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Replication and Transcription of Mammalian Mitochondrial Dna

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inferred← citeshttps://doi.org/10.1002/ece3.72935openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.73326openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03194602openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03356496openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-010-0530-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-005-0246-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-010-9322-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00294-011-0338-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00343-019-8364-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00411-010-0329-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00432-008-0439-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00439-022-02505-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00592-025-02546-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10528-020-09956-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10528-025-11213-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10709-018-0033-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10815-020-01853-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11010-012-1481-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11033-023-08928-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11427-013-4474-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11434-011-4917-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11756-026-02319-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11802-020-4409-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12041-012-0157-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13105-011-0083-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13277-016-4918-0openalex-snapshot
Manganese-superoxide dismutase (Mn-SOD) overexpression is a common event in colorectal cancers with mitochondrial microsatellite instability
inferred← citeshttps://doi.org/10.1007/s13364-025-00822-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64219-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-816193-7.00006-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-24836-8.00005-5openalex-snapshot
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Mitochondrial genotyping of cultured Piaractus brachypomus revealed low diversity and mutations in regions involved in metabolisms and proliferation
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Vascular smooth muscle cell proliferation is dependent upon upregulation of mitochondrial transcription factor A (mtTFA) expression in injured rat carotid artery
inferred← citeshttps://doi.org/10.1016/j.bbabio.2004.10.003openalex-snapshot
The transcription machinery in mammalian mitochondria
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inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.11.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbagrm.2012.03.002openalex-snapshot
Mitochondrial transcription factor A regulates mitochondrial transcription initiation, DNA packaging, and genome copy number
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The rat mitochondrial Ori L encodes a novel small RNA resembling an ancestral tRNA
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inferred← citeshttps://doi.org/10.1016/j.gene.2011.10.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2021.145868openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2022.147042openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2023.148054openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.10.285openalex-snapshot
Comparative analyses of the complete mitochondrial genomes of two southern African endemic guitarfish, Acroteriobatus annulatus and A. blochii
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Distinct hypoxia-induced translational profiles of embryonic and adult-derived macrophages
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inferred← citeshttps://doi.org/10.1016/j.jcz.2023.12.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jddst.2019.05.002openalex-snapshot
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Mitochondrial D310 D-Loop instability and histological subtypes in radiation-induced cutaneous basal cell carcinomas
inferred← citeshttps://doi.org/10.1016/j.jmb.2007.06.074openalex-snapshot
In vitro Reconstitution and Characterization of the Yeast Mitochondrial Degradosome Complex Unravels Tight Functional Interdependence
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2015.05.010openalex-snapshot
Dietary isoflavone daidzein promotes Tfam expression that increases mitochondrial biogenesis in C2C12 muscle cells
inferred← citeshttps://doi.org/10.1016/j.mad.2009.01.008openalex-snapshot
Region-specific changes in mitochondrial D-loop in aged rat CNS
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2015.01.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mce.2005.11.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mce.2019.110631openalex-snapshot
Testosterone induces up-regulation of mitochondrial gene expression in murine C2C12 skeletal muscle cells accompanied by an increase of nuclear respiratory factor-1 and its downstream effectors
inferred← citeshttps://doi.org/10.1016/j.mito.2007.07.001openalex-snapshot
