On the public citation graph

Mitochondrial transcription and translation: overview

https://doi.org/10.1042/ebc20170102

0 signed · 424 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-3-662-41088-2_7openalex-snapshot

Mitochondrial Nucleoid and Transcription Factor A

inferredcites →https://doi.org/10.1007/s00439-001-0610-5openalex-snapshot

Identification and characterization of two novel human mitochondrial elongation factor genes, hEFG2 and hEFG1, phylogenetically conserved through evolution

inferredcites →https://doi.org/10.1016/0092-8674(83)90145-9openalex-snapshot

The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units

inferredcites →https://doi.org/10.1016/0092-8674(84)90343-xopenalex-snapshot

Precise identification of individual promoters for transcription of each strand of human mitochondrial DNA

inferredcites →https://doi.org/10.1016/j.ajhg.2011.11.027openalex-snapshot

Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis

inferredcites →https://doi.org/10.1016/j.ajhg.2015.06.011openalex-snapshot

TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies

inferredcites →https://doi.org/10.1016/j.bbabio.2010.02.036openalex-snapshot

Human mitochondrial mRNAs—like members of all families, similar but different

inferredcites →https://doi.org/10.1016/j.bbrc.2010.07.019openalex-snapshot

LRPPRC is a mitochondrial matrix protein that is conserved in metazoans

inferredcites →https://doi.org/10.1016/j.cell.2005.09.040openalex-snapshot

Termination Factor-Mediated DNA Loop between Termination and Initiation Sites Drives Mitochondrial rRNA Synthesis

inferredcites →https://doi.org/10.1016/j.cell.2008.09.013openalex-snapshot

RNase P without RNA: Identification and Functional Reconstitution of the Human Mitochondrial tRNA Processing Enzyme

inferredcites →https://doi.org/10.1016/j.cell.2009.10.031openalex-snapshot

TFB2 Is a Transient Component of the Catalytic Site of the Human Mitochondrial RNA Polymerase

inferredcites →https://doi.org/10.1016/j.cell.2010.05.018openalex-snapshot

Helix Unwinding and Base Flipping Enable Human MTERF1 to Terminate Mitochondrial Transcription

inferredcites →https://doi.org/10.1016/j.cell.2016.09.003openalex-snapshot

Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein

inferredcites →https://doi.org/10.1016/j.cell.2017.09.035openalex-snapshot

Mechanism of Transcription Anti-termination in Human Mitochondria

inferredcites →https://doi.org/10.1016/j.cell.2017.10.036openalex-snapshot

Structural Basis of Mitochondrial Transcription Initiation

inferredcites →https://doi.org/10.1016/j.celrep.2015.01.030openalex-snapshot

Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis

inferredcites →https://doi.org/10.1016/j.celrep.2015.01.063openalex-snapshot

A Mitochondria-Specific Isoform of FASTK Is Present In Mitochondrial RNA Granules and Regulates Gene Expression and Function

inferredcites →https://doi.org/10.1016/j.cmet.2009.03.001openalex-snapshot

Methylation of 12S rRNA Is Necessary for In Vivo Stability of the Small Subunit of the Mammalian Mitochondrial Ribosome

inferredcites →https://doi.org/10.1016/j.cmet.2013.02.005openalex-snapshot

GRSF1 Regulates RNA Processing in Mitochondrial RNA Granules

inferredcites →https://doi.org/10.1016/j.cmet.2013.02.006openalex-snapshot

The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression

inferredcites →https://doi.org/10.1016/j.cmet.2013.03.006openalex-snapshot

MTERF1 Binds mtDNA to Prevent Transcriptional Interference at the Light-Strand Promoter but Is Dispensable for rRNA Gene Transcription Regulation

inferredcites →https://doi.org/10.1016/j.cmet.2016.08.017openalex-snapshot

A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation

inferredcites →https://doi.org/10.1016/j.jmb.2008.09.077openalex-snapshot

Roles of the N- and C-Terminal Domains of Mammalian Mitochondrial Initiation Factor 3 in Protein Biosynthesis

inferredcites →https://doi.org/10.1016/j.molcel.2004.06.044openalex-snapshot

Regulation of Nuclear Receptor Activity by a Pseudouridine Synthase through Posttranscriptional Modification of Steroid Receptor RNA Activator

inferredcites →https://doi.org/10.1016/j.molcel.2007.06.031openalex-snapshot

mtRF1a Is a Human Mitochondrial Translation Release Factor Decoding the Major Termination Codons UAA and UAG

inferredcites →https://doi.org/10.1016/j.molcel.2007.11.021openalex-snapshot

A Single Mammalian Mitochondrial Translation Initiation Factor Functionally Replaces Two Bacterial Factors

inferredcites →https://doi.org/10.1016/j.molcel.2009.06.028openalex-snapshot

EF-G2mt Is an Exclusive Recycling Factor in Mammalian Mitochondrial Protein Synthesis

inferredcites →https://doi.org/10.1016/j.molcel.2011.01.013openalex-snapshot

Structural Basis for Dimerization and Activity of Human PAPD1, a Noncanonical Poly(A) Polymerase

inferredcites →https://doi.org/10.1016/j.tibs.2017.02.003openalex-snapshot

Regulation of Mammalian Mitochondrial Gene Expression: Recent Advances

inferredcites →https://doi.org/10.1016/j.tig.2017.11.001openalex-snapshot

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized

inferredcites →https://doi.org/10.1016/s0021-9258(18)77393-6openalex-snapshot

Identification and initial characterization of translational initiation factor 2 from bovine mitochondria.

inferredcites →https://doi.org/10.1016/s0021-9258(18)83265-3openalex-snapshot

Interaction of bovine mitochondrial ribosomes with messenger RNA

inferredcites →https://doi.org/10.1016/s0092-8674(03)00762-1openalex-snapshot

Structure of the Mammalian Mitochondrial Ribosome Reveals an Expanded Functional Role for Its Component Proteins

inferredcites →https://doi.org/10.1016/s0378-1119(97)00279-5openalex-snapshot

The human mitochondrial elongation factor tu (EF-Tu) gene: cDNA sequence, genomic localization, genomic structure, and identification of a pseudogene

inferredcites →https://doi.org/10.1017/s135583829999043xopenalex-snapshot

Mutations in the highly conserved GGQ motif of class 1 polypeptide release factors abolish ability of human eRF1 to trigger peptidyl-tRNA hydrolysis

inferredcites →https://doi.org/10.1038/290457a0openalex-snapshot

Sequence and organization of the human mitochondrial genome

inferredcites →https://doi.org/10.1038/290470a0openalex-snapshot

tRNA punctuation model of RNA processing in human mitochondria

inferredcites →https://doi.org/10.1038/ejhg.2014.293openalex-snapshot

RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement

inferredcites →https://doi.org/10.1038/emboj.2010.14openalex-snapshot

A functional peptidyl‐tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome

inferredcites →https://doi.org/10.1038/emboj.2011.392openalex-snapshot

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

inferredcites →https://doi.org/10.1038/nature10435openalex-snapshot

Structure of human mitochondrial RNA polymerase

inferredcites →https://doi.org/10.1038/nature13895openalex-snapshot

The complete structure of the large subunit of the mammalian mitochondrial ribosome

