On the public citation graph

Horizontal Transfer of Entire Genomes via Mitochondrial Fusion in the Angiosperm Amborella

0 signed · 551 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9780470015902.a0025142openalex-snapshot

Mitochondrial Genome Evolution

inferredcites →https://doi.org/10.1002/tax.592019openalex-snapshot

A revised classification of Santalales

inferredcites →https://doi.org/10.1007/978-3-7091-1130-7_9openalex-snapshot

Plant Mitochondrial Genome Diversity: The Genomics Revolution

inferredcites →https://doi.org/10.1007/bf00029863openalex-snapshot

Rps3 and rpl16 genes do not overlap in Oenothera mitochondria: GTG as a potential translation initiation codon in plant mitochondria?

inferredcites →https://doi.org/10.1007/bf02143500openalex-snapshot

Plant mitochondrial DNA evolved rapidly in structure, but slowly in sequence

inferredcites →https://doi.org/10.1007/bf02669847openalex-snapshot

An improved method for the isolation of total RNA from spurce tissues

inferredcites →https://doi.org/10.1007/s00239-004-2606-yopenalex-snapshot

Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron

inferredcites →https://doi.org/10.1007/s00239-004-5951-yopenalex-snapshot

Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron

inferredcites →https://doi.org/10.1007/s00299-010-0897-6openalex-snapshot

Fusion of mitochondria in tobacco suspension cultured cells is dependent on the cellular ATP level but not on actin polymerization

inferredcites →https://doi.org/10.1007/s00438-002-0767-1openalex-snapshot

The complete sequence of the rice (Oryza sativa L.) mitochondrial genome: frequent DNA sequence acquisition and loss during the evolution of flowering plants

inferredcites →https://doi.org/10.1007/s00438-006-0139-3openalex-snapshot

Patterns of partial RNA editing in mitochondrial genes of Beta vulgaris

inferredcites →https://doi.org/10.1007/s13199-011-0129-zopenalex-snapshot

Origin of eukaryotic cells: 40 years on

inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot

Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate

inferredcites →https://doi.org/10.1016/0092-8674(81)90187-2openalex-snapshot

The mitochondrial genome is large and variable in a family of plants (Cucurbitaceae)

inferredcites →https://doi.org/10.1016/b978-0-12-394279-1.00003-xopenalex-snapshot

The Role of Horizontal Transfer in Shaping the Plant Mitochondrial Genome

inferredcites →https://doi.org/10.1016/j.bbamcr.2006.03.007openalex-snapshot

Structure, function and evolution of the mitochondrial division apparatus

inferredcites →https://doi.org/10.1016/j.cub.2012.01.054openalex-snapshot

Adaptive Evolution of C4 Photosynthesis through Recurrent Lateral Gene Transfer

inferredcites →https://doi.org/10.1016/j.ympev.2008.09.009openalex-snapshot

Relative rates of synonymous substitutions in the mitochondrial, chloroplast and nuclear genomes of seed plants

inferredcites →https://doi.org/10.1038/nature01743openalex-snapshot

Widespread horizontal transfer of mitochondrial genes in flowering plants

inferredcites →https://doi.org/10.1038/ng.654openalex-snapshot

The genome of the domesticated apple (Malus × domestica Borkh.)

inferredcites →https://doi.org/10.1038/nrm3013openalex-snapshot

Mitochondrial fusion and fission in cell life and death

inferredcites →https://doi.org/10.1038/sj.hdy.6800659openalex-snapshot

Molecular evolution: Lateral gene transfer and other possibilities

inferredcites →https://doi.org/10.1073/pnas.0401077101openalex-snapshot

Frequent fusion and fission of plant mitochondria with unequal nucleoid distribution

inferredcites →https://doi.org/10.1073/pnas.0408302101openalex-snapshot

Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants

inferredcites →https://doi.org/10.1073/pnas.0408336102openalex-snapshot

Massive horizontal transfer of mitochondrial genes from diverse land plant donors to the basal angiosperm Amborella

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.0507287103openalex-snapshot

FZL, an FZO-like protein in plants, is a determinant of thylakoid and chloroplast morphology

inferredcites →https://doi.org/10.1073/pnas.1001225107openalex-snapshot

An uncorrelated relaxed-clock analysis suggests an earlier origin for flowering plants

inferredcites →https://doi.org/10.1073/pnas.1221376110openalex-snapshot

Is junk DNA bunk? A critique of ENCODE

inferredcites →https://doi.org/10.1073/pnas.1833775100openalex-snapshot

Horizontal gene transfer from flowering plants to Gnetum

inferredcites →https://doi.org/10.1073/pnas.69.7.1830openalex-snapshot

Physicochemical Characterization of Mitochondrial DNA from Pea Leaves

inferredcites →https://doi.org/10.1073/pnas.95.24.14244openalex-snapshot

Explosive invasion of plant mitochondria by a group I intron

inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot

RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models

inferredcites →https://doi.org/10.1093/gbe/evr042openalex-snapshot

Structural and Content Diversity of Mitochondrial Genome in Beet: A Comparative Genomic Analysis

inferredcites →https://doi.org/10.1093/molbev/msg159openalex-snapshot

Analysis of the Amborella trichopoda Chloroplast Genome Sequence Suggests That Amborella Is Not a Basal Angiosperm

inferredcites →https://doi.org/10.1093/molbev/msm226openalex-snapshot

Modeling Sites of RNA Editing as a Fifth Nucleotide State Reveals Progressive Loss of Edited Sites from Angiosperm Mitochondria

inferredcites →https://doi.org/10.1093/molbev/msn129openalex-snapshot

Frequent, Phylogenetically Local Horizontal Transfer of the cox1 Group I Intron in Flowering Plant Mitochondria

inferredcites →https://doi.org/10.1093/molbev/msn226openalex-snapshot

Mitochondrial DNA of Vitis vinifera and the Issue of Rampant Horizontal Gene Transfer

inferredcites →https://doi.org/10.1093/molbev/msq029openalex-snapshot

Insights into the Evolution of Mitochondrial Genome Size from Complete Sequences of Citrullus lanatus and Cucurbita pepo (Cucurbitaceae)

inferredcites →https://doi.org/10.1093/nar/18.13.3689openalex-snapshot

Transfer RNAs of potato (Solanum tuberosum) mitochondria have different genetic origins

inferredcites →https://doi.org/10.1093/nar/gkr517openalex-snapshot

Transfection of plant mitochondria and in organello gene integration

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025768openalex-snapshot

Accelerated evolution of sites undergoing mRNA editing in plant mitochondria and chloroplasts

