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The Hows and Whys of Cytoplasmic Inheritance in Seed Plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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FINE STRUCTURE OF THE SPERMATOZOID OF ZAMIA: THE VIERERGRUPPE
inferredcites →https://doi.org/10.1002/j.1537-2197.1977.tb12359.xopenalex-snapshot
CHANGES IN PLASTID AND MITOCHONDRION CONTENT DURING MATURATION OF GENERATIVE CELLS OF SOLANUM (SOLANACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1980.tb07630.xopenalex-snapshot
DEVELOPMENTAL FEATURES OF THE SPERMATOGENOUS CELL IN GINKGO BILOBA
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08742.xopenalex-snapshot
PROTOPLAST FUSION: A NOVEL APPROACH TO ORGANELLE GENETICS IN HIGHER PLANTS
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb11219.xopenalex-snapshot
RAPID SCREENING METHOD TO DETECT POTENTIAL BIPARENTAL INHERITANCE OF PLASTID DNA AND RESULTS FOR OVER 200 ANGIOSPERM SPECIES
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15096.xopenalex-snapshot
ALLOPOLYPLOID SPECIATION IN TRAGOPOGON: INSIGHTS FROM CHLOROPLAST DNA
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb11399.xopenalex-snapshot
SEXUAL REPRODUCTION IN EPHEDRA NEVADENSIS (EPHEDRACEAE): FURTHER EVIDENCE OF DOUBLE FERTILIZATION IN A NONFLOWERING SEED PLANT
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13574.xopenalex-snapshot
CYTOLOGICAL BASIS FOR CYTOPLASMIC INHERITANCE IN PSEUDOTSUGA MENZIESII. I. POLLEN TUBE AND ARCHEGONIAL DEVELOPMENT
inferredcites →https://doi.org/10.1002/j.1537-2197.1991.tb11437.xopenalex-snapshot
CHLOROPLAST DNA VARIATION IN GLIRICIDIA SEPIUM (LEGUMINOSAE): INTRASPECIFIC PHYLOGENY AND TOKOGENY
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb13737.xopenalex-snapshot
IS ORGANELLE DNA STRICTLY MATERNALLY INHERITED? POWER ANALYSIS OF A BINOMIAL DISTRIBUTION
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb13808.xopenalex-snapshot
CPDNA INHERITANCE IN INTERSPECIFIC CROSSES AND EVOLUTIONARY INFERENCE IN LOUISIANA IRISES
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb15301.xopenalex-snapshot
GENETIC EVIDENCE FOR TRACE PATERNAL TRANSMISSION OF PLASTIDS IN LIRIODENDRON AND MAGNOLIA (MAGNOLIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11492.xopenalex-snapshot
C hloroplast ‐DNA restriction site analysis in the genus B romus (P oaceae )
inferredcites →https://doi.org/10.1007/bf00189808openalex-snapshot
Male cytoplasmic diminution and male germ unit in young and mature pollen of Cymbidium goeringii: a 3-dimensional and quantitative study
inferredcites →https://doi.org/10.1007/bf00191614openalex-snapshot
Populations of plastids and mitochondria during male reproductive cell maturation in Nicotiana tabacum L.: A cytological basis for occasional biparental inheritance
inferredcites →https://doi.org/10.1007/bf00196605openalex-snapshot
Quantitative, three-dimensional analysis of alfalfa egg cells in two genotypes: Implications for biparental plastid inheritance
inferredcites →https://doi.org/10.1007/bf00199758openalex-snapshot
Fertilization in Nicotiana tabacum: ultrastructural organization of propane-jet-frozen embryo sacs in vivo
inferredcites →https://doi.org/10.1007/bf00215042openalex-snapshot
Analysis of the mitochondrial DNA of the somatic hybrids of Solanum brevidens and S. tuberosum using non-radioactive digoxigenin-labelled DNA probes
inferredcites →https://doi.org/10.1007/bf00215717openalex-snapshot
Large-scale deletions of rice plastid DNA in anther culture
inferredcites →https://doi.org/10.1007/bf00223786openalex-snapshot