inferredcites →https://doi.org/10.1038/nchembio.2099openalex-snapshot

NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNAMet

inferredcites →https://doi.org/10.1038/ncomms12039openalex-snapshot

Deficient methylation and formylation of mt-tRNAMet wobble cytosine in a patient carrying mutations in NSUN3

inferredcites →https://doi.org/10.1038/ncomms3940openalex-snapshot

Codon-reading specificities of mitochondrial release factors and translation termination at non-standard stop codons

inferredcites →https://doi.org/10.1038/ng1064openalex-snapshot

Human mitochondrial transcription factor B1 methylates ribosomal RNA at a conserved stem-loop

inferredcites →https://doi.org/10.1038/ng909openalex-snapshot

Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA

inferredcites →https://doi.org/10.1038/nn1910openalex-snapshot

Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization

inferredcites →https://doi.org/10.1038/nsmb.1859openalex-snapshot

Human mitochondrial mTERF wraps around DNA through a left-handed superhelical tandem repeat

inferredcites →https://doi.org/10.1038/s41467-017-01221-zopenalex-snapshot

LRPPRC-mediated folding of the mitochondrial transcriptome

inferredcites →https://doi.org/10.1042/bj20100757openalex-snapshot

Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit

inferredcites →https://doi.org/10.1042/bj20131107openalex-snapshot

Glutamyl-tRNAGln amidotransferase is essential for mammalian mitochondrial translation in vivo

inferredcites →https://doi.org/10.1042/ebc20170100openalex-snapshot

Mitochondrial DNA replication in mammalian cells: overview of the pathway

inferredcites →https://doi.org/10.1042/ebc20170103openalex-snapshot

Mitochondrial DNA transcription and translation: clinical syndromes

inferredcites →https://doi.org/10.1073/pnas.0907602106openalex-snapshot

Biogenesis of glutaminyl-mt tRNA Gln in human mitochondria

inferredcites →https://doi.org/10.1073/pnas.1006026107openalex-snapshot

G-quadruplex structures in RNA stimulate mitochondrial transcription termination and primer formation

inferredcites →https://doi.org/10.1073/pnas.1321312111openalex-snapshot

Structural basis of reverse nucleotide polymerization

inferredcites →https://doi.org/10.1073/pnas.1401657111openalex-snapshot

Cryo-EM structure of the small subunit of the mammalian mitochondrial ribosome

inferredcites →https://doi.org/10.1073/pnas.1609338113openalex-snapshot

Human mitochondrial ribosomes can switch their structural RNA composition

inferredcites →https://doi.org/10.1073/pnas.79.23.7195openalex-snapshot

Identification of initiation sites for heavy-strand and light-strand transcription in human mitochondrial DNA.

inferredcites →https://doi.org/10.1074/jbc.271.10.5805openalex-snapshot

Expression, Purification, and Mechanistic Studies of Bovine Mitochondrial Translational Initiation Factor 2

inferredcites →https://doi.org/10.1074/jbc.c110.128918openalex-snapshot

Human Mitochondrial Transcription Revisited

inferredcites →https://doi.org/10.1074/jbc.c114.581868openalex-snapshot

Assignment of 2′-O-Methyltransferases to Modification Sites on the Mammalian Mitochondrial Large Subunit 16 S Ribosomal RNA (rRNA)

inferredcites →https://doi.org/10.1074/jbc.m001899200openalex-snapshot

Interaction of Mitochondrial Elongation Factor Tu with Aminoacyl-tRNA and Elongation Factor Ts

inferredcites →https://doi.org/10.1074/jbc.m006265200openalex-snapshot

The Human Lysyl-tRNA Synthetase Gene Encodes Both the Cytoplasmic and Mitochondrial Enzymes by Means of an Unusual Alternative Splicing of the Primary Transcript

inferredcites →https://doi.org/10.1074/jbc.m106202200openalex-snapshot

Identification and Characterization of Mammalian Mitochondrial tRNA nucleotidyltransferases

inferredcites →https://doi.org/10.1074/jbc.m109.098400openalex-snapshot

Mitochondrial and Nuclear Genomic Responses to Loss of LRPPRC Expression

inferredcites →https://doi.org/10.1074/jbc.m116.751008openalex-snapshot

Human Mitochondrial Transcription Factor B2 Is Required for Promoter Melting during Initiation of Transcription

inferredcites →https://doi.org/10.1074/jbc.m116.771105openalex-snapshot

The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules

inferredcites →https://doi.org/10.1074/jbc.m500216200openalex-snapshot

Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

inferredcites →https://doi.org/10.1074/jbc.m500804200openalex-snapshot

Human Mitochondrial mRNAs Are Stabilized with Polyadenylation Regulated by Mitochondria-specific Poly(A) Polymerase and Polynucleotide Phosphorylase

inferredcites →https://doi.org/10.1074/jbc.m602429200openalex-snapshot

Conserved Sequence Box II Directs Transcription Termination and Primer Formation in Mitochondria

inferredcites →https://doi.org/10.1074/jbc.r111.290585openalex-snapshot

Termination of Protein Synthesis in Mammalian Mitochondria

inferredcites →https://doi.org/10.1091/mbc.e10-01-0047openalex-snapshot

LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria

inferredcites →https://doi.org/10.1091/mbc.e14-01-0014openalex-snapshot

MRM2 and MRM3 are involved in biogenesis of the large subunit of the mitochondrial ribosome

inferredcites →https://doi.org/10.1093/emboj/17.14.4101openalex-snapshot

Structure of T7 RNA polymerase complexed to the transcriptional inhibitor T7 lysozyme

inferredcites →https://doi.org/10.1093/hmg/6.4.615openalex-snapshot

Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database

inferredcites →https://doi.org/10.1093/hmg/ddr397openalex-snapshot

The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation

inferredcites →https://doi.org/10.1093/hmg/ddt652openalex-snapshot

Loss of LRPPRC causes ATP synthase deficiency

inferredcites →https://doi.org/10.1093/hmg/ddu352openalex-snapshot

A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression

inferredcites →https://doi.org/10.1093/nar/gkh886openalex-snapshot

Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA

inferredcites →https://doi.org/10.1093/nar/gkh923openalex-snapshot

Identification of a novel human nuclear-encoded mitochondrial poly(A) polymerase

inferredcites →https://doi.org/10.1093/nar/gki1007openalex-snapshot

Role of the N- and C-terminal extensions on the activity of mammalian mitochondrial translational initiation factor 3

inferredcites →https://doi.org/10.1093/nar/gkn576openalex-snapshot

The human mitochondrial ribosome recycling factor is essential for cell viability

inferredcites →https://doi.org/10.1093/nar/gkp903openalex-snapshot

Human mitochondrial RNA turnover caught in flagranti: involvement of hSuv3p helicase in RNA surveillance

inferredcites →https://doi.org/10.1093/nar/gkq068openalex-snapshot

Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibition

inferredcites →https://doi.org/10.1093/nar/gkq1224openalex-snapshot

TEFM (c17orf42) is necessary for transcription of human mtDNA

inferredcites →https://doi.org/10.1093/nar/gkr470openalex-snapshot

PDE12 removes mitochondrial RNA poly(A) tails and controls translation in human mitochondria

