Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells (Q33689022)

28 July 2017

title

Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells (English)

1 reference

28 July 2017

1 reference

I Trounce

1

1 reference

28 July 2017

J Schmiedel

2

1 reference

28 July 2017

H C Yen

3

1 reference

28 July 2017

S Hosseini

4

1 reference

28 July 2017

M D Brown

5

1 reference

28 July 2017

J J Olson

6

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28 July 2017

D C Wallace

7

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28 July 2017

language of work or name

English

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publication date

1 May 2000

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28 July 2017

published in

Nucleic Acids Research

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28 July 2017

volume

28

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28 July 2017

issue

10

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28 July 2017

page(s)

2164-2170

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Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Sequence and gene organization of mouse mitochondrial DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Sequence and organization of the human mitochondrial genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

An established avian fibroblast cell line without mitochondrial DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Development and characterization of continuous avian cell lines depleted of mitochondrial DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

A rapid Percoll gradient procedure for isolation of synaptosomes directly from an S1 fraction: homogeneity and morphology of subcellular fractions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Diseases of the mitochondrial DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

THREE DEGREES OF GUANYLIC ACID--INOSINIC ACID PYROPHOSPHORYLASE DEFICIENCY IN MOUSE FIBROBLASTS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

DELETION OF THYMIDINE KINASE ACTIVITY FROM L CELLS RESISTANT TO BROMODEOXYURIDINE.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Human aging is associated with various point mutations in tRNA genes of mitochondrial DNA.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=105374

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10773087

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10773087

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Age-associated damage in mitochondrial DNA in human hearts

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10773087

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/28.10.2164

1 reference

28 July 2017

1 reference

28 July 2017

1 reference