Cargando…
PM373. Behavioral and neurochemical abnormalities in heterozygous Reelin Orleans mutant mouse model of schizophrenia
Autores principales: | Yamada, Kiyofumi, Sobue, Akira, Aoyama, Yuki, Wei, Shan, Nagai, Taku, Aleksic, Branko, Kushima, Itaru, Ozaki, Norio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616309/ http://dx.doi.org/10.1093/ijnp/pyw041.373 |
Ejemplares similares
-
Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia
por: Sobue, Akira, et al.
Publicado: (2018) -
Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions
por: Furukawa, Sawako, et al.
Publicado: (2023) -
PM338. Investigation of the association of rare single nucleotide variants in methyl-CpG-binding domain protein 5 (MBD5) with phenotypes of autism spectrum disorders and schizophrenia.
por: Ishizuka, Kanako, et al.
Publicado: (2016) -
Copy Number Variant in the Region of Adenosine Kinase (ADK) and Its Possible Contribution to Schizophrenia Susceptibility
por: Kimura, Hiroki, et al.
Publicado: (2017) -
Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia
por: Sawahata, Masahito, et al.
Publicado: (2020)