A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder (Q28254976): Difference between revisions

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scientific article

Language	Label	Description	Also known as
English	A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder	scientific article

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scholarly article

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A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder (English)

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author name string

N A Sachs

1

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A Sawa

2

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S E Holmes

3

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C A Ross

4

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L E DeLisi

5

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R L Margolis

6

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language of work or name

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publication date

August 2005

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Molecular Psychiatry

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10

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8

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758-64

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001667

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1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

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https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Evolutionary constraints on the Disrupted in Schizophrenia locus

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https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Disrupted in Schizophrenia 1 (DISC1) is a multicompartmentalized protein that predominantly localizes to mitochondria

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Chromosome 1 loci in Finnish schizophrenia families

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

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

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

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https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

A NUDEL-dependent mechanism of neurofilament assembly regulates the integrity of CNS neurons

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Yeast two-hybrid screens implicate DISC1 in brain development and function

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Nudel functions in membrane traffic mainly through association with Lis1 and cytoplasmic dynein

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness

1 reference

https://api.crossref.org/works/10.1038/SJ.MP.4001667

21 April 2017

Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

DISC1 (Disrupted in Schizophrenia-1) is expressed in limbic regions of the primate brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

Cloning and characterization of Disc1, the mouse ortholog of DISC1 (Disrupted-in-Schizophrenia 1).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

Expression of Disrupted-In-Schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

Expression of disrupted in schizophrenia 1 (DISC1) protein in the adult and developing mouse brain indicates its role in neurodevelopment.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001667

21 January 2018

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