Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of <i>Mecp2</i> Heterozygous Mouse Females
Rett Syndrome is an X-linked neurodevelopmental disorder (RTT; OMIM#312750) associated to <i>MECP2</i> 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 jurisdicti...
Main Authors: | , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-11-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/22/16249 |