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DXO gene

Known as: RAI1, DOM3Z, DXO 
 
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
The 5′→3′ exoribonucleases (XRNs) comprise a large family of conserved enzymes in eukaryotes with crucial functions in RNA… Expand
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2009
2009
Disorders with overlapping diagnostic features are grouped into a network module. Based on phenotypic similarities or… Expand
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2008
2008
The retinoic acid induced 1 (RAI1) gene when deleted or mutated results in Smith–Magenis syndrome (SMS), while duplication of… Expand
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Highly Cited
2007
Highly Cited
2007
Smith-Magenis syndrome (SMS) is associated with an approximately 3.7 Mb common deletion in 17p11.2 and characterized by its… Expand
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Highly Cited
2006
Highly Cited
2006
Purpose: Smith-Magenis syndrome (SMS) is a complex disorder that includes mental retardation, craniofacial and skeletal anomalies… Expand
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2006
2006
[1] After a base level drop, rivers are the first components of the landscape to respond by incising into topography. A base… Expand
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Highly Cited
2005
Highly Cited
2005
Retinoic acid induced 1 (RAI1) is among the 20 genes identified in the critical region of Smith-Magenis syndrome (SMS), a genomic… Expand
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Highly Cited
2004
Highly Cited
2004
High-throughput (HTP) protein-interaction assays, such as the yeast two-hybrid (Y2H) system, are enormously useful in predicting… Expand
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2001
2001
The human chromosomal band 17p11.2 is a genetically unstable interval. It has been shown to be deleted in patients suffering from… Expand
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Highly Cited
2000
Highly Cited
2000
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder caused by the expansion of a polymorphic (CAG)(n) tract… Expand
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