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Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-1878(200005)22:5<481::aid-bies10>3.0.co;2-topenalex-snapshot
Prokaryotic and eukaryotic chromosomes: what's the difference?
inferredcites →https://doi.org/10.1006/geno.2002.6798openalex-snapshot
Structure and Chromosomal Distribution of Human Mitochondrial Pseudogenes
inferredcites →https://doi.org/10.1007/bf00163806openalex-snapshot
Numt, a recent transfer and tandem amplification of mitochondrial DNA to the nuclear genome of the domestic cat
inferredcites →https://doi.org/10.1007/bf00222864openalex-snapshot
Tobacco nuclear DNA contains long tracts of homology to chloroplast DNA
inferredcites →https://doi.org/10.1007/bf00279648openalex-snapshot
Plastid DNA sequence homologies in the tobacco nuclear genome
inferredcites →https://doi.org/10.1007/bf01733906openalex-snapshot
Genetic and biochemical implications of the endosymbiotic origin of the chloroplast
inferredcites →https://doi.org/10.1007/bf01990603openalex-snapshot
Das Wesen und die Erblichkeitsverhältnisse der „Varietates albomarginatae hort.“ vonPelargonium zonale
inferredcites →https://doi.org/10.1007/s00239-002-2390-5openalex-snapshot
Evolutionary Dynamics of Large Numts in the Human Genome: Rarity of Independent Insertions and Abundance of Post-Insertion Duplications
inferredcites →https://doi.org/10.1007/s002940050241openalex-snapshot
The evolution of the Calvin cycle from prokaryotic to eukaryotic chromosomes: a case study of functional redundancy in ancient pathways through endosymbiosis
inferredcites →https://doi.org/10.1007/s002940050489openalex-snapshot
Mechanisms of mitochondrial DNA escape to the nucleus in the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s00438-002-0706-1openalex-snapshot
Genome sequencing of a 239-kb region of rice chromosome 10L reveals a high frequency of gene duplication and a large chloroplast DNA insertion
inferredcites →https://doi.org/10.1007/s00439-002-0892-2openalex-snapshot
Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer
inferredcites →https://doi.org/10.1016/0014-5793(93)81430-8openalex-snapshot
The mitochondrial genome on its way to the nucleus: different stages of gene transfer in higher plants
inferredcites →https://doi.org/10.1016/0921-8734(92)90026-lopenalex-snapshot
New evidence for the insertion of mitochondrial DNA into the human genome: significance for cancer and aging
inferredcites →https://doi.org/10.1016/j.gene.2004.01.008openalex-snapshot
An improved prediction of chloroplast proteins reveals diversities and commonalities in the chloroplast proteomes of Arabidopsis and rice
inferredcites →https://doi.org/10.1016/j.mib.2003.09.003openalex-snapshot
Evolutionary connections between bacterial and eukaryotic signaling systems: a genomic perspective
inferredcites →https://doi.org/10.1016/s0022-2836(83)80270-8openalex-snapshot
Mitochondrial DNA sequences in the nuclear genome of Strongylocentrotus pupuratus
inferredcites →https://doi.org/10.1016/s0074-7696(08)62223-8openalex-snapshot
Escape and Migration of Nucleic Acids between Chloroplasts, Mitochondria, and the Nucleus
inferredcites →https://doi.org/10.1016/s0168-9525(01)02312-5openalex-snapshot
How do mitochondrial genes get into the nucleus?
inferredcites →https://doi.org/10.1016/s0168-9525(02)00003-3openalex-snapshot
Chloroplast research in the genomic age
inferredcites →https://doi.org/10.1016/s0168-9525(03)00137-9openalex-snapshot
Evolutionary diversification of mitochondrial proteomes: implications for human disease
inferredcites →https://doi.org/10.1016/s0168-9525(98)01494-2openalex-snapshot
You are what you eat: a gene transfer ratchet could account for bacterial genes in eukaryotic nuclear genomes
inferredcites →https://doi.org/10.1016/s0168-9525(99)01766-7openalex-snapshot
Why have organelles retained genomes?
inferredcites →https://doi.org/10.1016/s0169-5347(01)02151-6openalex-snapshot
Mitochondrial pseudogenes: evolution's misplaced witnesses
inferredcites →https://doi.org/10.1016/s0378-1119(01)00613-8openalex-snapshot
The Arabidopsis chloroplast ribosomal protein L21 is encoded by a nuclear gene of mitochondrial origin
inferredcites →https://doi.org/10.1016/s0378-1119(03)00754-6openalex-snapshot
DNA transfer from chloroplast to nucleus is much rarer in Chlamydomonas than in tobacco
inferredcites →https://doi.org/10.1016/s0959-437x(98)80029-4openalex-snapshot
Early branching eukaryotes?
