| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | John F Allen | Q42557347 |
| P2093 | author name string | John F Allen | |
| P2860 | cites work | Reconstructing Early Events in Eukaryotic Evolution | Q44542208 |
| Sequence and analysis of chromosome 2 of the plant Arabidopsis thaliana | Q44963941 | ||
| The major light-harvesting complex of Photosystem II: aspects of its molecular and cell biology | Q46061193 | ||
| Gene transfer to the nucleus and the evolution of chloroplasts | Q47608344 | ||
| Redox conditions specify the proteins synthesised by isolated chloroplasts and mitochondria | Q47684234 | ||
| Redox control of gene expression and the function of chloroplast genomes - an hypothesis | Q47703407 | ||
| Sequence conservation of light-harvesting and stress-response proteins in relation to the three-dimensional molecular structure of LHCII. | Q47706961 | ||
| Structure of the protein subunits in the photosynthetic reaction centre of Rhodopseudomonas viridis at 3Å resolution | Q47743729 | ||
| Repeated, recent and diverse transfers of a mitochondrial gene to the nucleus in flowering plants | Q47810371 | ||
| An essential component of a novel bacterial protein export system with homologues in plastids and mitochondria | Q47860114 | ||
| Single gene circles in dinoflagellate chloroplast genomes | Q47946696 | ||
| Protein synthesis by isolated pea mitochondria is dependent on the activity of respiratory complex II. | Q47998358 | ||
| Protein disulfide isomerase as a regulator of chloroplast translational activation | Q48041388 | ||
| Transcription, splicing and editing of plastid RNAs in the nonphotosynthetic plant Epifagus virginiana | Q48069538 | ||
| A nuclear-encoded form II RuBisCO in dinoflagellates | Q48072795 | ||
| Gene transfer from mitochondrion to nucleus: novel mechanisms for gene activation from Cox2. | Q48307690 | ||
| Organisation and expression of the plastid genome of the dinoflagellate Amphidinium operculatum | Q48321822 | ||
| A family of selfish minicircular chromosomes with jumbled chloroplast gene fragments from a dinoflagellate | Q48351893 | ||
| Molecular chaperones encoded by a reduced nucleus: the cryptomonad nucleomorph | Q48354703 | ||
| Regulation of psbA and psaE expression by light quality in Synechocystis species PCC 6803. A redox control mechanism. | Q50506027 | ||
| Short- and long-term redox regulation of photosynthetic light energy distribution and photosystem stoichiometry by acetate metabolism in the green alga, Chlamydobotrys stellata. | Q50750697 | ||
| Separate sexes and the mitochondrial theory of ageing. | Q51016046 | ||
| A hydrogen-producing mitochondrion. | Q52567244 | ||
| Modification of a glnB-like gene product by photosynthetic electron transport in the cyanobacterium Synechococcus 6301. | Q52875718 | ||
| Tracing the Thread of Plastid Diversity through the Tapestry of Life. | Q55033359 | ||
| Mitochondrial and chloroplast genomes of maize have a 12-kilobase DNA sequence in common | Q56689111 | ||
| How many genes in Arabidopsis come from cyanobacteria? An estimate from 386 protein phylogenies | Q57179114 | ||
| Distribution and Nomenclature of Protein-coding Genes in 12 Sequenced Chloroplast Genomes | Q57179141 | ||
| Gene Transfer from Organelles to the Nucleus: How Much, What Happens, and Why? | Q57179145 | ||
| Sequence Analysis of the Genome of the Unicellular Cyanobacterium Synechocystis sp. Strain PCC6803. II. Sequence Determination of the Entire Genome and Assignment of Potential Protein-coding Regions | Q21994433 | ||
| Mitochondrial Genome Evolution and the Origin of Eukaryotes | Q22065393 | ||
| Mitochondrial evolution | Q22065556 | ||
| Effects of carbon source on expression of F0 genes and on the stoichiometry of the c subunit in the F1F0 ATPase of Escherichia coli | Q24522184 | ||
| Evolutionary analysis of Arabidopsis, cyanobacterial, and chloroplast genomes reveals plastid phylogeny and thousands of cyanobacterial genes in the nucleus | Q24535805 | ||
| On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells | Q24675851 | ||
| Balancing the two photosystems: photosynthetic electron transfer governs transcription of reaction centre genes in chloroplasts | Q24676149 | ||
| Chloroplast origin and integration | Q24679649 | ||
| A mitochondrial-like chaperonin 60 gene in Giardia lamblia: evidence that diplomonads once harbored an endosymbiont related to the progenitor of mitochondria | Q24682058 | ||
