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Plant mitochondrial DNA evolved rapidly in structure, but slowly in sequence
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4684-4988-4_2openalex-snapshot
The Mitochondrial Genome of Animals
inferredcites →https://doi.org/10.1007/978-1-4684-4988-4_3openalex-snapshot
Evolution of Chloroplast and Mitochondrial DNA in Plants and Algae
inferredcites →https://doi.org/10.1007/bf00251100openalex-snapshot
Comparison of the mitochondrial genome of Nicotiana tabacum with its progenitor species
inferredcites →https://doi.org/10.1007/bf00308062openalex-snapshot
Chloroplast DNA evolution and the origin of amphidiploid Brassica species
inferredcites →https://doi.org/10.1007/bf00330180openalex-snapshot
The tobacco mitochondrial ATPase subunit 9 gene is closely linked to an open reading frame for a ribosomal protein
inferredcites →https://doi.org/10.1007/bf00384620openalex-snapshot
Unicircular structure of the Brassica hirta mitochondrial genome
inferredcites →https://doi.org/10.1007/bf00433907openalex-snapshot
Physical and gene mapping of cauliflower (Brassica oleracea) mitochondrial DNA
inferredcites →https://doi.org/10.1007/bf01734101openalex-snapshot
Mitochondrial DNA sequences of primates: Tempo and mode of evolution
inferredcites →https://doi.org/10.1016/0076-6879(86)18072-4openalex-snapshot
Isolation and structural analysis of chloroplast DNA
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/10.1016/0092-8674(82)90337-3openalex-snapshot
The yeast plasmid 2μ circle
inferredcites →https://doi.org/10.1016/0092-8674(85)90041-8openalex-snapshot
Mitochondrial DNA rearrangements associated with fertile revertants of S-type male-sterile maize
inferredcites →https://doi.org/10.1016/0092-8674(86)90465-4openalex-snapshot
Novel recombinations in the maize mitochondrial genome produce a unique transcriptional unit in the texas male-sterile cytoplasm
inferredcites →https://doi.org/10.1016/0092-8674(86)90621-5openalex-snapshot
Mitochondrial genome rearrangement leads to extension and relocation of the cytochrome c oxidase subunit I gene in sorghum
inferredcites →https://doi.org/10.1016/0092-8674(87)90660-xopenalex-snapshot
A fused mitochondrial gene associated with cytoplasmic male sterility is developmentally regulated
inferredcites →https://doi.org/10.1016/0304-4211(81)90018-3openalex-snapshot
Sal 1 restriction enzyme analysis of chloroplast and mitochondrial DNAs in the genus Brassica
inferredcites →https://doi.org/10.1016/s0074-7696(08)62347-5openalex-snapshot
Molecular Biology of Higher Plant Mitochondrial DNA
inferredcites →https://doi.org/10.1038/301725a0openalex-snapshot
An unusual mitochondrial DNA plasmid in the genus Brassica
inferredcites →https://doi.org/10.1038/307437a0openalex-snapshot
Tripartite structure of the Brassica campestris mitochondrial genome
inferredcites →https://doi.org/10.1038/322501a0openalex-snapshot
Molecular botany: Wonders of chloroplast DNA
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.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.78.10.5953openalex-snapshot
Evolution of DNA sequence organization in mitochondrial genomes of Zea
inferredcites →https://doi.org/10.1073/pnas.84.20.7183openalex-snapshot
Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards.
inferredcites →https://doi.org/10.1073/pnas.84.24.9054openalex-snapshot
Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.
inferredcites →https://doi.org/10.1086/284690openalex-snapshot
Molecular Mechanisms of Mitochondrial-Genome Evolution in Higher Plants
inferredcites →https://doi.org/10.1093/genetics/106.4.735openalex-snapshot
THE NATURE OF NUCLEOTIDE SEQUENCE DIVERGENCE BETWEEN BARLEY AND MAIZE CHLOROPLAST DNA
inferredcites →https://doi.org/10.1093/genetics/112.3.649openalex-snapshot
MITOCHONDRIAL DNA SEQUENCE DIVERGENCE AMONG LYCOPERSICON AND RELATED SOLANUM SPECIES
inferredcites →https://doi.org/10.1093/genetics/118.2.341openalex-snapshot
Intraspecific variation and multicircularity in Brassica mitochondrial DNAs.
