Cargando…

Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility

Disabled 1 (DAB1) is an intracellular adaptor protein in the Reelin signaling pathway and plays an essential role in correct neuronal migration and layer formation in the developing brain. DAB1 has been repeatedly reported to be associated with neurodevelopmental disorders including schizophrenia (S...

Descripción completa

Detalles Bibliográficos
Autores principales:	Nawa, Yoshihiro, Kimura, Hiroki, Mori, Daisuke, Kato, Hidekazu, Toyama, Miho, Furuta, Sho, Yu, Yanjie, Ishizuka, Kanako, Kushima, Itaru, Aleksic, Branko, Arioka, Yuko, Morikawa, Mako, Okada, Takashi, Inada, Toshiya, Kaibuchi, Kozo, Ikeda, Masashi, Iwata, Nakao, Suzuki, Michio, Okahisa, Yuko, Egawa, Jun, Someya, Toshiyuki, Nishimura, Fumichika, Sasaki, Tsukasa, Ozaki, Norio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655853/ https://www.ncbi.nlm.nih.gov/pubmed/33298905 http://dx.doi.org/10.1038/s41439-020-00125-7

Ejemplares similares

Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder
por: Furuta, Sho, et al.
Publicado: (2022)

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder
por: Kato, Hidekazu, et al.
Publicado: (2020)

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
por: Ishizuka, Kanako, et al.
Publicado: (2020)

Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility
por: Yu, Yanjie, et al.
Publicado: (2018)

Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels
por: Toyama, Miho, et al.
Publicado: (2022)

Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia
por: Sawahata, Masahito, et al.
Publicado: (2020)

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders
por: Ishizuka, Kanako, et al.
Publicado: (2016)

Clinical characterization of patients with schizophrenia and 16p13.11 duplication: A case series
por: Kimura, Hiroki, et al.
Publicado: (2023)

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant
por: Arioka, Yuko, et al.
Publicado: (2018)

Clinical manifestations of schizophrenia in four patients with variants in voltage‐gated calcium channel‐encoding genes: a case series
por: Lo, Tzuyao, et al.
Publicado: (2022)

Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes
por: Kimura, Hiroki, et al.
Publicado: (2022)

Cell body shape and directional movement stability in human-induced pluripotent stem cell-derived dopaminergic neurons
por: Arioka, Yuko, et al.
Publicado: (2020)

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders
por: Ishizuka, K, et al.
Publicado: (2017)

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)

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)

Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia
por: Sobue, Akira, et al.
Publicado: (2018)

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk
por: Sekiguchi, Mariko, et al.
Publicado: (2020)

Copy Number Variant in the Region of Adenosine Kinase (ADK) and Its Possible Contribution to Schizophrenia Susceptibility
por: Kimura, Hiroki, et al.
Publicado: (2017)

Contribution of copy number variations to the risk of severe eating disorders
por: Kushima, Itaru, et al.
Publicado: (2022)

X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization
por: Kushima, Itaru, et al.
Publicado: (2022)

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population
por: Takasaki, Yuto, et al.
Publicado: (2016)

Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes
por: Ishizuka, Kanako, et al.
Publicado: (2016)

Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons
por: Arioka, Yuko, et al.
Publicado: (2020)

A Case Control Association Study and Cognitive Function Analysis of Neuropilin and Tolloid-Like 1 Gene and Schizophrenia in the Japanese Population
por: Banno, Masahiro, et al.
Publicado: (2011)

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility
por: Kimura, H, et al.
Publicado: (2017)

Relation Between Perinatal Depressive Symptoms, Harm Avoidance, and a History of Major Depressive Disorder: A Cohort Study of Pregnant Women in Japan
por: Kubota, Chika, et al.
Publicado: (2019)

Stable factor structure of the Edinburgh Postnatal Depression Scale during the whole peripartum period: Results from a Japanese prospective cohort study
por: Kubota, Chika, et al.
Publicado: (2018)

Validation and factor structure of the Japanese version of the inventory to diagnose depression, lifetime version for pregnant women
por: Kubota, Chika, et al.
Publicado: (2020)

The Risk Factors Predicting Suicidal Ideation Among Perinatal Women in Japan
por: Kubota, Chika, et al.
Publicado: (2020)

To Dab or Not to Dab: Rising Concerns Regarding the Toxicity of Cannabis Concentrates
por: Alzghari, Saeed K, et al.
Publicado: (2017)

White matter microstructure between the pre‐SMA and the cingulum bundle is related to response conflict in healthy subjects
por: Yamamoto, Maeri, et al.
Publicado: (2015)

PM373. Behavioral and neurochemical abnormalities in heterozygous Reelin Orleans mutant mouse model of schizophrenia
por: Yamada, Kiyofumi, et al.
Publicado: (2016)

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients
por: Yoshimi, Akira, et al.
Publicado: (2019)

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients
por: Yoshimi, Akira, et al.
Publicado: (2019)

Drug-induced Extrapyramidal Symptoms Scale (DIEPSS) Serbian Language version: Inter-rater and Test-retest Reliability
por: Peljto, Ami, et al.
Publicado: (2017)

Slovenian Version of the Drug-Induced Extrapyramidal Symptoms Scale: Evaluation of Interrater and Test-Retest Reliability
por: Senica, Nina, et al.
Publicado: (2023)

Association of the Myosin-binding Subunit of Myosin Phosphatase and Moesin: Dual Regulation of Moesin Phosphorylation by Rho-associated Kinase and Myosin Phosphatase
por: Fukata, Yuko, et al.
Publicado: (1998)

DAB2IP in cancer
por: Liu, Liang, et al.
Publicado: (2015)

Dabbing-Induced Hypersensitivity Pneumonitis
por: Haddad, Ibrahim, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_s4im4nn7kki12lsrc7s4f7s2se