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026201openalex-snapshot

Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference

inferredcites →https://doi.org/10.1098/rstb.2008.0122openalex-snapshot

New Caledonia: a very old Darwinian island?

inferredcites →https://doi.org/10.1101/gr.9.9.868openalex-snapshot

CAP3: A DNA Sequence Assembly Program

inferredcites →https://doi.org/10.1104/pp.104.044602openalex-snapshot

Sequence and Comparative Analysis of the Maize NB Mitochondrial Genome

inferredcites →https://doi.org/10.1105/tpc.111.087189openalex-snapshot

Origins and Recombination of the Bacterial-Sized Multichromosomal Mitochondrial Genome of Cucumber

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02561.xopenalex-snapshot

Mitochondria as a connected population: ensuring continuity of the mitochondrial genome during plant cell dedifferentiation through massive mitochondrial fusion

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04684.xopenalex-snapshot

A horizontally transferred tRNA Cys gene in the sugar beet mitochondrial genome: evidence that the gene is present in diverse angiosperms and its transcript is aminoacylated

inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05014.xopenalex-snapshot

The mitochondrial genome of Malus domestica and the import‐driven hypothesis of mitochondrial genome expansion in seed plants

inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04340.xopenalex-snapshot

Intraspecific variation in mitochondrial genome sequence, structure, and gene content in Silene vulgaris, an angiosperm with pervasive cytoplasmic male sterility

inferredcites →https://doi.org/10.1111/mec.12554openalex-snapshot

Phylogeography and niche modelling of the relict plant Amborella trichopoda (Amborellaceae) reveal multiple Pleistocene refugia in New Caledonia

inferredcites →https://doi.org/10.1126/science.1100671openalex-snapshot

Host-to-Parasite Gene Transfer in Flowering Plants: Phylogenetic Evidence from Malpighiales

inferredcites →https://doi.org/10.1126/science.1241089openalex-snapshot

The Amborella Genome and the Evolution of Flowering Plants

inferredcites →https://doi.org/10.1186/1471-2148-10-12openalex-snapshot

Erratum to: Phylogenetic analysis of mitochondrial substitution rate variation in the angiosperm tribe Sileneae

inferredcites →https://doi.org/10.1186/1471-2148-5-73openalex-snapshot

Multiple major increases and decreases in mitochondrial substitution rates in the plant family Geraniaceae

inferredcites →https://doi.org/10.1186/1471-2148-6-55openalex-snapshot

Pervasive survival of expressed mitochondrial rps14 pseudogenes in grasses and their relatives for 80 million years following three functional transfers to the nucleus.

inferredcites →https://doi.org/10.1186/1471-2148-7-135openalex-snapshot

Extensive variation in synonymous substitution rates in mitochondrial genes of seed plants

inferredcites →https://doi.org/10.1186/1471-2148-7-248openalex-snapshot

Mitochondrial DNA suggests at least 11 origins of parasitism in angiosperms and reveals genomic chimerism in parasitic plants

inferredcites →https://doi.org/10.1186/1471-2148-9-260openalex-snapshot

Phylogenetic analysis of mitochondrial substitution rate variation in the angiosperm tribe Sileneae

inferredcites →https://doi.org/10.1186/1471-2164-12-424openalex-snapshot

Determination of the melon chloroplast and mitochondrial genome sequences reveals that the largest reported mitochondrial genome in plants contains a significant amount of DNA having a nuclear origin

inferredcites →https://doi.org/10.1186/1471-2229-12-61openalex-snapshot

De novo assembly of the carrot mitochondrial genome using next generation sequencing of whole genomic DNA provides first evidence of DNA transfer into an angiosperm plastid genome

inferredcites →https://doi.org/10.1186/1741-7007-11-29openalex-snapshot

The “fossilized” mitochondrial genome of Liriodendron tulipifera: ancestral gene content and order, ancestral editing sites, and extraordinarily low mutation rate

inferredcites →https://doi.org/10.1186/1741-7007-4-31openalex-snapshot

An exceptional horizontal gene transfer in plastids: gene replacement by a distant bacterial paralog and evidence that haptophyte and cryptophyte plastids are sisters

inferredcites →https://doi.org/10.1186/1741-7007-8-150openalex-snapshot

Horizontal acquisition of multiple mitochondrial genes from a parasitic plant followed by gene conversion with host mitochondrial genes

inferredcites →https://doi.org/10.1186/gb-2011-12-5-r48openalex-snapshot

A physical map for the Amborella trichopodagenome sheds light on the evolution of angiosperm genome structure

inferredcites →https://doi.org/10.1371/journal.pbio.1001241openalex-snapshot

Rapid Evolution of Enormous, Multichromosomal Genomes in Flowering Plant Mitochondria with Exceptionally High Mutation Rates

inferredcites →https://doi.org/10.1371/journal.pgen.1003265openalex-snapshot

Massive Mitochondrial Gene Transfer in a Parasitic Flowering Plant Clade

inferredcites →https://doi.org/10.1371/journal.pone.0014048openalex-snapshot

The Agaricus bisporus cox1 Gene: The Longest Mitochondrial Gene and the Largest Reservoir of Mitochondrial Group I Introns

inferredcites →https://doi.org/10.1371/journal.pone.0023624openalex-snapshot

The GC-Rich Mitochondrial and Plastid Genomes of the Green Alga Coccomyxa Give Insight into the Evolution of Organelle DNA Nucleotide Landscape

inferredcites →https://doi.org/10.1371/journal.pone.0025836openalex-snapshot

The Mitochondrial Genomes of the Early Land Plants Treubia lacunosa and Anomodon rugelii: Dynamic and Conservative Evolution

inferredcites →https://doi.org/10.1371/journal.pone.0030531openalex-snapshot

The Complete Chloroplast and Mitochondrial Genome Sequences of Boea hygrometrica: Insights into the Evolution of Plant Organellar Genomes

inferredcites →https://doi.org/10.1371/journal.pone.0037164openalex-snapshot

A Complete Sequence and Transcriptomic Analyses of Date Palm (Phoenix dactylifera L.) Mitochondrial Genome