inferredcites →https://doi.org/10.1093/nar/gks1130openalex-snapshot

Human mitochondrial RNA decay mediated by PNPase–hSuv3 complex takes place in distinct foci

inferredcites →https://doi.org/10.1093/nar/gks506openalex-snapshot

LRPPRC/SLIRP suppresses PNPase-mediated mRNA decay and promotes polyadenylation in human mitochondria

inferredcites →https://doi.org/10.1093/nar/gkv105openalex-snapshot

TEFM is a potent stimulator of mitochondrial transcription elongation in vitro

inferredcites →https://doi.org/10.1093/nar/gkv861openalex-snapshot

Structure of mitochondrial poly(A) RNA polymerase reveals the structural basis for dimerization, ATP selectivity and the SPAX4 disease phenotype

inferredcites →https://doi.org/10.1093/nar/gkw1157openalex-snapshot

Human mitochondrial transcription factors TFAM and TFB2M work synergistically in promoter melting during transcription initiation

inferredcites →https://doi.org/10.1093/nar/gkw302openalex-snapshot

Mitochondrial transcription termination factor 1 directs polar replication fork pausing

inferredcites →https://doi.org/10.1093/nar/gkx164openalex-snapshot

FASTKD1 and FASTKD4 have opposite effects on expression of specific mitochondrial RNAs, depending upon their endonuclease-like RAP domain

inferredcites →https://doi.org/10.1093/nar/gky068openalex-snapshot

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease

inferredcites →https://doi.org/10.1093/nar/gky159openalex-snapshot

Polyadenylation and degradation of structurally abnormal mitochondrial tRNAs in human cells

inferredcites →https://doi.org/10.1126/science.1180674openalex-snapshot

Hungry Codons Promote Frameshifting in Human Mitochondrial Ribosomes

inferredcites →https://doi.org/10.1126/science.1258026openalex-snapshot

Structure of the large ribosomal subunit from human mitochondria

inferredcites →https://doi.org/10.1126/science.aaa0986openalex-snapshot

Replication-transcription switch in human mitochondria

inferredcites →https://doi.org/10.1126/science.aaa1193openalex-snapshot

The structure of the human mitochondrial ribosome

inferredcites →https://doi.org/10.1126/science.aaa3872openalex-snapshot

The complete structure of the 55 S mammalian mitochondrial ribosome

inferredcites →https://doi.org/10.1128/mcb.00946-08openalex-snapshot

Characterization of Human GTPBP3, a GTP-Binding Protein Involved in Mitochondrial tRNA Modification

inferredcites →https://doi.org/10.1128/mcb.01002-06openalex-snapshot

Mammalian Polynucleotide Phosphorylase Is an Intermembrane Space RNase That Maintains Mitochondrial Homeostasis

inferredcites →https://doi.org/10.1128/mcb.22.4.1116-1125.2002openalex-snapshot

A Human Mitochondrial Transcription Factor Is Related to RNA Adenine Methyltransferases and Binds S-Adenosylmethionine

inferredcites →https://doi.org/10.1186/1471-2199-11-72openalex-snapshot

Effects on mitochondrial transcription of manipulating mTERF protein levels in cultured human HEK293 cells

inferredcites →https://doi.org/10.1186/1745-6150-7-14openalex-snapshot

Structure based hypothesis of a mitochondrial ribosome rescue mechanism

inferredcites →https://doi.org/10.1186/gb-2012-13-2-r12openalex-snapshot

Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome c oxidase

inferredcites →https://doi.org/10.1196/annals.1293.007openalex-snapshot

Mitochondrial Nucleoid and Transcription Factor A

inferredcites →https://doi.org/10.1261/rna.035600.112openalex-snapshot

Trmt61B is a methyltransferase responsible for 1-methyladenosine at position 58 of human mitochondrial tRNAs

inferredcites →https://doi.org/10.1261/rna.052365.115openalex-snapshot

FASTKD2 is an RNA-binding protein required for mitochondrial RNA processing and translation

inferredcites →https://doi.org/10.1371/journal.pbio.1002557openalex-snapshot

Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates

inferredcites →https://doi.org/10.1371/journal.pgen.1000590openalex-snapshot

A Computational Screen for Regulators of Oxidative Phosphorylation Implicates SLIRP in Mitochondrial RNA Homeostasis

inferredcites →https://doi.org/10.1371/journal.pgen.1002910openalex-snapshot

A Combinatorial Amino Acid Code for RNA Recognition by Pentatricopeptide Repeat Proteins

inferredcites →https://doi.org/10.1371/journal.pgen.1004110openalex-snapshot

NSUN4 Is a Dual Function Mitochondrial Protein Required for Both Methylation of 12S rRNA and Coordination of Mitoribosomal Assembly

inferredcites →https://doi.org/10.1371/journal.pgen.1004424openalex-snapshot

Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA

inferredcites →https://doi.org/10.1371/journal.pgen.1004616openalex-snapshot

Ribosome Rescue and Translation Termination at Non-Standard Stop Codons by ICT1 in Mammalian Mitochondria

inferredcites →https://doi.org/10.1371/journal.pgen.1005227openalex-snapshot

Response to “Ribosome Rescue and Translation Termination at Non-standard Stop Codons by ICT1 in Mammalian Mitochondria”

inferredcites →https://doi.org/10.1371/journal.pgen.1005423openalex-snapshot

SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation

inferredcites →https://doi.org/10.1371/journal.pgen.1005964openalex-snapshot

Human Cells Require Non-stop Ribosome Rescue Activity in Mitochondria

inferredcites →https://doi.org/10.1371/journal.pgen.1006355openalex-snapshot

Mtu1-Mediated Thiouridine Formation of Mitochondrial tRNAs Is Required for Mitochondrial Translation and Is Involved in Reversible Infantile Liver Injury

inferredcites →https://doi.org/10.1371/journal.pone.0019152openalex-snapshot

Localization of Human RNase Z Isoforms: Dual Nuclear/Mitochondrial Targeting of the ELAC2 Gene Product by Alternative Translation Initiation

inferredcites →https://doi.org/10.15252/embj.201694885openalex-snapshot

NSUN3 and ABH1 modify the wobble position of mt‐tRNAMet to expand codon recognition in mitochondrial translation

inferredcites →https://doi.org/10.15252/embr.201643391openalex-snapshot

A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability

inferredcites →https://doi.org/10.3390/biom7010024openalex-snapshot

Dealing with an Unconventional Genetic Code in Mitochondria: The Biogenesis and Pathogenic Defects of the 5‐Formylcytosine Modification in Mitochondrial tRNAMet

inferredcites →https://doi.org/10.4161/cc.10.17.17060openalex-snapshot

RNA processing in human mitochondria

inferredcites →https://doi.org/10.4161/rna.8.4.15393openalex-snapshot

Involvement of human ELAC2 gene product in 3' end processing of mitochondrial tRNAs

inferredcites →https://doi.org/10.7554/elife.27596openalex-snapshot

Maturation of selected human mitochondrial tRNAs requires deadenylation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/zookeys.1221.129136zenodo-depositor-declared

