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RERE gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Heterozygous variants in the arginine‐glutamic acid dipeptide repeats gene (RERE) have been shown to cause neurodevelopmental… Expand
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
Tuberculosis (TB) is a serious health problem causing 1.5 million deaths worldwide. After the discovery of first-line anti-TB… Expand
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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Highly Cited
2013
Highly Cited
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
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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2007
2007
The transcriptional regulator RERE/Atrophin‐2 (RERE) is required for the normal patterning of the early vertebrate embryo… Expand
1998
1998
P-selectin is one of the adhesion molecules involved in leukocyte rolling during an inflammatory reaction. The aim of this study… Expand