Nuclear–mitochondrial interaction
inferred← citeshttps://doi.org/10.1016/j.mito.2008.09.001openalex-snapshot
Rat visceral yolk sac (VYS) and placenta mitochondrial features during the placentation period
inferred← citeshttps://doi.org/10.1016/j.mito.2009.01.012openalex-snapshot
Recombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression
inferred← citeshttps://doi.org/10.1016/j.mito.2012.06.010openalex-snapshot
D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria
inferred← citeshttps://doi.org/10.1016/j.mito.2012.10.009openalex-snapshot
Mitochondria: One of the destinations of miRNAs
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Association study of mitochondrial genetic polymorphisms in asthmatic children
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inferred← citeshttps://doi.org/10.1016/j.mito.2018.12.003openalex-snapshot
Circulating mitochondria DNA, a non-invasive cancer diagnostic biomarker candidate
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Identifying Pig Mitochondrial TSS: Structure and Functional Features
inferred← citeshttps://doi.org/10.1016/j.mito.2022.03.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcel.2006.11.024openalex-snapshot
Initiation and Beyond: Multiple Functions of the Human Mitochondrial Transcription Machinery
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Clonal expansion of different mtDNA variants without selective advantage in solid tumors
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High selenium diet protects against TNBS-induced acute inflammation, mitochondrial dysfunction, and secondary necrosis in rat colon
inferred← citeshttps://doi.org/10.1016/j.omtn.2025.102449openalex-snapshot
Development of a cell-penetrating peptide-based nanocomplex for long-term delivery of intact mitochondrial DNA into epithelial cells
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The complete mitochondrial genomes of the liver flukes Opisthorchis felineus and Clonorchis sinensis (Trematoda)
inferred← citeshttps://doi.org/10.1016/j.physrep.2013.03.005openalex-snapshot
Stochastic mechano-chemical kinetics of molecular motors: A multidisciplinary enterprise from a physicist’s perspective
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Mitochondrial encephalomyopathy: Towards diagnosis. A case report
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Altered mitochondrial biogenesis and its fusion gene expression is involved in the high-altitude adaptation of rat lung
inferred← citeshttps://doi.org/10.1016/j.rsma.2024.103580openalex-snapshot
Comparative mitogenomes of Lobotiformes provides insights into the phylogentic position of Hapalogenyidae
inferred← citeshttps://doi.org/10.1016/j.smallrumres.2023.106937openalex-snapshot
Study of Kosta goat (Capra hircus) mitochondrial DNA and their phylogenetic based on whole genome sequensing
inferred← citeshttps://doi.org/10.1016/j.snb.2020.128418openalex-snapshot
Real-time tracking of mitochondrial dynamics by a dual-sensitive probe
inferred← citeshttps://doi.org/10.1016/j.steroids.2011.04.009openalex-snapshot
Effects of ovariectomy and 17-β estradiol replacement on rat brown adipose tissue mitochondrial function
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.11.004openalex-snapshot
The Cellular Mitochondrial Genome Landscape in Disease
inferred← citeshttps://doi.org/10.1016/j.vph.2009.10.008openalex-snapshot
Thyroid hormone and myocardial mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1016/j.yexmp.2006.07.005openalex-snapshot
Nuclear and mitochondrial localization of the putative RNA helicase DHX32
inferred← citeshttps://doi.org/10.1016/j.yexmp.2006.10.009openalex-snapshot
Characterization of murine Dhx32
inferred← citeshttps://doi.org/10.1016/j.ygeno.2018.08.006openalex-snapshot
Complete mitochodrial genome of the crab spider Ebrechtella tricuspidata (Araneae: Thomisidae): A novel tRNA rearrangement and phylogenetic implications for Araneae
inferred← citeshttps://doi.org/10.1016/j.ygeno.2018.11.027openalex-snapshot
Comparative mitogenome analysis of three species and monophyletic inference of Catantopinae (Orthoptera: Acridoidea)
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.02.008openalex-snapshot
Complete mitochondrial genomes of three Oxya grasshoppers (Orthoptera) and their implications for phylogenetic reconstruction
inferred← citeshttps://doi.org/10.1016/j.yhbeh.2006.01.005openalex-snapshot
Energy metabolism, thermogenesis and body mass regulation in Brandt's voles (Lasiopodomys brandtii) during cold acclimation and rewarming
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.03.013openalex-snapshot
Multiple rearrangements in mitochondrial genomes of Isopoda and phylogenetic implications
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.10.020openalex-snapshot
Genetic aspects of mitochondrial genome evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.11.019openalex-snapshot
The impact of mitochondrial genome analyses on the understanding of deuterostome phylogeny
inferred← citeshttps://doi.org/10.1016/s0030-6657(08)70233-6openalex-snapshot
Mutacje mitochondrialnego DNA w rozwoju nowotworów głowy i szyi
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77001-6openalex-snapshot
The Role of the Mitochondrion in Sperm Function: Is There a Place for Oxidative Phosphorylation or Is This a Purely Glycolytic Process?