inferredcites →https://doi.org/10.1371/journal.pone.0049096openalex-snapshot

Frequent Gain and Loss of Introns in Fungal Cytochrome b Genes

inferredcites →https://doi.org/10.1371/journal.pone.0069476openalex-snapshot

The Complete Mitochondrial Genome of Gossypium hirsutum and Evolutionary Analysis of Higher Plant Mitochondrial Genomes

inferredcites →https://doi.org/10.1534/genetics.107.073312openalex-snapshot

Comparisons Among Two Fertile and Three Male-Sterile Mitochondrial Genomes of Maize

inferredcites →https://doi.org/10.3732/ajb.1000404openalex-snapshot

Angiosperm phylogeny: 17 genes, 640 taxa

inferredcites →https://doi.org/10.5252/a2012n2a1openalex-snapshot

Le référentiel taxonomique Florical et les caractéristiques de la flore vasculaire indigène de la Nouvelle-Calédonie

What points at this work

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

inferred← citeshttps://doi.org/10.1002/tax.13123zenodo-depositor-declared

A tough nutlet to crack: Resolving the phylogeny of Thesium (Thesiaceae), the largest genus in Santalales

inferred← citeshttps://doi.org/10.1002/1873-3468.14298openalex-snapshot

Mitochondria, energy, and metabolism in neuronal health and disease

inferred← citeshttps://doi.org/10.1002/9780470015902.a0026814openalex-snapshot

Genome Evolution in Plants

inferred← citeshttps://doi.org/10.1002/9781118906583.ch2openalex-snapshot

MITOCHONDRIAL DNA REPAIR AND GENOME EVOLUTION

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0544openalex-snapshot

Mitochondrial DNA Repair and Genome Evolution

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0689openalex-snapshot

A mborella– Bearing Witness to the Past?

inferred← citeshttps://doi.org/10.1002/ajb2.1016openalex-snapshot

Quartet Sampling distinguishes lack of support from conflicting support in the green plant tree of life

inferred← citeshttps://doi.org/10.1002/ajb2.1066openalex-snapshot

Organellar phylogenomics inform systematics in the green algal family Hydrodictyaceae (Chlorophyceae) and provide clues to the complex evolutionary history of plastid genomes in the green algal tree of life

inferred← citeshttps://doi.org/10.1002/biuz.201490027openalex-snapshot

Amborella trichopoda – das Schnabeltier unter den Pflanzen

inferred← citeshttps://doi.org/10.1002/ece3.7133openalex-snapshot

Phylogeny and evolution of chloroplast tRNAs in Adoxaceae

inferred← citeshttps://doi.org/10.1002/ece3.73758openalex-snapshot

Complex History of Organellar Introgression in Nothofagus Trees: Chloroplast and Mitochondrial Capture Facilitated by Natural Selection

inferred← citeshttps://doi.org/10.1002/iub.1894openalex-snapshot

Massive mitochondrial DNA content in diplonemid and kinetoplastid protists

inferred← citeshttps://doi.org/10.1007/7397_2016_20openalex-snapshot

Structural Genomics of Angiosperm Trees: Genome Duplications, Ploidy, and Repeat Sequences

inferred← citeshttps://doi.org/10.1007/7397_2016_26openalex-snapshot

Evolutionary Histories of Gene Families in Angiosperm Trees

inferred← citeshttps://doi.org/10.1007/978-1-0716-0997-2_6openalex-snapshot

Utility of the Mitochondrial Genome in Plant Taxonomic Studies

inferred← citeshttps://doi.org/10.1007/978-3-030-16057-9_6openalex-snapshot

Eukaryotes

inferred← citeshttps://doi.org/10.1007/978-3-319-22461-9_6openalex-snapshot

What Is the Meaning of Extreme Phylogenetic Diversity? The Case of Phylogenetic Relict Species

inferred← citeshttps://doi.org/10.1007/978-3-319-54064-1_2openalex-snapshot

Organelle Genomes and Endosymbionts

inferred← citeshttps://doi.org/10.1007/978-3-319-98836-8_11openalex-snapshot

Evolution of Prokaryote-Animal Endosymbiosis from a Genomics Perspective

inferred← citeshttps://doi.org/10.1007/s00122-018-3218-zopenalex-snapshot

Identification of a gene responsible for cytoplasmic male-sterility in onions (Allium cepa L.) using comparative analysis of mitochondrial genome sequences of two recently diverged cytoplasms

inferred← citeshttps://doi.org/10.1007/s00239-019-09916-1openalex-snapshot

Evolutionary Dynamics of Transferred Sequences Between Organellar Genomes in Cucurbita

inferred← citeshttps://doi.org/10.1007/s00239-020-09937-1openalex-snapshot

Horizontal Gene Transfer has Impacted cox1 Gene Evolution in Cassytha filiformis

inferred← citeshttps://doi.org/10.1007/s00239-020-09980-yopenalex-snapshot

Plant Mitochondria are a Riddle Wrapped in a Mystery Inside an Enigma

inferred← citeshttps://doi.org/10.1007/s00294-014-0448-8openalex-snapshot

The intraspecific variability of mitochondrial genes of Agaricus bisporus reveals an extensive group I intron mobility combined with low nucleotide substitution rates

inferred← citeshttps://doi.org/10.1007/s00294-015-0512-zopenalex-snapshot

The evolutionary conservation of rps3 introns and rps19-rps3-rpl16 gene cluster in Adiantum capillus-veneris mitochondria

inferred← citeshttps://doi.org/10.1007/s00294-016-0595-1openalex-snapshot

Completion of the mitochondrial genome sequence of onion (Allium cepa L.) containing the CMS-S male-sterile cytoplasm and identification of an independent event of the ccmF N gene split

inferred← citeshttps://doi.org/10.1007/s00294-016-0652-9openalex-snapshot

Hoarding and horizontal transfer led to an expanded gene and intron repertoire in the plastid genome of the diatom, Toxarium undulatum (Bacillariophyta)

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/s00425-024-04386-2openalex-snapshot

Assembly and comparative analysis of the first complete mitochondrial genome of Setaria italica

inferred← citeshttps://doi.org/10.1007/s00425-024-04449-4openalex-snapshot

Piece and parcel of gymnosperm organellar genomes

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/s00497-019-00371-yopenalex-snapshot