inferredcites →https://doi.org/10.1016/s0959-437x(98)80033-6openalex-snapshot
Plastid evolution: origins, diversity, trends
inferredcites →https://doi.org/10.1016/s0968-0004(02)02193-xopenalex-snapshot
Mitochondria as we don't know them
inferredcites →https://doi.org/10.1016/s1055-7903(03)00194-5openalex-snapshot
Evolution of mitochondrial gene content: gene loss and transfer to the nucleus
inferredcites →https://doi.org/10.1016/s1360-1385(00)01598-3openalex-snapshot
Membrane heredity and early chloroplast evolution
inferredcites →https://doi.org/10.1016/s1360-1385(99)01480-6openalex-snapshot
Alternative splicing and mitochondrial import
inferredcites →https://doi.org/10.1016/s1369-5266(02)00248-0openalex-snapshot
Engineering the plastid genome of higher plants
inferredcites →https://doi.org/10.1016/s1369-5266(02)00296-0openalex-snapshot
Protein import into chloroplasts
inferredcites →https://doi.org/10.1023/a:1025472709537openalex-snapshot
Abundance of plastid DNA insertions in nuclear genomes of rice and Arabidopsis
inferredcites →https://doi.org/10.1038/17624openalex-snapshot
Photosynthetic control of chloroplast gene expression
inferredcites →https://doi.org/10.1038/22099openalex-snapshot
Single gene circles in dinoflagellate chloroplast genomes
inferredcites →https://doi.org/10.1038/297197a0openalex-snapshot
Testing the theory of evolution by comparing phylogenetic trees constructed from five different protein sequences
inferredcites →https://doi.org/10.1038/299678a0openalex-snapshot
Promiscuous DNA—chloroplast genes inside plant mitochondria
inferredcites →https://doi.org/10.1038/299698a0openalex-snapshot
Mitochondrial and chloroplast genomes of maize have a 12-kilobase DNA sequence in common
inferredcites →https://doi.org/10.1038/301296a0openalex-snapshot
Rearranged mitochondrial genes in the yeast nuclear genome
inferredcites →https://doi.org/10.1038/30234openalex-snapshot
Gene transfer to the nucleus and the evolution of chloroplasts
inferredcites →https://doi.org/10.1038/305065a0openalex-snapshot
Sequence homology between spinach nuclear and chloroplast genomes
inferredcites →https://doi.org/10.1038/32096openalex-snapshot
The hydrogen hypothesis for the first eukaryote
inferredcites →https://doi.org/10.1038/346376a0openalex-snapshot
Escape of DNA from mitochondria to the nucleus in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/35042567openalex-snapshot
Repeated, recent and diverse transfers of a mitochondrial gene to the nucleus in flowering plants
inferredcites →https://doi.org/10.1038/35048692openalex-snapshot
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/387493a0openalex-snapshot
An ancestral mitochondrial DNA resembling a eubacterial genome in miniature
inferredcites →https://doi.org/10.1038/45471openalex-snapshot
Sequence and analysis of chromosome 2 of the plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/47076openalex-snapshot
Mitochondrial DNA repairs double-strand breaks in yeast chromosomes
inferredcites →https://doi.org/10.1038/nature01435openalex-snapshot
Direct measurement of the transfer rate of chloroplast DNA into the nucleus
inferredcites →https://doi.org/10.1038/nature01945openalex-snapshot
Mitochondrial remnant organelles of Giardia function in iron-sulphur protein maturation
inferredcites →https://doi.org/10.1038/nature02026openalex-snapshot
Global analysis of protein localization in budding yeast
inferredcites →https://doi.org/10.1038/nature02053openalex-snapshot
Genome-scale approaches to resolving incongruence in molecular phylogenies
inferredcites →https://doi.org/10.1038/nbt0503-489openalex-snapshot
Organelle evolution meets biotechnology
inferredcites →https://doi.org/10.1038/sj.embor.embor828openalex-snapshot
Covariations in the nuclear chloroplast transcriptome reveal a regulatory master‐switch
inferredcites →https://doi.org/10.1046/j.0014-2956.2001.02722.xopenalex-snapshot
Evolution of the enzymes of the citric acid cycle and the glyoxylate cycle of higher plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00485.xopenalex-snapshot
Transfer of rps14 from the mitochondrion to the nucleus in maize implied integration within a gene encoding the iron–sulphur subunit of succinate dehydrogenase and expression by alternative splicing
inferredcites →https://doi.org/10.1073/pnas.032658599openalex-snapshot
The origin of the eukaryotic cell: A genomic investigation
inferredcites →https://doi.org/10.1073/pnas.0335769100openalex-snapshot
Plant-like traits associated with metabolism of Trypanosoma parasites
inferredcites →https://doi.org/10.1073/pnas.0336115100openalex-snapshot
Unique mitochondrial genome architecture in unicellular relatives of animals
inferredcites →https://doi.org/10.1073/pnas.042694899openalex-snapshot
Punctuated evolution of mitochondrial gene content: High and variable rates of mitochondrial gene loss and transfer to the nucleus during angiosperm evolution
inferredcites →https://doi.org/10.1073/pnas.0831049100openalex-snapshot
Dynamin: The endosymbiosis ring of power?
inferredcites →https://doi.org/10.1073/pnas.091110398openalex-snapshot
Complex mtDNA constitutes an approximate 620-kb insertion on Arabidopsis thaliana chromosome 2: Implication of potential sequencing errors caused by large-unit repeats
inferredcites →https://doi.org/10.1073/pnas.122354399openalex-snapshot
Intracellular gene transfer: Reduced hydrophobicity facilitates gene transfer for subunit 2 of cytochrome c oxidase
inferredcites →https://doi.org/10.1073/pnas.1230951100openalex-snapshot
Lateral gene transfer and the evolution of plastid-targeted proteins in the secondary plastid-containing alga Bigelowiella natans
inferredcites →https://doi.org/10.1073/pnas.1430924100openalex-snapshot
High-frequency gene transfer from the chloroplast genome to the nucleus
inferredcites →https://doi.org/10.1073/pnas.1533499100openalex-snapshot
The genome sequence of Blochmannia floridanus : Comparative analysis of reduced genomes
inferredcites →https://doi.org/10.1073/pnas.1633606100openalex-snapshot
Gene transfer from organelles to the nucleus: Frequent and in big chunks
inferredcites →https://doi.org/10.1073/pnas.182432999openalex-snapshot
Evolutionary analysis of Arabidopsis , cyanobacterial, and chloroplast genomes reveals plastid phylogeny and thousands of cyanobacterial genes in the nucleus
inferredcites →https://doi.org/10.1073/pnas.222228199openalex-snapshot
Genome fragment of Wolbachia endosymbiont transferred to X chromosome of host insect
inferredcites →https://doi.org/10.1073/pnas.240454797openalex-snapshot
Isoprenoid biosynthesis: The evolution of two ancient and distinct pathways across genomes
inferredcites →https://doi.org/10.1073/pnas.87.12.4576openalex-snapshot
Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya.