Complete mitochondrial genome of Lepidocephalichthys berdmorei and its phylogenetic status within the family Cobitidae (Cypriniformes)

inferred← citeshttps://doi.org/10.1002/acn3.70065openalex-snapshot

Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome

inferred← citeshttps://doi.org/10.1002/advs.202408599openalex-snapshot

Enhanced Oxidative Phosphorylation Driven by TACO1 Mitochondrial Translocation Promotes Stemness and Cisplatin Resistance in Bladder Cancer

inferred← citeshttps://doi.org/10.1002/btpr.88502openalex-snapshot

Single‐cell RNA sequencing reveals population‐based shifts in gene expression heterogeneity in an unstable, clonally derived CHO cell line

inferred← citeshttps://doi.org/10.1002/ece3.72282openalex-snapshot

Mitochondrial Genomes of Three Species of the Family Camaenidae (Gastropoda: Stylommatophora): Structural Features, Codon Usage Patterns, and Phylogenetic Implications

inferred← citeshttps://doi.org/10.1002/humu.23777openalex-snapshot

Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3′‐end processing

inferred← citeshttps://doi.org/10.1002/jcla.24983openalex-snapshot

Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage

inferred← citeshttps://doi.org/10.1002/oby.23424openalex-snapshot

Mitochondrial genome variations, mitochondrial‐nuclear compatibility, and their association with metabolic diseases

inferred← citeshttps://doi.org/10.1002/pmic.202300058openalex-snapshot

Transcriptomic analysis and fusion gene identifications of midbody remnants released from colorectal cancer cells reveals they are molecularly distinct from exosomes and microparticles

inferred← citeshttps://doi.org/10.1002/pmic.70006openalex-snapshot

Memantine Administration Enhances Glutamatergic and GABAergic Pathways in the Human Hippocampus of Alzheimer's Disease Patients

inferred← citeshttps://doi.org/10.1002/prot.26654openalex-snapshot

The role of lysine acetylation in the function of mitochondrial ribosomal protein L12

inferred← citeshttps://doi.org/10.1002/ps.70027openalex-snapshot

Bifenazate as compatible acaricide for biocontrol agent Transeius montdorensis (Acari: Phytoseiidae)

inferred← citeshttps://doi.org/10.1002/ps.8065openalex-snapshot

A novel mutation in mitochondrial cytochrome b conferring resistance to bifenazate in two‐spotted spider mite Tetranychus urticae Koch (Acarina: Tetranychidae)

inferred← citeshttps://doi.org/10.1007/978-1-0716-3171-3_14openalex-snapshot

Reconstitution of Mammalian Mitochondrial Translation System Capable of Long Polypeptide Synthesis

inferred← citeshttps://doi.org/10.1007/978-3-030-32300-4_11openalex-snapshot

Genetic Aspects of Male Infertility

inferred← citeshttps://doi.org/10.1007/978-3-030-67727-5_45openalex-snapshot

Disorders of Replication, Transcription and Translation of Mitochondrial DNA

inferred← citeshttps://doi.org/10.1007/978-3-030-74811-1_21openalex-snapshot

Application of Computer-Aided Translation Software in Business English Translation

inferred← citeshttps://doi.org/10.1007/978-3-030-86684-6_3openalex-snapshot

Mitochondrial Biogenesis and Dynamics in Health and Disease

inferred← citeshttps://doi.org/10.1007/978-981-13-8367-0_13openalex-snapshot

Mitochondrial Genetics

inferred← citeshttps://doi.org/10.1007/978-981-96-6569-3_11openalex-snapshot

Innovative Elicitors in Plant Science

inferred← citeshttps://doi.org/10.1007/978-981-99-5162-8_7openalex-snapshot

Metabolomics in the Study of Human Mitochondrial Diseases

inferred← citeshttps://doi.org/10.1007/s10528-026-11440-zopenalex-snapshot

Complete Mitochondrial Genome Analysis of Atypopenaeus stenodactylus and Its Phylogenetic Significance Within Penaeidae

inferred← citeshttps://doi.org/10.1007/s10709-021-00121-xopenalex-snapshot

The signals of selective constraints on the mitochondrial non-coding control region: insights from comparative mitogenomics of Clupeoid fishes

inferred← citeshttps://doi.org/10.1007/s11010-024-05053-6openalex-snapshot

MALSU1-mediated regulation of mitochondrial function governs proliferation and doxorubicin resistance in triple-negative breast cancer cells

inferred← citeshttps://doi.org/10.1007/s11033-025-10297-6openalex-snapshot

Recent advancements in the understanding of the alterations in mitochondrial biogenesis in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1007/s11064-020-02993-5openalex-snapshot

The Novel Role of PPAR Alpha in the Brain: Promising Target in Therapy of Alzheimer’s Disease and Other Neurodegenerative Disorders

inferred← citeshttps://doi.org/10.1007/s12011-024-04198-1openalex-snapshot

Chronic Exposure to Arsenic and Fluoride Starting at Gestation Alters Liver Mitochondrial Protein Expression and Induces Early Onset of Liver Fibrosis in Male Mouse Offspring

inferred← citeshttps://doi.org/10.1007/s12035-023-03429-1openalex-snapshot

Role of Mutations of Mitochondrial Aminoacyl-tRNA Synthetases Genes on Epileptogenesis

inferred← citeshttps://doi.org/10.1016/b978-0-12-819656-4.00001-2openalex-snapshot

mtDNA replication, maintenance, and nucleoid organization

inferred← citeshttps://doi.org/10.1016/b978-0-12-819656-4.00002-4openalex-snapshot

Human mitochondrial transcription and translation

inferred← citeshttps://doi.org/10.1016/b978-0-12-819656-4.00015-2openalex-snapshot

Nuclear genetic disorders of mitochondrial DNA gene expression

inferred← citeshttps://doi.org/10.1016/b978-0-12-820552-5.00018-8openalex-snapshot

Metabolic Disorders With Associated Movement Abnormalities

inferred← citeshttps://doi.org/10.1016/b978-0-12-821562-3.00026-5openalex-snapshot

DNA transcription and translation in mitochondria

inferred← citeshttps://doi.org/10.1016/b978-0-12-821913-3.00007-xopenalex-snapshot

Neurodevelopmental, neurocognitive, and behavioral disorders

inferred← citeshttps://doi.org/10.1016/b978-0-443-15260-3.00015-6openalex-snapshot

The mitochondrial unfolded protein response in health and disease

inferred← citeshttps://doi.org/10.1016/b978-0-443-33351-4.00015-5openalex-snapshot

Role of mitochondria in sustaining cellular homeostasis in health and diseases

inferred← citeshttps://doi.org/10.1016/bs.vh.2023.01.011openalex-snapshot

The potential role of environmental factors in modulating mitochondrial DNA epigenetic marks

inferred← citeshttps://doi.org/10.1016/j.anireprosci.2026.108209openalex-snapshot

Seasonal conditions shape mitochondrial genome organization and functional resilience in mature bovine sperm

inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.166016openalex-snapshot

Cancer cell metabolism: Rewiring the mitochondrial hub

inferred← citeshttps://doi.org/10.1016/j.bbadis.2025.167731openalex-snapshot

A detailed review on the role of miRNAs in mitochondrial–nuclear cross talk during cancer progression

inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.11.005openalex-snapshot

The mammalian mitochondrial epitranscriptome

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119167openalex-snapshot

TFB2M and POLRMT are essential for mammalian mitochondrial DNA replication

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2026.120220openalex-snapshot

