NUFIP2 gene

Known as: MGC117262, nuclear fragile X mental retardation protein interacting protein 2, PIG1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2018
0119952018

Papers overview

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2018
2018
When exposed to ultraviolet radiation, the human skin produces profuse reactive oxygen species (ROS), which in turn activate a… (More)
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2016
2016
Microdeletions at 17q11.2 often encompass NF1 gene, is the cause for NF1 microdeletion syndrome. Microdeletion at 17q11.2 without… (More)
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2015
2015
Fragile X syndrome is caused by the lack of expression of fragile X mental retardation protein (FMRP), an RNA-binding protein… (More)
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2015
2015
DDX6 (p54/RCK) is a human RNA helicase with central roles in mRNA decay and translation repression. To help our understanding of… (More)
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2012
2012
BACKGROUND Melanosomes are specialized membrane-surrounded organelles, which are involved in the synthesis, storage and transport… (More)
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2011
2011
Oxidative stress caused by hydrogen peroxide (H(2)O(2)) leads to cell death and has been implicated in the pathogenesis of… (More)
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2008
2008
We describe a large germline deletion removing the NF1 locus, identified by heterozygosity mapping based on microsatellite… (More)
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Highly Cited
2002
Highly Cited
2002
Galectin-7 is normally expressed in all types of stratified epithelia, but is significantly down-regulated in squamous cell… (More)
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1998
1998
In a previous report, a plasmid, pIG1, which contained the loading domain from the Streptomyces avermitilis polyketide synthase… (More)
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1997
1997
The complete nucleotide sequence of a naturally occurring 5.36-kb streptomycin and sulphonamide resistance plasmid, designated… (More)
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