inferredcites →https://doi.org/10.1093/nar/12.15.6141openalex-snapshot
Recombination sequences in plant mitochondrial genomes: diversity and homologies to known mitochondrial genes
inferredcites →https://doi.org/10.1093/nar/14.24.9755openalex-snapshot
Tricircular mitochondrial genomes ofBrassicaandRaphanus: reversal of repeat configurations by inversiton
inferredcites →https://doi.org/10.1093/nar/15.13.5141openalex-snapshot
Extensive mitochondrial specific transcription of theBrassica campestrismitochondrial genome
inferredcites →https://doi.org/10.1093/nar/16.9.3787openalex-snapshot
Physical and gene organization of mitochondrial DNA in fertile and male sterile sunflower. CMS-associated alterations in structure and transcription of theatpA gene
inferredcites →https://doi.org/10.1111/j.1095-8312.1985.tb02048.xopenalex-snapshot
Mitochondrial DNA and two perspectives on evolutionary genetics
inferredcites →https://doi.org/10.1128/mcb.8.4.1474openalex-snapshot
Mitochondrial DNA Rearrangements and Transcriptional Alterations in the Male-Sterile Cytoplasm of Ogura Radish
inferredcites →https://doi.org/10.1146/annurev.bi.53.070184.003041openalex-snapshot
TRANSCRIPTION OF THE MAMMALIAN MITOCHONDRIAL GENOME
inferredcites →https://doi.org/10.1146/annurev.ge.19.120185.001545openalex-snapshot
COMPARATIVE ORGANIZATION OF CHLOROPLAST GENOMES
inferredcites →https://doi.org/10.1146/annurev.pp.38.060187.002135openalex-snapshot
Evolution of Higher-Plant Chloroplast DNA-Encoded Genes: Implications for Structure-Function and Phylogenetic Studies
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1002/iub.270openalex-snapshot
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Molecular Phylogenetic Studies of Brassica,Rorippa,Arabidopsis and Allied Genera Based on the Internal Transcribed Spacer Region of 18S–25S rDNA
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Plant Mitochondrial Genome Evolution and Gene Transfer to the Nucleus
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Mitochondrial Mutations in Plants
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Translational Machinery in Plant Organelles
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Cytoplasmic Male Sterility and Fertility Restoration by Nuclear Genes
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DNA and RNA from Ancient Plant Seeds
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Organization and Evolution of Mitochondrial DNA in Metazoa
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Contributions of Molecular Data to Papilionoid Legume Systematics
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Mitochondrial DNA in Plant Systematics: Applications and Limitations
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Molecular Systematics and Crop Evolution
inferred← citeshttps://doi.org/10.1007/978-1-4615-3304-7_35openalex-snapshot
Organization and Evolution of the Maize Mitochondrial Genome
inferred← citeshttps://doi.org/10.1007/978-1-4615-5419-6_1openalex-snapshot
Choosing an Approach and an Appropriate Gene for Phylogenetic Analysis
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Genetic Mapping as a Tool for Studying Speciation
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Probability Models for DNA Sequence Evolution
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Genome Rearrangement Problems with Single and Multiple Gene Copies: A Review
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Counting Sorting Scenarios and Intermediate Genomes for the Rank Distance
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Clustering Based on Rank Distance with Applications on DNA
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inferred← citeshttps://doi.org/10.1007/978-3-7091-9138-5_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-7091-9138-5_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-81-322-2283-5_8openalex-snapshot
Organellar Genomes of Flowering Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-0163-9_1openalex-snapshot
Mitochondrial genome organization