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77003-xopenalex-snapshot
Mitochondrial DNA in the Oocyte and the Developing Embryo
inferred← citeshttps://doi.org/10.1016/s0070-2153(06)77005-3openalex-snapshot
Mitochondrial Disease—Its Impact, Etiology, and Pathology
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)02222-2openalex-snapshot
Chapter 22 In Vivo and In Vitro Approaches for Studying the Yeast Mitochondrial RNA Degradosome Complex
inferred← citeshttps://doi.org/10.1017/s0016672305007718openalex-snapshot
A large-scale screening of the normalized mammalian mitochondrial gene expression profiles
inferred← citeshttps://doi.org/10.1017/s0029665119000533openalex-snapshot
Effects of obesity and weight loss on mitochondrial structure and function and implications for colorectal cancer risk
inferred← citeshttps://doi.org/10.1021/cr040463dopenalex-snapshot
DNA Polymerase γ in Mitochondrial DNA Replication and Repair
inferred← citeshttps://doi.org/10.1038/cr.2010.119openalex-snapshot
Identification of mouse liver mitochondria-associated miRNAs and their potential biological functions
inferred← citeshttps://doi.org/10.1038/cr.2013.37openalex-snapshot
The mitochondrial genome encodes abundant small noncoding RNAs
inferred← citeshttps://doi.org/10.1038/hdy.2016.120openalex-snapshot
Purifying selection and genetic drift shaped Pleistocene evolution of the mitochondrial genome in an endangered Australian freshwater fish
inferred← citeshttps://doi.org/10.1038/jhg.2012.17openalex-snapshot
The Amerindian mtDNA haplogroup B2 enhances the risk of HPV for cervical cancer: de-regulation of mitochondrial genes may be involved
inferred← citeshttps://doi.org/10.1038/mp.2017.48openalex-snapshot
Depression, telomeres and mitochondrial DNA: between- and within-person associations from a 10-year longitudinal study
inferred← citeshttps://doi.org/10.1038/npre.2008.2084.1openalex-snapshot
Recombinant Mitochondrial Transcription Factor A with N-terminal Mitochondrial Transduction Domain Increases Respiration and Mitochondrial Gene Expression in G11778A Leber's Hereditary Optic Neuropathy Cybrid Cells
inferred← citeshttps://doi.org/10.1038/nrg1606openalex-snapshot
Mitochondrial DNA mutations in human disease
inferred← citeshttps://doi.org/10.1038/s41392-024-02081-yopenalex-snapshot
Engineered mitochondria in diseases: mechanisms, strategies, and applications
inferred← citeshttps://doi.org/10.1038/s41422-026-01224-wopenalex-snapshot
Mitochondrial double-stranded RNA drives aging-associated cognitive decline
inferred← citeshttps://doi.org/10.1038/s41467-018-05007-9openalex-snapshot
Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria
inferred← citeshttps://doi.org/10.1038/s41598-017-01654-yopenalex-snapshot
The first two complete mitochondrial genomes for the family Triglidae and implications for the higher phylogeny of Scorpaeniformes
inferred← citeshttps://doi.org/10.1038/s41598-017-07977-0openalex-snapshot
Complete mitochondrial genomes of Anopheles stephensi and An. dirus and comparative evolutionary mitochondriomics of 50 mosquitoes
inferred← citeshttps://doi.org/10.1038/s41598-018-33684-5openalex-snapshot
Plasmid-normalized quantification of relative mitochondrial DNA copy number
inferred← citeshttps://doi.org/10.1038/s41598-020-60123-1openalex-snapshot
The distinct spatiotemporal distribution and effect of feed restriction on mtDNA copy number in broilers
inferred← citeshttps://doi.org/10.1038/s41598-020-76410-wopenalex-snapshot
Comparative analysis of the complete mitochondrial genomes in two limpets from Lottiidae (Gastropoda: Patellogastropoda): rare irregular gene rearrangement within Gastropoda
inferred← citeshttps://doi.org/10.1038/s41598-022-10547-8openalex-snapshot
Mitogenome-wise codon usage pattern from comparative analysis of the first mitogenome of Blepharipa sp. (Muga uzifly) with other Oestroid flies
inferred← citeshttps://doi.org/10.1038/s41598-022-14414-4openalex-snapshot
Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells
inferred← citeshttps://doi.org/10.1038/s41598-023-27806-xopenalex-snapshot
New Dielis species and structural dichotomy of the mitochondrial cox2 gene in Scoliidae wasps
inferred← citeshttps://doi.org/10.1038/s41598-025-05085-yopenalex-snapshot
Complete mitogenomes of venomous fish Paracentropogon rubripinnis and Inimicus japonicus elucidate phylogenetic relationships in Scorpaeniformes