inferredcites →https://doi.org/10.1073/pnas.92.20.9122openalex-snapshot
A nuclear gene of eubacterial origin in Euglena gracilis reflects cryptic endosymbioses during protist evolution.
inferredcites →https://doi.org/10.1073/pnas.93.15.7727openalex-snapshot
Exon shuffling and the origin of the mitochondrial targeting function in plant cytochrome c1 precursor.
inferredcites →https://doi.org/10.1073/pnas.95.11.6239openalex-snapshot
Genomic evidence for two functionally distinct gene classes
inferredcites →https://doi.org/10.1073/pnas.96.16.9207openalex-snapshot
A single nuclear transcript encoding mitochondrial RPS14 and SDHB of rice is processed by alternative splicing: Common use of the same mitochondrial targeting signal for different proteins
inferredcites →https://doi.org/10.1074/jbc.m010244200openalex-snapshot
Subunit II of Cytochrome c Oxidase in Chlamydomonad Algae Is a Heterodimer Encoded by Two Independent Nuclear Genes
inferredcites →https://doi.org/10.1080/15216540310001592834openalex-snapshot
Hydrogenosomes, Mitochondria and Early Eukaryotic Evolution
inferredcites →https://doi.org/10.1091/mbc.e02-08-0490openalex-snapshot
Interactions amongCOX1,COX2, andCOX3mRNA-specific Translational Activator Proteins on the Inner Surface of the Mitochondrial Inner Membrane ofSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/genetics/134.1.21openalex-snapshot
Nuclear mutations in Saccharomyces cerevisiae that affect the escape of DNA from mitochondria to the nucleus.
inferredcites →https://doi.org/10.1093/molbev/msh110openalex-snapshot
NUMTs in Sequenced Eukaryotic Genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003934openalex-snapshot
Mitochondrial Pseudogenes Are Pervasive and Often Insidious in the Snapping Shrimp Genus Alpheus
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003971openalex-snapshot
The Human Genome Project Reveals a Continuous Transfer of Large Mitochondrial Fragments to the Nucleus
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003987openalex-snapshot
Using Secondary Structure to Identify Ribosomal Numts: Cautionary Examples from the Human Genome
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004046openalex-snapshot
Prokaryotic Evolution in Light of Gene Transfer
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004060openalex-snapshot
Evolution of Mitochondrial Cytochrome b Pseudogene in Genus Nycticebus
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026271openalex-snapshot
Symbiotic Origin of a Novel Actin Gene in the Cryptophyte Pyrenomonas helgolandii
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026320openalex-snapshot
Frequent Assimilation of Mitochondrial DNA by Grasshopper Nuclear Genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026388openalex-snapshot
Multiple Nuclear Insertions of Mitochondrial Cytochrome b Sequences in Callitrichine Primates
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040258openalex-snapshot
Sampling properties of DNA sequence data in phylogenetic analysis.
inferredcites →https://doi.org/10.1098/rstb.2002.1183openalex-snapshot
On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells
inferredcites →https://doi.org/10.1098/rstb.2002.1185openalex-snapshot
How big is the iceberg of which organellar genes in nuclear genomes are but the tip?
inferredcites →https://doi.org/10.1098/rstb.2002.1191openalex-snapshot
The function of genomes in bioenergetic organelles
inferredcites →https://doi.org/10.1101/gr.132102openalex-snapshot
Genome Size Reduction through Illegitimate Recombination Counteracts Genome Expansion in Arabidopsis
inferredcites →https://doi.org/10.1101/gr.227202openalex-snapshot
Pattern of Organization of Human Mitochondrial Pseudogenes in the Nuclear Genome
inferredcites →https://doi.org/10.1104/pp.010908openalex-snapshot
The Treasure Trove of Algal Chloroplast Genomes. Surprises in Architecture and Gene Content, and Their Functional Implications
inferredcites →https://doi.org/10.1104/pp.118.1.9openalex-snapshot
Gene Transfer from Organelles to the Nucleus: How Much, What Happens, and Why?1
inferredcites →https://doi.org/10.1105/tpc.010009openalex-snapshot
Nuclear Genes That Encode Mitochondrial Proteins for DNA and RNA Metabolism Are Clustered in the Arabidopsis Genome[W]
inferredcites →https://doi.org/10.1105/tpc.010483openalex-snapshot
Genes for Two Mitochondrial Ribosomal Proteins in Flowering Plants Are Derived from Their Chloroplast or Cytosolic Counterparts
inferredcites →https://doi.org/10.1105/tpc.13.3.645openalex-snapshot
Many Parallel Losses of infA from Chloroplast DNA during Angiosperm Evolution with Multiple Independent Transfers to the Nucleus
inferredcites →https://doi.org/10.1111/j.1558-5646.1971.tb01930.xopenalex-snapshot
ORIGIN OF EUKARYOTIC CELLS
inferredcites →https://doi.org/10.1126/science.1071196openalex-snapshot
Rooting the Eukaryote Tree by Using a Derived Gene Fusion
inferredcites →https://doi.org/10.1126/science.1082192openalex-snapshot
The Division of Endosymbiotic Organelles
inferredcites →https://doi.org/10.1126/science.1083523openalex-snapshot
In-Depth View of Structure, Activity, and Evolution of Rice Chromosome 10
inferredcites →https://doi.org/10.1126/science.1085463openalex-snapshot
Reconstruction of the Proto-Mitochondrial Metabolism
inferredcites →https://doi.org/10.1126/science.1138359openalex-snapshot
Evolution of Organelles and Eukaryotic Genomes
inferredcites →https://doi.org/10.1126/science.283.5407.1476openalex-snapshot
Mitochondrial Evolution
inferredcites →https://doi.org/10.1128/mmbr.46.1.1-42.1982openalex-snapshot
Has the endosymbiont hypothesis been proven?
