| scholarly article | Q13442814 |
| P2093 | author name string | Trevor Williams | |
| Amy L Donner | |||
| P2860 | cites work | The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome | Q22011211 |
| Cloning and characterisation of the Sry-related transcription factor gene Sox8. | Q22253229 | ||
| Transformation and Stat activation by derivatives of FGFR1, FGFR3, and FGFR4 | Q22254704 | ||
| Cell responses to FGFR3 signalling: growth, differentiation and apoptosis | Q24297423 | ||
| A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene | Q24533335 | ||
| Transcription factor gene AP-2 gamma essential for early murine development | Q24537286 | ||
| From head to toes: the multiple facets of Sox proteins | Q24548730 | ||
| Targeted disruption of the mouse Stat3 gene leads to early embryonic lethality | Q24685515 | ||
| Structural basis for SRY-dependent 46-X,Y sex reversal: modulation of DNA bending by a naturally occurring point mutation | Q27634883 | ||
| Molecular basis of human 46X,Y sex reversal revealed from the three-dimensional solution structure of the human SRY-DNA complex | Q27730262 | ||
| Pairing SOX off: with partners in the regulation of embryonic development | Q28139502 | ||
| Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control | Q28141560 | ||
| Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators | Q28213186 | ||
| Roles of FGF signaling in skeletal development and human genetic diseases | Q28239936 | ||
| Solution structure of the sequence-specific HMG box of the lymphocyte transcriptional activator Sox-4 | Q28271290 | ||
| Gene targeting reveals a widespread role for the high-mobility-group transcription factor Sox11 in tissue remodeling | Q28504616 | ||
| A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo | Q28505232 | ||
| Transcription factor AP-2 essential for cranial closure and craniofacial development | Q28513302 | ||
| The high mobility group transcription factor Sox8 is a negative regulator of osteoblast differentiation | Q28586194 | ||
| AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice | Q28586197 | ||
| Sox9 is required for cartilage formation | Q28588649 | ||
| Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization | Q28590890 | ||
| Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta | Q28591284 | ||
| The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 | Q28593218 | ||
| Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 | Q28594321 | ||
| A series of normal stages in the development of the chick embryo | Q29037347 | ||
| A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells | Q29547557 | ||
| 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 | ||
| Hierarchy revealed in the specification of three skeletal fates by Sox9 and Runx2. | Q42635325 | ||
| Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice | Q43640386 | ||
| A Ser250Trp substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis | Q44589915 | ||
| Noradrenergic neurons in the zebrafish hindbrain are induced by retinoic acid and require tfap2a for expression of the neurotransmitter phenotype | Q44610891 | ||
| Stat1 controls postnatal bone formation by regulating fibroblast growth factor signaling in osteoblasts | Q44836661 | ||
| A zone of frontonasal ectoderm regulates patterning and growth in the face. | Q45999105 | ||
| Regulation of transcription factor AP-2 by the morphogen retinoic acid and by second messengers. | Q46001099 | ||
| AP2-dependent signals from the ectoderm regulate craniofacial development in the zebrafish embryo. | Q46172553 | ||
| Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region | Q47288623 | ||
| Delineation of two distinct 6p deletion syndromes | Q48267342 | ||
| Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse | Q48837214 | ||
| Comparative analysis of genes downstream of the Hoxd cluster in developing digits and external genitalia. | Q52047618 | ||
| Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture. | Q52050351 | ||
| Conserved molecular program regulating cranial and appendicular skeletogenesis. | Q52088161 | ||
| Shh and Fgf8 act synergistically to drive cartilage outgrowth during cranial development. | Q52088188 | ||
| Identification and regulation of tissue‐specific cis‐acting elements associated with the human AP‐2α gene | Q52099713 | ||
| The IIIc alternative of Fgfr2 is a positive regulator of bone formation. | Q52116911 | ||
| Transcription factor AP-2gamma is essential in the extra-embryonic lineages for early postimplantation development. | Q52119917 | ||
| An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. | Q52171813 | ||
| Chicken transcription factor AP-2: cloning, expression and its role in outgrowth of facial prominences and limb buds. | Q52192985 | ||
| STAT signaling is active during early mammalian development. | Q52196597 | ||
