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TFAP2A gene

Known as: AP2, TFAP2A, TRANSCRIPTION FACTOR AP2-ALPHA 
This gene is involved in transcriptional activation of genes which are required for development of ectodermal tissues. It also plays a role in the… 
National Institutes of Health

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Related topics

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Homo sapiensTranscription Factor AP-2 AlphaTranscriptional Regulationdna binding

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TFAP2A wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population
PurposeTranscription factor AP-2 alpha (TFAP2A) is an important transcriptional factor involved in various aspects of embryo… 
2017
2017
Distinct roles of Tfap2A & Tfap2B in the diversification of GABAergic neuronal subtypes in the cerebellum
2013
2013
REGULATION OF NEURAL CREST DEVELOPMENT REQUIRES FUNCTIONAL INTERACTIONS BETWEEN HDAC1, TFAP2A AND FOXD3
...............................................................................................ii Dedication… 
2012
2012
[Branchio-oculo-facial syndrome].
2011
2011
Table 2. [Recurrent TFAP2A Pathogenic Variants Revealing a Mutational Hotspot].
2010
2010
Additional clinical and molecular analyses of TFAP2A in patients with the branchio‐oculo‐facial syndrome
The branchio‐oculo‐facial syndrome (BOFS) is a rare disorder with approximately 50 sporadic and familial cases in the literature… 
2010
2010
Additional clinical and molecular analyses of TFAP2A in patients with the Branchio‐Oculo‐Facial syndrome: Previously reported patient
Additional Clinical and Molecular Analyses of TFAP2A in Patients With the Branchio-Oculo-Facial Syndrome: Previously Reported… 
2009
2009
A complex TFAP2A allele is associated with branchio‐oculo‐facial syndrome and inner ear malformation in a deaf child
We present a 4‐year‐old girl with congenital profound sensorineural deafness associated with inner ear malformation (incomplete… 
Highly Cited
2004
Highly Cited
2004
Skeletal and pigment cell defects in the lockjaw mutant reveal multiple roles for zebrafish tfap2a in neural crest development
Members of the AP‐2 transcription factor family have critical roles in many aspects of embryonic development. The zebrafish… 
2003
2003
Genetic variation analysis of MLP, TFAP2A, and CSK in patients with neural tube defects
Neural tube defects (NTDs) are congenital malformations which arise from incomplete closure of the neural tube during early… 
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