Genetic basis of non-syndromic anomalies of human tooth number
Authors:
- Gabriella GalluccioGabriella Galluccio
- Monica CastellanoMCMonica Castellano
- Camilla La MonacaCMCamilla La Monaca
- 1 July 2012
- journal article
- review article
- Published by Elsevier in Archives of Oral Biology
- Vol. 57 (7) , 918-930
Abstract
No abstract availableKeywords
This publication has 106 references indexed in Scilit:
- Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental developmentArchives of Oral Biology, 2009
- Morphogenetic fields within the human dentition: A new, clinically relevant synthesis of an old conceptArchives of Oral Biology, 2009
- Wnt/beta-catenin signaling plays an essential role in activation of odontogenic mesenchyme during early tooth developmentDevelopmental Biology, 2009
- Molecular genetics of tooth developmentCurrent Opinion in Genetics & Development, 2009
- Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesisEuropean Journal of Human Genetics, 2009
- Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9Human Molecular Genetics, 2009
- Primary cilia regulate Shh activity in the control of molar tooth numberDevelopment, 2009
- Revitalization of a diastemal tooth primordium in Spry2 null mice results from increased proliferation and decreased apoptosisJournal of Experimental Zoology Part B: Molecular and Developmental Evolution, 2009
- Identification and Functional Analysis of Two Novel PAX9 MutationsCells Tissues Organs, 2008
- THE WNT SIGNALING PATHWAY IN DEVELOPMENT AND DISEASEAnnual Review of Cell and Developmental Biology, 2004