Current understanding of male sterility systems in vegetable Brassicas and their exploitation in hybrid breeding

inferred← citeshttps://doi.org/10.1007/s10142-025-01548-7openalex-snapshot

Evolution of phenylalanine ammonia-lyase protein family from algae to angiosperm

inferred← citeshttps://doi.org/10.1007/s10142-025-01596-zopenalex-snapshot

Mitochondrial genome evolution in the orchid subfamily Cypripedioideae (Orchidaceae)

inferred← citeshttps://doi.org/10.1007/s10265-015-0744-5openalex-snapshot

In situ observations of the basal angiosperm Amborella trichopoda reveal a long fruiting cycle overlapping two annual flowering periods

inferred← citeshttps://doi.org/10.1007/s10709-025-00241-8openalex-snapshot

Assembly and characterization of the first mitochondrial genome of Phyllanthaceae: a case study of the ornamental aquatic plant Phyllanthus fluitans

inferred← citeshttps://doi.org/10.1007/s11103-018-0734-9openalex-snapshot

Towards a comprehensive picture of C-to-U RNA editing sites in angiosperm mitochondria

inferred← citeshttps://doi.org/10.1007/s11103-019-00869-zopenalex-snapshot

Elucidating genomic patterns and recombination events in plant cybrid mitochondria

inferred← citeshttps://doi.org/10.1007/s11103-019-00940-9openalex-snapshot

The dual-targeted RNA editing factor AEF1 is universally conserved among angiosperms and reveals only minor adaptations upon loss of its chloroplast or its mitochondrial target

inferred← citeshttps://doi.org/10.1007/s11103-020-01014-xopenalex-snapshot

Multichromosomal structure and foreign tracts in the Ombrophytum subterraneum (Balanophoraceae) mitochondrial genome

inferred← citeshttps://doi.org/10.1007/s11295-025-01707-8openalex-snapshot

First complete mitogenome assembly of Castanea sativa: structure, comparative genomics, and phylogeny

inferred← citeshttps://doi.org/10.1007/s11427-018-9450-1openalex-snapshot

Complete loss of RNA editing from the plastid genome and most highly expressed mitochondrial genes of Welwitschia mirabilis

inferred← citeshttps://doi.org/10.1007/s11676-022-01511-3openalex-snapshot

Assembly and analysis of the Populus deltoides mitochondrial genome: the first report of a multicircular mitochondrial conformation for the genus Populus

inferred← citeshttps://doi.org/10.1007/s11676-025-01869-0openalex-snapshot

Assembly and phylogenetic analysis of the complete mitochondrial genome of a widely planted hybrid eucalypt (Eucalyptus urophylla × E. grandis)

inferred← citeshttps://doi.org/10.1007/s11816-023-00841-wopenalex-snapshot

Loss of mitogenome-encoded respiratory genes complemented by nuclear transcripts in halophyte Pandanus odorifer (Forssk.) Kuntze

inferred← citeshttps://doi.org/10.1007/s12038-015-9514-8openalex-snapshot

Evolutionary change and phylogenetic relationships in light of horizontal gene transfer

inferred← citeshttps://doi.org/10.1016/b978-0-12-387731-4.00024-4openalex-snapshot

References

inferred← citeshttps://doi.org/10.1016/b978-0-12-811940-2.00016-2openalex-snapshot

Symbiosis: Why Was the Transition from Microbial Prokaryotes to Eukaryotic Organisms a Cosmic Gigayear Event?

inferred← citeshttps://doi.org/10.1016/b978-0-12-812553-3.00003-5openalex-snapshot

Building the Tree of Life

inferred← citeshttps://doi.org/10.1016/bs.abr.2016.01.002openalex-snapshot

Coevolution of Organelle RNA Editing and Nuclear Specificity Factors in Early Land Plants

inferred← citeshttps://doi.org/10.1016/j.aquabot.2014.05.013openalex-snapshot

Mixed evolutionary traits of Tolypella (section Rothia, Charales) compared with Chara and Nitella shown by ultrastructure of vegetative internodal cells

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2020.107671openalex-snapshot

Adaptive innovation of green plants by horizontal gene transfer

inferred← citeshttps://doi.org/10.1016/j.ceb.2016.05.008openalex-snapshot

From microbiology to cell biology: when an intracellular bacterium becomes part of its host cell

inferred← citeshttps://doi.org/10.1016/j.cell.2014.07.047openalex-snapshot

Sympatric Speciation in a Bacterial Endosymbiont Results in Two Genomes with the Functionality of One

inferred← citeshttps://doi.org/10.1016/j.compbiomed.2021.104682openalex-snapshot

Deepred-Mt: Deep representation learning for predicting C-to-U RNA editing in plant mitochondria

inferred← citeshttps://doi.org/10.1016/j.cpb.2014.08.002openalex-snapshot

Expression of a transferred nuclear gene in a mitochondrial genome

inferred← citeshttps://doi.org/10.1016/j.cub.2014.04.042openalex-snapshot

Horizontal Gene Transfer: Accidental Inheritance Drives Adaptation

inferred← citeshttps://doi.org/10.1016/j.cub.2014.05.008openalex-snapshot

Evolution: How a Barnacle Came to Parasitise a Shark

inferred← citeshttps://doi.org/10.1016/j.cub.2017.10.008openalex-snapshot

Idiosyncratic Genome Degradation in a Bacterial Endosymbiont of Periodical Cicadas

inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.032openalex-snapshot

The Life of an Insect Endosymbiont from the Cradle to the Grave

inferred← citeshttps://doi.org/10.1016/j.cub.2026.03.011openalex-snapshot

Amborella

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.03.033openalex-snapshot

The role of mitochondria in plant development and stress tolerance

inferred← citeshttps://doi.org/10.1016/j.gde.2023.102053openalex-snapshot

When and why are mitochondria paternally inherited?

