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Regulation of Kv11.1 Isoform Expression by Polyadenylate Binding Protein Nuclear 1

International journal of molecular sciences, 2021-01, Vol.22 (2), p.863

2021

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Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome

Gene, 2014-04, Vol.539 (2), p.190-197

2014

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Isoform-specific dominant-negative effects associated with hERG1 G628S mutation in long QT syndrome

PloS one, 2012-08, Vol.7 (8), p.e42552

2012

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Regulation of Kv11.1 potassium channel C-terminal isoform expression by the RNA-binding proteins HuR and HuD

The Journal of biological chemistry, 2018-12, Vol.293 (51), p.19624-19632

2018

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Upregulation of functional Kv11.1a isoform expression by modified U1 small nuclear RNA

Gene, 2018-01, Vol.641, p.220-225

2018

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Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndrome

Heart rhythm, 2011-08, Vol.8 (8), p.1200-1206

2011

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LQT2 nonsense mutations generate trafficking defective NH2-terminally truncated channels by the reinitiation of translation

American journal of physiology. Heart and circulatory physiology, 2013-11, Vol.305 (9), p.H1397-H1404

2013

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Mutational Analysis of the Stability of the H2A and H2B Histone Monomers

Journal of molecular biology, 2008-12, Vol.384 (5), p.1369-1383

2008

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Upregulation of functional Kv11.1 isoform expression by inhibition of intronic polyadenylation with antisense morpholino oligonucleotides

Journal of molecular and cellular cardiology, 2014-11, Vol.76, p.26-32

2014

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Inhibition of nonsense-mediated mRNA decay by antisense morpholino oligonucleotides restores functional expression of hERG nonsense and frameshift mutations in long-QT syndrome

Journal of molecular and cellular cardiology, 2011-01, Vol.50 (1), p.223-229

2011

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Early LQT2 nonsense mutation generates N-terminally truncated hERG channels with altered gating properties by the reinitiation of translation

Journal of molecular and cellular cardiology, 2012-11, Vol.53 (5), p.725-733

2012

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Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome

American journal of physiology. Heart and circulatory physiology, 2011-01, Vol.300 (1), p.H312-H318

2011

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Identification of Kv11.1 isoform switch as a novel pathogenic mechanism of long-QT syndrome

Circulation. Cardiovascular genetics, 2014-08, Vol.7 (4), p.482

2014

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Alternative Splicing and Polyadenylation Contribute to the Generation of hERG1 C-terminal Isoforms

The Journal of biological chemistry, 2010-10, Vol.285 (42), p.32233-32241

2010

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Mutational Studies Uncover Non-Native Structure in the Dimeric Kinetic Intermediate of the H2A–H2B Heterodimer

Journal of molecular biology, 2010-08, Vol.401 (3), p.518-531

2010

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Unique fluorophores in the dimeric archaeal histones hMfB and hPyA1 reveal the impact of nonnative structure in a monomeric kinetic intermediate

Protein science, 2008-02, Vol.17 (2), p.322-332

2008

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Regulation of KV11.1 C-Terminal Isoform Expression by HU Proteins

Biophysical journal, 2016-02, Vol.110 (3), p.281a-281a

2016

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Regulation of hERG C-Terminal Isoform Expression by Modified U1 Small Nuclear RNA

Biophysical journal, 2014-01, Vol.106 (2), p.139a-139a

2014

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LQT2 nonsense mutations generate trafficking defective NH 2 -terminally truncated channels by the reinitiation of translation

American journal of physiology. Heart and circulatory physiology, 2013-11, Vol.305 (9), p.H1397-H1404

2013

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LQT2 nonsense mutations generate trafficking defective NH^sub 2^-terminally truncated channels by the reinitiation of translation

American journal of physiology. Heart and circulatory physiology, 2013-11, Vol.305 (9), p.H1397

2013

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Regulation of hERG C-terminal Isoform Expression by KCNH2 Intronic Elements

Biophysical journal, 2018-02, Vol.114 (3), p.130a-131a

2018

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Multiple splicing defects caused by hERG splice site mutation 2592+ 1G>A associated with long QT syndrome

American journal of physiology. Heart and circulatory physiology, 2011, Vol.69 (1)

2011

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Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome

American Journal of Physiology: Cell Physiology, 2011-01, Vol.300 (1), p.H312-H318

2011

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LQT2 Nonsense Mutation Escapes NMD by the Reinitiation of Translation to Generate N-Terminally Truncated hERG Channels

Biophysical journal, 2012-01, Vol.102 (3), p.678a-678a

2012

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Mutations at the Intron 9 Donor Splice Site in hERG Lead to Cryptic Splicing in LQT2

Biophysical journal, 2010-01, Vol.98 (3), p.116a-116a

2010

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Regulation of Kv11.1 Isoform Expression by Polyadenylate Binding Protein Nuclear 1

Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome

Isoform-specific dominant-negative effects associated with hERG1 G628S mutation in long QT syndrome

Regulation of Kv11.1 potassium channel C-terminal isoform expression by the RNA-binding proteins HuR and HuD

Upregulation of functional Kv11.1a isoform expression by modified U1 small nuclear RNA

Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndrome

LQT2 nonsense mutations generate trafficking defective NH2-terminally truncated channels by the reinitiation of translation

Mutational Analysis of the Stability of the H2A and H2B Histone Monomers

Upregulation of functional Kv11.1 isoform expression by inhibition of intronic polyadenylation with antisense morpholino oligonucleotides

Inhibition of nonsense-mediated mRNA decay by antisense morpholino oligonucleotides restores functional expression of hERG nonsense and frameshift mutations in long-QT syndrome

Early LQT2 nonsense mutation generates N-terminally truncated hERG channels with altered gating properties by the reinitiation of translation

Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome

Identification of Kv11.1 isoform switch as a novel pathogenic mechanism of long-QT syndrome

Alternative Splicing and Polyadenylation Contribute to the Generation of hERG1 C-terminal Isoforms

Mutational Studies Uncover Non-Native Structure in the Dimeric Kinetic Intermediate of the H2A–H2B Heterodimer

Unique fluorophores in the dimeric archaeal histones hMfB and hPyA1 reveal the impact of nonnative structure in a monomeric kinetic intermediate

Regulation of KV11.1 C-Terminal Isoform Expression by HU Proteins

Regulation of hERG C-Terminal Isoform Expression by Modified U1 Small Nuclear RNA

LQT2 nonsense mutations generate trafficking defective NH 2 -terminally truncated channels by the reinitiation of translation

LQT2 nonsense mutations generate trafficking defective NH^sub 2^-terminally truncated channels by the reinitiation of translation

Regulation of hERG C-terminal Isoform Expression by KCNH2 Intronic Elements

Multiple splicing defects caused by hERG splice site mutation 2592+ 1G>A associated with long QT syndrome

Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome

LQT2 Nonsense Mutation Escapes NMD by the Reinitiation of Translation to Generate N-Terminally Truncated hERG Channels

Mutations at the Intron 9 Donor Splice Site in hERG Lead to Cryptic Splicing in LQT2

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