Impact of F1Fo-ATP-synthase dimer assembly factors on mitochondrial function and organismic aging
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: Microbial Cell 5.2018, No. 4, S. 198-207, doi:10.15698/mic2018.04.625
- Event
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Veröffentlichung
- (where)
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Frankfurt am Main
- (who)
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Universitätsbibliothek Johann Christian Senckenberg
- (when)
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2018
- Creator
- URN
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urn:nbn:de:hebis:30:3-525542
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:57 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Rampello, Nadia Giusi
- Stenger, Maria
- Westermann, Benedikt
- Osiewacz, Heinz D.
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2018
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The mitochondrial Hsp70 controls the assembly of the F1FO-ATP synthase
The cristae modulator Optic atrophy 1 requires mitochondrial ATP synthase oligomers to safeguard mitochondrial function
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mitochondrial‐derived vesicles retain membrane potential and contain a functional ATP synthase
Inhibition of ATP synthase reverse activity restores energy homeostasis in mitochondrial pathologies
Structure of a complete ATP synthase dimer reveals the molecular basis of inner mitochondrial membrane morphology
The role of mitochondrial ATP synthase in cancer
The mitochondrial ATP synthase as an ATP consumer—a surprising therapeutic target
Variants in mitochondrial ATP synthase cause variable neurologic phenotypes
The mitochondrial chaperone TRAP1 regulates F-ATP synthase channel formation
BNIP3 regulates bioenergetics in cardiomyocytes by interaction with mitochondrial ATP synthase
The mitochondrial Hsp70 controls the assembly of the F1FO-ATP synthase
The cristae modulator Optic atrophy 1 requires mitochondrial ATP synthase oligomers to safeguard mitochondrial function
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mitochondrial‐derived vesicles retain membrane potential and contain a functional ATP synthase
Inhibition of ATP synthase reverse activity restores energy homeostasis in mitochondrial pathologies
Structure of a complete ATP synthase dimer reveals the molecular basis of inner mitochondrial membrane morphology
The role of mitochondrial ATP synthase in cancer
The mitochondrial ATP synthase as an ATP consumer—a surprising therapeutic target
Variants in mitochondrial ATP synthase cause variable neurologic phenotypes
The mitochondrial chaperone TRAP1 regulates F-ATP synthase channel formation
BNIP3 regulates bioenergetics in cardiomyocytes by interaction with mitochondrial ATP synthase
The mitochondrial Hsp70 controls the assembly of the F1FO-ATP synthase
The cristae modulator Optic atrophy 1 requires mitochondrial ATP synthase oligomers to safeguard mitochondrial function
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mechanism of proton-powered c-ring rotation in a mitochondrial ATP synthase
Mitochondrial‐derived vesicles retain membrane potential and contain a functional ATP synthase