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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
MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.
BACKGROUND A hemizygous deletion of 1.5-3 Mb in 22q11.2 causes a distinct clinical syndrome with variable congenital defects… 
2015
2015
MALDI-TOF-MS Assay to Detect the Hemizygous 22 q 11 . 2 Deletion in DNA from Dried Blood Spots
BACKGROUND: A hemizygous deletion of 1.5–3 Mb in 22q11.2 causes a distinct clinical syndrome with variable congenital defects… 
2013
2013
Polymorphisms in schizophrenia candidate gene UFD1L may contribute to cognitive deficits
Review
2005
Review
2005
Molekulargenetische Studien bikuspider Aortenklappen
ZusammenfassungHintergrund:Die kongenitale bikuspide Aortenklappe (BAV) ist die häufigste Herzmissbildung. Sie tritt bei ca. 1–2… 
2003
2003
Functional Attenuation of Ufd1l, a 22q11.2 Deletion Syndrome Candidate Gene, Leads to Cardiac Outflow Septation Defects in Chicken Embryos
Microdeletion of chromosome 22q11.2 is commonly associated with congenital cardiovascular defects that involve development of… 
2001
2001
Characterization of the bi-directional transcriptional control region between the human UFD1L and CDC45L genes.
The human UFD1L and CDC45L genes, adjacently located in the head-to-head direction on chromosome 22q11, are separated by a 884… 
2001
2001
PII: S0925-4773(01)00489-0
Two to three megabase deletions on chromosome 22q11 are the cytogenetic findings most commonly associated with cardiac and… 
2000
2000
No association of the -277A variant allele of the UFD1L promoter polymorphism and schizophrenia
2000
2000
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotype
5 Thomas, T. et al. (1998) A signaling cascade in-volving endothelin-1, dHAND and Msx1 regulatesdevelopment of neural crest… 
1998
1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).
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