inferred← citeshttps://doi.org/10.1007/978-94-011-0163-9_17openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-0163-9_3openalex-snapshot
Mitochondrial Transfer RNAs and RNA Editing
inferred← citeshttps://doi.org/10.1007/978-94-011-1094-5_4openalex-snapshot
Recombination of Plant Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1007/978-94-011-2442-3_3openalex-snapshot
Organelle DNA isolation and RFLP analysis
inferred← citeshttps://doi.org/10.1007/978-981-16-6974-3_12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-92-3309-0_4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00015551openalex-snapshot
Comparison of the wheat mitochondrial atp9 gene sequence with mitochondrial and chloroplast homologues from other plants
inferred← citeshttps://doi.org/10.1007/bf00017914openalex-snapshot
Patterns of mitochondrial DNA instability in Brassica campestris cultured cells
inferred← citeshttps://doi.org/10.1007/bf00020232openalex-snapshot
Genetic correlation of the orf224/atp6 gene region with Polima CMS in Brassica somatic hybrids
inferred← citeshttps://doi.org/10.1007/bf00032959openalex-snapshot
Protoplast culture and regeneration from Brassica oleracea ?rapid cycling? and other varieties
inferred← citeshttps://doi.org/10.1007/bf00049333openalex-snapshot
Transcript mapping and processing of mitochondrial RNA in the chlorophyte alga Prototheca wickerhamii
inferred← citeshttps://doi.org/10.1007/bf00051926openalex-snapshot
Mitochondrial DNA RFLP in genus Oryza and cultivated rice
inferred← citeshttps://doi.org/10.1007/bf00162974openalex-snapshot
Genetic code and phylogenetic origin of oomycetous mitochondria
inferred← citeshttps://doi.org/10.1007/bf00163803openalex-snapshot
Promiscuous mitochondrial group II intron sequences in plant nuclear genomes
inferred← citeshttps://doi.org/10.1007/bf00221138openalex-snapshot
A high frequency of intergenomic mitochondrial recombination and an overall biased segregation of B. campestris or recombined B. campestris mitochondria were found in somatic hybrids made within Brassicaceae
inferred← citeshttps://doi.org/10.1007/bf00222879openalex-snapshot
Intraspecific heterogeneity of the Vicia faba mitochondrial genome: evidence for multiregional rearrangements in the mitochondrial chromosome associated with coxII-orf192 chimeric gene formation
inferred← citeshttps://doi.org/10.1007/bf00223638openalex-snapshot
A unique cytoplasmic male sterility (CMS) determinant is present in three Phaseolus species characterized by different mitochondrial genomes
inferred← citeshttps://doi.org/10.1007/bf00223895openalex-snapshot
Phylogenetic relationships within Hevea brasiliensis as deduced from a polymorphic mitochondrial DNA region
inferred← citeshttps://doi.org/10.1007/bf00224188openalex-snapshot
Mitochondrial DNA polymorphisms of Malawian bean lines: further evidence for two major gene pools
inferred← citeshttps://doi.org/10.1007/bf00224191openalex-snapshot
Analysis of chloroplast and mitochondrial segregation in three different combinations of somatic hybrids produced within Brassicaceae
inferred← citeshttps://doi.org/10.1007/bf00225017openalex-snapshot
Organellar segregation, rearrangement and recombination in protoplast fusion-derived Brassica oleracea calli
inferred← citeshttps://doi.org/10.1007/bf00225892openalex-snapshot
Relationships among Cichorium species and related genera as determined by analysis of mitochondrial RFLPs
inferred← citeshttps://doi.org/10.1007/bf00226214openalex-snapshot
Variability and uniformity of mitochondrial DNA in populations of putative diploid ancestors of common wheat
inferred← citeshttps://doi.org/10.1007/bf00226252openalex-snapshot
Atrazine-resistant cytoplasmic male-sterile-nigra broccoli obtained by protoplast fusion between cytoplasmic male-sterile Brassica oleracea and atrazine-resistant Brassica campestris
inferred← citeshttps://doi.org/10.1007/bf00227319openalex-snapshot
Differences between, and possible origins of, the cytoplasms found in fertile and male-sterile onions (Allium cepa L.)
