Reference : Teeth. Where and how to make them.
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/10993/1320
Teeth. Where and how to make them.
English
Peters, H. [> >]
Balling, Rudi mailto [> >]
1999
Trends in Genetics
Elsevier Trends Journals
15
2
59-65
Yes (verified by ORBilu)
0168-9525
Cambridge
United Kingdom
[en] Animals ; Bone Morphogenetic Protein 4 ; Bone Morphogenetic Proteins/genetics/physiology ; DNA-Binding Proteins/genetics/physiology ; Embryonic Induction ; Epithelium/embryology ; Eye Proteins ; Fibroblast Growth Factors/deficiency/genetics/physiology ; Gene Expression Regulation, Developmental ; Genes, Homeobox ; Gestational Age ; Growth Substances/genetics/physiology ; Homeodomain Proteins/genetics/physiology ; MSX1 Transcription Factor ; Mesoderm/physiology ; Mice ; Mice, Knockout ; Morphogenesis ; Odontogenesis/genetics/physiology ; PAX9 Transcription Factor ; Paired Box Transcription Factors ; Repressor Proteins ; Signal Transduction ; Transcription Factors/genetics/physiology
[en] Organs have to develop at precisely determined sites to ensure functionality of the whole organism. Organogenesis is typically regulated by a series of interactions between morphologically distinct tissues. The developing tooth of the mouse is an excellent model to study these processes and we are beginning to understand the networks regulating reciprocal tissue interactions at the molecular level. Synergistic and antagonistic effects of signaling molecules including FGFs and BMPs are recursively used to induce localized responses in the adjacent tissue layer (mesenchyme or epithelium). However, at different phases of odontogenesis these secreted growth factors have distinct effects and at the same time they are regulated by different upstream factors. The mesenchymal transcription factors Msx1 and Pax9 are initially regulated by epithelial FGFs and BMPs, but subsequently they function upstream of these signaling molecules. This cascade provides a molecular model by which reciprocal tissue interactions are controlled.
http://hdl.handle.net/10993/1320

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