inferred← citeshttps://doi.org/10.1016/j.gene.2022.147081openalex-snapshot

Polymeric structure of the Cannabis sativa L. mitochondrial genome identified with an assembly graph model

inferred← citeshttps://doi.org/10.1016/j.gene.2024.148869openalex-snapshot

Analysis of the complete mitochondrial genome of Panax quinquefolius reveals shifts from cis-splicing to trans-splicing of intron cox2i373

inferred← citeshttps://doi.org/10.1016/j.gene.2026.150210openalex-snapshot

The first complete multichromosomal mitogenome of Cunninghamia lanceolata (Chinese fir): assembly, characterization and comparative analysis

inferred← citeshttps://doi.org/10.1016/j.genrep.2026.102600openalex-snapshot

A unified nomenclature system for plant mitochondrial genomes: Resolving structural, coding, and non-coding annotation challenges

inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119382openalex-snapshot

Comprehensive analysis of the mitochondrial genome of Populus tomentosa ‘GM107’ and the dynamic expression of mitochondrial ATP synthase genes

inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121544openalex-snapshot

Comparative organellar genomics of four Jasminum accessions reveals adaptive divergence and phylogenomic conflicts in Oleaceae

inferred← citeshttps://doi.org/10.1016/j.jgg.2025.04.016openalex-snapshot

Near-gapless telomere-to-telomere reference nuclear genome and variable mitochondrial genome of Amborella trichopoda

inferred← citeshttps://doi.org/10.1016/j.jia.2025.02.018openalex-snapshot

Multiple chromosomal configurations and phylogenetic implications in Saccharum mitochondrial genomes

inferred← citeshttps://doi.org/10.1016/j.mito.2014.04.005openalex-snapshot

RNA editing in plant mitochondria —Connecting RNA target sequences and acting proteins

inferred← citeshttps://doi.org/10.1016/j.mito.2019.06.005openalex-snapshot

Do angiosperms with highly divergent mitochondrial genomes have altered mitochondrial function?

inferred← citeshttps://doi.org/10.1016/j.mito.2020.03.007openalex-snapshot

Interchangeable parts: The evolutionarily dynamic tRNA population in plant mitochondria

inferred← citeshttps://doi.org/10.1016/j.mito.2020.03.008openalex-snapshot

Mitochondria in parasitic plants

inferred← citeshttps://doi.org/10.1016/j.pbi.2015.05.008openalex-snapshot

Horizontal gene transfer in parasitic plants

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.01.013openalex-snapshot

Mitochondria of Cedrus atlantica and allied species: A new chapter in the horizontal gene transfer history

inferred← citeshttps://doi.org/10.1016/j.pld.2016.04.002openalex-snapshot

An acyltransferase gene that putatively functions in anthocyanin modification was horizontally transferred from Fabaceae into the genus Cuscuta

inferred← citeshttps://doi.org/10.1016/j.pld.2023.02.004openalex-snapshot

Mitochondrial RNA editing sites affect the phylogenetic reconstruction of gymnosperms

inferred← citeshttps://doi.org/10.1016/j.pld.2023.11.001openalex-snapshot

The first mitogenome of Lauraceae (Cinnamomum chekiangense)

inferred← citeshttps://doi.org/10.1016/j.pld.2025.12.013openalex-snapshot

Exploring the evolutionary landscape of mitochondrial genomes in the sunflower family (Asteraceae)

inferred← citeshttps://doi.org/10.1016/j.plgene.2026.100586openalex-snapshot

Mitochondrial genome characterization and comparative study in shallots (Allium cepa L. var. aggregatum)

inferred← citeshttps://doi.org/10.1016/j.scienta.2021.109928openalex-snapshot

Overexpression of JrAMT2 in walnut (Juglans regia L.) rootstock enhances nitrogen level in grafted wild-type walnut scions

inferred← citeshttps://doi.org/10.1016/j.tplants.2015.11.008openalex-snapshot

Rootstocks: Diversity, Domestication, and Impacts on Shoot Phenotypes

inferred← citeshttps://doi.org/10.1016/j.tplants.2023.12.014openalex-snapshot

Plant organellar genomes: much done, much more to do

inferred← citeshttps://doi.org/10.1016/j.tplants.2025.10.002openalex-snapshot

Land plant evolution: from microbial interaction to horizontal gene transfer

inferred← citeshttps://doi.org/10.1016/j.tree.2014.10.002openalex-snapshot

Relict species: a relict concept?

inferred← citeshttps://doi.org/10.1016/j.ygeno.2024.110859openalex-snapshot

Assembly and comparative analysis of the complete mitochondrial genome of white towel gourd (Luffa cylindrica)

inferred← citeshttps://doi.org/10.1016/j.ygeno.2024.110935openalex-snapshot

Structural analysis of the mitochondrial genome of Santalum album reveals a complex branched configuration

inferred← citeshttps://doi.org/10.1016/j.ygeno.2026.111248openalex-snapshot

The first mitochondrial genome in Zingiber: Structural and evolutionary characterization of ginger (Zingiber officinale)

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.04.009openalex-snapshot

Gene tree discordance and coalescent methods support ancient intergeneric hybridisation between Dasymaschalon and Friesodielsia (Annonaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.12.006openalex-snapshot

Genome-scale transfer of mitochondrial DNA from legume hosts to the holoparasite Lophophytum mirabile (Balanophoraceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.012openalex-snapshot

The complete organelle genomes of Physochlaina orientalis: Insights into short sequence repeats across seed plant mitochondrial genomes

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.022openalex-snapshot

Incongruence between gene trees and species trees and phylogenetic signal variation in plastid genes

inferred← citeshttps://doi.org/10.1038/hdy.2014.118openalex-snapshot

Horizontal gene transfer from a flowering plant to the insular pine Pinus canariensis (Chr. Sm. Ex DC in Buch)

inferred← citeshttps://doi.org/10.1038/ismej.2017.144openalex-snapshot

Tremblaya phenacola PPER: an evolutionary beta-gammaproteobacterium collage

inferred← citeshttps://doi.org/10.1038/nature.2013.14426openalex-snapshot

Shrub genome reveals secrets of flower power

inferred← citeshttps://doi.org/10.1038/nature15205openalex-snapshot

Gene transfer in complex cells

inferred← citeshttps://doi.org/10.1038/nrg3657openalex-snapshot

A genome conserved and a genome expanded

inferred← citeshttps://doi.org/10.1038/nrg3962openalex-snapshot

Horizontal gene transfer: building the web of life

inferred← citeshttps://doi.org/10.1038/s41437-018-0153-3openalex-snapshot

Recombination and intraspecific polymorphism for the presence and absence of entire chromosomes in mitochondrial genomes

