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RANGRF gene

Known as: HSPC165, MOG1 homolog (S. cerevisiae), RANGNRF 
National Institutes of Health

Papers overview

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2014
2014
Sudden unexplained nocturnal death syndrome (SUNDS) remains an enigma to both forensic pathologists and physicians. Previous… Expand
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2013
2013
Background—Loss-of-function mutations in Nav1.5 cause sodium channelopathies, including Brugada syndrome, dilated cardiomyopathy… Expand
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2012
2012
BACKGROUND Brugada syndrome (BrS) is a primary arrhythmia syndrome characterized by the occurrence of malignant ventricular… Expand
Highly Cited
2011
Highly Cited
2011
Background— Brugada syndrome (BrS) is caused mainly by mutations in the SCN5A gene, which encodes the &agr;-subunit of the… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND The protein MOG1 is a cofactor of the cardiac sodium channel, Nav1.5. Overexpression of MOG1 in Nav1.5-expressing… Expand
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Highly Cited
2008
Highly Cited
2008
The cardiac sodium channel Nav1.5 is essential for the physiological function of the heart and contributes to lethal cardiac… Expand
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2001
2001
Many of the proteins that mediate transport into and out of the nucleus have been structurally and functionally conserved… Expand
2001
2001
Mog1 is a nuclear protein that interacts with Ran, the Ras family GTPase that confers directionality to nuclear import and export… Expand
2001
2001
We have cloned and characterized the Schizosaccharomyces pombe gene mog1(+), which encodes a protein with homology to the… Expand
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Highly Cited
1998
Highly Cited
1998
  • M. Oki, T. Nishimoto
  • Proceedings of the National Academy of Sciences…
  • 1998
  • Corpus ID: 11295044
We previously isolated 25 temperature-sensitive gsp1 alleles of Saccharomyces cerevisiae Ran homologue, each of which possesses… Expand