(Q37732176)

22 August 2017

1 reference

title

DISCopathies: brain disorders related to DISC1 dysfunction (English)

1 reference

22 August 2017

Carsten Korth

1

1 reference

22 August 2017

publication date

1 January 2009

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Reviews in the Neurosciences

22 August 2017

published in

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22 August 2017

volume

20

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22 August 2017

issue

5-6

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22 August 2017

page(s)

321-330

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Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

22 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1, PDE4B, and NDE1 at the centrosome and synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Understanding the role of DISC1 in psychiatric disease and during normal development

21 January 2018

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Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

The DISC locus in psychiatric illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Behavioral phenotypes of Disc1 missense mutations in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disrupted-In-Schizophrenia 1 regulates integration of newly generated neurons in the adult brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Chromosome 1 loci in Finnish schizophrenia families

21 January 2018

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https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Development of hippocampal mossy fiber synaptic outputs by new neurons in the adult brain

21 January 2018

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https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Filamentous nerve cell inclusions in neurodegenerative diseases: tauopathies and alpha-synucleinopathies

21 January 2018

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https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology

21 January 2018

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https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

A novel DISC1-interacting partner DISC1-Binding Zinc-finger protein: implication in the modulation of DISC1-dependent neurite outgrowth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disruption of GW bodies impairs mammalian RNA interference

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1-NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association of DISC1 with autism and Asperger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1 immunoreactivity at the light and ultrastructural level in the human neocortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disc1 is mutated in the 129S6/SvEv strain and modulates working memory in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Microtubule-associated protein tau (tau) is a major antigenic component of paired helical filaments in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

A mutation in mouse Disc1 that models a schizophrenia risk allele leads to specific alterations in neuronal architecture and cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Insolubility of disrupted-in-schizophrenia 1 disrupts oligomer-dependent interactions with nuclear distribution element 1 and is associated with sporadic mental disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Specific developmental disruption of disrupted-in-schizophrenia-1 function results in schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disruption of two novel genes by a translocation co-segregating with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1 localizes to the centrosome by binding to kendrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Isoform-selective susceptibility of DISC1/phosphodiesterase-4 complexes to dissociation by elevated intracellular cAMP levels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Inducible expression of mutant human DISC1 in mice is associated with brain and behavioral abnormalities reminiscent of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Positive association of the Disrupted-in-Schizophrenia-1 gene (DISC1) with schizophrenia in the Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Schizophrenia-related neural and behavioral phenotypes in transgenic mice expressing truncated Disc1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association within a family of a balanced autosomal translocation with major mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Toxic proteins in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association between genotype at an exonic SNP in DISC1 and normal cognitive aging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association of variants in DISC1 with psychosis-related traits in a large population cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

From neuropathology to neurodevelopment

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

Genomewide Linkage Scan in Schizoaffective Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FREVNEURO.2009.20.5-6.321

10.1515/REVNEURO.2009.20.5-6.321

21 January 2018

Identifiers

DOI

1 reference

22 August 2017

1 reference