Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia-Reference-Cited by-同舟云学术

Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia

Published:2018-09-07 Issue:9 Volume:13 Page:e0202989
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Bonczek Ondřej,Bielik Peter,Krejčí Přemysl,Zeman Tomáš,Izakovičová-Hollá Lýdie,Šoukalová Jana,Vaněk Jiří,Gerguri Tereza,Balcar Vladimir J.,Šerý Omar^ORCID

Funder

Internal Grant Agency of the Czech Ministry of Health of The Czech Republic

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference54 articles.

1. Neural crest and the origin of ectomesenchyme: neural fold heterogeneity suggests an alternative hypothesis;JA Weston;Dev Dyn,2004

2. Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages;M Jussila;Cold Spring Harb Perspect Biol,2012

3. Molecular genetics of tooth morphogenesis and patterning: the right shape in the right place;AS Tucker;J Dent Res,1999

4. The cutting-edge of mammalian development; how the embryo makes teeth;A Tucker;Nat Rev Genet,2004

5. Genome-wide analysis of gene expression in human embryonic tooth germ;Z Huang;J Mol Histol,2014

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