(Q44079651)

29 November 2017

title

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1352971

17 September 2022

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1352971

17 September 2022

author name string

V. Petruzzella

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1352971

17 September 2022

X. Chen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1352971

17 September 2022

E. A. Schon

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1352971

17 September 2022

language of work or name

English

0 references

publication date

1 July 1992

1 reference

29 November 2017

15 July 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1352971

Biochemical and Biophysical Research Communications

17 September 2022

published in

1 reference

29 November 2017

volume

186

1 reference

29 November 2017

issue

1

1 reference

29 November 2017

page(s)

491-497

1 reference

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

29 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Detection of a specific mitochondrial DNA deletion in tissues of older humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Sequence and organization of the human mitochondrial genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Identification of point mutations by mispairing PCR as exemplified in MERRF disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Cytochrome oxidase deficiency in Alzheimer's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Alzheimer's disease: a cell biological perspective

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Mitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980834-4

10.1016/S0006-291X(05)80834-4

7 January 2021

Identifiers

DOI

1 reference

29 November 2017

1 reference