in lymphocyte activation.
- Published in:
- Journal of Cell Biology, 2007, v. 179, n. 5, p. 923, doi. 10.1083/jcb.200708200
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- Publication type:
- Article
A Homolog of FHM2 Is Involved in Modulation of Excitatory Neurotransmission by Serotonin in C. elegans.
- Published in:
- PLoS ONE, 2010, v. 5, n. 4, p. 1, doi. 10.1371/journal.pone.0010368
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- Publication type:
- Article
Functional Interactions between KCNE1 C-Terminus and the KCNQ1 Channel.
- Published in:
- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005143
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- Publication type:
- Article
A-kinase anchoring protein targeting of protein kinase A and regulation of HERG channels.
- Published in:
- 2008
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- Publication type:
- journal article
Phenotypic Variability in iPSC-Induced Cardiomyocytes and Cardiac Fibroblasts Carrying Diverse LMNA Mutations.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.778982
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- Publication type:
- Article
14-3-3 amplifies and prolongs adrenergic stimulation of HERG K<sup>+</sup> channel activity.
- Published in:
- EMBO Journal, 2002, v. 21, n. 8, p. 1889, doi. 10.1093/emboj/21.8.1889
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- Publication type:
- Article
A minK-HERG complex regulates the cardiac potassium current I subscript Kr.
- Published in:
- Nature, 1997, v. 388, n. 6639, p. 289, doi. 10.1038/40882
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- Publication type:
- Article
Perceptions of an Implantable Cardioverter-Defibrillator: A Qualitative Study of Families with a History of Sudden, Life-Threatening Cardiac Events, and Recommendations to Improve Care.
- Published in:
- Einstein Journal of Biology & Medicine, 2013, v. 29, n. 1/2, p. 3
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- Publication type:
- Article
Express with caution: Epitope tags and cDNA variants effects on hERG channel trafficking, half-life and function.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2017, v. 28, n. 9, p. 1070, doi. 10.1111/jce.13259
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- Publication type:
- Article
Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.
- Published in:
- Pacing & Clinical Electrophysiology, 2017, v. 40, n. 6, p. 703, doi. 10.1111/pace.13087
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- Publication type:
- Article
Partially Dominant Mutant Channel Defect Corresponding with Intermediate LQT2 Phenotype.
- Published in:
- Pacing & Clinical Electrophysiology, 2012, v. 35, n. 1, p. 3, doi. 10.1111/j.1540-8159.2011.03222.x
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- Publication type:
- Article
A Dual Mechanism for I<sub>Ks</sub> Current Reduction by the Pathogenic Mutation KCNQ1-S277L.
- Published in:
- Pacing & Clinical Electrophysiology, 2011, v. 34, n. 12, p. 1652, doi. 10.1111/j.1540-8159.2011.03190.x
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- Publication type:
- Article
Corrigendum.
- Published in:
- Human Mutation, 2019, v. 40, n. 3, p. 357, doi. 10.1002/humu.23711
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- Publication type:
- Article
An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome.
- Published in:
- Human Mutation, 2015, v. 36, n. 8, p. 764, doi. 10.1002/humu.22805
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- Publication type:
- Article
Characterization of two putative potassium channels in Plasmodium falciparum.
- Published in:
- Malaria Journal, 2008, v. 7, p. 1, doi. 10.1186/1475-2875-7-19
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- Publication type:
- Article
Functional testing for variant prioritization in a family with long QT syndrome.
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- Molecular Genetics & Genomics, 2021, v. 296, n. 4, p. 823, doi. 10.1007/s00438-021-01780-3
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- Publication type:
- Article
Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC‐neurons and cardiomyocytes.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2093
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- Publication type:
- Article
Compound heterozygous CASQ2 mutations and long-term course of catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 6, p. 788, doi. 10.1002/mgg3.323
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- Publication type:
- Article
Development of a Targeted Multi-Disorder High-Throughput Sequencing Assay for the Effective Identification of Disease-Causing Variants.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133742
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- Publication type:
- Article