| The 6p deletion syndrome: a new orofacial clefting syndrome and its implications for antenatal screening. | Q53458116 | ||
| STAT1 mediates the increased apoptosis and reduced chondrocyte proliferation in mice overexpressing FGF2 | Q57054880 | ||
| Transcriptional mechanisms in osteoblast differentiation and bone formation | Q73763993 | ||
| Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families | Q75382701 | ||
| MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data | Q29547902 | ||
| Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis | Q33515610 | ||
| Interactions between Sox9 and beta-catenin control chondrocyte differentiation | Q33775735 | ||
| Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder | Q33864543 | ||
| The transcription factors L-Sox5 and Sox6 are essential for cartilage formation | Q33955940 | ||
| Cloning and expression of AP-2, a cell-type-specific transcription factor that activates inducible enhancer elements | Q34164797 | ||
| Patterning Systems—From One End of the Limb to the Other | Q34189919 | ||
| Genetics of craniofacial development and malformation | Q34271559 | ||
| Induction of neural crest in Xenopus by transcription factor AP2alpha | Q34470119 | ||
| FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease | Q34702208 | ||
| A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes | Q35042862 | ||
| Pattern formation: old models out on a limb. | Q35057541 | ||
| Deciphering skeletal patterning: clues from the limb | Q35128223 | ||
| The genetic basis for skeletal diseases | Q35128232 | ||
| About face: signals and genes controlling jaw patterning and identity in vertebrates | Q35136052 | ||
| Genetically altered mouse models: the good, the bad, and the ugly | Q35150807 | ||
| FGF signaling inhibits chondrocyte proliferation and regulates bone development through the STAT-1 pathway | Q35198364 | ||
| Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest | Q35234587 | ||
| Cellular and molecular mechanisms of development of the external genitalia | Q35594470 | ||
| Molecular and genetic regulation of testis descent and external genitalia development | Q35769881 | ||
| Gene-regulatory interactions in neural crest evolution and development | Q35885247 | ||
| Stat1 functions as a cytoplasmic attenuator of Runx2 in the transcriptional program of osteoblast differentiation | Q35967234 | ||
| New insights into craniofacial morphogenesis | Q36037960 | ||
| FGF signaling in the developing endochondral skeleton | Q36111408 | ||
| Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes. | Q37346093 | ||
| A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis. | Q37493982 | ||
| Regulation of Hoxc-8 during mouse embryonic development: identification and characterization of critical elements involved in early neural tube expression. | Q38288443 | ||
| Cell type-specific regulation of expression of transcription factor AP-2 in neuroectodermal cells | Q38303639 | ||
| The DNA-binding specificity of SOX9 and other SOX proteins. | Q38328342 | ||
| A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors | Q38329519 | ||
| 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 | ||
| Transcription factor Ap-2alpha is necessary for development of embryonic melanophores, autonomic neurons and pharyngeal skeleton in zebrafish. | Q38346507 | ||
| lockjaw encodes a zebrafish tfap2a required for early neural crest development. | Q38349455 | ||
| SOX9 enhances aggrecan gene promoter/enhancer activity and is up-regulated by retinoic acid in a cartilage-derived cell line, TC6. | Q40831754 | ||
| Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus | Q40881151 | ||
| Activation of Stat1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia type II dwarfism | Q41120368 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 1358-1370 | |
| P577 | publication date | 2006-05-01 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins | |
| P478 | volume | 235 |
| Q39483974 | Ablation of the Sox11 Gene Results in Clefting of the Secondary Palate Resembling the Pierre Robin Sequence |
| Q28654627 | Functional analysis of limb transcriptional enhancers in the mouse |
| Q57444461 | Genetic Dissection of a Supergene Implicates in Craniofacial Evolution of Threespine Sticklebacks |
| Q28592776 | Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme |
| Q41577826 | Limb-Enhancer Genie: An accessible resource of accurate enhancer predictions in the developing limb. |
| Q35673892 | Morphological integration of soft-tissue facial morphology in Down Syndrome and siblings |
| Q37668700 | Roles of AP-2 transcription factors in the regulation of cartilage and skeletal development |
| Q64085553 | The biological characteristics of transcription factors AP-2α and AP-2γ and their importance in various types of cancers |
| Q37383066 | The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models |
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