| Literature DB >> 29655165 |
Mengjia Weng1, Zhengxi Chen1, Qian Xiao2, Ruomei Li1, Zhenqi Chen3.
Abstract
The fibroblast growth factors (FGFs) play a critical role during palatogenesis by mediating a variety of cellular responses. Extensive epidemiological and genetic studies over several decades in humans have revealed members of the FGF family function as candidate genes for syndromic and nonsyndromic cleft lip and cleft palate. The findings that FGFs signaling work delicately in the development of palate have been confirmed in mice carrying targeted mutations. Here we try to review recent progress toward a detailed understanding of FGF signaling including FGF7, FGF8, FGF9, FGF10, FGF18 and their receptors FGFR1, FGFR2 in palate development studies and discuss how they interact with other factors on the basis of animal studies regarding cleft palate.Entities:
Keywords: Cleft palate; FGF signaling; Palatogenesis; Teratogens
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Year: 2018 PMID: 29655165 DOI: 10.1016/j.biopha.2018.04.026
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529