inferred← citeshttps://doi.org/10.1007/bf00228686openalex-snapshot
Comparison of the organization of the mitochondrial genome in tomato somatic hybrids and cybrids
inferred← citeshttps://doi.org/10.1007/bf00232384openalex-snapshot
Protoplast fusion-derived Ogura male sterile cauliflower with cold tolerance
inferred← citeshttps://doi.org/10.1007/bf00261233openalex-snapshot
A specific rearrangement of mitochondrial DNA induced by tissue culture
inferred← citeshttps://doi.org/10.1007/bf00277131openalex-snapshot
Identification of the entire set of transferred chloroplast DNA sequences in the mitochondrial genome of rice
inferred← citeshttps://doi.org/10.1007/bf00277349openalex-snapshot
RNA editing of a conserved reading frame in plant mitochondria increases its similarity to two overlapping reading frames in Escherichia coli
inferred← citeshttps://doi.org/10.1007/bf00292310openalex-snapshot
Rearrangement, amplification, and assortment of mitochondrial DNA molecules in cultured cells of Brassica campestris
inferred← citeshttps://doi.org/10.1007/bf00309541openalex-snapshot
Three mitochondrial unassigned open reading frames of Podospora anserina represent remnants of a viral-type RNA polymerase gene
inferred← citeshttps://doi.org/10.1007/bf00309559openalex-snapshot
Polymorphism for ribosomal RNA gene arrangement in the mitochondrial genome of fall rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.1007/bf00312646openalex-snapshot
Occurrence and transcription of genes for nad1, nad3, nad4L, and nad6, coding for NADH dehydrogenase subunits 1, 3, 4L, and 6, in liverwort mitochondria
inferred← citeshttps://doi.org/10.1007/bf00313082openalex-snapshot
An internal part of the chloroplast atpA gene sequence is present in the mitochondrial genome of Triticum aestivum: molecular organisation and evolutionary aspects
inferred← citeshttps://doi.org/10.1007/bf00313246openalex-snapshot
A gene for cytochrome c oxidase subunit III (COXIII) in broad bean mitochondrial DNA: structural features and sequence evolution
inferred← citeshttps://doi.org/10.1007/bf00313247openalex-snapshot
Structure and transcription of the gene coding for subunit 3 of cytochrome oxidase in wheat mitochondria
inferred← citeshttps://doi.org/10.1007/bf00314882openalex-snapshot
Physical organization of the 18S and 5S ribosomal RNA genes in the mitochondrial genome of rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.1007/bf00318471openalex-snapshot
Large size and complex structure of mitochondrial DNA in two nonflowering land plants
inferred← citeshttps://doi.org/10.1007/bf00318475openalex-snapshot
Different organization and altered transcription of the mitochondrial atp6 gene in the male-sterile cytoplasm of rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.1007/bf00326232openalex-snapshot
Contrasting mutation rates in mitochondrial and nuclear genes of yeasts versus mammals
inferred← citeshttps://doi.org/10.1007/bf00336485openalex-snapshot
The role of coxI-associated repeated sequences in plant mitochondrial DNA rearrangements and radish cytoplasmic male sterility
inferred← citeshttps://doi.org/10.1007/bf00336783openalex-snapshot
Characterization of expression of a mitochondrial gene region associated with the Brassica “Polima” CMS: developmental influences
inferred← citeshttps://doi.org/10.1007/bf00351504openalex-snapshot
Comparative analysis of a recombining-repeat-sequence family in the mitochondrial genomes of wheat (Triticum aestivum L.) and rye (Secale cereale L.)
