FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model

Crouzon syndrome with acanthosis nigricans (CAN, a rare type of craniosynostosis characterized by premature suture fusion and neurological impairments) has been linked to a gain-of-function mutation (p.Ala391Glu) in fibroblast growth factor receptor 3 (FGFR3). To characterize the CAN mutation’s impa...

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Detalles Bibliográficos
Autores principales: Cornille, Maxence, Moriceau, Stéphanie, Khonsari, Roman H., Heuzé, Yann, Loisay, Léa, Boitez, Valérie, Morice, Anne, Arnaud, Eric, Collet, Corinne, Bensidhoum, Morad, Kaci, Nabil, Boddaert, Nathalie, Paternoster, Giovanna, Rauschendorfer, Theresa, Werner, Sabine, Mansour, Suzanne L., Di Rocco, Federico, Oury, Franck, Legeai-Mallet, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Brief Definitive Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906494/
https://www.ncbi.nlm.nih.gov/pubmed/35254402
http://dx.doi.org/10.1084/jem.20201879

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906494/
https://www.ncbi.nlm.nih.gov/pubmed/35254402
http://dx.doi.org/10.1084/jem.20201879

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