| Literature DB >> 26322171 |
Noriko Funato1, Masataka Nakamura1, Hiromi Yanagisawa1.
Abstract
Cleft palate, including complete or incomplete cleft palates, soft palate clefts, and submucosal cleft palates, is the most frequent congenital craniofacial anomaly in humans. Multifactorial conditions, including genetic and environmental factors, induce the formation of cleft palates. The process of palatogenesis is temporospatially regulated by transcription factors, growth factors, extracellular matrix proteins, and membranous molecules; a single ablation of these molecules can result in a cleft palate in vivo. Studies on knockout mice were reviewed in order to identify genetic errors that lead to cleft palates. In this review, we systematically describe these mutant mice and discuss the molecular mechanisms of palatogenesis.Entities:
Keywords: Incomplete cleft palate; Knockout mice; Palatal shelf; Palatogenesis; Submucosal cleft palate; Tbx1
Year: 2015 PMID: 26322171 PMCID: PMC4549757 DOI: 10.4331/wjbc.v6.i3.121
Source DB: PubMed Journal: World J Biol Chem ISSN: 1949-8454