inferredcites →https://doi.org/10.1146/annurev.biochem.66.1.863openalex-snapshot
PROTEIN IMPORT INTO MITOCHONDRIA
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.351openalex-snapshot
Mitochondrial Genome Evolution and the Origin of Eukaryotes
inferredcites →https://doi.org/10.1146/annurev.genet.35.102401.090231openalex-snapshot
The Inheritance of Genes in Mitochondria and Chloroplasts: Laws, Mechanisms, and Models
inferredcites →https://doi.org/10.1146/annurev.pp.32.060181.000551openalex-snapshot
Chloroplast Proteins: Synthesis, Transport, and Assembly
inferredcites →https://doi.org/10.1186/1471-2148-1-4openalex-snapshot
A genomic timescale for the origin of eukaryotes
inferredcites →https://doi.org/10.1242/jcs.111.16.2455openalex-snapshot
Escape of mitochondrial DNA to the nucleus in ymel yeast is mediated by vacuolar-dependent turnover of abnormal mitochondrial compartments
inferredcites →https://doi.org/10.1515/bc.2001.187openalex-snapshot
An Overview of Endosymbiotic Models for the Origins of Eukaryotes, Their ATP-Producing Organelles (Mitochondria and Hydrogenosomes), and Their Heterotrophic Lifestyle
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Bangiomorpha pubescensn. gen., n. sp.: implications for the evolution of sex, multicellularity, and the Mesoproterozoic/Neoproterozoic radiation of eukaryotes
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Protein Import into Hydrogenosomes and Mitosomes
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Hydrogenosomes of Anaerobic Chytrids: An Alternative Way to Adapt to Anaerobic Environments
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The Evolutionary Origins of Plant Organelles
inferred← citeshttps://doi.org/10.1007/978-1-4020-4061-0_2openalex-snapshot
Chloroplast Development: Whence and Whither
inferred← citeshttps://doi.org/10.1007/978-1-4614-7780-8openalex-snapshot
Lateral Gene Transfer in Evolution
inferred← citeshttps://doi.org/10.1007/978-1-4614-7780-8_2openalex-snapshot
Lateral Gene Transfer and the Evolution of Photosynthesis in Eukaryotes
inferred← citeshttps://doi.org/10.1007/978-1-4614-8087-7_11openalex-snapshot
Sequencing and Assembly of the Transgenic Papaya Genome
inferred← citeshttps://doi.org/10.1007/978-1-4614-8087-7_16openalex-snapshot
Genomics of Papaya Sex Chromosomes
inferred← citeshttps://doi.org/10.1007/978-1-4939-1136-3_11openalex-snapshot
Protein Transport into Plastids of Secondarily Evolved Organisms
inferred← citeshttps://doi.org/10.1007/978-1-4939-2288-8_18openalex-snapshot
Allotopic Expression of ATP6 in the Mouse as a Transgenic Model of Mitochondrial Disease
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_1openalex-snapshot
Primary Endosymbiosis: Emergence of the Primary Chloroplast and the Chromatophore, Two Independent Events
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_4openalex-snapshot
Diversity and Plasticity of Plastids in Land Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-9074-0_9openalex-snapshot
The Methodology Behind Network Thinking: Graphs to Analyze Microbial Complexity and Evolution
inferred← citeshttps://doi.org/10.1007/978-1-59745-466-7_30openalex-snapshot
Phylogenetic Analysis to Uncover Organellar Origins of Nuclear-Encoded Genes
inferred← citeshttps://doi.org/10.1007/978-1-60327-853-9_28openalex-snapshot
Horizontal Gene Transfer in Eukaryotic Parasites: A Case Study of Entamoeba histolytica and Trichomonas vaginalis
inferred← citeshttps://doi.org/10.1007/978-1-61779-237-3_7openalex-snapshot
Use of Transcriptomics to Analyze Chloroplast Processes in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-62703-995-6_1openalex-snapshot
The Plastid Genomes of Flowering Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-03389-7_12openalex-snapshot
Carrot Organelle Genomes: Organization, Diversity, and Inheritance
inferred← citeshttps://doi.org/10.1007/978-3-030-11045-1_10openalex-snapshot
Duckweed Chloroplast Genome Sequencing and Annotation
inferred← citeshttps://doi.org/10.1007/978-3-030-17941-0_2openalex-snapshot
The Evolution of Oxygen-Independent Energy Metabolism in Eukaryotes with Hydrogenosomes and Mitosomes
inferred← citeshttps://doi.org/10.1007/978-3-030-21862-1_12openalex-snapshot
Role of Horizontal Gene Transfer in Evolution of the Plant Genome
inferred← citeshttps://doi.org/10.1007/978-3-030-51849-3_13openalex-snapshot
The Photosynthetic Adventure of Paulinella Spp
inferred← citeshttps://doi.org/10.1007/978-3-030-65317-0_4openalex-snapshot
Holistic Fitness: Microbiomes are Part of the Holobiont’s Fitness
inferred← citeshttps://doi.org/10.1007/978-3-030-90383-1_4openalex-snapshot
