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English
Mitochondrial disease: mtDNA and protein segregation mysteries in iPSCs
scientific article published on December 2013
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scholarly article
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Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
title
Mitochondrial disease: mtDNA and protein segregation mysteries in iPSCs
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
main subject
mitochondrial disease
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inferred from title
author
Alicia M Pickrell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
author name string
Richard J Youle
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
language of work or name
English
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publication date
1 December 2013
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
published in
Current Biology
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
volume
23
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
issue
23
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
page(s)
R1052-4
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
cites work
The accumulation of misfolded proteins in the mitochondrial matrix is sensed by PINK1 to induce PARK2/Parkin-mediated mitophagy of polarized mitochondria
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=4746723
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Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.
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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=4746723
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30 September 2017
Mitochondrial regulation in pluripotent stem cells
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PubMed Central
reference URL
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30 September 2017
The PINK1-Parkin pathway promotes both mitophagy and selective respiratory chain turnover in vivo
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PubMed Central
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30 September 2017
A defect in the mitochondrial complex III, but not complex IV, triggers early ROS-dependent damage in defined brain regions.
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PubMed Central
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30 September 2017
Somatic oxidative bioenergetics transitions into pluripotency-dependent glycolysis to facilitate nuclear reprogramming.
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The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions
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30 September 2017
Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations
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30 September 2017
New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice
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Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
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Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.
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Premature ageing in mice expressing defective mitochondrial DNA polymerase
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The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle
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30 September 2017
Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24309284
retrieved
12 December 2020
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inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.CUB.2013.10.048
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
PMC publication ID
4746723
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
PubMed publication ID
24309284
1 reference
stated in
Europe PubMed Central
PMC publication ID
4746723
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24309284%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020
ResearchGate publication ID
259204662
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