| scholarly article | Q13442814 |
| P2093 | author name string | Williams T | |
| Nelson DK | |||
| P2860 | cites work | Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome | Q24310222 |
| Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome | Q24311679 | ||
| Mutations of the TWIST gene in the Saethre-Chotzen syndrome | Q24311736 | ||
| A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome | Q24314986 | ||
| Craniosynostosis in transgenic mice overexpressing Nell-1 | Q24553230 | ||
| Generalized lacZ expression with the ROSA26 Cre reporter strain | Q27860837 | ||
| A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis | Q28249477 | ||
| Characterization of a dimerization motif in AP-2 and its function in heterologous DNA-binding proteins | Q28266897 | ||
| Analysis of the DNA-binding and activation properties of the human transcription factor AP-2 | Q28271397 | ||
| Transcription factor AP-2 essential for cranial closure and craniofacial development | Q28513302 | ||
| Tgf-beta1, Tgf-beta2, Tgf-beta3 and Msx2 expression is elevated during frontonasal suture morphogenesis and during active postnatal facial growth | Q28567708 | ||
| 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 | ||
| Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 | Q28594321 | ||
| Sonic hedgehog mediates the polarizing activity of the ZPA | Q29616565 | ||
| Expression of the T-box gene Eomesodermin during early mouse development. | Q30630109 | ||
| Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis | Q33515610 | ||
| From head to toe: conservation of molecular signals regulating limb and craniofacial morphogenesis | Q33592088 | ||
| Cranial sutures as intramembranous bone growth sites | Q34085716 | ||
| Mechanisms balancing skeletal matrix synthesis and degradation | Q34129759 | ||
| Positive and negative regulation of transcription in vitro: enhancer-binding protein AP-2 is inhibited by SV40 T antigen | Q34163571 | ||
| Angiogenesis and bone growth | Q34204716 | ||
| Genetics of craniofacial development and malformation | Q34271559 | ||
| Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome | Q34308670 | ||
| Mechanisms of normal and tumor-derived angiogenesis | Q34592513 | ||
| FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease | Q34702208 | ||
| Mechanobiology of craniofacial sutures | Q35009879 | ||
| Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disorders | Q35787010 | ||
| Contrasting roles for c-Myc and L-Myc in the regulation of cellular growth and differentiation in vivo. | Q37694376 | ||
| Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects | Q38344566 | ||
| Neurobehavioral evidence for the involvement of the vomeronasal system in mammalian reproduction | Q39855349 | ||
| Characterization of the endothelium-specific murine vascular endothelial growth factor receptor-2 (Flk-1) promoter | Q41181627 | ||
| Transforming growth factor-alpha-induced transcriptional activation of the vascular permeability factor (VPF/VEGF) gene requires AP-2-dependent DNA binding and transactivation. | Q41916797 | ||
| Altered fracture repair in the absence of MMP9 | Q42641175 | ||
| Tissue origins and interactions in the mammalian skull vault | Q43849664 | ||
| Immunochemical and mechanical characterization of cartilage subtypes in rabbit. | Q44074259 | ||
| Impaired angiogenesis and endochondral bone formation in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188. | Q46288581 | ||
| Identification and regulation of tissue‐specific cis‐acting elements associated with the human AP‐2α gene | Q52099713 | ||
| Postnatal Msx1 expression pattern in craniofacial, axial, and appendicular skeleton of transgenic mice from the first week until the second year. | Q52135229 | ||
| Epithelia are interchangeable between facial primordia of chick embryos and morphogenesis is controlled by the mesenchyme. | Q52244290 | ||
| Use of bromodeoxyuridine-immunohistochemistry to examine the proliferation, migration and time of origin of cells in the central nervous system. | Q52250604 | ||
| Restricted growth at the frontonasal suture: alterations in craniofacial growth in rabbits | Q69772907 | ||
| The relationship between masticatory function and craniofacial morphology. I. A cephalometric longitudinal analysis in the growing rat fed a soft diet | Q69850668 | ||
| Modulation of bovine articular chondrocyte gene expression in vitro by oxygen tension | Q73998897 | ||
| Effects of insulin-like growth factor-I on nasopremaxillary growth under different masticatory loadings in growing mice | Q74269142 | ||
| Strain induced osteogenesis of the craniofacial suture upon controlled delivery of low-frequency cyclic forces | Q78586446 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 72-92 | |
| P577 | publication date | 2004-03-01 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Frontonasal process-specific disruption of AP-2alpha results in postnatal midfacial hypoplasia, vascular anomalies, and nasal cavity defects | |
| P478 | volume | 267 |
| Q46256632 | A Cre transgene active in developing endodermal organs, heart, limb, and extra-ocular muscle |
| Q28587729 | AP-2 factors act in concert with Notch to orchestrate terminal differentiation in skin epidermis |
| Q37566996 | Activation of Hedgehog signaling by loss of GNAS causes heterotopic ossification |
| Q28588584 | An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda |
| Q37045093 | Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain |
| Q40006898 | BCL11B regulates sutural patency in the mouse craniofacial skeleton |
| Q36404257 | Comparative ontogeny and phylogeny of the upper jaw skeleton in amniotes |
| Q24811874 | Conditional knockdown of Fgfr2 in mice using Cre-LoxP induced RNA interference |
| Q35740259 | Cre-mediated recombination can induce apoptosis in vivo by activating the p53 DNA damage-induced pathway |
| Q35567806 | FGF8 is essential for formation of the ductal system in the male reproductive tract |
| Q38641260 | From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models |
| Q37334244 | Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins |
| Q57444461 | Genetic Dissection of a Supergene Implicates in Craniofacial Evolution of Threespine Sticklebacks |
| Q50193517 | Hydronephrosis in the Wnt5a-ablated kidney is caused by an abnormal ureter-bladder connection |
| Q28592776 | Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme |
| Q39186926 | Long-range enhancers regulating Myc expression are required for normal facial morphogenesis |
| Q28589447 | Loss of AP-2alpha impacts multiple aspects of ventral body wall development and closure |
| Q36586217 | Molecular mechanisms of midfacial developmental defects |
| Q21563367 | Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects |
| Q28083779 | Receptor tyrosine kinase signaling: regulating neural crest development one phosphate at a time |
| Q54780420 | Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome. |
| Q46596456 | Stage-dependent craniofacial defects resulting from Sprouty2 overexpression |
| Q24655671 | TFAP2A mutations result in branchio-oculo-facial syndrome |
| Q34818278 | Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage. |
| Q21184171 | The AP-2 family of transcription factors |
| Q39949448 | Variation in the Developmental and Morphological Interaction Between the Nasal Septum and Facial Skeleton |
| Q38344566 | Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects |
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