High transmission of paternal plastid DNA in alfalfa plants demonstrated by restriction fragment polymorphic analysis
inferredcites →https://doi.org/10.1007/bf00225959openalex-snapshot
Chloroplast DNA in Pinus monticola
inferredcites →https://doi.org/10.1007/bf00226107openalex-snapshot
Quantitative cytology of the alfalfa generative cell and its relation to male plastid inheritance patterns in three genotypes
inferredcites →https://doi.org/10.1007/bf00226220openalex-snapshot
Inheritance of chloroplast and mitochondrial DNA in Picea and composition of hybrids from introgression zones
inferredcites →https://doi.org/10.1007/bf00227580openalex-snapshot
The effect of genotype on pollen transmission of mitochondria in rapeseed (Brassica napus)
inferredcites →https://doi.org/10.1007/bf00229388openalex-snapshot
Variation in generative cell plastid nucleoids and male fertility in Medicago sativa
inferredcites →https://doi.org/10.1007/bf00232294openalex-snapshot
Transmission of paternal chloroplasts in tobacco (Nicotiana tabacum)
inferredcites →https://doi.org/10.1007/bf00247543openalex-snapshot
Quantitative cytology of the egg and central cell of Plumbago zeylanica and its impact on cytoplasmic inheritance patterns
inferredcites →https://doi.org/10.1007/bf00260905openalex-snapshot
Biparental inheritance of chloroplast DNA and the existence of heteroplasmic cells in alfalfa
inferredcites →https://doi.org/10.1007/bf00266189openalex-snapshot
Paternal inheritance of chloroplast DNA and maternal inheritance of mitochondrial DNA in loblolly pine
inferredcites →https://doi.org/10.1007/bf00266656openalex-snapshot
Inheritance of plastids in interspecific hybrids of blue spruce and white spruce
inferredcites →https://doi.org/10.1007/bf00266672openalex-snapshot
Paternal inheritance of plastids in Medicago sativa
inferredcites →https://doi.org/10.1007/bf00267882openalex-snapshot
Unequal distribution of plastids during generative cell formation in Impatiens
inferredcites →https://doi.org/10.1007/bf00268112openalex-snapshot
The deficiency of soluble proteins and plastid ribosomal RNA in the albino pollen plantlets of rice
inferredcites →https://doi.org/10.1007/bf00275175openalex-snapshot
Variations of chloroplast DNAs in the genus Pelargonium and their biparental inheritance
inferredcites →https://doi.org/10.1007/bf00283034openalex-snapshot
Paternal inheritance of mitochondria in rapeseed (Brassica napus)
inferredcites →https://doi.org/10.1007/bf00309602openalex-snapshot
Paternal plastid inheritance in alfalfa: plastid nucleoid number within generative cells correlates poorly with plastid number and male plastid transmission trength
inferredcites →https://doi.org/10.1007/bf00309912openalex-snapshot
Analysis of mitochondrial DNA and its inheritance in Populus
inferredcites →https://doi.org/10.1007/bf00318524openalex-snapshot
Plastid genome structure and plastid-related transcript levels in albino barley plants derived from anther culture
inferredcites →https://doi.org/10.1007/bf00332951openalex-snapshot
Recombination between chloroplast DNAs does not occur in sexual crosses of Oenothera
inferredcites →https://doi.org/10.1007/bf00334525openalex-snapshot
Plastid DNA is not detectable in the male gametes and pollen tubes of an angiosperm (Antirrhinum majus) that is maternal for plastid inheritance
inferredcites →https://doi.org/10.1007/bf00337947openalex-snapshot
Restriction endonuclease analysis of plastid DNA from tomato, potato and some of their somatic hybrids
inferredcites →https://doi.org/10.1007/bf00351474openalex-snapshot
Maternal transmission of mitochondrial DNA in interspecific hybrids of Populus
