(Q38344570)

English

Frontonasal process-specific disruption of AP-2alpha results in postnatal midfacial hypoplasia, vascular anomalies, and nasal cavity defects

scientific article published on March 2004

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scholarly article

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Europe PubMed Central

2 September 2017

Frontonasal process-specific disruption of AP-2alpha results in postnatal midfacial hypoplasia, vascular anomalies, and nasal cavity defects (English)

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Europe PubMed Central

2 September 2017

author name string

Nelson DK

1

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Europe PubMed Central

2 September 2017

Williams T

2

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Europe PubMed Central

2 September 2017

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publication date

1 March 2004

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Europe PubMed Central

2 September 2017

Developmental Biology

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Europe PubMed Central

2 September 2017

267

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Europe PubMed Central

2 September 2017

1

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Europe PubMed Central

2 September 2017

72-92

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Europe PubMed Central

2 September 2017

Tgf-beta1, Tgf-beta2, Tgf-beta3 and Msx2 expression is elevated during frontonasal suture morphogenesis and during active postnatal facial growth

1 reference

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Restricted growth at the frontonasal suture: alterations in craniofacial growth in rabbits

1 reference

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7 January 2021

Mechanisms balancing skeletal matrix synthesis and degradation

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Requirement for AP-2alpha in cardiac outflow tract morphogenesis

1 reference

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Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects

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Expression of the T-box gene Eomesodermin during early mouse development.

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Altered fracture repair in the absence of MMP9

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Mutations of the TWIST gene in the Saethre-Chotzen syndrome

1 reference

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Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disorders

1 reference

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Angiogenesis and bone growth

1 reference

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7 January 2021

Transforming growth factor-alpha-induced transcriptional activation of the vascular permeability factor (VPF/VEGF) gene requires AP-2-dependent DNA binding and transactivation.

1 reference

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7 January 2021

Modulation of bovine articular chondrocyte gene expression in vitro by oxygen tension

1 reference

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Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

1 reference

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

1 reference

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Tissue origins and interactions in the mammalian skull vault

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The relationship between masticatory function and craniofacial morphology. I. A cephalometric longitudinal analysis in the growing rat fed a soft diet

1 reference

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Impaired angiogenesis and endochondral bone formation in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188.

1 reference

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7 January 2021

Mechanobiology of craniofacial sutures

1 reference

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Strain induced osteogenesis of the craniofacial suture upon controlled delivery of low-frequency cyclic forces

1 reference

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Use of bromodeoxyuridine-immunohistochemistry to examine the proliferation, migration and time of origin of cells in the central nervous system.

1 reference

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7 January 2021

Positive and negative regulation of transcription in vitro: enhancer-binding protein AP-2 is inhibited by SV40 T antigen

1 reference

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7 January 2021

Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis

1 reference

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7 January 2021

Contrasting roles for c-Myc and L-Myc in the regulation of cellular growth and differentiation in vivo.

1 reference

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7 January 2021

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

1 reference

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7 January 2021

Immunochemical and mechanical characterization of cartilage subtypes in rabbit.

1 reference

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AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

1 reference

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Cranial sutures as intramembranous bone growth sites

1 reference

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7 January 2021

Postnatal Msx1 expression pattern in craniofacial, axial, and appendicular skeleton of transgenic mice from the first week until the second year.

1 reference

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FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease

1 reference

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Mechanisms of normal and tumor-derived angiogenesis

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Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

1 reference

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Epithelia are interchangeable between facial primordia of chick embryos and morphogenesis is controlled by the mesenchyme.

1 reference

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Sonic hedgehog mediates the polarizing activity of the ZPA

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Characterization of the endothelium-specific murine vascular endothelial growth factor receptor-2 (Flk-1) promoter

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From head to toe: conservation of molecular signals regulating limb and craniofacial morphogenesis

1 reference

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Transcription factor AP-2 essential for cranial closure and craniofacial development

1 reference

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7 January 2021

Generalized lacZ expression with the ROSA26 Cre reporter strain

1 reference

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Effects of insulin-like growth factor-I on nasopremaxillary growth under different masticatory loadings in growing mice

1 reference

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Genetics of craniofacial development and malformation

1 reference

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

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Analysis of the DNA-binding and activation properties of the human transcription factor AP-2

1 reference

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Characterization of a dimerization motif in AP-2 and its function in heterologous DNA-binding proteins

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Neurobehavioral evidence for the involvement of the vomeronasal system in mammalian reproduction

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Identification and regulation of tissue‐specific cis‐acting elements associated with the human AP‐2α gene

1 reference

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Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2

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Craniosynostosis in transgenic mice overexpressing Nell-1

1 reference

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7 January 2021

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10.1016/J.YDBIO.2003.10.033

1 reference

Europe PubMed Central

2 September 2017

1 reference

Europe PubMed Central

2 September 2017

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