| Crystal structure of photosystem II from Synechococcus elongatus at 3.8 A resolution | Q27629975 | ||
| Three-dimensional structure of cyanobacterial photosystem I at 2.5 A resolution | Q27632715 | ||
| Different import pathways through the mitochondrial intermembrane space for inner membrane proteins | Q27931734 | ||
| Endosymbiosis and evolution of the plant cell | Q28140982 | ||
| Mitochondrial gene therapy: an arena for the biomedical use of inteins | Q28143675 | ||
| The mitosome, a novel organelle related to mitochondria in the amitochondrial parasite Entamoeba histolytica | Q28199058 | ||
| A mitochondrial remnant in the microsporidian Trachipleistophora hominis | Q28218819 | ||
| A briefly argued case that mitochondria and plastids are descendants of endosymbionts, but that the nuclear compartment is not | Q28765971 | ||
| Reducing the genome size of organelles favours gene transfer to the nucleus | Q29042311 | ||
| Phylogenetic classification and the universal tree | Q29547749 | ||
| The hydrogen hypothesis for the first eukaryote | Q29618266 | ||
| The alpha and the beta: protein translocation across mitochondrial and plastid outer membranes | Q30168484 | ||
| Conserved properties of hydrogenosomal and mitochondrial ADP/ATP carriers: a common origin for both organelles | Q31038846 | ||
| Protein translocation into and across the bacterial plasma membrane and the plant thylakoid membrane | Q33543963 | ||
| Non-mitochondrial ATP transport | Q33546890 | ||
| Why have organelles retained genomes? | Q33719441 | ||
| The histidine protein kinase superfamily. | Q33740391 | ||
| How membrane proteins travel across the mitochondrial intermembrane space | Q33763330 | ||
| Mechanisms for redox control of gene expression | Q33765970 | ||
| Evolution of organellar genomes | Q33801588 | ||
| Many Parallel Losses of infA from Chloroplast DNA during Angiosperm Evolution with Multiple Independent Transfers to the Nucleus | Q57252801 | ||
| Structure and function of the plant light-harvesting complex, LHC-II | Q57807258 | ||
| The doors to organelles | Q58997048 | ||
| Photosynthetic control of chloroplast gene expression | Q59054958 | ||
| Mitochondrial genes on the move | Q59072853 | ||
| Genetic functions of isolated maize mitochondria under model changes of redox conditions | Q59106324 | ||
| Control mechanisms of plastid gene expression | Q59303741 | ||
| Cardiac arrest can be less of a gamble | Q60283042 | ||
| A novel protein transport system involved in the biogenesis of bacterial electron transfer chains | Q60359099 | ||
| A vesicle transport system inside chloroplasts | Q60544979 | ||
| Mitochondrial protein import machinery and targeting information | Q61914252 | ||
| Evolution of Organelles and Eukaryotic Genomes | Q66941318 | ||
| Maize mitochondrial DNA contains a sequence homologous to the ribulose-1,5-bisphosphate carboxylase large subunit gene of chloroplast DNA | Q70289428 | ||
| NAD turnover and utilisation of metabolites for RNA synthesis in a reaction sensing the redox state of the cytochrome b6f complex in isolated chloroplasts | Q71604123 | ||
| Redox control of RNA synthesis in potato mitochondria | Q71858000 | ||
| Limitations to in vivo import of hydrophobic proteins into yeast mitochondria. The case of a cytoplasmically synthesized apocytochrome b | Q72209568 | ||
| Light-regulated translation of chloroplast messenger RNAs through redox potential | Q72886749 | ||
| Redox control in development and evolution: evidence from colonial hydroids | Q73211696 | ||
| A mitochondrial model for premature ageing of somatically cloned mammals | Q73347940 | ||
| Organelle genes--do they jump or are they pushed? | Q73396973 | ||
| TspO of rhodobacter sphaeroides. A structural and functional model for the mammalian peripheral benzodiazepine receptor | Q73462971 | ||
| From redox flow to gene regulation: role of the PrrC protein of Rhodobacter sphaeroides 2.4.1. | Q73469208 | ||
| Direct transcriptional control of the chloroplast genes psbA and psaAB adjusts photosynthesis to light energy distribution in plants | Q73483502 | ||
| The mitochondrial hsp70 chaperone system. Effect of adenine nucleotides, peptide substrate, and mGrpE on the oligomeric state of mhsp70 | Q73575509 | ||
| Redox state, reactive oxygen species and adaptive growth in colonial hydroids | Q74147695 | ||