inferred← citeshttps://doi.org/10.1007/bf00351732openalex-snapshot
Novel mitochondrial genomes in Brassica napus somatic hybrids
inferred← citeshttps://doi.org/10.1007/bf00351745openalex-snapshot
The higher plant nad5 mitochondrial gene: a conserved discontinuous transcription pattern
inferred← citeshttps://doi.org/10.1007/bf00521276openalex-snapshot
Location, identity, amount and serial entry of chloroplast DNA sequences in crucifer mitochondrial DNAs
inferred← citeshttps://doi.org/10.1007/bf01037584openalex-snapshot
Both chloroplast and mitochondrial NADH dehydrogenase subunit 5 genes are transcribed in pea
inferred← citeshttps://doi.org/10.1007/bf02106051openalex-snapshot
Cytoplasmic male sterility inBeta is associated with structural rearrangements of the mitochondrial DNA and is not due to interspecific organelle transfer
inferred← citeshttps://doi.org/10.1007/bf02173775openalex-snapshot
The rapeseed mitochondrial gene encoding a homologue of the bacterial protein Ccl1 is divided into two independently transcribed reading frames
inferred← citeshttps://doi.org/10.1007/bf02190618openalex-snapshot
Mitochondrial genome size variation and restriction fragment length polymorphisms in threePhaseolus species
inferred← citeshttps://doi.org/10.1007/bf03194652openalex-snapshot
The selection of mosaic (MSC) phenotype after passage of cucumber (Cucumis sativus L.) through cell culture — a method to obtain plant mitochondrial mutants
inferred← citeshttps://doi.org/10.1007/bfb0015244openalex-snapshot
Towards a computational theory of genome rearrangements
inferred← citeshttps://doi.org/10.1007/pl00006290openalex-snapshot
Evolution of the Plant Mitochondrial Genome: Dynamics of Duplication and Deletion of Sequences
inferred← citeshttps://doi.org/10.1007/pl00006502openalex-snapshot
Rates of Nucleotide Substitution in Angiosperm Mitochondrial DNA Sequences and Dates of Divergence Between Brassica and Other Angiosperm Lineages
inferred← citeshttps://doi.org/10.1007/s00122-002-0868-6openalex-snapshot
Combination of chloroplast and mitochondrial DNA polymorphisms to study cytoplasm genetic differentiation in the olive complex (Olea europaea L.)
inferred← citeshttps://doi.org/10.1007/s00122-003-1284-2openalex-snapshot
Characterization of a mosaic minisatellite locus in the mitochondrial DNA of Norway spruce [Picea abies (L.) Karst.]
inferred← citeshttps://doi.org/10.1007/s00122-004-1595-yopenalex-snapshot
Chloroplast and mitochondrial molecular tests identify European×Japanese larch hybrids
inferred← citeshttps://doi.org/10.1007/s00122-004-1895-2openalex-snapshot
Phylogenetic analysis of Oryza species, based on simple sequence repeats and their flanking nucleotide sequences from the mitochondrial and chloroplast genomes
inferred← citeshttps://doi.org/10.1007/s00122-005-1965-0openalex-snapshot
Reproduction and cytogenetic characterization of interspecific hybrids derived from crosses between Brassica carinata and B. rapa
inferred← citeshttps://doi.org/10.1007/s00122-008-0909-xopenalex-snapshot
Identification of a novel chimeric gene, orf725, and its use in development of a molecular marker for distinguishing among three cytoplasm types in onion (Allium cepa L.)
inferred← citeshttps://doi.org/10.1007/s001220050084openalex-snapshot
Estimating genetic diversity of Arabidopsis thaliana ecotypes with amplified fragment length polymorphisms (AFLP)
inferred← citeshttps://doi.org/10.1007/s001220050512openalex-snapshot
Phylogenetic analysis in the Festuca-Lolium complex using molecular markers and ITS rDNA
inferred← citeshttps://doi.org/10.1007/s001220050875openalex-snapshot
Differential transmission of the Cucumis organellar genomes
inferred← citeshttps://doi.org/10.1007/s001220051383openalex-snapshot
Cytoplasmic male sterility in the olive (Olea europaea L.)