inferred← citeshttps://doi.org/10.1038/s41467-023-38836-4openalex-snapshot

The genome of Acorus deciphers insights into early monocot evolution

inferred← citeshttps://doi.org/10.1038/s41477-018-0349-9openalex-snapshot

Genome structure and evolution of Antirrhinum majus L

inferred← citeshttps://doi.org/10.1038/s41477-025-01982-2openalex-snapshot

The biology of grafting and its applications in studying information exchange between plants

inferred← citeshttps://doi.org/10.1038/s41598-017-07886-2openalex-snapshot

Horizontal transfer of a ß-1,6-glucanase gene from an ancestral species of fungal endophyte to a cool-season grass host

inferred← citeshttps://doi.org/10.1038/s41598-018-30297-wopenalex-snapshot

Complete sequence of kenaf (Hibiscus cannabinus) mitochondrial genome and comparative analysis with the mitochondrial genomes of other plants

inferred← citeshttps://doi.org/10.1038/s41598-019-41377-wopenalex-snapshot

Evidence of mitochondrial DNA in the chloroplast genome of Convallaria keiskei and its subsequent evolution in the Asparagales

inferred← citeshttps://doi.org/10.1038/s41598-020-76478-4openalex-snapshot

Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer

inferred← citeshttps://doi.org/10.1038/s41598-020-80149-9openalex-snapshot

Comparative analysis of nuclear, chloroplast, and mitochondrial genomes of watermelon and melon provides evidence of gene transfer

inferred← citeshttps://doi.org/10.1038/s41598-024-55150-1openalex-snapshot

Comparative analysis of chloroplast and mitochondrial genomes of sweet potato provides evidence of gene transfer

inferred← citeshttps://doi.org/10.1038/s41598-024-75324-1openalex-snapshot

Assembly and analysis of the complete mitochondrial genome of Carya illinoinensis to provide insights into the conserved sequences of tRNA genes

inferred← citeshttps://doi.org/10.1038/s42003-023-04659-8openalex-snapshot

Rickettsial DNA and a trans-splicing rRNA group I intron in the unorthodox mitogenome of the fern Haplopteris ensiformis

inferred← citeshttps://doi.org/10.1038/s42003-025-07525-xopenalex-snapshot

Genome assembly of Stewartia sinensis reveals origin and evolution of orphan genes in Theaceae

inferred← citeshttps://doi.org/10.1038/s42003-025-08418-9openalex-snapshot

Evolution of mitochondrial RNA editing sites and stop codon-lacking transcripts in angiosperms

inferred← citeshttps://doi.org/10.1038/srep09040openalex-snapshot

The location and translocation of ndh genes of chloroplast origin in the Orchidaceae family

inferred← citeshttps://doi.org/10.1038/srep23744openalex-snapshot

Reconstructing the complex evolutionary history of mobile plasmids in red algal genomes

inferred← citeshttps://doi.org/10.1038/srep30158openalex-snapshot

The mitochondrial genome map of Nelumbo nucifera reveals ancient evolutionary features

inferred← citeshttps://doi.org/10.1038/srep30192openalex-snapshot

Two hAT transposon genes were transferred from Brassicaceae to broomrapes and are actively expressed in some recipients

inferred← citeshttps://doi.org/10.1038/srep43402openalex-snapshot

Foreign Plastid Sequences in Plant Mitochondria are Frequently Acquired Via Mitochondrion-to-Mitochondrion Horizontal Transfer

inferred← citeshttps://doi.org/10.1071/sb19019openalex-snapshot

Advances in legume research in the genomics era

inferred← citeshttps://doi.org/10.1073/pnas.1319929111openalex-snapshot

Horizontal transfer of an adaptive chimeric photoreceptor from bryophytes to ferns

inferred← citeshttps://doi.org/10.1073/pnas.1421386112openalex-snapshot

Genome expansion via lineage splitting and genome reduction in the cicada endosymbiont Hodgkinia

inferred← citeshttps://doi.org/10.1073/pnas.1421391112openalex-snapshot

Maternal transmission, sex ratio distortion, and mitochondria

inferred← citeshttps://doi.org/10.1073/pnas.1421397112openalex-snapshot

The massive mitochondrial genome of the angiosperm Silene noctiflora is evolving by gain or loss of entire chromosomes

inferred← citeshttps://doi.org/10.1073/pnas.1422049112openalex-snapshot

Mitochondrial and plastid genome architecture: Reoccurring themes, but significant differences at the extremes

inferred← citeshttps://doi.org/10.1073/pnas.1504491112openalex-snapshot

Miniaturized mitogenome of the parasitic plant Viscum scurruloideum is extremely divergent and dynamic and has lost all nad genes

inferred← citeshttps://doi.org/10.1073/pnas.1513346112openalex-snapshot

Symbiosis becoming permanent: Survival of the luckiest

inferred← citeshttps://doi.org/10.1073/pnas.1518644113openalex-snapshot

Cell-to-cell movement of mitochondria in plants

inferred← citeshttps://doi.org/10.1073/pnas.1608765113openalex-snapshot

Horizontal gene transfer is more frequent with increased heterotrophy and contributes to parasite adaptation

inferred← citeshttps://doi.org/10.1073/pnas.1613375114openalex-snapshot

Multiple horizontal transfers of nuclear ribosomal genes between phylogenetically distinct grass lineages

inferred← citeshttps://doi.org/10.1073/pnas.1712321115openalex-snapshot

Multiple origins of interdependent endosymbiotic complexes in a genus of cicadas

inferred← citeshttps://doi.org/10.1073/pnas.1810031116openalex-snapshot

Lateral transfers of large DNA fragments spread functional genes among grasses

inferred← citeshttps://doi.org/10.1080/07352689.2017.1327762openalex-snapshot

Plant Mitochondrial Genome Evolution and Cytoplasmic Male Sterility

inferred← citeshttps://doi.org/10.1080/23802359.2019.1591242openalex-snapshot

The complete mitochondrial genome of tulip tree, Liriodendron tulipifera L. (Magnoliaceae): intra-species variations on mitochondrial genome

inferred← citeshttps://doi.org/10.1080/24701394.2017.1334772openalex-snapshot

Diversity of mitochondrial plastid DNAs (MTPTs) in seed plants

inferred← citeshttps://doi.org/10.1086/726005openalex-snapshot

Mitochondrial Genome Sequencing and Analysis of the Invasive Microstegium vimineum: A Resource for Systematics, Invasion History, and Management