| Redox flow as an instrument of gene regulation | Q77745539 | ||
| The biogenesis and assembly of photosynthetic proteins in thylakoid membranes1 | Q95297449 | ||
| Adjustments of photosystem stoichiometry in chloroplasts improve the quantum efficiency of photosynthesis | Q33815681 | ||
| The Tat protein export pathway | Q33826511 | ||
| Light intensity regulation of cab gene transcription is signaled by the redox state of the plastoquinone pool | Q33828613 | ||
| The twin-arginine translocation system: a novel means of transporting folded proteins in chloroplasts and bacteria | Q33880915 | ||
| Translation of chloroplast psbA mRNA is regulated by signals initiated by both photosystems II and I | Q33947192 | ||
| Microbial genes in the human genome: lateral transfer or gene loss? | Q33947327 | ||
| Photosynthesis of ATP-electrons, proton pumps, rotors, and poise | Q33960845 | ||
| Redox control and the evolution of multicellularity | Q34031122 | ||
| Alternative respiratory pathways of Escherichia coli: energetics and transcriptional regulation in response to electron acceptors | Q34064912 | ||
| The rotary mechanism of ATP synthase | Q34103409 | ||
| Toc, Tic, and chloroplast protein import | Q34105694 | ||
| An overview of endosymbiotic models for the origins of eukaryotes, their ATP-producing organelles (mitochondria and hydrogenosomes), and their heterotrophic lifestyle | Q34107198 | ||
| Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus | Q34121380 | ||
| Evolution of the mitochondrial genetic system: an overview | Q34133371 | ||
| Protein phosphorylation in regulation of photosynthesis | Q34233371 | ||
| Versatility of the mitochondrial protein import machinery | Q34238028 | ||
| Protein targeting by the twin-arginine translocation pathway | Q34238035 | ||
| Redox signalling in chloroplasts and mitochondria: genomic and biochemical evidence for two-component regulatory systems in bioenergetic organelles | Q34332362 | ||
| Control of gene expression by redox potential and the requirement for chloroplast and mitochondrial genomes | Q34336183 | ||
| Complete gene map of the plastid-like DNA of the malaria parasite Plasmodium falciparum | Q34392458 | ||
| Pathways of plastid-to-nucleus signaling | Q34394363 | ||
| Molecular chaperones involved in chloroplast protein import | Q34466794 | ||
| Plastid evolution: origins, diversity, trends | Q34488794 | ||
| Chloroplast evolution: secondary symbiogenesis and multiple losses | Q34511116 | ||
| Reaction centres: the structure and evolution of biological solar power. | Q34536467 | ||
| REDOX regulation of early embryo development. | Q34577154 | ||
| Does complexity constrain organelle evolution? | Q34598180 | ||
| Signal transduction between the chloroplast and the nucleus | Q34667571 | ||
| One, two, three: nature's tool box for building plastids | Q34721977 | ||
| Assembly of membrane-bound respiratory complexes by the Tat protein-transport system | Q34736353 | ||
| Mitochondrial protein import: two membranes, three translocases | Q34970740 | ||
| Will the real LHC II kinase please step forward? | Q34977365 | ||
| Redox and light regulation of gene expression in photosynthetic prokaryotes | Q35069325 | ||
| Relocation of the plastid rbcL gene to the nucleus yields functional ribulose-1,5-bisphosphate carboxylase in tobacco chloroplasts | Q35084322 | ||
| The Evolutionary Origin of the Mitochondrion: A Nonsymbiotic Model | Q35225456 | ||
| The endosymbiont hypothesis revisited | Q35549580 | ||
| Complex mtDNA constitutes an approximate 620-kb insertion on Arabidopsis thaliana chromosome 2: implication of potential sequencing errors caused by large-unit repeats. | Q35864168 | ||
| Mutational analysis of signal transduction by ArcB, a membrane sensor protein responsible for anaerobic repression of operons involved in the central aerobic pathways in Escherichia coli | Q36112544 | ||
| Hydrogenosomes: convergent adaptations of mitochondria to anaerobic environments | Q36340720 | ||
| Systematic changes in gene expression patterns following adaptive evolution in yeast | Q36430518 | ||
| Has the endosymbiont hypothesis been proven? | Q37066187 | ||
| Chaperone function: the assembly of ribulose bisphosphate carboxylase-oxygenase | Q37608536 | ||
| On the microassembly of integral membrane proteins | Q37938179 | ||
| Biogenesis of mitochondria | Q38195055 | ||