inferred← citeshttps://doi.org/10.1007/s00216-016-9595-8openalex-snapshot
Advances in DNA metabarcoding for food and wildlife forensic species identification
inferred← citeshttps://doi.org/10.1007/s00239-004-2606-yopenalex-snapshot
Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron
inferred← citeshttps://doi.org/10.1007/s00239-010-9346-yopenalex-snapshot
Testing for Selection on Synonymous Sites in Plant Mitochondrial DNA: The Role of Codon Bias and RNA Editing
inferred← citeshttps://doi.org/10.1007/s00239-012-9508-1openalex-snapshot
Quantifying the Elevation of Mitochondrial DNA Evolutionary Substitution Rates Over Nuclear Rates in the Intertidal Copepod Tigriopus californicus
inferred← citeshttps://doi.org/10.1007/s00239-015-9704-xopenalex-snapshot
Are Synonymous Substitutions in Flowering Plant Mitochondria Neutral?
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/s00239-021-10000-wopenalex-snapshot
The Journal of Molecular Evolution Turns 50
inferred← citeshttps://doi.org/10.1007/s00285-026-02450-xopenalex-snapshot
Genome rearrangements as double coset Markov chains
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/s002940050176openalex-snapshot
A mitochondrial sub-stoichiometric orf87-nad3-nad1 exonA co-transcription unit present in Solanaceae was amplified in the genus Nicotiana
inferred← citeshttps://doi.org/10.1007/s002940050212openalex-snapshot
Brassica nap cytoplasmic male sterility is associated with expression of a mtDNA region containing a chimeric gene similar to the pol CMS-associated orf224 gene
inferred← citeshttps://doi.org/10.1007/s002940050213openalex-snapshot
The rapeseed mitochondrial gene for subunit 2 of the NADH dehydrogenase complex: a trans-spliced structure is conserved in one of the smallest plant mitochondrial genomes
inferred← citeshttps://doi.org/10.1007/s002940050402openalex-snapshot
Rapeseed mitochondrial ccb206, a gene involved in cytochrome c biogenesis, is co-transcribed with the nad3 and rps12 genes: organization, transcription, and RNA editing of the nad3/rps12/ccb206 locus
inferred← citeshttps://doi.org/10.1007/s002940050532openalex-snapshot
Phage T4-like intermediates of DNA replication and recombination in the mitochondria of the higher plant Chenopodium album (L.)
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/s00425-023-04245-6openalex-snapshot
Multiple configurations of the plastid and mitochondrial genomes of Caragana spinosa
inferred← citeshttps://doi.org/10.1007/s00425-023-04316-8openalex-snapshot
Demographic dynamics and molecular evolution of the rare and endangered subsect. Gerardianae of Pinus: insights from chloroplast genomes and mitochondrial DNA markers
inferred← citeshttps://doi.org/10.1007/s00425-025-04629-wopenalex-snapshot
The Taihangia mitogenome provides new insights into its adaptation and organelle genome evolution in Rosaceae
inferred← citeshttps://doi.org/10.1007/s00438-002-0740-zopenalex-snapshot
Complex organization of the mitochondrial genome of petaloid CMS carrot
inferred← citeshttps://doi.org/10.1007/s00438-017-1353-xopenalex-snapshot
Whole genome comparative analysis of four Georgian grape cultivars
inferred← citeshttps://doi.org/10.1007/s004380050478openalex-snapshot
Homologous recombination involving cox2 is responsible for a mutation in the CMS-specific mitochondrial locus of Petunia
inferred← citeshttps://doi.org/10.1007/s004380050761openalex-snapshot
Cis- and trans-splicing and RNA editing are required for the expression of nad2 in wheat mitochondria
inferred← citeshttps://doi.org/10.1007/s00453-021-00814-xopenalex-snapshot
Sorting a Permutation by Best Short Swaps
inferred← citeshttps://doi.org/10.1007/s00468-014-1136-5openalex-snapshot
Development of mitochondrial SNP markers in different Populus species
inferred← citeshttps://doi.org/10.1007/s00521-013-1468-xopenalex-snapshot