inferred← citeshttps://doi.org/10.1093/aob/mcad108openalex-snapshot

Invited Review Beyond parasitic convergence: unravelling the evolution of the organellar genomes in holoparasites

inferred← citeshttps://doi.org/10.1093/aob/mcaf084openalex-snapshot

Mitoplastomic discordance in Brassicaceae phylogenomics confirms the complex evolutionary history of the family

inferred← citeshttps://doi.org/10.1093/botlinnean/boad019openalex-snapshot

The origin and fate of fungal mitochondrial horizontal gene transferred sequences in orchids (Orchidaceae)

inferred← citeshttps://doi.org/10.1093/gbe/evab124openalex-snapshot

Genomic Rearrangements and Sequence Evolution across Brown Algal Organelles

inferred← citeshttps://doi.org/10.1093/gbe/evad155openalex-snapshot

The Mitochondrial Genome of the Holoparasitic PlantThonningia sanguineaProvides Insights into the Evolution of the Multichromosomal Structure

inferred← citeshttps://doi.org/10.1093/gbe/evae184openalex-snapshot

New Insights into the Diversity of Mitochondrial Plastid DNA

inferred← citeshttps://doi.org/10.1093/gbe/evu165openalex-snapshot

Ancient Nuclear Plastid DNA in the Yew Family (Taxaceae)

inferred← citeshttps://doi.org/10.1093/gbe/evu253openalex-snapshot

History of Plastid DNA Insertions Reveals Weak Deletion and AT Mutation Biases in Angiosperm Mitochondrial Genomes

inferred← citeshttps://doi.org/10.1093/gbe/evv244openalex-snapshot

Organellar Genomes of White Spruce (Picea glauca): Assembly and Annotation

inferred← citeshttps://doi.org/10.1093/gbe/evv251openalex-snapshot

The Plastomes of Two Species in the Endoparasite GenusPilostyles(Apodanthaceae) Each Retain Just Five or Six Possibly Functional Genes

inferred← citeshttps://doi.org/10.1093/gbe/evv256openalex-snapshot

Detecting and Characterizing the Highly Divergent Plastid Genome of the Nonphotosynthetic Parasitic PlantHydnora visseri(Hydnoraceae)

inferred← citeshttps://doi.org/10.1093/gbe/evw003openalex-snapshot

Linear Plasmids and the Rate of Sequence Evolution in Plant Mitochondrial Genomes

inferred← citeshttps://doi.org/10.1093/gbe/evw233openalex-snapshot

Loss of aTrans-Splicingnad1Intron from Geraniaceae and Transfer of the Maturase GenematRto the Nucleus inPelargonium

inferred← citeshttps://doi.org/10.1093/gbe/evy179openalex-snapshot

PacBio-Based Mitochondrial Genome Assembly of Leucaena trichandra (Leguminosae) and an Intrageneric Assessment of Mitochondrial RNA Editing

inferred← citeshttps://doi.org/10.1093/gbe/evz063openalex-snapshot

Evolution and Diversification of Kiwifruit Mitogenomes through Extensive Whole-Genome Rearrangement and Mosaic Loss of Intergenic Sequences in a Highly Variable Region

inferred← citeshttps://doi.org/10.1093/gbe/evz229openalex-snapshot

The Mitochondrial Genome of Eleusine indica and Characterization of Gene Content Within Poaceae

inferred← citeshttps://doi.org/10.1093/gbe/evz263openalex-snapshot

The Mitogenome of Norway Spruce and a Reappraisal of Mitochondrial Recombination in Plants

inferred← citeshttps://doi.org/10.1093/hr/uhae023openalex-snapshot

PMAT: an efficient plant mitogenome assembly toolkit using low-coverage HiFi sequencing data

inferred← citeshttps://doi.org/10.1093/hr/uhae141openalex-snapshot

Genome assembly and resequencing shed light on evolution, population selection, and sex identification in Vernicia montana

inferred← citeshttps://doi.org/10.1093/jxb/erad104openalex-snapshot

Break-induced replication is the primary recombination pathway in plant somatic hybrid mitochondria: a model for mitochondrial horizontal gene transfer

inferred← citeshttps://doi.org/10.1093/jxb/erx057openalex-snapshot

Non-coding RNA may be associated with cytoplasmic male sterility in Silene vulgaris

inferred← citeshttps://doi.org/10.1093/jxb/erx297openalex-snapshot

Hybrids and horizontal transfer: introgression allows adaptive allele discovery

inferred← citeshttps://doi.org/10.1093/jxb/erz456openalex-snapshot

Diverse trajectories of plastome degradation in holoparasitic Cistanche and genomic location of the lost plastid genes

inferred← citeshttps://doi.org/10.1093/molbev/msab255openalex-snapshot

Rapid Shifts in Mitochondrial tRNA Import in a Plant Lineage with Extensive Mitochondrial tRNA Gene Loss

inferred← citeshttps://doi.org/10.1093/molbev/msaf025openalex-snapshot

Fungal-Derived tRNAs Are Expressed and Aminoacylated in Orchid Mitochondria

inferred← citeshttps://doi.org/10.1093/molbev/msaf082openalex-snapshot

Unequally Abundant Chromosomes and Unusual Collections of Transferred Sequences Characterize Mitochondrial Genomes of Gastrodia (Orchidaceae), One of the Largest Mycoheterotrophic Plant Genera

inferred← citeshttps://doi.org/10.1093/molbev/msu199openalex-snapshot

350 My of Mitochondrial Genome Stasis in Mosses, an Early Land Plant Lineage

inferred← citeshttps://doi.org/10.1093/molbev/msu324openalex-snapshot

Horizontal Gene Transfer of Chlamydial-Like tRNA Genes into Early Vascular Plant Mitochondria

inferred← citeshttps://doi.org/10.1093/molbev/msv127openalex-snapshot

Extensive Horizontal Transfer and Homologous Recombination Generate Highly Chimeric Mitochondrial Genomes in Yeast

inferred← citeshttps://doi.org/10.1093/molbev/msv201openalex-snapshot

Multiple Origins of Eukaryoticcox15Suggest Horizontal Gene Transfer from Bacteria to Jakobid Mitochondrial DNA

inferred← citeshttps://doi.org/10.1093/molbev/msw024openalex-snapshot

GinkgoandWelwitschiaMitogenomes Reveal Extreme Contrasts in Gymnosperm Mitochondrial Evolution