Metabolic regulation of mitochondrial DNA (mtDNA) homeostasis

inferred← citeshttps://doi.org/10.1016/j.bbrc.2023.02.051openalex-snapshot

RETRACTED: Epidermal growth factor receptor promotes high-fructose nonalcoholic fatty liver disease by inducing mitochondrial fission in zebrafish

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2022.121947openalex-snapshot

Mitochondrial dysfunction-targeted nanosystems for precise tumor therapeutics

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113033openalex-snapshot

A STAT3 protein complex required for mitochondrial mRNA stability and cancer

inferred← citeshttps://doi.org/10.1016/j.cyto.2023.156285openalex-snapshot

The tale of antibiotics beyond antimicrobials: Expanding horizons

inferred← citeshttps://doi.org/10.1016/j.dnarep.2020.102916openalex-snapshot

Consequences of compromised mitochondrial genome integrity

inferred← citeshttps://doi.org/10.1016/j.ebiom.2022.104397openalex-snapshot

Sustained activation of EGFR-ERK1/2 signaling limits the response to tigecycline-induced mitochondrial respiratory deficiency in liver cancer

inferred← citeshttps://doi.org/10.1016/j.ejbt.2025.04.001openalex-snapshot

Application of mitochondrial genomes to species identification and evolution

inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175883openalex-snapshot

TIMELESS promotes the proliferation and migration of lung adenocarcinoma cells by activating EGFR through AMPK and SPHK1 regulation

inferred← citeshttps://doi.org/10.1016/j.fertnstert.2019.05.005openalex-snapshot

Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency

inferred← citeshttps://doi.org/10.1016/j.fsigen.2026.103489openalex-snapshot

RNA-STR/SNP: A mirror of forensic DNA-STR/SNP

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144870openalex-snapshot

On-call Mito-Firefighter: Dual-activated nanoparticles based on carboxymethyl chitosan/β-cyclodextrin to achieve mitochondria targeting and destruction/PTT/PDT cascade anticancer treatment

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111970openalex-snapshot

Differences in nature killer cell response and interference with mitochondrial DNA induced apoptosis in moxifloxacin environment

inferred← citeshttps://doi.org/10.1016/j.isci.2022.105410openalex-snapshot

Cytosolic and mitochondrial tRNA synthetase inhibitors increase lifespan in a GCN4/atf-4-dependent manner

inferred← citeshttps://doi.org/10.1016/j.isci.2024.108883openalex-snapshot

Deficient tRNA posttranscription modification dysregulated the mitochondrial quality controls and apoptosis

inferred← citeshttps://doi.org/10.1016/j.isci.2024.110560openalex-snapshot

Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies

inferred← citeshttps://doi.org/10.1016/j.jaci.2021.03.033openalex-snapshot

CD4+ T-cell differentiation and function: Unifying glycolysis, fatty acid oxidation, polyamines NAD mitochondria

inferred← citeshttps://doi.org/10.1016/j.jad.2025.03.116openalex-snapshot

Genetic insights into the role of mitochondria-related genes in mental disorders: An integrative multi-omics analysis

inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101788openalex-snapshot

Methyltransferase METTL8 is required for 3-methylcytosine modification in human mitochondrial tRNAs

inferred← citeshttps://doi.org/10.1016/j.jbc.2026.111455openalex-snapshot

Role of mitochondrial translation in modulating inflammatory disease outcome: Current knowledge and future perspectives

inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113174openalex-snapshot

Higher-order structural organization of mitochondrial metabolism

inferred← citeshttps://doi.org/10.1016/j.jbiotec.2019.04.019openalex-snapshot

Ultracentrifugation enrichment protocol followed by total RNA sequencing allows assembly of the complete mitochondrial genome

inferred← citeshttps://doi.org/10.1016/j.jmb.2021.166922openalex-snapshot

Expression Regulation, Protein Chemistry and Functional Biology of the Guanine-Rich Sequence Binding Factor 1 (GRSF1)

inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169198openalex-snapshot

Interplay Between tRNA Modifications and Processing

inferred← citeshttps://doi.org/10.1016/j.jphotochemrev.2023.100619openalex-snapshot

Recent Developments in Mitochondrial G‐Quadruplex Recognising Fluorescent Probes: A Review

inferred← citeshttps://doi.org/10.1016/j.mad.2020.111345openalex-snapshot

Mitochondrial biogenesis in organismal senescence and neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.mito.2021.09.001openalex-snapshot

Repeated mild traumatic brain injuries perturb the mitochondrial biogenesis via DNA methylation in the hippocampus of rat

inferred← citeshttps://doi.org/10.1016/j.mito.2023.06.003openalex-snapshot

NUDT6 and NUDT9, two mitochondrial members of the NUDIX family, have distinct hydrolysis activities

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2020.04.004openalex-snapshot

Diverse roles of mtDNA in schizophrenia: Implications in its pathophysiology and as biomarker for cognitive impairment

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105411openalex-snapshot

Increased metabolism in combination with the novel cytochrome b target-site mutation L258F confers cross-resistance between the Qo inhibitors acequinocyl and bifenazate in Tetranychus urticae

inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.105964openalex-snapshot

Mode of inheritance for pesticide resistance, importance and prevalence: A review

inferred← citeshttps://doi.org/10.1016/j.redox.2020.101778openalex-snapshot

Accelerated FASTK mRNA degradation induced by oxidative stress is responsible for the destroyed myocardial mitochondrial gene expression and respiratory function in alcoholic cardiomyopathy

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.161738openalex-snapshot

Fluoride impairs mitochondrial translation by targeting miR-221-3p/c-Fos/RMND1 axis contributing to neurodevelopment defects

inferred← citeshttps://doi.org/10.1016/j.str.2026.02.009openalex-snapshot

Molecular mechanism underlying the specific RNA recognition of mitochondrial helicase DDX28 and its critical role in mitoribosomal biogenesis

inferred← citeshttps://doi.org/10.1016/j.tcb.2020.03.001openalex-snapshot

Folding the Mitochondrial UPR into the Integrated Stress Response

inferred← citeshttps://doi.org/10.1016/j.tranon.2021.101280openalex-snapshot

Curcumin derivative 1, 2-bis [(3E, 5E)-3, 5-bis [(2-chlorophenyl) methylene]-4-oxo-1-piperidyl] ethane-1, 2-dione (ST03) induces mitochondria mediated apoptosis in ovarian cancer cells and inhibits tumor progression in EAC mouse model

inferred← citeshttps://doi.org/10.1016/j.yexcr.2020.112369openalex-snapshot

PGC1α regulates mitochondrial oxidative phosphorylation involved in cisplatin resistance in ovarian cancer cells via nucleo-mitochondrial transcriptional feedback

inferred← citeshttps://doi.org/10.1016/j.ymgmr.2020.100616openalex-snapshot

Improved lactate control with dichloroacetate in a case with severe neonatal lactic acidosis due to MTFMT mitochondrial translation disorder

inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00687openalex-snapshot

Synthetic Biology of Plants and Microbes for Agriculture, Environment, and Future Applications

inferred← citeshttps://doi.org/10.1021/acschembio.8b00951openalex-snapshot

Metabolic Regulation of the Epitranscriptome

inferred← citeshttps://doi.org/10.1021/acsnano.0c01388openalex-snapshot

Perimitochondrial Enzymatic Self-Assembly for Selective Targeting the Mitochondria of Cancer Cells

inferred← citeshttps://doi.org/10.1021/jacs.3c09230openalex-snapshot

Collision-Induced Unfolding Reveals Disease-Associated Stability Shifts in Mitochondrial Transfer Ribonucleic Acids

inferred← citeshttps://doi.org/10.1038/s12276-023-01121-xopenalex-snapshot

Mitochondrial nucleic acids in innate immunity and beyond

inferred← citeshttps://doi.org/10.1038/s41392-023-01546-wopenalex-snapshot

Mitochondrial heterogeneity in diseases

inferred← citeshttps://doi.org/10.1038/s41401-022-00864-zopenalex-snapshot

Mitochondria homeostasis: Biology and involvement in hepatic steatosis to NASH

inferred← citeshttps://doi.org/10.1038/s41420-025-02803-3openalex-snapshot

Identification of a novel minor-groove DNA binder that represses mitochondrial gene expression and induces apoptosis in highly aggressive leiomyosarcoma cells

inferred← citeshttps://doi.org/10.1038/s41420-026-03075-1openalex-snapshot

TUFM: a central regulator in mitochondrial quality control and beyond

inferred← citeshttps://doi.org/10.1038/s41421-023-00634-zopenalex-snapshot

Structural insights into the specific recognition of mitochondrial ribosome-binding factor hsRBFA and 12 S rRNA by methyltransferase METTL15

inferred← citeshttps://doi.org/10.1038/s41437-023-00650-5openalex-snapshot

Mitochondrially mediated RNA interference, a retrograde signaling system affecting nuclear gene expression

inferred← citeshttps://doi.org/10.1038/s41467-020-17853-7openalex-snapshot

Mechanism of ribosome rescue by alternative ribosome-rescue factor B

inferred← citeshttps://doi.org/10.1038/s41467-022-32544-1openalex-snapshot

Structural basis for shape-selective recognition and aminoacylation of a D-armless human mitochondrial tRNA

inferred← citeshttps://doi.org/10.1038/s41467-023-36277-7openalex-snapshot

TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease

inferred← citeshttps://doi.org/10.1038/s41467-023-37291-5openalex-snapshot

A defect in mitochondrial protein translation influences mitonuclear communication in the heart

inferred← citeshttps://doi.org/10.1038/s41467-023-40600-7openalex-snapshot

MTH1 protects platelet mitochondria from oxidative damage and regulates platelet function and thrombosis

inferred← citeshttps://doi.org/10.1038/s41467-024-48163-xopenalex-snapshot

Mitoribosome structure with cofactors and modifications reveals mechanism of ligand binding and interactions with L1 stalk

inferred← citeshttps://doi.org/10.1038/s41467-026-71511-yopenalex-snapshot

A framework for the exploration of subcellular compartmentalization of RNA-binding proteins

inferred← citeshttps://doi.org/10.1038/s41576-023-00645-2openalex-snapshot

RNA modifications in physiology and disease: towards clinical applications

inferred← citeshttps://doi.org/10.1038/s41580-020-0220-5openalex-snapshot

The mitochondrial tRNA conundrum

inferred← citeshttps://doi.org/10.1038/s41580-021-00430-1openalex-snapshot

Cellular origins of dsRNA, their recognition and consequences

inferred← citeshttps://doi.org/10.1038/s41582-021-00455-2openalex-snapshot

Applying genomic and transcriptomic advances to mitochondrial medicine

inferred← citeshttps://doi.org/10.1038/s41586-023-06643-yopenalex-snapshot

Structures illustrate step-by-step mitochondrial transcription initiation

inferred← citeshttps://doi.org/10.1038/s41589-024-01776-1openalex-snapshot

Mitochondria-localized MBD2c facilitates mtDNA transcription and drug resistance

inferred← citeshttps://doi.org/10.1038/s41594-021-00637-yopenalex-snapshot

Structural basis of RNA processing by human mitochondrial RNase P

inferred← citeshttps://doi.org/10.1038/s41594-024-01445-wopenalex-snapshot

Molecular basis of human nuclear and mitochondrial tRNA 3′ processing

inferred← citeshttps://doi.org/10.1038/s41596-021-00517-1openalex-snapshot

Monitoring mammalian mitochondrial translation with MitoRiboSeq

inferred← citeshttps://doi.org/10.1038/s41598-019-47145-0openalex-snapshot

Comparative mitogenomics of the Decapoda reveals evolutionary heterogeneity in architecture and composition

inferred← citeshttps://doi.org/10.1038/s41598-019-56231-2openalex-snapshot

MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus

inferred← citeshttps://doi.org/10.1038/s41598-023-41053-0openalex-snapshot

Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6

inferred← citeshttps://doi.org/10.1038/s41598-023-50213-1openalex-snapshot

The mitochondrial DNA common deletion as a potential biomarker of cancer-associated fibroblasts from skin basal and squamous cell carcinomas

inferred← citeshttps://doi.org/10.1038/s42003-025-07645-4openalex-snapshot

TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA

inferred← citeshttps://doi.org/10.1042/bcj20260185openalex-snapshot

Re-evaluating the rationale for targeting oxidative phosphorylation in acute myeloid leukemia

inferred← citeshttps://doi.org/10.1042/bst20190265openalex-snapshot

Mammalian mitochondrial translation — revealing consequences of divergent evolution

inferred← citeshttps://doi.org/10.1042/ebc20170103openalex-snapshot

Mitochondrial DNA transcription and translation: clinical syndromes

inferred← citeshttps://doi.org/10.1073/pnas.2023752118openalex-snapshot

Fever supports CD8 + effector T cell responses by promoting mitochondrial translation

inferred← citeshttps://doi.org/10.1073/pnas.2534946123openalex-snapshot

Expression of four mitochondrial tRNAs from only two loci

inferred← citeshttps://doi.org/10.1074/jbc.ra120.012618openalex-snapshot

Differential processing and localization of human Nocturnin controls metabolism of mRNA and nicotinamide adenine dinucleotide cofactors

inferred← citeshttps://doi.org/10.1080/15384101.2019.1646563openalex-snapshot

Beyond the unwinding: role of TOP1MT in mitochondrial translation

inferred← citeshttps://doi.org/10.1080/15476286.2021.1935572openalex-snapshot

Mitochondrial noncoding RNAs: new wine in an old bottle

inferred← citeshttps://doi.org/10.1080/15592294.2023.2241010openalex-snapshot

Genome-wide methylation profile of mitochondrial DNA across bovine preimplantation development

inferred← citeshttps://doi.org/10.1080/19490976.2019.1592421openalex-snapshot

Gut bacteria signaling to mitochondria in intestinal inflammation and cancer

inferred← citeshttps://doi.org/10.1080/23802359.2026.2654107openalex-snapshot

The complete mitochondrial genome of the Perinereis linea (Polychaeta: Nereididae) and Nereididae phylogenetic implications