| The Organelle Genome Database Project (GOBASE). | Q38554662 | ||
| How do mitochondrial genes get into the nucleus? | Q38577569 | ||
| A redox-responsive regulator of photosynthesis gene expression in the cyanobacterium Synechocystis sp. Strain PCC 6803. | Q39538988 | ||
| Why mitochondria need a genome | Q39730093 | ||
| Redox signaling: globalization of gene expression | Q40370532 | ||
| Mitochondrial DNA mutations associated with aging and degenerative diseases | Q40412592 | ||
| Expression of a plastidic ATP/ADP transporter gene in Escherichia coli leads to a functional adenine nucleotide transport system in the bacterial cytoplasmic membrane | Q40858622 | ||
| Redox control of transcription: sensors, response regulators, activators and repressors | Q40862281 | ||
| Free-radical-induced mutation vs redox regulation: costs and benefits of genes in organelles | Q41004644 | ||
| Organelle genomes: going, going, gone! | Q41350783 | ||
| Coordination of nuclear and chloroplast gene expression in plant cells. | Q41649296 | ||
| Genome-wide analysis of mRNAs targeted to yeast mitochondria | Q42012883 | ||
| Changes in photosystem stoichiometry in response to environmental conditions for cell growth observed with the cyanophyte Synechocystis PCC 6714. | Q42439249 | ||
| The complete mitochondrial DNA sequences of Nephroselmis olivacea and Pedinomonas minor. Two radically different evolutionary patterns within green algae | Q42477626 | ||
| Cyanobacterial ycf27 gene products regulate energy transfer from phycobilisomes to photosystems I and II. | Q42614900 | ||
| Small single-copy region of plastid DNA in the non-photosynthetic angiosperm Epifagus virginiana contains only two genes. Differences among dicots, monocots and bryophytes in gene organization at a non-bioenergetic locus | Q42617686 | ||
| Sequence analysis of the genome of the unicellular cyanobacterium Synechocystis sp. strain PCC6803. II. Sequence determination of the entire genome and assignment of potential protein-coding regions (supplement). | Q42643336 | ||
| The mitochondrial genome of Arabidopsis thaliana contains 57 genes in 366,924 nucleotides | Q42647751 | ||
| Photosynthetic electron flow regulates transcription of the psaB gene in pea (Pisum sativum L.) chloroplasts through the redox state of the plastoquinone pool | Q43510937 | ||
| A novel mechanism of nuclear photosynthesis gene regulation by redox signals from the chloroplast during photosystem stoichiometry adjustment | Q43684836 | ||
| Searching limiting steps in the expression of chloroplast-encoded proteins: relations between gene copy number, transcription, transcript abundance and translation rate in the chloroplast of Chlamydomonas reinhardtii. | Q44066514 | ||
| The ycf27 genes from cyanobacteria and eukaryotic algae: distribution and implications for chloroplast evolution | Q44120409 | ||
| The mitochondrial genome of Arabidopsis is composed of both native and immigrant information | Q44497661 | ||
| P433 | issue | 1429 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 19-37; discussion 37-8 | |
| P577 | publication date | 2003-01-29 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | The function of genomes in bioenergetic organelles | |
| P478 | volume | 358 |
| Q26748864 | An Evolutionary Framework for Understanding the Origin of Eukaryotes |
| Q28728648 | Biochemistry and evolution of anaerobic energy metabolism in eukaryotes |
| Q38208795 | Bioenergetic constraints on the evolution of complex life |
| Q30645106 | Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases |
| Q33569824 | Burrowers from the past: mitochondrial signatures of Ordovician bivalve infaunalization |
| Q42575518 | C-Terminal Region of Sulfite Reductase Is Important to Localize to Chloroplast Nucleoids in Land Plants |
| Q33283632 | Chloroplast His-to-Asp signal transduction: a potential mechanism for plastid gene regulation in Heterosigma akashiwo (Raphidophyceae) |
| Q24649959 | Chloroplast two-component systems: evolution of the link between photosynthesis and gene expression |
| Q28596339 | Comparative Large-Scale Mitogenomics Evidences Clade-Specific Evolutionary Trends in Mitochondrial DNAs of Bivalvia |
| Q22066362 | Complete nucleotide sequence of the chlorarachniophyte nucleomorph: nature's smallest nucleus |
| Q59711092 | Concordant divergence of mitogenomes and a mitonuclear gene cluster in bird lineages inhabiting different climates |
