(Q48396289)

11 February 2018

title

No association of mutations and mRNA expression of WFS1/wolframin with bipolar disorder in humans. (English)

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11 February 2018

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8

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11 February 2018

author name string

Tadafumi Kato

1

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11 February 2018

Kazuya Iwamoto

2

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11 February 2018

Shinsuke Washizuka

3

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11 February 2018

Kanako Mori

4

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11 February 2018

Osamu Tajima

5

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11 February 2018

Tsuyoshi Akiyama

6

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11 February 2018

Shinichiro Nanko

7

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11 February 2018

Nobumasa Kato

9

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11 February 2018

language of work or name

English

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publication date

1 February 2003

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11 February 2018

published in

Neuroscience Letters

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11 February 2018

volume

338

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11 February 2018

issue

1

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11 February 2018

page(s)

21-24

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11 February 2018

A locus for bipolar affective disorder on chromosome 4p

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Regulation of ER stress proteins by valproate: therapeutic implications.

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7 January 2021

Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.

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7 January 2021

Molecular genetics of bipolar disorder.

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7 January 2021

The other, forgotten genome: mitochondrial DNA and mental disorders

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

Increased levels of a mitochondrial DNA deletion in the brain of patients with bipolar disorder.

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7 January 2021

Chromosome 4 Workshop Summary: Sixth World Congress on Psychiatric Genetics, Bonn, Germany, October 6-10, 1998.

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7 January 2021

Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene.

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7 January 2021

Organic mood syndrome in two siblings with Wolfram syndrome

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7 January 2021

WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

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7 January 2021

Psychiatric disorders in 36 families with Wolfram syndrome

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7 January 2021

Psychiatric findings in Wolfram syndrome homozygotes

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7 January 2021

WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901334-4

7 January 2021

Mutation screening of the Wolfram syndrome gene in psychiatric patients

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The stanley foundation brain collection and neuropathology consortium

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7 January 2021

10.1016/S0304-3940(02)01334-4

Identifiers

DOI

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11 February 2018

PubMed ID

12565131

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11 February 2018