Lack of FAM20A, Ectopic Gingival Mineralization and Chondro/Osteogenic Modifications in Enamel Renal Syndrome.

Fam20A calcification cell death enamel renal syndrome fibroblast gingiva osteoblast

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2020
Historique:
received: 11 09 2020
accepted: 16 11 2020
entrez: 11 1 2021
pubmed: 12 1 2021
medline: 12 1 2021
Statut: epublish

Résumé

Enamel renal syndrome (ERS) is a rare recessive disorder caused by loss-of-function mutations in

Identifiants

pubmed: 33425910
doi: 10.3389/fcell.2020.605084
pmc: PMC7793853
doi:

Types de publication

Journal Article

Langues

eng

Pagination

605084

Informations de copyright

Copyright © 2020 Simancas Escorcia, Diarra, Naveau, Dessombz, Felizardo, Cannaya, Chatziantoniou, Quentric, Vikkula, Cases, Berdal, De La Dure-Molla and Kozyraki.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

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Auteurs

Victor Simancas Escorcia (V)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Abdoulaziz Diarra (A)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Adrien Naveau (A)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Arnaud Dessombz (A)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Rufino Felizardo (R)

CRMR O-RARES, Hôpital Rothshild, UFR d'Odontologie-Garancière, Université de Paris, Paris, France.

Vidjeacoumary Cannaya (V)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Christos Chatziantoniou (C)

UMRS1155, INSERM, Sorbonne Université, Paris, France.

Mickaël Quentric (M)

Department of Human Genetics, De Duve Institute, Université catholique de Louvain, Brussels, Belgium.

Miikka Vikkula (M)

Department of Human Genetics, De Duve Institute, Université catholique de Louvain, Brussels, Belgium.

Olivier Cases (O)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.

Ariane Berdal (A)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.
CRMR O-RARES, Hôpital Rothshild, UFR d'Odontologie-Garancière, Université de Paris, Paris, France.

Muriel De La Dure-Molla (M)

CRMR O-RARES, Hôpital Rothshild, UFR d'Odontologie-Garancière, Université de Paris, Paris, France.
Institut des maladies génétiques, Imagine, Paris, France.

Renata Kozyraki (R)

Centre de Recherche des Cordeliers, Sorbonne Université, INSERM, Université de Paris, Laboratory of Oral Molecular Pathophysiology, Paris, France.
CRMR O-RARES, Hôpital Rothshild, UFR d'Odontologie-Garancière, Université de Paris, Paris, France.

Classifications MeSH