FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?-Reference-Cited by-同舟云学术

FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?

Published:2017-05-03 Issue: Volume:8 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Lignon Guilhem,Beres Fleur,Quentric Mickael,Rouzière Stephan,Weil Raphael,De La Dure-Molla Muriel,Naveau Adrien,Kozyraki Renata,Dessombz Arnaud,Berdal Ariane

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference48 articles.

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2. Disruption of enamel crystal formation quantified by synchrotron microdiffraction;Al-Jawad;J. Dent.,2012

3. A Mutation in the Mouse Amelx Tri-Tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta;Barron;Hum. Mol. Genet.,2010

4. Revisiting the Localisation of Zn2+ cations sorbed on pathological apatite calcifications made through X-Ray absorption spectroscopy;Bazin;Biochimie,2009

5. The status of strontium in biological apatites: an XANES/EXAFS investigation;Bazin;J. Synchrotron Radiat.,2014

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1. Role of amelogenin phosphorylation in regulating dental enamel formation;Matrix Biology;2024-08

2. FAM20A: a potential diagnostic biomarker for lung squamous cell carcinoma;Frontiers in Immunology;2024-06-25

3. Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG;Oral Diseases;2023-09-24

4. FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome;International Endodontic Journal;2023-05-16

5. Molecular‐based phenotype variations in amelogenesis imperfecta;Oral Diseases;2023-05-08