Clustering based on median and closest string via rank distance with applications on DNA
inferred← citeshttps://doi.org/10.1007/s00606-010-0371-5openalex-snapshot
Genetic diversity and relationships in Solanum subg. Archaesolanum (Solanaceae) based on RAPD and chloroplast PCR-RFLP analyses
inferred← citeshttps://doi.org/10.1007/s10126-008-9129-2openalex-snapshot
Comparative Analyses of Coding and Noncoding DNA Regions Indicate that Acropora (Anthozoa: Scleractina) Possesses a Similar Evolutionary Tempo of Nuclear vs. Mitochondrial Genomes as in Plants
inferred← citeshttps://doi.org/10.1007/s10142-026-01851-xopenalex-snapshot
Comparisons of mitochondrial genomes of CMS line and its nuclear and cytoplasmic donors uncover the genome rearrangement and CMS associated candidate gene in eggplant
inferred← citeshttps://doi.org/10.1007/s10462-020-09951-1openalex-snapshot
Biological computation and computational biology: survey, challenges, and discussion
inferred← citeshttps://doi.org/10.1007/s10531-017-1324-xopenalex-snapshot
Phylogeography of endangered Dendrobium moniliforme in East Asia based on mitochondrial DNA sequence variations
inferred← citeshttps://doi.org/10.1007/s10681-023-03207-zopenalex-snapshot
Cases of paternal inheritance and recombination of mitochondrial DNA in peas (Pisum L.)
inferred← citeshttps://doi.org/10.1007/s10722-006-9179-0openalex-snapshot
Molecular phylogeny of Chinese vegetable mustard (Brassica juncea) based on the internal transcribed spacers (ITS) of nuclear ribosomal DNA
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/s10878-007-9077-1openalex-snapshot
On the inapproximability of the exemplar conserved interval distance problem of genomes
inferred← citeshttps://doi.org/10.1007/s10910-006-9095-8openalex-snapshot
Estimate the Distance of Genome Rearrangements by Reversals
inferred← citeshttps://doi.org/10.1007/s10910-006-9145-2openalex-snapshot
An algorithm for reversal median problem
inferred← citeshttps://doi.org/10.1007/s11032-011-9656-9openalex-snapshot
Chloroplast and mitochondrial SSR help to distinguish allo-cytoplasmic male sterile types in cabbage (Brassica oleracea L. var. capitata)
inferred← citeshttps://doi.org/10.1007/s11032-013-9993-yopenalex-snapshot
Mitotype-specific sequences related to cytoplasmic male sterility in Oryza species
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/s11103-018-0734-9openalex-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/s12374-025-09501-8openalex-snapshot
On the Plant Mitochondrial Genome Assembly Pipelines Focusing on High-Accuracy Long-Read Data
inferred← citeshttps://doi.org/10.1007/s12374-026-09525-8openalex-snapshot
The History and Future of Plant Molecular Ecology
inferred← citeshttps://doi.org/10.1007/s12892-009-0146-0openalex-snapshot
In silico-selection of Brassica rapa organelle genome-derived BACs using their end sequences and sequence level comparative analysis of the 124 kb mitochondrial genome sequences in the family Brassicaceae
inferred← citeshttps://doi.org/10.1007/s13580-013-0026-xopenalex-snapshot
SSRs mining of Brassica species in mitochondrial genomes: Bioinformatic approaches
inferred← citeshttps://doi.org/10.1007/s13721-016-0113-xopenalex-snapshot
New approximations for block sorting
inferred← citeshttps://doi.org/10.1007/s40290-019-00266-3openalex-snapshot
ITS2: An Ideal DNA Barcode for the Arid Medicinal Plant Rhazya Stricta
inferred← citeshttps://doi.org/10.1007/s44372-026-00476-5openalex-snapshot
Mitochondrial genome of the North American Morus rubra L. (red mulberry) reveals plastome gene transfer and essence of RNA editing
inferred← citeshttps://doi.org/10.1016/0168-9452(94)03977-1openalex-snapshot
Biased mitochondrial segregation, independent of cell type used for fusion and of hybrid nuclear DNA content, was found in Brassica napus (+) B. oleracea somatic hybrids
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