Cargando…

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

Detalles Bibliográficos
Autores principales:	Yoshimi, Akira, Yamada, Shinnosuke, Kunimoto, Shohko, Aleksic, Branko, Hirakawa, Akihiro, Ohashi, Mitsuki, Matsumoto, Yurie, Hada, Kazuhiro, Itoh, Norimichi, Arioka, Yuko, Kimura, Hiroki, Kushima, Itaru, Nakamura, Yukako, Shiino, Tomoko, Mori, Daisuke, Tanaka, Satoshi, Hamada, Shuko, Noda, Yukihiro, Nagai, Taku, Yamada, Kiyofumi, Ozaki, Norio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2019
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499804/ https://www.ncbi.nlm.nih.gov/pubmed/31053702 http://dx.doi.org/10.1038/s41398-019-0479-5

Ejemplares similares

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

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia
por: Aleksic, Branko, et al.
Publicado: (2013)

Methylation analysis for postpartum depression: a case control study
por: Nakamura, Yukako, et al.
Publicado: (2019)

Resequencing and Association Analysis of PTPRA, a Possible Susceptibility Gene for Schizophrenia and Autism Spectrum Disorders
por: Xing, Jingrui, et al.
Publicado: (2014)

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

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)

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

Mice carrying a schizophrenia-associated mutation of the Arhgap10 gene are vulnerable to the effects of methamphetamine treatment on cognitive function: association with morphological abnormalities in striatal neurons
por: Hada, Kazuhiro, et al.
Publicado: (2021)

Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients
por: Koide, Takayoshi, et al.
Publicado: (2012)

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

Correction: Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients
por: Koide, Takayoshi, et al.
Publicado: (2012)

Factor Structure of the Japanese Version of the Edinburgh Postnatal Depression Scale in the Postpartum Period
por: Kubota, Chika, et al.
Publicado: (2014)

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)

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

Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions
por: Furukawa, Sawako, et al.
Publicado: (2023)

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

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

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

Innate immune activation of astrocytes impairs neurodevelopment via upregulation of follistatin-like 1 and interferon-induced transmembrane protein 3
por: Yamada, Shinnosuke, et al.
Publicado: (2018)

Overexpression of astroglial major histocompatibility complex class I in the medial prefrontal cortex impairs visual discrimination learning in mice
por: Wulaer, Bolati, et al.
Publicado: (2020)

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

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population
por: Kimura, Hiroki, et al.
Publicado: (2015)

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

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

Relationship between social support during pregnancy and postpartum depressive state: a prospective cohort study
por: Morikawa, Mako, et al.
Publicado: (2015)

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)

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)

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)

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

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

Evaluation of Factors Affecting Continuous Performance Test Identical Pairs Version Score of Schizophrenic Patients in a Japanese Clinical Sample
por: Koide, Takayoshi, et al.
Publicado: (2012)

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)

ACUTE SCHIZOPHRENIC EPISODES—ARE THEY SCHIZOPHRENIC?
por: Singh, Gurmeet, et al.
Publicado: (1981)

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

Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics
por: Nakajima, Mizuho, et al.
Publicado: (2006)

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

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder
por: Wang, Chenyao, et al.
Publicado: (2022)

Dysfunction of Serotonergic and Dopaminergic Neuronal Systems in the Antidepressant-Resistant Impairment of Social Behaviors Induced by Social Defeat Stress Exposure as Juveniles
por: Hasegawa, Sho, et al.
Publicado: (2018)

PM346. Social defeat stress as juveniles impairs persistent social behaviors and neurogenesis
por: Noda, Yukihiro, et al.
Publicado: (2016)

PS134. A strategy for treating in deficits of social behaviors induced by exposure to social defeat stress as juveniles
por: Hasegawa, Sho, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_ikggks7vjgdrfr89ab4asaa8th