Marine Protists: A Hitchhiker’s Guide to their Role in the Marine Microbiome
inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_5openalex-snapshot
Structure and Evolution of Diatom Nuclear Genes and Genomes
inferred← citeshttps://doi.org/10.1007/978-3-031-29199-9_3openalex-snapshot
The Evolution of Mitochondrial Genomes in Fungi
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_4openalex-snapshot
Chloroplast Translation Machinery
inferred← citeshttps://doi.org/10.1007/978-3-031-70098-9_6openalex-snapshot
The Genetic Engineering Toolbox for Transformation of Higher Plant Plastids
inferred← citeshttps://doi.org/10.1007/978-3-319-28637-2_9openalex-snapshot
Mitochondria, the Synapse, and Neurodegeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-39126-7_5openalex-snapshot
Regulation of Carotenoid Biosynthesis in Photosynthetic Organs
inferred← citeshttps://doi.org/10.1007/978-3-319-54064-1_2openalex-snapshot
Organelle Genomes and Endosymbionts
inferred← citeshttps://doi.org/10.1007/978-3-540-38502-8_3openalex-snapshot
Origin, Function, and Transmission of Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-540-38502-8_4openalex-snapshot
Mitochondria and Their Host: Morphology to Molecular Phylogeny
inferred← citeshttps://doi.org/10.1007/978-3-540-38502-8_7openalex-snapshot
Hydrogenosomes (and Related Organelles, Either) Are Not the Same
inferred← citeshttps://doi.org/10.1007/978-3-540-72954-9_4openalex-snapshot
Extranuclear Inheritance: Plastid—Nuclear Cooperation in Photosystem I Assembly in Photosynthetic Eukaryotes
inferred← citeshttps://doi.org/10.1007/978-3-540-74250-0_9openalex-snapshot
Frequent DNA Transfer Among Mitochondrial, Plastid and Nuclear Genomes of Rice During Evolution
inferred← citeshttps://doi.org/10.1007/978-3-642-00952-5_16openalex-snapshot
Why Phylogenetic Trees are Often Quite Robust Against Lateral Transfers
inferred← citeshttps://doi.org/10.1007/978-3-642-01085-9_14openalex-snapshot
Transgenetic Algorithm: A New Endosymbiotic Approach for Evolutionary Algorithms
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_13openalex-snapshot
Introns, Mobile Elements, and Plasmids
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_18openalex-snapshot
Erratum to: Mitochondria, Hydrogenosomes and Mitosomes in Relation to the CoRR Hypothesis for Genome Function and Evolution
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_5openalex-snapshot
Mitochondria, Hydrogenosomes and Mitosomes in Relation to the CoRR Hypothesis for Genome Function and Evolution
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_6openalex-snapshot
Evolutionary Rate Variation in Organelle Genomes: The Role of Mutational Processes
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_7openalex-snapshot
Gene Transfer to the Nucleus
inferred← citeshttps://doi.org/10.1007/978-3-642-45218-5_3openalex-snapshot
3 Phylogenomics for the Study of Fungal Biology
inferred← citeshttps://doi.org/10.1007/978-3-662-45425-1_7openalex-snapshot
Co-expression of Cellulases in the Chloroplasts of Nicotiana tabacum
inferred← citeshttps://doi.org/10.1007/978-3-662-53389-5_7openalex-snapshot
Chloroplast and Mitochondrial Genomes of Tomato
inferred← citeshttps://doi.org/10.1007/978-3-7091-1303-5_14openalex-snapshot
Endosymbioses in Sacoglossan Seaslugs: Plastid-Bearing Animals that Keep Photosynthetic Organelles Without Borrowing Genes
inferred← citeshttps://doi.org/10.1007/978-3-7091-1303-5_2openalex-snapshot
Modifications and Innovations in the Evolution of Mitochondrial Protein Import Pathways
inferred← citeshttps://doi.org/10.1007/978-3-7091-1303-5_3openalex-snapshot
The Single Primary Endosymbiotic Event
inferred← citeshttps://doi.org/10.1007/978-3-7091-1303-5_4openalex-snapshot
Insertion of Metabolite Transporters into the Endosymbiont Membrane(s) as a Prerequisite for Primary Endosymbiosis
inferred← citeshttps://doi.org/10.1007/978-4-431-55130-0_1openalex-snapshot
Protistan Diversity in Environmental Molecular Surveys
inferred← citeshttps://doi.org/10.1007/978-81-322-2172-2_15openalex-snapshot
Plant Physiomics: Photoelectrochemical and Molecular Retrograde Signalling in Plant Acclimatory and Defence Responses
inferred← citeshttps://doi.org/10.1007/978-90-481-3795-4_10openalex-snapshot
Plastid Evolution and the Nuclear Genomic “Footprint” of Red and Green Algal Endosymbionts
inferred← citeshttps://doi.org/10.1007/978-90-481-3795-4_9openalex-snapshot
Coordination of Nuclear and Plastid Gene Expression in Red Algae and Green Plants
inferred← citeshttps://doi.org/10.1007/978-90-481-9449-0_3openalex-snapshot
Problems and Progress in Understanding the Origins of Mitochondria and Plastids
inferred← citeshttps://doi.org/10.1007/978-90-481-9449-0_8openalex-snapshot
