Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death (Q24323900)

GOA release 2020-03-11

Nucleoporin 155

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GOA release 2020-03-11

author name string

Xianqin Zhang

1

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Shenghan Chen

2

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Shin Yoo

3

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Susmita Chakrabarti

4

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Teng Zhang

5

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Tie Ke

6

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Carlos Oberti

7

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Sandro L Yong

8

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Fang Fang

9

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Lin Li

10

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Roberto de la Fuente

11

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Lejin Wang

12

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Qiuyun Chen

13

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Qing Kenneth Wang

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA

14

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language of work or name

English

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publication date

12 December 2008

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published in

Cell

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volume

135

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page(s)

1017-27

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issue

6

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cites work

1 reference

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Architecture and design of the nuclear pore complex

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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Association of high intracellular, but not serum, heat shock protein 70 with postoperative atrial fibrillation

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Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes

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Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice

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Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo.

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Atrial electrophysiological remodeling caused by rapid atrial activation: underlying mechanisms and clinical relevance to atrial fibrillation

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Regulating access to the genome: nucleocytoplasmic transport throughout the cell cycle

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Genomic organization, transcript variants and comparative analysis of the human nucleoporin 155 (NUP155) gene

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ACC/AHA/ESC guidelines for the management of patients with atrial fibrillation: executive summary. A Report of the American College of Cardiology/ American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Co

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Low preoperative HSP70 atrial myocardial levels correlate significantly with high incidence of postoperative atrial fibrillation after cardiac surgery

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Cell biology: popping out of the nucleus.

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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

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Nuclear pore association confers optimal expression levels for an inducible yeast gene

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Determining the architectures of macromolecular assemblies

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The molecular architecture of the nuclear pore complex

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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Nup155 regulates nuclear envelope and nuclear pore complex formation in nematodes and vertebrates

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Atrial fibrillation in patients with congestive heart failure

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The mRNA export factor human Gle1 interacts with the nuclear pore complex protein Nup155

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Nup155 is a novel nuclear pore complex protein that contains neither repetitive sequence motifs nor reacts with WGA

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Interaction between the shuttling mRNA export factor Gle1 and the nucleoporin hCG1: a conserved mechanism in the export of Hsp70 mRNA.

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Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy

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Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program

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Beat shock proteins and atrial fibrillation.

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

release_dv2qlspq5nbsrjywndkcxbb7qe

2835765

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/dv2qlspq5nbsrjywndkcxbb7qe

24 November 2022

mapped directly with Wikidata item

2835765

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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