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RANGRF gene

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

Papers overview

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2016
2016
MOG1 was initially identified as a protein that interacts with the small GTPase Ran involved in transport of macromolecules into… Expand
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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 Na(v)1.5 cause sodium channelopathies, including Brugada syndrome, dilated… Expand
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2012
2012
BACKGROUND Brugada syndrome (BrS) is a primary arrhythmia syndrome characterized by the occurrence of malignant ventricular… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Brugada syndrome (BrS) is caused mainly by mutations in the SCN5A gene, which encodes the α-subunit of the cardiac… Expand
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2011
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 Nav 1.5 is essential for the physiological function of the heart and contributes to lethal cardiac… Expand
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2001
2001
Mog1 is a nuclear protein that interacts with Ran, the Ras family GTPase that confers directionality to nuclear import and export… 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
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1998
1998
We previously isolated 25 temperature-sensitive gsp1 alleles of Saccharomyces cerevisiae Ran homologue, each of which possesses… Expand
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