Cnidarian–Dinoflagellate Symbiosis-Mediated Adaptation to Environmental Perturbations
inferred← citeshttps://doi.org/10.1007/978-94-007-2445-7_13openalex-snapshot
Varieties of Living Things: Life at the Intersection of Lineage and Metabolism
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_1openalex-snapshot
Origins of Mitochondria and Plastids
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_5openalex-snapshot
Plastid Genomes of Seed Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_9openalex-snapshot
Promiscuous Organellar DNA
inferred← citeshttps://doi.org/10.1007/978-94-007-5724-0_11openalex-snapshot
Development-Dependent Changes in the Amount and Structural Organization of Plastid DNA
inferred← citeshttps://doi.org/10.1007/978-94-007-5724-0_12openalex-snapshot
The Ins and Outs of Chloroplast Protein Transport
inferred← citeshttps://doi.org/10.1007/978-94-007-5724-0_22openalex-snapshot
Plastid Signaling During the Plant Life Cycle
inferred← citeshttps://doi.org/10.1007/978-94-007-5724-0_4openalex-snapshot
The Biogenesis of the Thylakoid Membrane: Photosystem II, a Case Study
inferred← citeshttps://doi.org/10.1007/978-94-017-9118-2_12openalex-snapshot
Horizontal Gene Transfer in Microbial Ecosystems
inferred← citeshttps://doi.org/10.1007/978-94-017-9484-8_7openalex-snapshot
An Evolutionary Perspective on the Plant Hormone Ethylene
inferred← citeshttps://doi.org/10.1007/978-981-10-8372-3_4openalex-snapshot
Reprogramming of Cells by Lactic Acid Bacteria
inferred← citeshttps://doi.org/10.1007/978-981-15-5228-1_3openalex-snapshot
The Multifaceted Connections Between Photosynthesis and Respiratory Metabolism
inferred← citeshttps://doi.org/10.1007/978-981-16-6974-3_12openalex-snapshot
Genetics of Plant Organelles: Plastid and Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1007/978-981-97-3169-5_15openalex-snapshot
Chloroplast Genomics and Their Uses in Crop Improvement
inferred← citeshttps://doi.org/10.1007/s00018-005-4539-zopenalex-snapshot
Lateral gene transfer in eukaryotes
inferred← citeshttps://doi.org/10.1007/s00018-010-0523-3openalex-snapshot
Function of chloroplast RNA-binding proteins
inferred← citeshttps://doi.org/10.1007/s00018-013-1424-zopenalex-snapshot
A metabolic scenario for the evolutionary origin of peroxisomes from the endomembranous system
inferred← citeshttps://doi.org/10.1007/s00018-013-1437-7openalex-snapshot
Evolution and biology of supernumerary B chromosomes
inferred← citeshttps://doi.org/10.1007/s00122-005-0107-zopenalex-snapshot
Characteristics of the tomato nuclear genome as determined by sequencing undermethylated EcoRI digested fragments
inferred← citeshttps://doi.org/10.1007/s00203-006-0200-yopenalex-snapshot
Biochemical characterization of isocitrate dehydrogenase from Methylococcus capsulatus reveals a unique NAD+-dependent homotetrameric enzyme
inferred← citeshttps://doi.org/10.1007/s00203-026-05044-9openalex-snapshot
Comparative mitochondrial genomics of Ophiocordycipitaceae fungi reveals AT bias and site-specific positive selection in the nad4 gene
inferred← citeshttps://doi.org/10.1007/s00239-005-0200-6openalex-snapshot
The Discriminatory Transfer Routes of tRNA Genes Among Organellar and Nuclear Genomes in Flowering Plants: A Genome-Wide Investigation of indica Rice
inferred← citeshttps://doi.org/10.1007/s00239-005-0254-5openalex-snapshot
Sequence of the Tomato Chloroplast DNA and Evolutionary Comparison of Solanaceous Plastid Genomes
inferred← citeshttps://doi.org/10.1007/s00239-009-9277-7openalex-snapshot
The Conflict Between Horizontal Gene Transfer and the Safeguard of Identity: Origin of Meiotic Sexuality
inferred← citeshttps://doi.org/10.1007/s00239-016-9768-2openalex-snapshot
Quest for Ancestors of Eukaryal Cells Based on Phylogenetic Analyses of Aminoacyl-tRNA Synthetases
inferred← citeshttps://doi.org/10.1007/s00253-018-8831-xopenalex-snapshot
Two or three domains: a new view of tree of life in the genomics era
inferred← citeshttps://doi.org/10.1007/s00284-018-1482-4openalex-snapshot
Cross-Reactivity of Prokaryotic 16S rDNA-Specific Primers to Eukaryotic DNA: Mistaken Microbial Community Profiling in Environmental Samples
inferred← citeshttps://doi.org/10.1007/s00294-004-0522-8openalex-snapshot
The mitochondrial DNA of land plants: peculiarities in phylogenetic perspective
inferred← citeshttps://doi.org/10.1007/s00294-006-0082-1openalex-snapshot
Heteroplasmy as a common state of mitochondrial genetic information in plants and animals
inferred← citeshttps://doi.org/10.1007/s00294-006-0088-8openalex-snapshot
Mitochondria, hydrogenosomes and mitosomes: products of evolutionary tinkering!