inferredcites →https://doi.org/10.1007/bf00351478openalex-snapshot
Cell type determines plastid transmission in tomato intergeneric somatic hybrids
inferredcites →https://doi.org/10.1007/bf00365653openalex-snapshot
Plastid inheritance in Oenothera: organelle genome modifies the extent of biparental plastid transmission
inferredcites →https://doi.org/10.1007/bf00393450openalex-snapshot
Ultrastructure of the sperm of Plumbago zeylanica
inferredcites →https://doi.org/10.1007/bf00406648openalex-snapshot
Cotton embryogenesis: The entrance and discharge of the pollen tube in the embryo sac
inferredcites →https://doi.org/10.1007/bf00425497openalex-snapshot
Transmission of paternal chloroplasts in Nicotiana
inferredcites →https://doi.org/10.1007/bf00425775openalex-snapshot
Übertragung von Plastiden durch den Pollen bei Antirrhinum majus
inferredcites →https://doi.org/10.1007/bf00449820openalex-snapshot
Deleted forms of plastid DNA in albino plants from cereal anther culture
inferredcites →https://doi.org/10.1007/bf01273229openalex-snapshot
Quantitative ultrastructural analysis of barley sperm
inferredcites →https://doi.org/10.1007/bf01279731openalex-snapshot
Ultrastructural studies on plastids of generative and vegetative cells inLiliaceae 3. Plastid distribution during the pollen development inGasteria verrucosa (Mill.) Duval
inferredcites →https://doi.org/10.1007/bf01280294openalex-snapshot
The zygote and proembryo of alfalfa: quantitative, three-dimensional analysis and implications for biparental plastid inheritance
inferredcites →https://doi.org/10.1007/bf01297349openalex-snapshot
Epifluorescent microscopic studies on the mechanism of preferential destruction of chloroplast nucleoids of male origin in young zygotes ofChlamydomonas reinhardtii
inferredcites →https://doi.org/10.1007/bf01322625openalex-snapshot
Organization of the early post-fertilization megagametophyte ofPopulus deltoides
inferredcites →https://doi.org/10.1007/bf01323275openalex-snapshot
Generative cell composition and its relation to male plastid inheritance patterns inMedicago sativa
inferredcites →https://doi.org/10.1007/bf01332652openalex-snapshot
Behavior of organelle nuclei (nucleoids) in generative and vegetative cells during maturation of pollen inLilium longiflorum andPelargonium zonale
inferredcites →https://doi.org/10.1007/bf01343371openalex-snapshot
Fluorescence microscopy of plastid nucleoids and a survey of nuclease C in higher plants with respect to mode of plastid inheritance
inferredcites →https://doi.org/10.1007/bf01353997openalex-snapshot
Quantitative, three-dimensional ultrastructure of isolated corn (Zea mays) sperm cells
inferredcites →https://doi.org/10.1007/bf01403723openalex-snapshot
Ultrastructural characterization and three-dimensional reconstruction of isolated maize (Zea mays L.) egg cell protoplasts
inferredcites →https://doi.org/10.1007/bf01417530openalex-snapshot
Ultrastructural analysis of the sperm cells of mature pollen of maize,Zea mays
inferredcites →https://doi.org/10.1007/bf01544749openalex-snapshot
Elimination of mitochondrial elements and improved viability in hybrid cells
inferredcites →https://doi.org/10.1007/bf01637253openalex-snapshot
Disappearance of plastid and mitochondrial nucleoids during the formation of generative cells of higher plants revealed by fluorescence microscopy
inferredcites →https://doi.org/10.1007/bf01666263openalex-snapshot
Sperm cells in pollen tubes ofNicotians tabacum L.: three-dimensional reconstruction, cytoplasmic diminution, and quantitative cytology
