| scholarly article | Q13442814 |
| P356 | DOI | 10.1128/MCB.01168-07 |
| P8608 | Fatcat ID | release_axl6jqdh2fd3rfc6ihey3uhyd4 |
| P932 | PMC publication ID | 2223317 |
| P698 | PubMed publication ID | 17984226 |
| P2093 | author name string | Jian Zhang | |
| Jian Huang | |||
| Trevor Williams | |||
| Weiguo Feng | |||
| P2860 | cites work | Highly conserved non-coding sequences are associated with vertebrate development | Q21092819 |
| The AP-2 family of transcription factors | Q21184171 | ||
| A new generation of JASPAR, the open-access repository for transcription factor binding site profiles | Q25255984 | ||
| Repeated morphological evolution through cis-regulatory changes in a pleiotropic gene | Q28235451 | ||
| The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages | Q28504916 | ||
| Transcription factor AP-2 essential for cranial closure and craniofacial development | Q28513302 | ||
| Requirement for AP-2alpha in cardiac outflow tract morphogenesis | Q28584763 | ||
| AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice | Q28586197 | ||
| AP-2alpha transcription factor is required for early morphogenesis of the lens vesicle | Q28587027 | ||
| Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 | Q28594321 | ||
| MatInspector and beyond: promoter analysis based on transcription factor binding sites | Q29616314 | ||
| Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis | Q33515610 | ||
| Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting | Q33681429 | ||
| Comparative genomics: genome-wide analysis in metazoan eukaryotes | Q34187800 | ||
| Making digit patterns in the vertebrate limb | Q34496736 | ||
| Comparative and functional analysis of the AP2 promoter indicates that conserved octamer and initiator elements are critical for activity | Q34602256 | ||
| Applied bioinformatics for the identification of regulatory elements | Q35766840 | ||
| Comparative genomics at the vertebrate extremes | Q35778678 | ||
| Retinoid-induced limb malformations | Q35867179 | ||
| The developing limb and the control of the number of digits | Q36023736 | ||
| Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics | Q36559423 | ||
| Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins | Q37334244 | ||
| A long-range regulatory element of Hoxc8 identified by using the pClasper vector | Q37694251 | ||
| Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects | Q38344566 | ||
| Frontonasal process-specific disruption of AP-2alpha results in postnatal midfacial hypoplasia, vascular anomalies, and nasal cavity defects | Q38344570 | ||
| lockjaw encodes a zebrafish tfap2a required for early neural crest development. | Q38349455 | ||
| SELEX and missing phosphate contact analyses reveal flexibility within the AP-2[alpha] protein: DNA binding complex | Q39728282 | ||
| Shuffling of cis-regulatory elements is a pervasive feature of the vertebrate lineage | Q41852340 | ||
| An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development | Q41902872 | ||
| Amphioxus and lamprey AP-2 genes: implications for neural crest evolution and migration patterns. | Q42527237 | ||
| Noradrenergic neurons in the zebrafish hindbrain are induced by retinoic acid and require tfap2a for expression of the neurotransmitter phenotype | Q44610891 | ||
| An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice | Q44924708 | ||
| The AP-2 transcription factor is required for joint formation and cell survival in Drosophila leg development. | Q47071789 | ||
| Drosophila transcription factor AP-2 in proboscis, leg and brain central complex development | Q47072053 | ||
| Enhancer sequence conservation between vertebrates is favoured in developmental regulator genes | Q48144721 | ||
| Delineation of two distinct 6p deletion syndromes | Q48267342 | ||
| Identification and regulation of tissue‐specific cis‐acting elements associated with the human AP‐2α gene | Q52099713 | ||
| Overexpression of transcription factor AP-2alpha suppresses mammary gland growth and morphogenesis. | Q52107622 | ||
| Chicken transcription factor AP-2: cloning, expression and its role in outgrowth of facial prominences and limb buds. | Q52192985 | ||
| Comparative analysis of AP-2 alpha and AP-2 beta gene expression during murine embryogenesis. | Q52197891 | ||
| The 6p deletion syndrome: a new orofacial clefting syndrome and its implications for antenatal screening. | Q53458116 | ||
| AP-2.2, a novel gene related to AP-2, is expressed in the forebrain, limbs and face during mouse embryogenesis | Q62818027 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Transcription factor AP-2, alpha | Q21982739 |
| P304 | page(s) | 315–325 | |
| P577 | publication date | 2008-01-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme | |
| P478 | volume | 28 |
| Q90291182 | A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population |
| Q33857851 | Conservation in first introns is positively associated with the number of exons within genes and the presence of regulatory epigenetic signals |
| Q37178305 | Control elements in the neighboring ATPase gene influence spatiotemporal expression of the human agouti-related protein |
| Q81752916 | Expression levels of FAS are regulated through an evolutionary conserved element in intron 2, which modulates cystic fibrosis disease severity |
| Q28654627 | Functional analysis of limb transcriptional enhancers in the mouse |
| Q57444461 | Genetic Dissection of a Supergene Implicates in Craniofacial Evolution of Threespine Sticklebacks |
| Q35853942 | Hip geometry variation is associated with bone mineralization pathway gene variants: The Framingham Study. |
| Q33889301 | Intronic elements in the Na+/I- symporter gene (NIS) interact with retinoic acid receptors and mediate initiation of transcription |
| Q41696586 | Mllt10 knockout mouse model reveals critical role of Af10-dependent H3K79 methylation in midfacial development |
| Q47271603 | Modulation of FOXD3 activity in human embryonic stem cells directs pluripotency and paraxial mesoderm fates |
| Q36586217 | Molecular mechanisms of midfacial developmental defects |
| Q34876963 | Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators |
| Q37668700 | Roles of AP-2 transcription factors in the regulation of cartilage and skeletal development |
| Q24655671 | TFAP2A mutations result in branchio-oculo-facial syndrome |
| Q31039716 | The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data |
| Q35217337 | cis-regulatory mutations are a genetic cause of human limb malformations |
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