Cargando…

Copy Number Variant in the Region of Adenosine Kinase (ADK) and Its Possible Contribution to Schizophrenia Susceptibility

BACKGROUND: Adenosine kinase (ADK) is supposed to be a schizophrenia susceptibility gene based on the findings that ADK is an enzyme that catalyzes transfer of the gamma-phosphate from ATP to adenosine, which interacts with dopamine and glutamate neurotransmitters. However, no reports of schizophren...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kimura, Hiroki, Kushima, Itaru, Yohimi, Akira, Aleksic, Branko, Ozaki, Norio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2017
Materias:	Regular Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932473/ https://www.ncbi.nlm.nih.gov/pubmed/29126171 http://dx.doi.org/10.1093/ijnp/pyx103

Ejemplares similares

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

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

Polygenic risk scores in schizophrenia with clinically significant copy number variants
por: Taniguchi, Satoru, et al.
Publicado: (2019)

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

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

Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes
por: Ishizuka, Kanako, 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)

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)

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)

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

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

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

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

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)

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

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders
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)

Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress
por: Yoshikawa, Akane, et al.
Publicado: (2021)

Beginning Android ADK with Arduino
por: Böhmer, Mario
Publicado: (2012)

Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility
por: Nawa, Yoshihiro, et al.
Publicado: (2020)

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

Stable Knockdown of Adenosine Kinase by Lentiviral Anti-ADK miR-shRNAs in Wharton’s Jelly Stem Cells
por: Estiri, Hajar, et al.
Publicado: (2018)

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

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

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)

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)

In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN
por: Ishii, Takaya, et al.
Publicado: (2019)

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)

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)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

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

Involvement of cerebellar and subcortical connector hubs in schizophrenia
por: Yamamoto, Maeri, et al.
Publicado: (2022)

New Copy Number Variations in Schizophrenia
por: Magri, Chiara, et al.
Publicado: (2010)

Resistance of Leishmania infantum to allopurinol is associated with chromosome and gene copy number variations including decrease in the S-adenosylmethionine synthetase (METK) gene copy number
por: Yasur-Landau, Daniel, et al.
Publicado: (2018)

Genome-Wide Identification and Expression Analysis of Tomato ADK Gene Family during Development and Stress
por: Yang, Lu, et al.
Publicado: (2021)

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

Turner syndrome presenting with idiopathic regression: A case report
por: Mizobuchi, Kosuke, et al.
Publicado: (2022)

Aryl diketoacids (ADK) selectively inhibit duplex DNA-unwinding activity of SARS coronavirus NTPase/helicase
por: Lee, Chaewoon, et al.
Publicado: (2009)

Copy Number Variants in German Patients with Schizophrenia
por: Priebe, Lutz, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_65hg3o9o62aro2bl27va8h47f2