inferredcites →https://doi.org/10.1007/bf01917436openalex-snapshot
Über Plastidenkonkurrenz bei Oenothera
inferredcites →https://doi.org/10.1007/bf02675411openalex-snapshot
Mechanisms of maternal inheritance of plastids and mitochondria: Developmental and ultrastructural evidence
inferredcites →https://doi.org/10.1016/0022-5193(82)90371-xopenalex-snapshot
Sex is dangerous in a world of potential symbionts or the basis of selection for uniparental inheritance
inferredcites →https://doi.org/10.1016/0092-8674(84)90014-xopenalex-snapshot
Chloroplast DNA deletions associated with wheat plants regenerated from pollen: possible basis for maternal inheritance of chloroplasts
inferredcites →https://doi.org/10.1016/0147-619x(80)90063-3openalex-snapshot
Elimination of plastids during spermatogenesis and fertilization in the plant kingdom
inferredcites →https://doi.org/10.1016/0168-9452(87)90123-3openalex-snapshot
Why are plastids maternally inherited in epilobium? Ultrastructural observations during microgametogenesis
inferredcites →https://doi.org/10.1016/0959-437x(93)90009-eopenalex-snapshot
Origin and ,evolution of organelle genomes
inferredcites →https://doi.org/10.1016/1047-8477(92)90066-jopenalex-snapshot
Mitochondrial derivatives of Culex quinquefasciatus (culicidae) spermatozoon: Some new aspects evidenced by cytochemistry and image processing
inferredcites →https://doi.org/10.1016/s0012-1606(05)80024-7openalex-snapshot
Monitoring by epifluorescence microscopy of organelle DNA fate during pollen development in five angiosperm species
inferredcites →https://doi.org/10.1016/s0074-7696(08)61094-3openalex-snapshot
Cytoskeleton and Cytoplasmic Organization of Pollen and Pollen Tubes
inferredcites →https://doi.org/10.1016/s0074-7696(08)61095-5openalex-snapshot
The Male Germ Unit: Concept, Composition, and Significance
inferredcites →https://doi.org/10.1016/s0367-2530(17)31601-8openalex-snapshot
Ultrastructural Studies on Plastids of Generative and Vegetative Cells in Liliaceae. 7. Plastid distribution during generative cell development in Tulbaghia violacea Harv.
inferredcites →https://doi.org/10.1038/hdy.1973.1openalex-snapshot
The control of plastid inheritance in Pelargonium II
inferredcites →https://doi.org/10.1038/hdy.1989.86openalex-snapshot
Variation in plastid inheritance between pelargonium cultivars and their hybrids
inferredcites →https://doi.org/10.1073/pnas.82.18.6129openalex-snapshot
Preferential fertilization in Plumbago : Ultrastructural evidence for gamete-level recognition in an angiosperm
inferredcites →https://doi.org/10.1073/pnas.82.20.6960openalex-snapshot
Interspecific chloroplast recombination in a Nicotiana somatic hybrid
inferredcites →https://doi.org/10.1073/pnas.84.7.2097openalex-snapshot
Chloroplast DNA polymorphisms in lodgepole and jack pines and their hybrids.
inferredcites →https://doi.org/10.1073/pnas.85.8.2594openalex-snapshot
Exclusion of male mitochondria and plastids during syngamy in barley as a basis for maternal inheritance
inferredcites →https://doi.org/10.1073/pnas.86.23.9347openalex-snapshot
Chloroplast and mitochondrial DNA are paternally inherited in Sequoia sempervirens D. Don Endl
inferredcites →https://doi.org/10.1080/00087114.1973.10797127openalex-snapshot
Sur L'Origine Paternelle des Organites du Proembryon duChamaecyparis LawsonianaA. Murr. (Cupressacèes)
inferredcites →https://doi.org/10.1086/411855openalex-snapshot
Evolutionary Consequences of Intracellular Organelle Competition
inferredcites →https://doi.org/10.1093/genetics/133.4.989openalex-snapshot
Plastome-genome interactions affect plastid transmission in Oenothera.