inferred← citeshttps://doi.org/10.1038/s41598-025-30310-zopenalex-snapshot
Adaptive evolution and phylogeny of cerithioid gastropods with six new mitogenomes
inferred← citeshttps://doi.org/10.1038/s41598-026-46786-2openalex-snapshot
Complete mitochondrial genomes of Pipistrellus pipistrellus and Pipistrellus nathusii, along with the resolution of the taxonomic positions of Pipistrellus and Nyctalus
inferred← citeshttps://doi.org/10.1038/s42003-020-01322-4openalex-snapshot
Retrograde signaling by a mtDNA-encoded non-coding RNA preserves mitochondrial bioenergetics
inferred← citeshttps://doi.org/10.1038/sj.emboj.7600257openalex-snapshot
Reconstitution of a minimal mtDNA replisome in vitro
inferred← citeshttps://doi.org/10.1038/sj.embor.7400878openalex-snapshot
Herpes simplex virus eliminates host mitochondrial DNA
inferred← citeshttps://doi.org/10.1039/c8nj00381eopenalex-snapshot
Multiple cation-doped linear polymers toward ATP sensing and a cell imaging application
inferred← citeshttps://doi.org/10.1042/bj20071615openalex-snapshot
Cisplatin-mediated impairment of mitochondrial DNA metabolism inversely correlates with glutathione levels
inferred← citeshttps://doi.org/10.1042/ebc20170101openalex-snapshot
Mitochondrial DNA replication: clinical syndromes
inferred← citeshttps://doi.org/10.1046/j.1439-0531.2003.00448.xopenalex-snapshot
The Mitochondrial Genome in Embryo Technologies
inferred← citeshttps://doi.org/10.1071/rd10133openalex-snapshot
Effect of maternal age on mitochondrial DNA copy number, ATP content and IVF outcome of bovine oocytes
inferred← citeshttps://doi.org/10.1073/pnas.1314970111openalex-snapshot
Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging
inferred← citeshttps://doi.org/10.1074/jbc.m109.092676openalex-snapshot
Identification of Multiple Rate-limiting Steps during the Human Mitochondrial Transcription Cycle in Vitro
inferred← citeshttps://doi.org/10.1080/00305316.2024.2359443openalex-snapshot
Characterisation of the complete mitochondrial genomes and phylogenetic analysis of ten Oedipodinae grasshoppers (Orthoptera: Acrididae) from Algeria
inferred← citeshttps://doi.org/10.1080/03014460.2022.2144447openalex-snapshot
Forensic evaluation of mitochondrial DNA heteroplasmy in Gujarat population, India
inferred← citeshttps://doi.org/10.1080/15287394.2012.699841openalex-snapshot
Radon-Induced Reduced Apoptosis in Human Bronchial Epithelial Cells with Knockdown of Mitochondria DNA
inferred← citeshttps://doi.org/10.1080/15476286.2016.1194161openalex-snapshot
Insights into the transcriptional and translational mechanisms of linear organellar chromosomes in the box jellyfish Alatina alata (Cnidaria: Medusozoa: Cubozoa)
inferred← citeshttps://doi.org/10.1080/15476286.2018.1521212openalex-snapshot
Single-molecule long-read transcriptome profiling of Platysternon megacephalum mitochondrial genome with gene rearrangement and control region duplication
inferred← citeshttps://doi.org/10.1080/15476286.2019.1709746openalex-snapshot
Precise annotation of human, chimpanzee, rhesus macaque and mouse mitochondrial genomes leads to insight into mitochondrial transcription in mammals
inferred← citeshttps://doi.org/10.1080/19768354.2015.1105866openalex-snapshot
The complete mitogenome of the wood-feeding cockroachCryptocercus kyebangensis(Blattodea: Cryptocercidae) and phylogenetic relations among cockroach families
inferred← citeshttps://doi.org/10.1080/19768354.2016.1150877openalex-snapshot
Complete mitochondrial genome sequence of the Indian pipistrellePipistrellus coromandra(Vespertilioninae)
inferred← citeshttps://doi.org/10.1080/23802359.2016.1219627openalex-snapshot
The complete mitochondrial genome of the servant mouse, Mus famulus
inferred← citeshttps://doi.org/10.1080/24701394.2016.1238902openalex-snapshot
The novel primers for mammal species identification-based mitochondrial cytochrome b sequence: implication for reserved wild animals in Thailand and endangered mammal species in Southeast Asia
inferred← citeshttps://doi.org/10.1080/24701394.2018.1461852openalex-snapshot
Cancer-specific SNPs originate from low-level heteroplasmic variants in human mitochondrial genomes of a matched cell line pair
inferred← citeshttps://doi.org/10.1086/bblv218n2p122openalex-snapshot