| Q28659001 | Conflicting phylogenies for early land plants are caused by composition biases among synonymous substitutions |
| Q36861754 | Coordination of gene expression between organellar and nuclear genomes |
| Q47406483 | Covariation of mitochondrial genome size with gene lengths: evidence for gene length reduction during mitochondrial evolution |
| Q57743381 | Cytonuclear integration and co-evolution |
| Q47438561 | DNA transfer from chloroplast to nucleus is much rarer in Chlamydomonas than in tobacco. |
| Q36154260 | Degenerate mitochondria |
| Q28603252 | Detecting and Characterizing the Highly Divergent Plastid Genome of the Nonphotosynthetic Parasitic Plant Hydnora visseri (Hydnoraceae) |
| Q24625702 | Do red and green make brown?: perspectives on plastid acquisitions within chromalveolates |
| Q28741296 | Early evolution without a tree of life |
| Q28608537 | Endosymbiosis and its implications for evolutionary theory |
| Q35542476 | Endosymbiosis and the design of eukaryotic electron transport |
| Q29618487 | Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes |
| Q26795689 | Endosymbiotic theories for eukaryote origin |
| Q28741658 | Energetics and genetics across the prokaryote-eukaryote divide |
| Q36072163 | Energy transduction anchors genes in organelles |
| Q36937111 | Energy, ageing, fidelity and sex: oocyte mitochondrial DNA as a protected genetic template |
| Q43110849 | Energy, genes and evolution: introduction to an evolutionary synthesis |
| Q38543456 | Eukaryotic Components Remodeled Chloroplast Nucleoid Organization during the Green Plant Evolution |
| Q38124025 | Evolution and cell physiology. 2. The evolution of cell signaling: from mitochondria to Metazoa |
| Q34399599 | Evolution of chloroplast transcript processing in Plasmodium and its chromerid algal relatives |
| Q36534537 | Evolution of malaria parasite plastid targeting sequences |
| Q28748402 | Evolution: like any other science it is predictable |
| Q37685824 | Evolutionary origins of metabolic compartmentalization in eukaryotes. |
| Q28742027 | Evolutionary patterns of the mitochondrial genome in Metazoa: exploring the role of mutation and selection in mitochondrial protein coding genes |
| Q28475587 | Evolutionary pressure on mitochondrial cytochrome b is consistent with a role of CytbI7T affecting longevity during caloric restriction |
| Q42161828 | Evolutionary rewiring: a modified prokaryotic gene-regulatory pathway in chloroplasts. |
| Q34807488 | From chloroplasts to "cryptic" plastids: evolution of plastid genomes in parasitic plants. |
| Q37174970 | Function and regulation of local axonal translation |
| Q36688667 | Gene therapy of the other genome: the challenges of treating mitochondrial DNA defects |
| Q35170156 | Gene transfer from organelles to the nucleus: frequent and in big chunks |
| Q21999777 | Genomics and chloroplast evolution: what did cyanobacteria do for plants? |
| Q37538139 | Getting a better picture of microbial evolution en route to a network of genomes |
| Q42207612 | Higher plant photosystem II light-harvesting antenna, not the reaction center, determines the excited-state lifetime-both the maximum and the nonphotochemically quenched |
| Q99727099 | Holliday junction resolvase MOC1 maintains plastid and mitochondrial genome integrity in algae and bryophytes |
| Q40832509 | Implications of mutation of organelle genomes for organelle function and evolution |
| Q39170182 | Integrating the UPRmt into the mitochondrial maintenance network |
| Q24669538 | Integration of chloroplast nucleic acid metabolism into the phosphate deprivation response in Chlamydomonas reinhardtii |
| Q28085209 | Integration of plastids with their hosts: Lessons learned from dinoflagellates |
| Q41849131 | Massively convergent evolution for ribosomal protein gene content in plastid and mitochondrial genomes |
| Q34636052 | MitoCOGs: clusters of orthologous genes from mitochondria and implications for the evolution of eukaryotes |
| Q47145383 | Mitochondrial DNA density homeostasis accounts for a threshold effect in a cybrid model of a human mitochondrial disease |
| Q91973409 | Mitochondrial Dysfunctions: A Thread Sewing Together Alzheimer's Disease, Diabetes, and Obesity |
| Q61809068 | Mitochondrial Heterogeneity |
| Q35619766 | Mitochondrial activity in gametes and transmission of viable mtDNA |