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a109517openalex-snapshot
Organelle transmission in higher plants: organelle alteration vs. physical exclusion
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110163openalex-snapshot
Transmission of chlorophyll deficiencies in Medicago sativa
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110443openalex-snapshot
Pollen Transmission of Plastid–DNA Under Genotypic Control in Petunia hybrida Hort
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110838openalex-snapshot
Influence of Parental Genotype on Plastid Inheritance in Medicago sativa
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110906openalex-snapshot
Paternal Chloroplast DNA Inheritance in a Diallel Cross of Jack Pine (Pinus banksiana Lamb.)
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111023openalex-snapshot
Paternal Inheritance of Plastids in Engelmann Spruce X Blue Spruce Hybrids
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111228openalex-snapshot
Discordant Inheritance of Mitochondrial and Plastid DNA in Diverse Alfalfa Genotypes
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111430openalex-snapshot
Biparental Inheritance of the Chloroplast Genome in Coreopsis (Asteraceae)
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111480openalex-snapshot
Relaxed and Stringent Genomes: Why Cytoplasmic Genes Don't Obey Mendel's Laws
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111481openalex-snapshot
The Salvage/Turnover/Repair (STOR) Model for Uniparental Inheritance in Chlamydomonas: DNA as a Source of Sustenance
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a076932openalex-snapshot
Nuclease C Polymorphism of Calcium-Dependent Nucleases in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077328openalex-snapshot
Survey of Ca2+-Dependent Nuclease in Green Plants
inferredcites →https://doi.org/10.1098/rspb.1992.0044openalex-snapshot
Intracellular symbionts and the evolution of uniparental cytoplasmic inheritance
inferredcites →https://doi.org/10.1111/j.1365-3180.1985.tb00612.xopenalex-snapshot
Physical basis for the maternal inheritance of triazine resistance inAmaranthus hybridus
inferredcites →https://doi.org/10.1111/j.1469-185x.1982.tb00373.xopenalex-snapshot
ULTRASTRUCTURE OF PLASTID INHERITANCE: GREEN ALGAE TO ANGIOSPERMS
inferredcites →https://doi.org/10.1111/j.1558-5646.1991.tb02641.xopenalex-snapshot
MITOCHONDRIAL INHERITANCE PATTERNS ACROSS A COTTONWOOD HYBRID ZONE: CYTONUCLEAR DISEQUILIBRIA AND HYBRID ZONE DYNAMICS
inferredcites →https://doi.org/10.1126/science.208.4440.196openalex-snapshot
Organelle Alteration as a Mechanism for Maternal Inheritance
inferredcites →https://doi.org/10.1126/science.6353578openalex-snapshot
Relaxed Cellular Controls and Organelle Heredity
inferredcites →https://doi.org/10.1139/b76-173openalex-snapshot
Anther and pollen infection in relation to the pollen and seed transmissibility of two strains of barley stripe mosaic virus in barley
inferredcites →https://doi.org/10.1139/x86-205openalex-snapshot
Paternal inheritance of chloroplast DNA in Douglas-fir
inferredcites →https://doi.org/10.1139/x88-209openalex-snapshot
Chloroplast DNA variation within individual trees of a Pinusbanksiana–Pinusconforta sympatric region
inferredcites →https://doi.org/10.1139/x91-100openalex-snapshot
Inheritance of chloroplast and mitochondrial DNA in incense-cedar (Calocedrusdecurrens)
inferredcites →https://doi.org/10.1139/x92-010openalex-snapshot
The inheritance of mitochondrial DNA in Douglas-fir (Pseudotsugamenziesii)
inferredcites →https://doi.org/10.1242/jcs.89.4.551openalex-snapshot
Insemination of the archegonium and fertilization in Taxus baccata L
inferredcites →https://doi.org/10.1242/jcs.99.1.21openalex-snapshot
Microtubule-determined plastid distribution during microsporogenesis in Lilium longiflorum