inferred← citeshttps://doi.org/10.1080/24701394.2026.2622715openalex-snapshot

Characterisation and comparative analysis of the complete mitochondrial genomes of two whiprays, Himantura leoparda and H. uarnak, occurring in the Southwest Indian Ocean

inferred← citeshttps://doi.org/10.1089/ars.2019.7921openalex-snapshot

Anaerobic Transcription by OxyR: A Novel Paradigm for Nitrosative Stress

inferred← citeshttps://doi.org/10.1089/hum.2024.073openalex-snapshot

Unconstrained Precision Mitochondrial Genome Editing with αDdCBEs

inferred← citeshttps://doi.org/10.1093/ajh/hpab133openalex-snapshot

Maternally Inherited Essential Hypertension: Adding Further Complexity to an Already Complex Condition

inferred← citeshttps://doi.org/10.1093/gbe/evac023openalex-snapshot

New Insights into Mitochondrial–Nuclear Interactions Revealed through Analysis of Small RNAs

inferred← citeshttps://doi.org/10.1093/gbe/evaf208openalex-snapshot

SmithRNAs: A Common Feature among Metazoa

inferred← citeshttps://doi.org/10.1093/genetics/iyab116openalex-snapshot

Mitochondrial mutations in Caenorhabditis elegans show signatures of oxidative damage and an AT-bias

inferred← citeshttps://doi.org/10.1093/hmg/ddaa014openalex-snapshot

DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism

inferred← citeshttps://doi.org/10.1093/hmg/ddz093openalex-snapshot

MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy

inferred← citeshttps://doi.org/10.1093/icb/icz025openalex-snapshot

Mitochondria and the Origin of Species: Bridging Genetic and Ecological Perspectives on Speciation Processes

inferred← citeshttps://doi.org/10.1093/jeb/voaf130openalex-snapshot

Matching mitochondrial respiration to changing environments through acclimatization and the evolution of fixed genetic differences

inferred← citeshttps://doi.org/10.1093/nar/gkaa860openalex-snapshot

Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts

inferred← citeshttps://doi.org/10.1093/nar/gkab404openalex-snapshot

YbeY is required for ribosome small subunit assembly and tRNA processing in human mitochondria

inferred← citeshttps://doi.org/10.1093/nar/gkab865openalex-snapshot

The structural and functional workings of KEOPS

inferred← citeshttps://doi.org/10.1093/nar/gkad343openalex-snapshot

The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development

inferred← citeshttps://doi.org/10.1093/nar/gkad713openalex-snapshot

Cleavage kinetics of human mitochondrial RNase P and contribution of its non-nuclease subunits

inferred← citeshttps://doi.org/10.1093/nar/gkaf021openalex-snapshot

Selection of initiator tRNA and start codon by mammalian mitochondrial initiation factor 3 in leaderless mRNA translation

inferred← citeshttps://doi.org/10.1093/nar/gkz277openalex-snapshot

The mitochondrial R-loop

inferred← citeshttps://doi.org/10.1093/nar/gkz575openalex-snapshot

Mammalian NSUN2 introduces 5-methylcytidines into mitochondrial tRNAs

inferred← citeshttps://doi.org/10.1093/nar/gkz735openalex-snapshot

METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis

inferred← citeshttps://doi.org/10.1093/narcan/zcac034openalex-snapshot

Prostate cancer resistance leads to a global deregulation of translation factors and unconventional translation

inferred← citeshttps://doi.org/10.1093/narmme/ugag040openalex-snapshot

SLIRP differentially modulates RNA binding of pathogenic LRPPRC variants

inferred← citeshttps://doi.org/10.1096/fj.202300623ropenalex-snapshot

Loss of FUT8 in renal tubules ameliorates ischemia‐reperfusion injury‐induced renal interstitial inflammation transition to fibrosis via the TLR3 – NF‐κB pathway

inferred← citeshttps://doi.org/10.1097/nnr.0000000000000598openalex-snapshot

Exploratory Analysis of Associations Between Whole Blood Mitochondrial Gene Expression and Cancer-Related Fatigue Among Breast Cancer Survivors

inferred← citeshttps://doi.org/10.1097/txd.0000000000001065openalex-snapshot

Rejection-associated Mitochondrial Impairment After Heart Transplantation

inferred← citeshttps://doi.org/10.1098/rstb.2020.0159openalex-snapshot

Molluscan mitochondrial genomes break the rules

inferred← citeshttps://doi.org/10.1101/2021.01.05.425492openalex-snapshot

Prostate cancer resistance leads to a global deregulation of translation factors and unconventional translation of long non-coding RNAs

inferred← citeshttps://doi.org/10.1101/2021.05.02.442361openalex-snapshot

METTL8 is required for 3-methylcytosine modification in human mitochondrial tRNAs

inferred← citeshttps://doi.org/10.1101/2023.05.24.542018openalex-snapshot

Structure of mitoribosome reveals mechanism of mRNA binding, tRNA interactions with L1 stalk, roles of cofactors and rRNA modifications

inferred← citeshttps://doi.org/10.1101/2023.10.26.564187openalex-snapshot

Activation of the mitochondrial unfolded protein response regulates the formation of stress granules

inferred← citeshttps://doi.org/10.1101/2024.03.28.587146openalex-snapshot

SLIRP promotes autoimmune diseases by amplifying antiviral signaling via positive feedback regulation

inferred← citeshttps://doi.org/10.1101/2024.08.29.610400openalex-snapshot

Determining the off-target activity of antibiotics and novel translation initiation sites in mitochondria

inferred← citeshttps://doi.org/10.1101/2025.06.02.657529openalex-snapshot

Z-Form Stabilization By The Zα Domain Of Adar1p150 Has Subtle Effects On A-To-I Editing

inferred← citeshttps://doi.org/10.1101/2025.06.10.658430openalex-snapshot

A survey of dietary effects on tRNA abundance and modifications

inferred← citeshttps://doi.org/10.1101/2025.10.15.682593openalex-snapshot

Integrated Metabolic Complex Genetic Interaction Network of Chromosome 4p Loss in Basal Breast Cancer

inferred← citeshttps://doi.org/10.1101/696559openalex-snapshot

ReCappable Seq: Comprehensive Determination of Transcription Start Sites derived from all RNA polymerases

inferred← citeshttps://doi.org/10.1101/gr.275784.121openalex-snapshot

Comprehensive determination of transcription start sites derived from all RNA polymerases using ReCappable-seq

inferred← citeshttps://doi.org/10.1101/gr.276139.121openalex-snapshot

Low-input RNase footprinting for simultaneous quantification of cytosolic and mitochondrial translation

inferred← citeshttps://doi.org/10.1101/gr.281159.125openalex-snapshot

Dietary effects on cytosolic and mitochondrial tRNA abundance and modification patterns across mouse tissues

inferred← citeshttps://doi.org/10.1104/pp.18.01252openalex-snapshot

The Role of Plastidic Trigger Factor Serving Protein Biogenesis in Green Algae and Land Plants

