Fgfr3 Is a Positive Regulator of Osteoblast Expansion and Differentiation During Zebrafish Skull Vault Development-Reference-Cited by-同舟云学术

Fgfr3 Is a Positive Regulator of Osteoblast Expansion and Differentiation During Zebrafish Skull Vault Development

Published:2020-05-26 Issue:9 Volume:35 Page:1782-1797
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Dambroise Emilie¹,Ktorza Ivan¹,Brombin Alessandro²³,Abdessalem Ghaith⁴,Edouard Joanne⁵⁶,Luka Marine⁴,Fiedler Imke⁷,Binder Olivia¹,Pelle Olivier⁸,Patton E Elizabeth²³,Busse Björn⁷^ORCID,Menager Mickaël⁴,Sohm Frederic⁵⁶⁷⁸⁹,Legeai‐Mallet Laurence¹^ORCID

Affiliation:

1. Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, INSERM UMR 1163 Université de Paris, Imagine Institute Paris France

2. MRC Human Genetics Unit MRC Institute of Genetics and Molecular Medicine, University of Edinburgh Edinburgh UK

3. Cancer Research UK Edinburgh Centre MRC Institute of Genetics and Molecular Medicine, University of Edinburgh Edinburgh UK

4. Laboratory of Inflammatory Responses and Transcriptomic Networks in Diseases, INSERM UMR 1163 Université de Paris, Imagine Institute Paris France

5. UMS AMAGEN, CNRS, INRA Université Paris‐Saclay Gif‐sur‐Yvette France

6. Institute for Integrative Biology of the Cell (I2BC)–CNRS Gif‐sur‐Yvette France

7. Department of Osteology and Biomechanics University Medical Center Hamburg‐Eppendorf Hamburg Germany

8. Flow Cytometry Core Facility Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633 Paris France

9. Functional Genomics Institute of Lyon University of Lyon, CNRS, INRA, Ecole Normale Supérieure de Lyon Lyon France

Funder

Agence Nationale de la Recherche

H2020 European Research Council

Institut National de la Santé et de la Recherche Médicale

Union des Blessés de la Face et de la Tête

Melanoma Research Alliance

Seventh Framework Programme

Institut Curie

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbmr.4042

Reference65 articles.

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3. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome;Muenke M;Am J Hum Genet.,1997

4. FGFR3 mutation causes abnormal membranous ossification in achondroplasia

5. A Novel Homozygous Mutation in FGFR3 Causes Tall Stature, Severe Lateral Tibial Deviation, Scoliosis, Hearing Impairment, Camptodactyly, and Arachnodactyly

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