inferredcites →https://doi.org/10.18174/201610openalex-snapshot
Pollen tube - pistil interaction and fertilization in Lilium longiflorum
inferredcites →https://doi.org/10.2307/1223218openalex-snapshot
Chloroplast DNA and biosystematics: The effects of intraspecific diversity and plastid transmission
inferredcites →https://doi.org/10.2307/2445640openalex-snapshot
Evidence from Chloroplast DNA Restriction Site Analysis on the Relationships of Scalesia (Asteraceae: Heliantheae)
inferredcites →https://doi.org/10.5281/zenodo.16047652openalex-snapshot
Loss of the Paternal Mitochondrion during Fertilization
inferredcites →https://doi.org/10.5586/asbp.1988.024openalex-snapshot
Ultrastructural transformations in the cytoplasm of differentiating Hyacinthus orientalis L. pollen cells
inferredcites →https://doi.org/10.5685/plmorphol.5.19openalex-snapshot
Cytological study on plastid inheritance of Cryptomeria japonica D.Don
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A new hybrid from Taiwan, Elatostema ×hybrida (Urticaceae), is the first confirmed natural hybrid for Urticaceae
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Plant Interspecific Hybridization: Outcomes and Issues at the Intersection of Species
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Biological Containment Strategies for Transgenic Crops
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Multi‐locus phylogenetics, lineage sorting, and reticulation in Pinus subsection Australes
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Plastid genomes reveal recurrent formation of allopolyploid Fragaria
inferred← citeshttps://doi.org/10.1002/bies.201400110openalex-snapshot
Why are most organelle genomes transmitted maternally?
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Population Genomics Approaches Identify a Cryptic, Emerging Generalist Pest Complex
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Node ages, relationships, and phylogenomic incongruence in an ancient gymnosperm lineage – Phylogeny of Ephedra revisited
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Molecular systematics of Cuscuta subgenus Monogynella (Convolvulaceae) based on plastid and nuclear sequences
inferred← citeshttps://doi.org/10.1002/tax.612009openalex-snapshot
A dated species–tree approach to the trans–Pacific disjunction of the genus Jovellana (Calceolariaceae, Lamiales)
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Chloroplast DNA variation and hybridization between invasive populations of Japanese knotweed and giant knotweed (Fallopia, Polygonaceae)
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Transgenic Plastids in Basic Research and Plant Biotechnology
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Plant phylogeography based on organelle genes: an introduction
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Microspore Embryo Induction and Development in Higher Plants: Cytological and Ultrastructural Aspects
inferred← citeshttps://doi.org/10.1007/4735_2007_0223openalex-snapshot
Structure, function, and inheritance of plastid genomes
inferred← citeshttps://doi.org/10.1007/4735_2007_0226openalex-snapshot
Plastid biogenesis and differentiation
inferred← citeshttps://doi.org/10.1007/978-1-4020-3166-3_16openalex-snapshot
Chloroplast Genetic Engineering
inferred← citeshttps://doi.org/10.1007/978-1-4020-8854-4_11openalex-snapshot
Programmed Cell Death and Microspore Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4020-9602-0_7openalex-snapshot
Syngamy, Embryo Development and Seed Dispersal
inferred← citeshttps://doi.org/10.1007/978-3-642-02301-9_14openalex-snapshot
Fertilization in Angiosperms
inferred← citeshttps://doi.org/10.1007/978-3-642-19454-2_11openalex-snapshot
Small RNA Pathways and Their Function in the Male Gametophyte
inferred← citeshttps://doi.org/10.1007/978-3-642-57203-6_4openalex-snapshot
