TFAP2A wt Allele

Known as: AP2 Gene, AP2TF, AP-2 
Human TFAP2A wild-type allele is located in the vicinity of 6p24 and is approximately 24 kb in length. This allele, which encodes transcription… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1989-2017
012319892017

Papers overview

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2017
2017
Mutations in the gene encoding transcription factor TFAP2A result in pigmentation anomalies in model organisms and premature hair… (More)
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2013
2013
Malignant melanoma is one of the most aggressive human cancers, but the mechanisms governing its metastatic dissemination are not… (More)
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2013
2013
Malignant melanoma is one of the most aggressive human cancers, but the mechanisms governing its metastatic dissemination are not… (More)
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Review
2012
Review
2012
In recent years, knowledge regarding the genetic and epigenetic programmes governing specification, maintenance and… (More)
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2010
2010
BACKGROUND Friedreich ataxia is an autosomal recessive neurodegenerative disease caused by reduced expression levels of the… (More)
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2008
2008
Mutations in the gene encoding the TFAP2B transcription factor can cause Char syndrome with cardiac, craniofacial, and hand… (More)
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Highly Cited
2004
Highly Cited
2004
Malformations of the septum, outflow tract and aortic arch are the most common congenital cardiovascular defects and occur in… (More)
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2001
2001
BACKGROUND Very little is known about the identity of genetic factors involved in the complex etiology of nonsyndromic neural… (More)
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1999
1999
Nine samples of pure, feed-grade (FP) and agricultural-grade (AP) phosphates were evaluated at seven laboratories (six in Brazil… (More)
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Highly Cited
1989
Highly Cited
1989
We have examined the floral morphology and ontogeny of three mutants of Arabidopsis thaliana, Ap2-5, Ap2-6, and Ap2-7, that… (More)
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