Mutant C. elegans mitofusin leads to selective removal of mtDNA heteroplasmic deletions across generations to maintain fitness
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1741-7007
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Mutant C. elegans mitofusin leads to selective removal of mtDNA heteroplasmic deletions across generations to maintain fitness ; volume:20 ; number:1 ; day:9 ; month:2 ; year:2022 ; pages:1-17 ; date:12.2022
BMC biology ; 20, Heft 1 (9.2.2022), 1-17, 12.2022
- Creator
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Meshnik, Lana
Bar-Yaacov, Dan
Kasztan, Dana
Neiger, Tali
Cohen, Tal
Kishner, Mor
Valenci, Itay
Dadon, Sara
Klein, Christopher J.
Vance, Jeffery M.
Nevo, Yoram
Züchner, Stephan
Ovadia, Ofer
Mishmar, Dan
Ben-Zvi, Anat
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1186/s12915-022-01241-2
- URN
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urn:nbn:de:101:1-2022051520482902237492
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:28 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Meshnik, Lana
- Bar-Yaacov, Dan
- Kasztan, Dana
- Neiger, Tali
- Cohen, Tal
- Kishner, Mor
- Valenci, Itay
- Dadon, Sara
- Klein, Christopher J.
- Vance, Jeffery M.
- Nevo, Yoram
- Züchner, Stephan
- Ovadia, Ofer
- Mishmar, Dan
- Ben-Zvi, Anat
- SpringerLink (Online service)
Other Objects (12)
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Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
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Large-scale genetic analysis reveals mammalian mtDNA heteroplasmy dynamics and variance increase through lifetimes and generations
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Increased levels of large scale deletions of mtDNA of skin fibroblasts result in increased collagen degradation in dermal skin equivalents
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ALS spinal neurons show varied and reduced mtDNA gene copy numbers and increased mtDNA gene deletions
Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
Letters to future generations
Another Reason to Maintain Friendly Relations
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
Erratum to: Unraveling overlapping deletions by agglomerative clustering
New CACNA1A deletions are associated to migraine phenotypes
Large-scale genetic analysis reveals mammalian mtDNA heteroplasmy dynamics and variance increase through lifetimes and generations
Simple circuits to maintain isocapnia regardless of ventilation
Increased levels of large scale deletions of mtDNA of skin fibroblasts result in increased collagen degradation in dermal skin equivalents
Modulating Wnt signaling in chondrocytes to maintain phenotypic stability
ALS spinal neurons show varied and reduced mtDNA gene copy numbers and increased mtDNA gene deletions
Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
Letters to future generations
Another Reason to Maintain Friendly Relations
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
Erratum to: Unraveling overlapping deletions by agglomerative clustering
New CACNA1A deletions are associated to migraine phenotypes
Large-scale genetic analysis reveals mammalian mtDNA heteroplasmy dynamics and variance increase through lifetimes and generations
Simple circuits to maintain isocapnia regardless of ventilation
Increased levels of large scale deletions of mtDNA of skin fibroblasts result in increased collagen degradation in dermal skin equivalents