Extranuclear Inheritance: Plastid Genetics: Manipulation of Plastid Genomes and Biotechnological Applications
inferred← citeshttps://doi.org/10.1007/978-3-642-59940-8_2openalex-snapshot
Recombination:Organelle DNA of Plants and Fungi: Inheritance and Recombination
inferred← citeshttps://doi.org/10.1007/978-3-642-59969-9_7openalex-snapshot
Double Fertilization in Flowering Plants: Origin, Mechanisms and New Information from in vitro Fertilization
inferred← citeshttps://doi.org/10.1007/978-3-642-59985-9_20openalex-snapshot
Androgenesis and albinism in Poaceae: influence of genotype and carbohydrates
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_11openalex-snapshot
Plastome Mutants of Higher Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_5openalex-snapshot
Plastid Genomes of Seed Plants
inferred← citeshttps://doi.org/10.1007/978-94-017-1203-3_21openalex-snapshot
Inheritance of Cytoplasmic Traits — Embryological Perspectives
inferred← citeshttps://doi.org/10.1007/978-94-017-2311-4_14openalex-snapshot
Variation in Woody Plants; Molecular Markers, Evolutionary Processes and Conservation Biology
inferred← citeshttps://doi.org/10.1007/bf01276641openalex-snapshot
Emerging data on pollen tube growth and fertilization in flowering plants, 1990?1995
inferred← citeshttps://doi.org/10.1007/bf01279096openalex-snapshot
Differential development of plastids during microspore embryogenesis in barley
inferred← citeshttps://doi.org/10.1007/bf02344555openalex-snapshot
Spatial distribution of cpDNA and mtDNA haplotypes in a hybrid zone betweenPinus pumila andP. parviflora var.pentaphylla (Pinaceae)
inferred← citeshttps://doi.org/10.1007/pl00013867openalex-snapshot
Extensive Mitochondrial Introgression from Pinus pumila to P. parviflora var. pentaphylla (Pinaceae)
inferred← citeshttps://doi.org/10.1007/s00114-004-0571-3openalex-snapshot
The evolutionary processes of mitochondrial and chloroplast genomes differ from those of nuclear genomes
inferred← citeshttps://doi.org/10.1007/s00122-003-1424-8openalex-snapshot
Low frequency transmission of a plastid-encoded trait in Setaria italica
inferred← citeshttps://doi.org/10.1007/s00122-004-1800-zopenalex-snapshot
Chloroplast DNA inheritance and variation in Leucadendron species (Proteaceae) as revealed by PCR-RFLP
inferred← citeshttps://doi.org/10.1007/s00122-006-0436-6openalex-snapshot
Inheritance of organelle DNA markers in a pea cross associated with nuclear-cytoplasmic incompatibility
inferred← citeshttps://doi.org/10.1007/s00122-012-1930-7openalex-snapshot
Spectinomycin resistance mutations in the rrn16 gene are new plastid markers in Medicago sativa
inferred← citeshttps://doi.org/10.1007/s00122-023-04398-8openalex-snapshot
Molecular genetics of cytoplasmic male sterility and restorer-of-fertility for the fine tuning of pollen production in crops
inferred← citeshttps://doi.org/10.1007/s001220100663openalex-snapshot
New mitochondrial genome organization in three interspecific somatic hybrids of Medicago sativa including the parent-specific amplification of substoichiometric mitochondrial DNA units
inferred← citeshttps://doi.org/10.1007/s00299-009-0733-zopenalex-snapshot
Microspore embryogenesis and programmed cell death in barley: effects of copper on albinism in recalcitrant cultivars
inferred← citeshttps://doi.org/10.1007/s00343-020-0298-9openalex-snapshot
Development of organelle single nucleotide polymorphism (SNP) markers and their application for the identification of cytoplasmic inheritance patterns in Pyropia yezoensis (Bangiales, Rhodophyta)
inferred← citeshttps://doi.org/10.1007/s00425-002-0853-yopenalex-snapshot
Reduction in amounts of mitochondrial DNA in the sperm cells as a mechanism for maternal inheritance in Hordeum vulgare
inferred← citeshttps://doi.org/10.1007/s00425-012-1768-xopenalex-snapshot
