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Why mitochondria must fuse to maintain their genome integrity
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3700062
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retrieved
22 February 2020
review article
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title
Why mitochondria must fuse to maintain their genome integrity
(English)
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Europe PubMed Central
PMC publication ID
3700062
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22 February 2020
main subject
mitochondrion
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Michela Rugolo
series ordinal
3
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Europe PubMed Central
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3700062
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22 February 2020
Emmanuelle Sarzi
series ordinal
4
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Europe PubMed Central
PMC publication ID
3700062
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
Guy Lenaers
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5
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Europe PubMed Central
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3700062
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22 February 2020
author name string
Sara Vidoni
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1
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Crossref
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Europe PubMed Central
PMC publication ID
3700062
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
Claudia Zanna
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2
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Crossref
stated in
Europe PubMed Central
PMC publication ID
3700062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
language of work or name
English
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publication date
28 March 2013
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Europe PubMed Central
PMC publication ID
3700062
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
published in
Antioxidants & Redox Signaling
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Europe PubMed Central
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3700062
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22 February 2020
volume
19
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PubMed
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Europe PubMed Central
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3700062
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
issue
4
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PubMed
stated in
Europe PubMed Central
PMC publication ID
3700062
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22 February 2020
page(s)
379-388
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Europe PubMed Central
PMC publication ID
3700062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
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22 February 2020
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Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery
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28 September 2017
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28 September 2017
Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans
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28 September 2017
Bioenergetics of mitochondrial diseases associated with mtDNA mutations
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28 September 2017
An electron microscope study of the mitochondrial structure
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PubMed Central
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28 September 2017
Oxidative stress, mitochondrial DNA mutation, and impairment of antioxidant enzymes in aging.
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28 September 2017
Transcomplementation between different types of respiration-deficient mitochondria with different pathogenic mutant mitochondrial DNAs
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28 September 2017
MITOMAP: a human mitochondrial genome database--1998 update
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28 September 2017
Dynamics of mitochondria in living cells: shape changes, dislocations, fusion, and fission of mitochondria
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28 September 2017
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
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31 May 2018
A lethal defect of mitochondrial and peroxisomal fission
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
31 May 2018
MFN2, a new gene responsible for mitochondrial DNA depletion
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Mitochondrial DNA mutations in disease and aging.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Hereditary optic neuropathies share a common mitochondrial coupling defect.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
Identification of a fission yeast dynamin-related protein involved in mitochondrial DNA maintenance.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3700062
retrieved
28 November 2018
OPA1 cleavage depends on decreased mitochondrial ATP level and bivalent metals
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23350575
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Twinkle helicase(PEO1)gene mutation causes mitochondrial DNA depletion
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23350575
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Transmembrane segments of the dynamin Msp1p uncouple its functions in the control of mitochondrial morphology and genome maintenance
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23350575
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1089/ARS.2012.4800
1 reference
stated in
Europe PubMed Central
PMC publication ID
3700062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 February 2020
PMC publication ID
3700062
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
3700062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 February 2020
PubMed publication ID
23350575
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
3700062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23350575%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 February 2020
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