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UFD1L gene

Known as: ubiquitin fusion degradation 1 like (yeast), UFD1L, UBIQUITIN FUSION DEGRADATION 1-LIKE 
National Institutes of Health

Papers overview

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2016
2016
BACKGROUND A hemizygous deletion of 1.5-3 Mb in 22q11.2 causes a distinct clinical syndrome with variable congenital defects… 
2015
2015
BACKGROUND: A hemizygous deletion of 1.5–3 Mb in 22q11.2 causes a distinct clinical syndrome with variable congenital defects… 
2004
2004
DGCR6 is the most centromeric gene in the human DiGeorge critical region and is the only gene in the region with a second… 
2003
2003
Microdeletion of chromosome 22q11.2 is commonly associated with congenital cardiovascular defects that involve development of… 
2001
2001
The human UFD1L and CDC45L genes, adjacently located in the head-to-head direction on chromosome 22q11, are separated by a 884… 
1997
1997
Abstract Poly(A) polymerase is responsible for the addition of the adenylate tail to the 3′ ends of mRNA. Using the two-hybrid…