Unequal and Genotype-Dependent Expression of Mitochondrial Genes in Larvae of the Pacific Oyster Crassostrea gigas
inferred← citeshttps://doi.org/10.1089/rej.2007.0626openalex-snapshot
Caloric Restriction Retards the Age-Related Decline in Mitochondrial Function of Brown Adipose Tissue
inferred← citeshttps://doi.org/10.1093/carcin/bgt023openalex-snapshot
Reduced mitochondrial DNA copy number in peripheral blood leukocytes increases the risk of soft tissue sarcoma
inferred← citeshttps://doi.org/10.1093/cid/ciaa983openalex-snapshot
Mitochondria and Human Immunodeficiency Virus: A Troubled Relationship Enters Its Fourth Decade
inferred← citeshttps://doi.org/10.1093/gbe/evt119openalex-snapshot
Evolution Along the Mutation Gradient in the Dynamic Mitochondrial Genome of Salamanders
inferred← citeshttps://doi.org/10.1093/hmg/ddh140openalex-snapshot
Gene expression profiles of transcripts in amyloid precursor protein transgenic mice: up-regulation of mitochondrial metabolism and apoptotic genes is an early cellular change in Alzheimer's disease
inferred← citeshttps://doi.org/10.1093/humupd/dmi042openalex-snapshot
The transmission of OXPHOS disease and methods to prevent this
inferred← citeshttps://doi.org/10.1093/jisesa/ieaa021openalex-snapshot
Characterization of the Complete Mitochondrial Genome of Epicauta impressicornis (Coleoptera: Meloidae) and Its Phylogenetic Implications for the Infraorder Cucujiformia
inferred← citeshttps://doi.org/10.1093/jisesa/iew023openalex-snapshot
Complete Mitochondrial Genome ofHelicoverpa zea(Lepidoptera: Noctuidae) and Expression Profiles of Mitochondrial-Encoded Genes in Early and Late Embryos
inferred← citeshttps://doi.org/10.1093/jmammal/gyab117openalex-snapshot
A genomic portrait of Sturnira parvidens : mitochondrial chromosome, repetitive elements, and microsatellite discovery
inferred← citeshttps://doi.org/10.1093/jmcb/mjae029openalex-snapshot
Sterile activation of RNA-sensing pathways in autoimmunity
inferred← citeshttps://doi.org/10.1093/jnci/djn213openalex-snapshot
Mitochondrial DNA Content: Its Genetic Heritability and Association With Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.1093/med/9780197574522.003.0014openalex-snapshot
Mitochondrial genetics and bipolar disorder
inferred← citeshttps://doi.org/10.1093/med/9780199797608.003.0094openalex-snapshot
Mitochondrial Genetics and Bipolar Disorder
inferred← citeshttps://doi.org/10.1093/molbev/msq026openalex-snapshot
ND6 Gene "Lost" and Found: Evolution of Mitochondrial Gene Rearrangement in Antarctic Notothenioids
inferred← citeshttps://doi.org/10.1093/molbev/mss238openalex-snapshot
High Levels of Gene Expression Explain the Strong Evolutionary Constraint of Mitochondrial Protein-Coding Genes
inferred← citeshttps://doi.org/10.1093/molehr/gal112openalex-snapshot
mtDNA point mutations are present at various levels of heteroplasmy in human oocytes
inferred← citeshttps://doi.org/10.1093/mutage/gel048openalex-snapshot
Mitochondrial dysfunction, persistently elevated levels of reactive oxygen species and radiation-induced genomic instability: a review
inferred← citeshttps://doi.org/10.1093/nar/gkaa302openalex-snapshot
Human REXO2 controls short mitochondrial RNAs generated by mtRNA processing and decay machinery to prevent accumulation of double-stranded RNA
inferred← citeshttps://doi.org/10.1093/nar/gkad835openalex-snapshot
A conserved isoleucine in the binding pocket of RIG-I controls immune tolerance to mitochondrial RNA
inferred← citeshttps://doi.org/10.1093/nar/gkg717openalex-snapshot
Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNA
inferred← citeshttps://doi.org/10.1093/nar/gkh528openalex-snapshot
Phosphorylation of rat mitochondrial transcription termination factor (mTERF) is required for transcription termination but not for binding to DNA
inferred← citeshttps://doi.org/10.1093/nar/gkm676openalex-snapshot
The mitochondrial transcription termination factor mTERF modulates replication pausing in human mitochondrial DNA
inferred← citeshttps://doi.org/10.1093/nar/gkm863openalex-snapshot
Expression of a novel non-coding mitochondrial RNA in human proliferating cells
inferred← citeshttps://doi.org/10.1093/nar/gkp903openalex-snapshot
Human mitochondrial RNA turnover caught in flagranti: involvement of hSuv3p helicase in RNA surveillance
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