FAQ

TBX1 wt Allele

Known as: T-Box 1 wt Allele, CAFS, TGA 
Human TBX1 wild-type allele is located in the vicinity of 22q11.21 and is approximately 27 kb in length. This allele, which encodes T-box… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1964-2018
0500100019642018

Related topics

Related topics

10 relations
22q11.21CONOTRUNCAL HEART MALFORMATIONS (disorder)Cell ProliferationDGCR gene
(More)

Related mentions per year

Related mentions per year

1937-2018
19401960198020002020
TBX1 wt Allele
Cell Proliferation
Transcription, Genetic
dna binding
Homo sapiens
Transcriptional Regulation

Papers overview

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Highly Cited
2009
Highly Cited
2009
A novel class of small RNAs: tRNA-derived RNA fragments (tRFs).
New types of small RNAs distinct from microRNAs (miRNAs) are progressively being discovered in various organisms. In order to… (More)
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Highly Cited
2006
Highly Cited
2006
Tuning the structure and parameters of a neural network by using hybrid Taguchi-genetic algorithm
In this paper, a hybrid Taguchi-genetic algorithm (HTGA) is applied to solve the problem of tuning both network structure and… (More)
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Highly Cited
2001
Highly Cited
2001
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
The DiGeorge/velocardiofacial syndrome (DGS/VCFS) is a relatively common human disorder, usually associated with deletions of… (More)
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Highly Cited
2000
Highly Cited
2000
The Arabidopsis NPR1/NIM1 protein enhances the DNA binding activity of a subgroup of the TGA family of bZIP transcription factors.
The Arabidopsis NPR1 gene is essential in activating systemic, inducible plant defense responses. To gain a better understanding… (More)
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Highly Cited
1999
Highly Cited
1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Mutations in SCN5A, the gene encoding the cardiac Na(+) channel, have been identified in 2 distinct diseases associated with… (More)
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Highly Cited
1999
Highly Cited
1999
Detection of transposition of the great arteries in fetuses reduces neonatal morbidity and mortality.
BACKGROUND Transposition of the great arteries (TGA) is a life-threatening malformation in neonates, but it is amenable to… (More)
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Highly Cited
1997
Highly Cited
1997
Positional cloning of the APECED gene
Autoimmune polyglandular syndrome type I (APS 1, also called APECED) is an autosomal-recessive disorder that maps to human… (More)
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Highly Cited
1991
Highly Cited
1991
Selective perturbation of visual input during prehension movements
1. Subjects were instructed to reach and grasp cylindrical objects, using a precision grip. The objects were two concentric… (More)
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Highly Cited
1991
Highly Cited
1991
Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment
Reports describing short (< 20 bp) gene deletions causing human genetic disease were collated in order to study underlying… (More)
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Highly Cited
1985
Highly Cited
1985
The mitochondrial DNA molecule ofDrosophila yakuba: Nucleotide sequence, gene organization, and genetic code
The sequence of the 16,019 nucleotide-pair mitochondrial DNA (mtDNA) molecule ofDrosophila yakuba is presented. This molecule… (More)
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