Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of Mecp2 Heterozygous Mouse Females

Rett Syndrome is an X-linked neurodevelopmental disorder (RTT; OMIM#312750) associated to MECP2 mutations. MeCP2 dysfunction is seen as one cause for the deficiencies found in brain-derived neurotrophic factor (BDNF) signaling, since BDNF is one of the genes under MeCP2 jurisdiction. BDNF signaling...

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Detalles Bibliográficos
Autores principales: Miranda-Lourenço, Catarina, Rosa, Jéssica, Rei, Nádia, Belo, Rita F., Lopes, Ana Luísa, Silva, Diogo, Vieira, Cátia, Magalhães-Cardoso, Teresa, Viais, Ricardo, Correia-de-Sá, Paulo, Sebastião, Ana M., Diógenes, Maria J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671708/
https://www.ncbi.nlm.nih.gov/pubmed/38003438
http://dx.doi.org/10.3390/ijms242216249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671708/
https://www.ncbi.nlm.nih.gov/pubmed/38003438
http://dx.doi.org/10.3390/ijms242216249

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