Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms (Q48942369)

From Wikidata

Jump to navigation Jump to search

scientific article published on December 24, 2010

edit

Language	Label	Description	Also known as
English	Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms	scientific article published on December 24, 2010

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

title

Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

main subject

mitochondrial DNA

0 references

sequence deletion

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21185889

retrieved

20 November 2024

author

Shu-Ichi Ueno

series ordinal

7

object named as

Shu-ichi Ueno

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21185889

retrieved

20 November 2024

Akira Sano

series ordinal

8

object named as

Akira Sano

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21185889

retrieved

20 November 2024

author name string

Maiko Kato

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

Masayuki Nakamura

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

Mio Ichiba

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

Akiyuki Tomiyasu

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

Hirochika Shimo

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

Itsuro Higuchi

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

21185889

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21185889

retrieved

20 November 2024

publication date

24 December 2010

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

full work available at URL

https://api.elsevier.com/content/article/PII:S0168010210028828?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

https://api.elsevier.com/content/article/PII:S0168010210028828?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

published in

Neuroscience Research

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

volume

69

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

page(s)

331-336

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

cites work

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

series ordinal

1

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Neuroanatomical pattern of mitochondrial complex I pathology varies between schizophrenia, bipolar disorder and major depression

series ordinal

3

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers

series ordinal

4

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

MtDNA mutations in aging and apoptosis

series ordinal

5

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

series ordinal

6

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome

series ordinal

7

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

State-dependent alterations in mitochondrial complex I activity in platelets: a potential peripheral marker for schizophrenia

series ordinal

8

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Alterations of mitochondrial function and correlations with personality traits in selected major depressive disorder patients

series ordinal

9

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

series ordinal

10

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution

series ordinal

11

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood

series ordinal

12

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

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

series ordinal

13

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Mitochondrial complex I subunits expression is altered in schizophrenia: a postmortem study

series ordinal

14

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

The other, forgotten genome: mitochondrial DNA and mental disorders

series ordinal

15

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Role of adenine nucleotide translocator 1 in mtDNA maintenance

series ordinal

16

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

series ordinal

17

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: Report of a family

series ordinal

18

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Evidence for a mitochondrial oxidative phosphorylation defect in brains from patients with schizophrenia

series ordinal

19

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

series ordinal

20

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Advanced Telomere Shortening in Respiratory Chain Disorders

series ordinal

21

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

series ordinal

22

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Mitochondrial disease

series ordinal

23

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

series ordinal

24

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

series ordinal

25

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

series ordinal

27

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

series ordinal

28

1 reference

stated in

Crossref

DOI

10.1016/J.NEURES.2010.12.013

reference URL

https://api.crossref.org/works/10.1016/J.NEURES.2010.12.013

retrieved

20 November 2024

Identifiers

DOI

10.1016/J.NEURES.2010.12.013

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

PubMed publication ID

21185889

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21185889

retrieved

17 February 2018

reference URL

http://europepmc.org/abstract/MED/21185889

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48942369&oldid=2277647687"