| scholarly article | Q13442814 |
| P50 | author | Nils-Göran Larsson | Q5938385 |
| Stefan Jakobs | Q28355517 | ||
| Kjell Hultenby | Q28468914 | ||
| Bianca Habermann | Q30504194 | ||
| Arnaud Mourier | Q56944202 | ||
| Inge Kühl | Q57511218 | ||
| Eduardo Silva Ramos | Q58527426 | ||
| Assa Yeroslaviz | Q63679449 | ||
| Benedetta Ruzzenente | Q88166316 | ||
| Christian Brüser | Q92562054 | ||
| Elisa Motori | Q99407800 | ||
| Johanna H K Kauppila | Q125252094 | ||
| P2093 | author name string | Jakob D Busch | |
| P2860 | cites work | OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 | Q24290356 |
| Control of mitochondrial morphology by a human mitofusin | Q24290831 | ||
| LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs | Q24295176 | ||
| Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. | Q24541558 | ||
| Reconstitution of a minimal mtDNA replisome in vitro | Q24564147 | ||
| Gene Expression Omnibus: NCBI gene expression and hybridization array data repository | Q27860523 | ||
| Fast gapped-read alignment with Bowtie 2 | Q27860699 | ||
| The Sequence Alignment/Map format and SAMtools | Q27860966 | ||
| Mitochondrial DNA maintenance in yeast requires a protein containing a region related to the GTP-binding domain of dynamin | Q27934616 | ||
| Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae | Q27935307 | ||
| ER-associated mitochondrial division links the distribution of mitochondria and mitochondrial DNA in yeast | Q27935426 | ||
| The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria | Q27938333 | ||
| Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy | Q28140286 | ||
| Mutation spectrum and splicing variants in the OPA1 gene | Q28216607 | ||
| Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number | Q28290165 | ||
| Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance | Q28510356 | ||
| Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis | Q28511104 | ||
| In vivo occupancy of mitochondrial single-stranded DNA binding protein supports the strand displacement mode of DNA replication | Q28542495 | ||
| Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development | Q28594513 | ||
| Fast and accurate long-read alignment with Burrows-Wheeler transform | Q29547193 | ||
| Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A | Q29616547 | ||
| Disruption of fusion results in mitochondrial heterogeneity and dysfunction | Q29616566 | ||
| Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice | Q29617092 | ||
| ER tubules mark sites of mitochondrial division | Q29619991 | ||
| Dynamics of nucleoid structure regulated by mitochondrial fission contributes to cristae reformation and release of cytochrome c. | Q30541662 | ||
| Age-Associated Loss of OPA1 in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence. | Q33773474 | ||
| Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations | Q33877979 | ||
| Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice | Q34201844 | ||
| Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels. | Q35094282 | ||
| Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA. | Q35170688 | ||
| Mitochondrial fusion is essential for organelle function and cardiac homeostasis | Q35613447 | ||
| Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid | Q35754971 | ||
| Scalable Isolation of Mammalian Mitochondria for Nucleic Acid and Nucleoid Analysis | Q35831104 | ||
| Mitofusins 1 and 2 are essential for postnatal metabolic remodeling in heart | Q36455449 | ||
| Two-dimensional intact mitochondrial DNA agarose electrophoresis reveals the structural complexity of the mammalian mitochondrial genome. | Q36619848 | ||
| TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication | Q36787217 | ||
| Over-expression of the catalytic core of mitochondrial DNA (mtDNA) polymerase in the nervous system of Drosophila melanogaster reduces median life span by inducing mtDNA depletion | Q36860874 | ||
| OPA1 mutations and mitochondrial DNA damage: keeping the magic circle in shape | Q37068436 | ||
| POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. | Q37155771 | ||
| The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice | Q37365414 | ||
| Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria. | Q51760035 | ||
| A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy. | Q52137131 | ||
| Overexpression of the catalytic subunit of DNA polymerase gamma results in depletion of mitochondrial DNA in Drosophila melanogaster. | Q52583090 | ||
| POLRMT does not transcribe nuclear genes. | Q54316761 | ||
| Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function | Q80146686 | ||
| ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells | Q38758060 | ||
| Maintenance and Expression of Mammalian Mitochondrial DNA. | Q38792624 | ||
| Loss of LRPPRC causes ATP synthase deficiency | Q38806341 | ||
| Superresolution fluorescence imaging of mitochondrial nucleoids reveals their spatial range, limits, and membrane interaction | Q39665381 | ||
| Dynamics of mitochondria in living cells: shape changes, dislocations, fusion, and fission of mitochondria | Q40763148 | ||
| MtDNA-maintenance defects: syndromes and genes | Q40955181 | ||
| A hybrid G-quadruplex structure formed between RNA and DNA explains the extraordinary stability of the mitochondrial R-loop | Q41517167 | ||
| Dynamics of mitochondrial DNA nucleoids regulated by mitochondrial fission is essential for maintenance of homogeneously active mitochondria during neonatal heart development | Q41888127 | ||
| The accessory subunit B of DNA polymerase gamma is required for mitochondrial replisome function | Q42942782 | ||
| Subnormal levels of POLγA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and progressive external ophthalmoplegia [corrected]. | Q45852433 | ||
| OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions. | Q46398821 | ||
| Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA. | Q47228285 | ||
| Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals | Q47408311 | ||
| The short variant of the mitochondrial dynamin OPA1 maintains mitochondrial energetics and cristae structure | Q47948450 | ||
| Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons | Q48401711 | ||
| Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations | Q48474475 | ||
| The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. | Q48762457 | ||
| SnapShot: Mitochondrial Nucleoid | Q50065273 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e1008085 | |
| P577 | publication date | 2019-06-06 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Mitochondrial fusion is required for regulation of mitochondrial DNA replication | |
| P478 | volume | 15 |
| Q93103041 | Functional Interplay between Cristae Biogenesis, Mitochondrial Dynamics and Mitochondrial DNA Integrity |
| Q92970985 | MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement |
| Q96954758 | Mitochondrial Function in Muscle Stem Cell Fates |
| Q99407805 | Neuronal metabolic rewiring promotes resilience to neurodegeneration caused by mitochondrial dysfunction |
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