| Q38059778 | Mitochondrial disorders as windows into an ancient organelle |
| Q36974037 | Mitochondrial energy and redox signaling in plants |
| Q43455834 | Mitochondrial genome function and maternal inheritance |
| Q28084988 | Mitonuclear Ecology |
| Q28748935 | Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes |
| Q43206380 | Non-coding RNAs' partitioning in the evolution of photosynthetic organisms via energy transduction and redox signaling |
| Q37685822 | Organization and expression of organellar genomes. |
| Q28660547 | Origin and evolution of plastids and photosynthesis in eukaryotes |
| Q41978279 | Oxa1-ribosome complexes coordinate the assembly of cytochrome C oxidase in mitochondria |
| Q37873545 | Oxidation-reduction signalling components in regulatory pathways of state transitions and photosystem stoichiometry adjustment in chloroplasts |
| Q36052586 | Parasite plastids: approaching the endgame |
| Q38609310 | Peeping at TOMs-Diverse Entry Gates to Mitochondria Provide Insights into the Evolution of Eukaryotes |
| Q33961671 | Phylogenomic evidence for a myxococcal contribution to the mitochondrial fatty acid beta-oxidation |
| Q33352003 | Piecing together the puzzle of parasitic plant plastome evolution |
| Q28246136 | Planctomycetes and eukaryotes: a case of analogy not homology |
| Q34162450 | Plastids, genomes, and the probability of gene transfer |
| Q50626264 | Plastocyanin-ferredoxin oxidoreduction and endosymbiotic gene transfer. |
| Q41357442 | Probing the nucleotide-binding activity of a redox sensor: two-component regulatory control in chloroplasts. |
| Q40864134 | Proposal of a Twin Arginine Translocator System-Mediated Constraint against Loss of ATP Synthase Genes from Nonphotosynthetic Plastid Genomes. [Corrected]. |
| Q24633418 | Pulsing of membrane potential in individual mitochondria: a stress-induced mechanism to regulate respiratory bioenergetics in Arabidopsis |
| Q50088613 | Pyrenoid loss in Chlamydomonas reinhardtii causes limitations in CO2 supply, but not thylakoid operating efficiency. |
| Q94602414 | Recent advances in understanding mitochondrial genome diversity |
| Q46287365 | Reductive evolution of chloroplasts in non-photosynthetic plants, algae and protists |
| Q89810213 | Relaxed sequence constraints favor mutational freedom in idiosyncratic metazoan mitochondrial tRNAs |
| Q34327464 | Secondary loss of chloroplasts in trypanosomes |
| Q34206637 | Stability of mitochondrial membrane proteins in terrestrial vertebrates predicts aerobic capacity and longevity |
| Q37145158 | Structure, transcription, and variability of metazoan mitochondrial genome: perspectives from an unusual mitochondrial inheritance system |
| Q47680044 | The Isolation of a Functional Cytochrome b (6) f Complex: from Lucky Encounter to Rewarding Experiences |
| Q57178955 | The N-Terminal Sequences of Four Major Hydrogenosomal Proteins Are Not Essential for Import into Hydrogenosomes ofTrichomonas vaginalis |
| Q45641890 | The TOM complex is involved in the release of superoxide anion from mitochondria. |
| Q24657324 | The ancestral symbiont sensor kinase CSK links photosynthesis with gene expression in chloroplasts |
| Q28658605 | The drive to life on wet and icy worlds |
| Q29615412 | The energetics of genome complexity |
| Q88785549 | The energy expansions of evolution |
| Q55039234 | The evolutionary processes of mitochondrial and chloroplast genomes differ from those of nuclear genomes. |
| Q41869079 | The neglected genome |
| Q28752004 | The network of life: genome beginnings and evolution. Introduction |
| Q24642705 | The origin of plastids |
| Q64072133 | Thinking twice about the evolution of photosynthesis |
| Q42557292 | Transcriptional control of photosynthesis genes: the evolutionarily conserved regulatory mechanism in plastid genome function. |
| Q61812574 | What's in a name? How organelles of endosymbiotic origin can be distinguished from endosymbionts |
| Q26796678 | Why chloroplasts and mitochondria retain their own genomes and genetic systems: Colocation for redox regulation of gene expression |
| Q38113552 | Why did eukaryotes evolve only once? Genetic and energetic aspects of conflict and conflict mediation |
| Q24812320 | Why genes persist in organelle genomes |
| Q5137543 | CoRR hypothesis | described by source | P1343 |
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