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RERE gene

Known as: RE REPEATS-ENCODING GENE, KIAA0458, RERE 
 
National Institutes of Health

Papers overview

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2016
2016
Deletions of chromosome 1p36 affect approximately 1 in 5,000 newborns and are associated with developmental delay, intellectual… Expand
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Review
2015
Review
2015
Deletions of chromosome 1p36 affect approximately 1 in 5,000 newborns and are the most common terminal deletions in humans… Expand
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2013
2013
Individuals with terminal and interstitial deletions of chromosome 1p36 have a spectrum of defects that includes eye anomalies… Expand
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Highly Cited
2011
Highly Cited
2011
Large alterations in transcription accompany neurodegeneration in polyglutamine (polyQ) diseases. These pathologies manifest both… Expand
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2011
2011
This paper proposes a novel ARP authentication scheme based on an ARP authentication trailer and a new technique for hiding the… Expand
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Highly Cited
2010
Highly Cited
2010
One of the most notable features of the vertebrate body plan organization is its bilateral symmetry, evident at the level of… Expand
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Highly Cited
2010
Highly Cited
2010
Polyglutamine pathologies are neurodegenerative diseases that manifest both general polyglutamine toxicity and mutant protein… Expand
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2010
2010
Apple’s iMac computers are promoted by the Apple Inc. to be secure, safe, virus free and fast computers. In this experimental… Expand
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2007
2007
The transcriptional regulator RERE/Atrophin‐2 (RERE) is required for the normal patterning of the early vertebrate embryo… Expand
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1998
1998
P-selectin is one of the adhesion molecules involved in leukocyte rolling during an inflammatory reaction. The aim of this study… Expand
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