inferred← citeshttps://doi.org/10.1093/molbev/msx170openalex-snapshot

Mitochondrial Retroprocessing Promoted Functional Transfers of rpl5 to the Nucleus in Grasses

inferred← citeshttps://doi.org/10.1093/molbev/msy176openalex-snapshot

High and Variable Rates of Repeat-Mediated Mitochondrial Genome Rearrangement in a Genus of Plants

inferred← citeshttps://doi.org/10.1093/molbev/msz198openalex-snapshot

Ancient Mitochondrial Gene Transfer between Fungi and the Orchids

inferred← citeshttps://doi.org/10.1093/pcp/pcaf131openalex-snapshot

Systemic organellar genome reconfiguration along the parasitic continuum in the broomrape family (Orobanchaceae)

inferred← citeshttps://doi.org/10.1093/pcp/pcz111openalex-snapshot

Evolutionary Model of Plastidial RNA Editing in Angiosperms Presumed from Genome-Wide Analysis of Amborella trichopoda

inferred← citeshttps://doi.org/10.1093/sysbio/syu049openalex-snapshot

Mitochondrial Phylogenomics of Early Land Plants: Mitigating the Effects of Saturation, Compositional Heterogeneity, and Codon-Usage Bias

inferred← citeshttps://doi.org/10.1098/rspb.2025.2955openalex-snapshot

A structural solution to functional HGT: gene chimaerism bypasses mitochondrial expression barriers in parasitic plants

inferred← citeshttps://doi.org/10.1101/2021.03.02.433321openalex-snapshot

An updated assembly strategy helps parsing the cryptic mitochondrial genome evolution in plants

inferred← citeshttps://doi.org/10.1101/2022.01.18.476766openalex-snapshot

Expansion and Adaptive Evolution of the mTERF Gene Family in Plants

inferred← citeshttps://doi.org/10.1101/2022.12.23.521604openalex-snapshot

New mitochondrial genomes of leptosporangiate ferns allow modeling the mitogenomic inflation syndrome across all land plant lineages

inferred← citeshttps://doi.org/10.1101/2023.01.07.523103openalex-snapshot

Break-induced replication is the primary recombination pathway in plant somatic hybrid mitochondria: a model for mt-HGT

inferred← citeshttps://doi.org/10.1101/2023.02.10.527995openalex-snapshot

Mitochondrial genome sequencing and analysis of the invasive Microstegium vimineum : a resource for systematics, invasion history, and management

inferred← citeshttps://doi.org/10.1101/2024.02.01.578514openalex-snapshot

The Origin and Evolution of Orphan Genes: A Case Study in Tea Plant Family

inferred← citeshttps://doi.org/10.1101/2024.08.05.606707openalex-snapshot

Evolutionary rates of nuclear and organellar genomes are linked in land plants

inferred← citeshttps://doi.org/10.1101/2024.11.05.621957openalex-snapshot

R-Loop control and mitochondria genome stability require the 5’-3’ exonuclease/flap endonuclease OEX1

inferred← citeshttps://doi.org/10.1101/2025.06.25.661533openalex-snapshot

Circle-Mediated HGT shapes the multichromosomal mitochondrial genome of the endoparasite Mitrastemon yamamotoi

inferred← citeshttps://doi.org/10.1101/2025.11.14.688545openalex-snapshot

A structural solution to functional HGT: Gene chimerism bypasses mitochondrial expression barriers in parasitic plants

inferred← citeshttps://doi.org/10.1101/681718openalex-snapshot

Mitochondrial genome of non-photosynthetic mycoheterotrophic plant Hypopitys monotropa ,its structure, gene expression and RNA editing

inferred← citeshttps://doi.org/10.1101/gr.276885.122openalex-snapshot

Hybridization drives mitochondrial DNA degeneration and metabolic shift in a species with biparental mitochondrial inheritance

inferred← citeshttps://doi.org/10.1104/pp.114.243824openalex-snapshot

FRIENDLY Regulates Mitochondrial Distribution, Fusion, and Quality Control in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.17.01025openalex-snapshot

Fission and Fusion of Plant Mitochondria, and Genome Maintenance

inferred← citeshttps://doi.org/10.1105/tpc.114.123620openalex-snapshot

Evolutionary Origins of a Bioactive Peptide Buried within Preproalbumin

inferred← citeshttps://doi.org/10.1111/1755-0998.13584openalex-snapshot

ORTHOSKIM: In silico sequence capture from genomic and transcriptomic libraries for phylogenomic and barcoding applications

inferred← citeshttps://doi.org/10.1111/2041-210x.70419openalex-snapshot

HGTScanner : Detecting horizontal gene transfer at the fine scale using whole organelle genomes

inferred← citeshttps://doi.org/10.1111/cla.12578openalex-snapshot

PSA: an effective method for predicting horizontal gene transfers through parsimonious phylogenetic networks

inferred← citeshttps://doi.org/10.1111/jse.12655openalex-snapshot

Genomic architectural variation of plant mitochondria—A review of multichromosomal structuring

inferred← citeshttps://doi.org/10.1111/jse.12706openalex-snapshot

Exploring the impact of RNA editing on mitochondrial phylogenetic analyses in liverworts, an early land plant lineage

inferred← citeshttps://doi.org/10.1111/jse.12708openalex-snapshot

Mitochondrial genes from 18 angiosperms fill sampling gaps for phylogenomic inferences of the early diversification of flowering plants

inferred← citeshttps://doi.org/10.1111/jse.12833openalex-snapshot

Systematics of Mukdenia and Oresitrophe (Saxifragaceae): Insights from genome skimming data

inferred← citeshttps://doi.org/10.1111/mec.13742openalex-snapshot

The mutational hazard hypothesis of organelle genome evolution: 10 years on

inferred← citeshttps://doi.org/10.1111/nph.12835openalex-snapshot

Using plants to elucidate the mechanisms of cytonuclear co‐evolution

inferred← citeshttps://doi.org/10.1111/nph.13188openalex-snapshot

Homologous recombination and retention of a single form of most genes shape the highly chimeric mitochondrial genome of a cybrid plant

inferred← citeshttps://doi.org/10.1111/nph.13321openalex-snapshot

When two is a crowd: mitochondrial genome merger and its aftermath

showing the first 200 of 473

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.