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RNASE12 gene

Known as: RAI1, RNASE12, ribonuclease A family member 12 (inactive) 
National Institutes of Health

Related topics

Related topics

1 relation
Ribonucleases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome
Highly Cited
2012
Highly Cited
2012
Dxo1 is a novel eukaryotic enzyme with both decapping and 5′-3′ exoribonuclease activity
Recent studies showed that Rai1 is a crucial component of the mRNA 5′-end-capping quality-control mechanism in yeast. The yeast… 
2012
2012
A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men
The functional contribution of CNV to human biology and disease pathophysiology has undergone limited exploration. Recent… 
Highly Cited
2008
Highly Cited
2008
How much is too much? Phenotypic consequences of Rai1 overexpression in mice
The retinoic acid induced 1 (RAI1) gene when deleted or mutated results in Smith–Magenis syndrome (SMS), while duplication of… 
Highly Cited
2007
Highly Cited
2007
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.
Smith-Magenis syndrome (SMS) is associated with an approximately 3.7 Mb common deletion in 17p11.2 and characterized by its… 
Highly Cited
2006
Highly Cited
2006
Search on Chromosome 17 Centromere Reveals TNFRSF13B as a Susceptibility Gene for Intracranial Aneurysm: A Preliminary Study
Background— Our previous studies have shown a significant linkage of intracranial aneurysms (IAs) to chromosome 17. Methods and… 
Highly Cited
2005
Highly Cited
2005
Rat1p and Rai1p function with the nuclear exosome in the processing and degradation of rRNA precursors.
Exoribonucleases function in the processing and degradation of a variety of RNAs in all organisms. These enzymes play a… 
2004
2004
Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.
Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome associated with del(17)(p11.2p11.2… 
Highly Cited
2001
Highly Cited
2001
RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients.
Highly Cited
2000
Highly Cited
2000
Saccharomyces cerevisiae RAI1 (YGL246c) Is Homologous to Human DOM3Z and Encodes a Protein That Binds the Nuclear Exoribonuclease Rat1p
ABSTRACT The RAT1 gene of Saccharomyces cerevisiaeencodes a 5′→3′ exoribonuclease which plays an essential role in yeast RNA… 
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