inferred← citeshttps://doi.org/10.1111/ahg.70056openalex-snapshot

Decoding the Genetic and Phenotypic Spectrum of MT‐TI Mitochondrial Diseases

inferred← citeshttps://doi.org/10.1111/jpy.70080openalex-snapshot

Mitochondrial mRNA oligocitydylation occurs in Chlorophyceae and Ulvales but not Bryopsidales or Trebouxiophyceae

inferred← citeshttps://doi.org/10.1111/pbi.13985openalex-snapshot

Transgene insertion into the plastid genome alters expression of adjacent native chloroplast genes at the transcriptional and translational levels

inferred← citeshttps://doi.org/10.1111/rda.13786openalex-snapshot

Mitoepigenetics: Methylation of mitochondrial DNA is strand‐biased in bovine oocytes and embryos

inferred← citeshttps://doi.org/10.1111/zsc.12695openalex-snapshot

A non‐monophyly of ‘crowned’ Daphnia (Ctenodaphnia) Dybowski et Grochowski, 1895 (Cladocera: Daphniidae): From genomes to morphology

inferred← citeshttps://doi.org/10.1113/ep093325openalex-snapshot

Mitochondrial capacities and quality control following short‐ and long‐term weight restoration after simulated anorexia nervosa

inferred← citeshttps://doi.org/10.1139/cjm-2024-0179openalex-snapshot

Comparative mitogenomics of Leptographium procerum, Leptographium terebrantis, and Leptographium wingfieldii, an invasive fungal species in Canadian forests

inferred← citeshttps://doi.org/10.1146/annurev-biochem-071322-021330openalex-snapshot

Polyamines in Parkinson's Disease: Balancing Between Neurotoxicity and Neuroprotection

inferred← citeshttps://doi.org/10.1152/ajpgi.00031.2020openalex-snapshot

Perturbed mitochondrial dynamics, an emerging aspect of epithelial-microbe interactions

inferred← citeshttps://doi.org/10.1161/cir.0000000000001393openalex-snapshot

Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association

inferred← citeshttps://doi.org/10.1161/circulationaha.123.065546openalex-snapshot

AGO2 Protects Against Diabetic Cardiomyopathy by Activating Mitochondrial Gene Translation

inferred← citeshttps://doi.org/10.1161/circulationaha.123.066039openalex-snapshot

Raising NAD + Level Stimulates Short-Chain Dehydrogenase/Reductase Proteins to Alleviate Heart Failure Independent of Mitochondrial Protein Deacetylation

inferred← citeshttps://doi.org/10.1177/19476035241302954openalex-snapshot

Genomic Effects of Biomechanical Loading in Adolescent Human Growth Plate Cartilage: A Pilot Study

inferred← citeshttps://doi.org/10.1186/s12859-024-05909-0openalex-snapshot

SmithHunter: a workflow for the identification of candidate smithRNAs and their targets

inferred← citeshttps://doi.org/10.1186/s12862-022-01976-0openalex-snapshot

Complex mitogenomic rearrangements within the Pectinidae (Mollusca: Bivalvia).

inferred← citeshttps://doi.org/10.1186/s12915-019-0668-yopenalex-snapshot

Mitochondrial DNA: the overlooked oncogenome?

inferred← citeshttps://doi.org/10.1186/s12915-022-01267-6openalex-snapshot

GATD3A, a mitochondrial deglycase with evolutionary origins from gammaproteobacteria, restricts the formation of advanced glycation end products

inferred← citeshttps://doi.org/10.1186/s12967-022-03685-0openalex-snapshot

Current advances in gene therapy of mitochondrial diseases

inferred← citeshttps://doi.org/10.1186/s13020-023-00808-7openalex-snapshot

Z-ligustilide preferentially caused mitochondrial dysfunction in AML HL-60 cells by activating nuclear receptors NUR77 and NOR1

inferred← citeshttps://doi.org/10.1186/s13024-020-00376-6openalex-snapshot

Mitochondria dysfunction in the pathogenesis of Alzheimer’s disease: recent advances

inferred← citeshttps://doi.org/10.1186/s13104-020-05177-0openalex-snapshot

Functional conservation of mitochondrial RNA levels despite divergent mtDNA organization

inferred← citeshttps://doi.org/10.1210/endocr/bqaa166openalex-snapshot

Prenatal Androgenization Alters the Development of GnRH Neuron and Preoptic Area RNA Transcripts in Female Mice

inferred← citeshttps://doi.org/10.1210/endocr/bqac047openalex-snapshot

Jumonji Domain–containing Protein-3 (JMJD3/Kdm6b) Is Critical for Normal Ovarian Function and Female Fertility

inferred← citeshttps://doi.org/10.1242/bio.059844openalex-snapshot

Defective COX1 expression in aging mice liver

inferred← citeshttps://doi.org/10.1242/jcs.231811openalex-snapshot

Rescuing stalled mammalian mitoribosomes – what can we learn from bacteria?

inferred← citeshttps://doi.org/10.1242/jcs.263548openalex-snapshot

Activation of the mitochondrial unfolded protein response regulates the dynamic formation of stress granules

inferred← citeshttps://doi.org/10.1261/rna.080254.124openalex-snapshot

Mitochondrial mRNA and the small subunit rRNA in budding yeasts undergo 3′-end processing at conserved species-specific elements

inferred← citeshttps://doi.org/10.12688/f1000research.21490.1openalex-snapshot

Recent advances in understanding mitochondrial genome diversity

inferred← citeshttps://doi.org/10.1371/journal.pgen.1008923openalex-snapshot

RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPases

inferred← citeshttps://doi.org/10.1371/journal.pgen.1009873openalex-snapshot

The FASTK family proteins fine-tune mitochondrial RNA processing

inferred← citeshttps://doi.org/10.1371/journal.pone.0271380openalex-snapshot

Identification of the shared gene signatures and pathways between polycystic ovary syndrome and endometrial cancer: An omics data based combined approach

inferred← citeshttps://doi.org/10.1523/jneurosci.1936-25.2026openalex-snapshot

Mitochondrially Transcribed DsRNA Mediates Manganese-Induced Neuroinflammation

inferred← citeshttps://doi.org/10.15252/embj.2022113256openalex-snapshot

Ribonucleotide synthesis by NME6 fuels mitochondrial gene expression

inferred← citeshttps://doi.org/10.1530/rep-22-0424openalex-snapshot

DOHaD: A Menagerie of Adaptations and Perspectives: The interplay between early embryo metabolism and mitoepigenetic programming of development

inferred← citeshttps://doi.org/10.17582/journal.pjz/20230207150234openalex-snapshot

Genotoxicity and Anti-Cancer Activity of Tamoxifen and Ivermectin Loaded Chitosan Nanoparticles Against MCF-7 Cell Line

inferred← citeshttps://doi.org/10.17582/journal.pjz/20230323090320openalex-snapshot

Effect of Ginseng on Blood Lipid Profile, Testosterone Level and Epididymal Sperm Quality of Aged BALB/C Mice

inferred← citeshttps://doi.org/10.17582/journal.pjz/20230410070427openalex-snapshot

Molecular Identification of Predatory Birds Through Analysis of Mitochondrial ND2 Gene

showing the first 200 of 296 · page through all 296

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.