inferred← citeshttps://doi.org/10.1007/s00294-006-0118-6openalex-snapshot
DNA markers define plastid haplotypes in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00294-011-0342-6openalex-snapshot
Distinguishing authentic mitochondrial and plastid DNAs from similar DNA sequences in the nucleus using the polymerase chain reaction
inferred← citeshttps://doi.org/10.1007/s00299-023-03020-xopenalex-snapshot
Plastid engineering using episomal DNA
inferred← citeshttps://doi.org/10.1007/s00299-023-03039-0openalex-snapshot
Chimeric deletion mutation of rpoC2 underlies the leaf-patterning of Clivia miniata var. variegata
inferred← citeshttps://doi.org/10.1007/s00299-023-03102-wopenalex-snapshot
Remarkable mitochondrial genome heterogeneity in Meniocus linifolius (Brassicaceae)
inferred← citeshttps://doi.org/10.1007/s00299-024-03256-1openalex-snapshot
Unraveling the complex evolutionary features of the Cinnamomum camphora mitochondrial genome
inferred← citeshttps://doi.org/10.1007/s00299-024-03326-4openalex-snapshot
Assembly and comparative analysis of the mitochondrial genome in diploid potatoes
inferred← citeshttps://doi.org/10.1007/s00425-012-1752-5openalex-snapshot
How to build functional thylakoid membranes: from plastid transcription to protein complex assembly
inferred← citeshttps://doi.org/10.1007/s00425-012-1788-6openalex-snapshot
What remains after 2 months of starvation? Analysis of sequestered algae in a photosynthetic slug, Plakobranchus ocellatus (Sacoglossa, Opisthobranchia), by barcoding
inferred← citeshttps://doi.org/10.1007/s00425-012-1802-zopenalex-snapshot
The amount and integrity of mtDNA in maize decline with development
inferred← citeshttps://doi.org/10.1007/s00425-012-1819-3openalex-snapshot
Proteomic analysis of the Cyanophora paradoxa muroplast provides clues on early events in plastid endosymbiosis
inferred← citeshttps://doi.org/10.1007/s00425-018-2924-8openalex-snapshot
PAP genes are tissue- and cell-specific markers of chloroplast development
inferred← citeshttps://doi.org/10.1007/s00425-023-04245-6openalex-snapshot
Multiple configurations of the plastid and mitochondrial genomes of Caragana spinosa
inferred← citeshttps://doi.org/10.1007/s00425-025-04778-yopenalex-snapshot
Mutation in maize chloroplastic polypeptide chain release factor (ZmcpRF1) affects chloroplast development and leaf color
inferred← citeshttps://doi.org/10.1007/s00425-025-04860-5openalex-snapshot
Complete mitochondrial genome assembly and structural feature analysis of Thinopyrum elongatum (Poaceae)
inferred← citeshttps://doi.org/10.1007/s00435-012-0184-xopenalex-snapshot
Phagocytosis of algal chloroplasts by digestive gland cells in the photosynthesis-capable slug Elysia timida (Mollusca, Opisthobranchia, Sacoglossa)
inferred← citeshttps://doi.org/10.1007/s00438-004-1102-9openalex-snapshot
Fate of mitochondrially located S19 ribosomal protein genes after transfer of a functional copy to the nucleus in cereals
inferred← citeshttps://doi.org/10.1007/s00438-005-0075-7openalex-snapshot
Constancy of organellar genome copy numbers during leaf development and senescence in higher plants
inferred← citeshttps://doi.org/10.1007/s00438-013-0747-7openalex-snapshot
Organelle DNA accumulation in the recently evolved papaya sex chromosomes
inferred← citeshttps://doi.org/10.1007/s00439-020-02119-5openalex-snapshot
Mitonuclear genomics and aging
inferred← citeshttps://doi.org/10.1007/s00606-007-0608-0openalex-snapshot
An update on chloroplast genomes
inferred← citeshttps://doi.org/10.1007/s00606-013-0887-6openalex-snapshot
Comparative structure of the pollen in species of Passiflora: insights from the pollen wall and cytoplasm contents
inferred← citeshttps://doi.org/10.1007/s00709-017-1098-8openalex-snapshot
Review: origin of complex algae by secondary endosymbiosis: a journey through time
inferred← citeshttps://doi.org/10.1007/s10126-009-9197-yopenalex-snapshot
Characterization and Localization of a Hybrid Non-ribosomal Peptide Synthetase and Polyketide Synthase Gene from the Toxic Dinoflagellate Karenia brevis
inferred← citeshttps://doi.org/10.1007/s10142-011-0237-0openalex-snapshot
Recent insertion of a 52-kb mitochondrial DNA segment in the wheat lineage
inferred← citeshttps://doi.org/10.1007/s10142-013-0345-0openalex-snapshot
Horizontal gene transfer in plants
inferred← citeshttps://doi.org/10.1007/s10142-014-0422-zopenalex-snapshot
Plastid DNA insertions in plant nuclear genomes: the sites, abundance and ages, and a predicted promoter analysis
inferred← citeshttps://doi.org/10.1007/s10142-024-01511-yopenalex-snapshot
Unraveling the organellar genomic landscape of the therapeutic and entheogenic plant Mimosa tenuiflora: insights into genetic, structural, and evolutionary dynamics
inferred← citeshttps://doi.org/10.1007/s10265-016-0804-5openalex-snapshot
Plastid genome sequences of Gymnochlora stellata, Lotharella vacuolata, and Partenskyella glossopodia reveal remarkable structural conservation among chlorarachniophyte species
inferred← citeshttps://doi.org/10.1007/s10265-024-01547-yopenalex-snapshot
