TBX1 gene

Known as: TBX1, CATCH22, T-Box 1 Gene 
This gene plays a role in transcription and proliferation.
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
About 35% of patients with 22q11 deletion syndrome (22q11DS), which includes DiGeorge and velocardiofacial syndromes, develops… (More)
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Highly Cited
2004
Highly Cited
2004
Dysmorphogenesis of the cardiac outflow tract (OFT) causes many congenital heart defects, including those associated with… (More)
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Highly Cited
2004
Highly Cited
2004
Velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS) is associated with de novo hemizygous 22q11.2 deletions and is… (More)
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Highly Cited
2004
Highly Cited
2004
Formation and remodeling of the pharyngeal arches play central roles in craniofacial development. TBX1, encoding a T-box… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Del22q11.2 syndrome is the most frequent known chromosomal microdeletion syndrome, with an incidence of 1 in 4000-5000… (More)
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Highly Cited
2002
Highly Cited
2002
TBX1 is the major candidate gene for DiGeorge syndrome (DGS). Mouse studies have shown that the Tbx1 gene is haploinsufficient… (More)
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Highly Cited
2002
Highly Cited
2002
Tbx1 haploinsufficiency causes aortic arch abnormalities in mice because of early growth and remodeling defects of the fourth… (More)
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Highly Cited
2001
Highly Cited
2001
The DiGeorge/velocardiofacial syndrome (DGS/VCFS) is a relatively common human disorder, usually associated with deletions of… (More)
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Highly Cited
2001
Highly Cited
2001
Velo-cardio-facial syndrome (VCFS)/DiGeorge syndrome (DGS) is a human disorder characterized by a number of phenotypic features… (More)
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Highly Cited
1996
Highly Cited
1996
A novel family of genes, characterized by the presence of a region of homology to the DNA-binding domain of the Brachyury (T… (More)
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