Cargando…
Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility
In schizophrenia (SCZ) and autism spectrum disorder (ASD), the dysregulation of glutamate transmission through N-methyl-d-aspartate receptors (NMDARs) has been implicated as a potential etiological mechanism. Previous studies have accumulated evidence supporting NMDAR-encoding genes' role in et...
Autores principales: | Yu, Yanjie, Lin, Yingni, Takasaki, Yuto, Wang, Chenyao, Kimura, Hiroki, Xing, Jingrui, Ishizuka, Kanako, Toyama, Miho, Kushima, Itaru, Mori, Daisuke, Arioka, Yuko, Uno, Yota, Shiino, Tomoko, Nakamura, Yukako, Okada, Takashi, Morikawa, Mako, Ikeda, Masashi, Iwata, Nakao, Okahisa, Yuko, Takaki, Manabu, Sakamoto, Shinji, Someya, Toshiyuki, Egawa, Jun, Usami, Masahide, Kodaira, Masaki, Yoshimi, Akira, Oya-Ito, Tomoko, Aleksic, Branko, Ohno, Kinji, Ozaki, Norio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802496/ https://www.ncbi.nlm.nih.gov/pubmed/29317596 http://dx.doi.org/10.1038/s41398-017-0061-y |
Ejemplares similares
-
Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders
por: Xing, Jingrui, et al.
Publicado: (2016) -
Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders
por: Ishizuka, Kanako, et al.
Publicado: (2016) -
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population
por: Takasaki, Yuto, et al.
Publicado: (2016) -
Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder
por: Furuta, Sho, et al.
Publicado: (2022) -
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
por: Ishizuka, Kanako, et al.
Publicado: (2020)