Showing results (21-30 of 31) with videos related to
Sort By:
Pageof 4
Brain & Development|March 27, 2025
Diffuse but Non-homogeneous Brain Atrophy: Identification of Specific Brain Regions and Their Correlation with Clinical Severity in Rett SyndromeHajime Narita, Jun Natsume, Takeshi Suzuki, et al.Cell Reports|May 19, 2021
MeCP2 controls neural stem cell fate specification through miR-199a-mediated inhibition of BMP-Smad signalingHideyuki Nakashima, Keita Tsujimura, Koichiro Irie, et al.Scientific Reports|July 24, 2024
Gnao1 is a molecular switch that regulates the Rho signaling pathway in differentiating neuronsRyoji Taira, Satoshi Akamine, Sayaka Okuzono, et al.Cerebral Cortex (New York, N.Y. : 1991)|March 20, 2025
Structural pathways related to the subventricular zone are decreased in volume with altered microstructure in young adult males with autism spectrum disorderKeita Tsujimura, Alpen Ortug, José Luis Alatorre Warren, et al.Cerebral Cortex (New York, N.Y. : 1991)|March 8, 2025
Structural pathways related to the subventricular zone are decreased in volume with altered microstructure in young adult males with autism spectrum disorderKeita Tsujimura, Alpen Ortug, José Luis Alatorre Warren, et al.Frontiers in Neuroscience|February 23, 2023
Integration of structural MRI and epigenetic analyses hint at linked cellular defects of the subventricular zone and insular cortex in autism: Findings from a case studyEmi Takahashi, Nina Allan, Rafael Peres, et al.Diagnostics (Basel, Switzerland)|September 9, 2023
A Brain Morphometry Study with Across-Site Harmonization Using a ComBat-Generalized Additive Model in Children and AdolescentsTadashi Shiohama, Norihide Maikusa, Masahiro Kawaguchi, et al.Iscience|November 17, 2025
miR-199a functions downstream of MeCP2 in neurons of MECP2 duplication syndrome modelsYuichi Akaba, Satoru Takahashi, Shota Adachi, et al.Clinical Immunology (Orlando, Fla.)|September 7, 2023
Heterogeneity and mitochondrial vulnerability configurate the divergent immunoreactivity of human induced microglia-like cellsKousuke Yonemoto, Fumihiko Fujii, Ryoji Taira, et al.Translational Psychiatry|December 6, 2020
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorderHidekazu Kato, Itaru Kushima, Daisuke Mori, et al.Pageof 4