Plastome structure, phylogeny and evolution of plastid genes in Reevesia (Helicteroideae, Malvaceae)
inferred← citeshttps://doi.org/10.1007/s10509-006-9239-0openalex-snapshot
Plant Seeds as Model Vectors for the Transfer of Life Through Space
inferred← citeshttps://doi.org/10.1007/s10535-017-0759-yopenalex-snapshot
The complete chloroplast genome sequence of Pseudoroegneria libanotica, genomic features, and phylogenetic relationship with Triticeae species
inferred← citeshttps://doi.org/10.1007/s10709-005-5701-0openalex-snapshot
Accumulation of chloroplast DNA sequences on the Y chromosome of Silene latifolia
inferred← citeshttps://doi.org/10.1007/s10722-013-0018-9openalex-snapshot
Cytoplasmic diversity of the cotton genus as revealed by chloroplast microsatellite markers
inferred← citeshttps://doi.org/10.1007/s10722-026-02766-zopenalex-snapshot
Deciphering the chromosomal mitochondrial genome of Limnanthes douglasii
inferred← citeshttps://doi.org/10.1007/s10722-026-02855-zopenalex-snapshot
First plastome assembly of rice cytoplasmic male sterility (CMS) A/B lines reveals wild maternal origin
inferred← citeshttps://doi.org/10.1007/s10725-025-01282-xopenalex-snapshot
Mutations in the plant-conserved uL1m mitochondrial ribosomal protein significantly affect development, growth and abiotic stress tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11032-016-0538-zopenalex-snapshot
Toward the elucidation of cytoplasmic diversity in North American grape breeding programs
inferred← citeshttps://doi.org/10.1007/s11033-026-11737-7openalex-snapshot
Comparative analysis of mitochondrial genomes of Iris lactea reveals gene transfer and RNA-editing events
inferred← citeshttps://doi.org/10.1007/s11103-007-9171-xopenalex-snapshot
Protein targeting into complex diatom plastids: functional characterisation of a specific targeting motif
inferred← citeshttps://doi.org/10.1007/s11103-011-9762-4openalex-snapshot
The evolution of the plastid chromosome in land plants: gene content, gene order, gene function
inferred← citeshttps://doi.org/10.1007/s11103-011-9764-2openalex-snapshot
Introducing an RNA editing requirement into a plastid-localised transgene reduces but does not eliminate functional gene transfer to the nucleus
inferred← citeshttps://doi.org/10.1007/s11103-012-9874-5openalex-snapshot
Voltage-dependent-anion-channels (VDACs) in Arabidopsis have a dual localization in the cell but show a distinct role in mitochondria
inferred← citeshttps://doi.org/10.1007/s11103-019-00872-4openalex-snapshot
Structure, evolution and diverse physiological roles of SWEET sugar transporters in plants
inferred← citeshttps://doi.org/10.1007/s11103-022-01266-9openalex-snapshot
Cytonuclear coevolution in a holoparasitic plant with highly disparate organellar genomes
inferred← citeshttps://doi.org/10.1007/s11120-008-9333-yopenalex-snapshot
Plastocyanin–ferredoxin oxidoreduction and endosymbiotic gene transfer
inferred← citeshttps://doi.org/10.1007/s11120-010-9576-2openalex-snapshot
Structural and functional diversification of the light-harvesting complexes in photosynthetic eukaryotes
inferred← citeshttps://doi.org/10.1007/s11120-013-9811-8openalex-snapshot
The circadian regulation of photosynthesis
inferred← citeshttps://doi.org/10.1007/s11120-015-0161-6openalex-snapshot
Dysfunctional chloroplasts up-regulate the expression of mitochondrial genes in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1007/s11229-021-03271-9openalex-snapshot
From idealizations to social practices in science: the case of phylogenetic trees
inferred← citeshttps://doi.org/10.1007/s11240-013-0387-yopenalex-snapshot
Chloroplast expression of an HIV envelop-derived multiepitope protein: towards a multivalent plant-based vaccine
inferred← citeshttps://doi.org/10.1007/s11274-018-2567-8openalex-snapshot
Manipulation of the microalgal chloroplast by genetic engineering for biotechnological utilization as a green biofactory
inferred← citeshttps://doi.org/10.1007/s11295-022-01574-7openalex-snapshot
Chloroplast genome assembly and phylogenetic analysis of Pterocarpus dalbergioides Roxb., an endemic timber species
inferred← citeshttps://doi.org/10.1007/s11427-009-0108-2openalex-snapshot
Maize ZmFDR3 localized in chloroplasts is involved in iron transport
inferred← citeshttps://doi.org/10.1007/s11430-018-9326-1openalex-snapshot
Archaea, the tree of life, and cellular evolution in eukaryotes
inferred← citeshttps://doi.org/10.1007/s11434-007-0375-xopenalex-snapshot
Transfer of a eubacteria-type cell division site-determining factor CrMinD gene to the nucleus from the chloroplast genome in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1007/s11515-011-1139-1openalex-snapshot
Evolution of the chloroplast division machinery
inferred← citeshttps://doi.org/10.1007/s11676-017-0531-3openalex-snapshot
Analysis and characterization of the Salix suchowensis chloroplast genome
inferred← citeshttps://doi.org/10.1007/s11738-020-03089-xopenalex-snapshot
The chloroplast genome: a review
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