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"The DNA sequence and analysis of human chromosome 6."
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Nature425:805-811(2003) [PubMed] [Europe PMC] [Abstract]

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"Characterisation of the human AP-2beta and AP-2gamma genes."
Hasleton M.D. , Skinner A. , Hurst H.C.
Submitted (2000-06) to the EMBL/GenBank/DDBJ databases

"Chromosomal mapping of the human and mouse homologues of two new members of the AP-2 family of transcription factors."
Williamson J.A. , Bosher J.M. , Skinner A. , Sheer D. , Williams T. , Hurst H.C.
Genomics35:262-264(1996) [PubMed] [Europe PMC] [Abstract]

"Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator."
Bamforth S.D. , Braganca J. , Eloranta J.J. , Murdoch J.N. , Marques F.I. , Kranc K.R. , Farza H. , Henderson D.J. , Hurst H.C. , Bhattacharya S.
Nat. Genet.29:469-474(2001) [PubMed] [Europe PMC] [Abstract]

"Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2."
Braganca J. , Swingler T. , Marques F.I.R. , Jones T. , Eloranta J.J. , Hurst H.C. , Shioda T. , Bhattacharya S.
J. Biol. Chem.277:8559-8565(2002) [PubMed] [Europe PMC] [Abstract]

"Transcription factor AP-2 interacts with the SUMO-conjugating enzyme UBC9 and is sumolated in vivo."
Eloranta J.J. , Hurst H.C.
J. Biol. Chem.277:30798-30804(2002) [PubMed] [Europe PMC] [Abstract]

"Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2."
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J. Biol. Chem.278:16021-16029(2003) [PubMed] [Europe PMC] [Abstract]

"The interaction of KCTD1 with transcription factor AP-2alpha inhibits its transactivation."
Ding X. , Luo C. , Zhou J. , Zhong Y. , Hu X. , Zhou F. , Ren K. , Gan L. , He A. , Zhu J. , Gao X. , Zhang J.
J. Cell. Biochem.106:285-295(2009) [PubMed] [Europe PMC] [Abstract]

"Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus."
Satoda M. , Zhao F. , Diaz G.A. , Burn J. , Goodship J. , Davidson H.R. , Pierpont M.E.M. , Gelb B.D.
Nat. Genet.25:42-46(2000) [PubMed] [Europe PMC] [Abstract]

"Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation."
Zhao F. , Weismann C.G. , Satoda M. , Pierpont M.E.M. , Sweeney E. , Thompson E.M. , Gelb B.D.
Am. J. Hum. Genet.69:695-703(2001) [PubMed] [Europe PMC] [Abstract]