Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility. (Q35369750)

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21 February 2020

title

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility (English)

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21 February 2020

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21 February 2020

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21 February 2020

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21 February 2020

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21 February 2020

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21 February 2020

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21 February 2020

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21 February 2020

Tomoko Toyota

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21 February 2020

Yoshimi Iwayama

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21 February 2020

Masashi Ikeda

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21 February 2020

Branko Aleksic

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21 February 2020

Takayoshi Koide

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21 February 2020

Itaru Kushima

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21 February 2020

Yukako Nakamura

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21 February 2020

Hiroshi Ujike

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21 February 2020

Akira Yoshimi

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21 February 2020

Jingrui Xing

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21 February 2020

Chenyao Wang

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21 February 2020

Hiroki Kimura

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21 February 2020

Yuto Takasaki

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21 February 2020

Shohko Kunimoto

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21 February 2020

Yota Uno

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21 February 2020

Toshiya Inada

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21 February 2020

Daisuke Tsuboi

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21 February 2020

Noriko Yamamoto

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21 February 2020

Mami Yoshida

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21 February 2020

Michio Suzuki

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21 February 2020

Takeo Yoshikawa

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21 February 2020

Kozo Kaibuchi

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21 February 2020

language of work or name

English

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publication date

20 October 2014

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21 February 2020

published in

Schizophrenia Bulletin

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21 February 2020

volume

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21 February 2020

issue

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21 February 2020

page(s)

744-753

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Copy number variation in schizophrenia in Sweden

21 February 2020

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1 reference

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

27 July 2018

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27 July 2018

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Coupling PAF signaling to dynein regulation: structure of LIS1 in complex with PAF-acetylhydrolase

27 July 2018

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Mitotic spindle regulation by Nde1 controls cerebral cortical size

27 July 2018

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Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

27 July 2018

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A systematic genomewide linkage study in 353 sib pairs with schizophrenia

27 July 2018

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Missense Mutations in hMLH1 and hMSH2 Are Associated with Exonic Splicing Enhancers

27 July 2018

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14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome

27 July 2018

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A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

27 July 2018

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Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

27 July 2018

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27 July 2018

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A polygenic burden of rare disruptive mutations in schizophrenia

27 July 2018

1 reference

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The mitosis and neurodevelopment proteins NDE1 and NDEL1 form dimers, tetramers, and polymers with a folded back structure in solution.

26 September 2018

1 reference

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Genetic architectures of psychiatric disorders: the emerging picture and its implications

26 September 2018

1 reference

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SpliceAid 2: a database of human splicing factors expression data and RNA target motifs

26 September 2018

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Mutation surveyor: an in silico tool for sequencing analysis

26 September 2018

1 reference

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SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.

26 September 2018

1 reference

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Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

26 September 2018

1 reference

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Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4393687

Copy number variation in schizophrenia in the Japanese population

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4393687

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

26 September 2018

1 reference

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Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia

26 September 2018

1 reference

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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

26 September 2018

1 reference

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DISC1 regulates the transport of the NUDEL/LIS1/14-3-3epsilon complex through kinesin-1

26 September 2018

1 reference

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

26 September 2018

1 reference

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Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation

26 September 2018

1 reference

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Recruitment of katanin p60 by phosphorylated NDEL1, an LIS1 interacting protein, is essential for mitotic cell division and neuronal migration

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4393687

Coupling PAF Signaling to Dynein Regulation

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4393687

Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU147

21 January 2018

Identifiers

DOI

10.1093/SCHBUL/SBU147

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25332407%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25332407%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

PubMed publication ID

25332407

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25332407%20AND%20SRC:MED&resulttype=core&format=json