Biparental inheritance of organelles in Pelargonium: evidence for intergenomic recombination of mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/s00425-017-2706-8openalex-snapshot
Chondriokinesis during microsporogenesis in plants
inferred← citeshttps://doi.org/10.1007/s004250050606openalex-snapshot
The selective increase or decrease of organellar DNA in generative cells just after pollen mitosis one controls cytoplasmic inheritance
inferred← citeshttps://doi.org/10.1007/s00438-009-0488-9openalex-snapshot
Biparental inheritance of plastidial and mitochondrial DNA and hybrid variegation in Pelargonium
inferred← citeshttps://doi.org/10.1007/s00438-011-0653-9openalex-snapshot
Maternal inheritance of plastids and mitochondria in Cycas L. (Cycadaceae)
inferred← citeshttps://doi.org/10.1007/s00438-012-0732-6openalex-snapshot
Maternal inheritance of mitochondrial genomes and complex inheritance of chloroplast genomes in Actinidia Lind.: evidences from interspecific crosses
inferred← citeshttps://doi.org/10.1007/s004970000041openalex-snapshot
Western white pine ( Pinus monticola Dougl.) reproduction: II. Fertilisation and cytoplasmic inheritance
inferred← citeshttps://doi.org/10.1007/s004970000042openalex-snapshot
Western white pine ( Pinus monticola Dougl.) reproduction: I. Gametophyte development
inferred← citeshttps://doi.org/10.1007/s004970000043openalex-snapshot
Plastid differentiation during androgenesis in albino and non-albino producing cultivars of barley ( Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1007/s004970050194openalex-snapshot
In vitro double fertilization in Nicotiana tabacum (L.): fusion behavior and gamete interaction traced by video-enhanced microscopy
inferred← citeshttps://doi.org/10.1007/s00606-002-0264-3openalex-snapshot
Phylogenetic split of Larix : evidence from paternally inherited cpDNA trn T- trn F region
inferred← citeshttps://doi.org/10.1007/s00606-008-0123-yopenalex-snapshot
Genetic variation of Pinus uncinata (Pinaceae) in the Pyrenees determined with cpSSR markers
inferred← citeshttps://doi.org/10.1007/s00606-009-0168-6openalex-snapshot
Edraianthus × lakusicii (Campanulaceae) a new intersectional natural hybrid: morphological and molecular evidence
inferred← citeshttps://doi.org/10.1007/s00606-009-0250-0openalex-snapshot
Mitochondrial DNA reveals complex genetic structuring in a stenoendemic conifer Picea omorika [(Panč.) Purk.] caused by its long persistence within the refugial Balkan region
inferred← citeshttps://doi.org/10.1007/s00606-013-0800-3openalex-snapshot
Genetic differentiation and delimitation of Pugionium dolabratum and Pugionium cornutum (Brassicaceae)
inferred← citeshttps://doi.org/10.1007/s00606-013-0840-8openalex-snapshot
Chloroplast microsatellite diversity of Opisthopappus Shih (Asteraceae) endemic to China
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/s00606-015-1226-xopenalex-snapshot
Reproduction biology and chloroplast inheritance in Bromeliaceae: a case study in Fosterella (Pitcairnioideae)
inferred← citeshttps://doi.org/10.1007/s00606-016-1289-3openalex-snapshot
Determining the extent and direction of introgression between three spruce species based on molecular markers from three genomes with different rates of gene flow
inferred← citeshttps://doi.org/10.1007/s00606-020-01671-xopenalex-snapshot
Phylogenetic relationships within the subtribe Cynoglossinae (Cynoglossoideae: Boraginaceae): new insights from nuclear and plastid DNA sequence data
inferred← citeshttps://doi.org/10.1007/s006060200024openalex-snapshot
Chloroplast DNA phylogeography of Fagus crenata (Fagaceae) in Japan
inferred← citeshttps://doi.org/10.1007/s00709-002-0050-7openalex-snapshot
Cytological evidence for preservation of mitochondrial and plastid DNA in the mature generative cells of Chlorophytum spp. (Liliaceae)
inferred← citeshttps://doi.org/10.1007/s00709-004-0065-3openalex-snapshot
Presence of plastid and absence of mitochondrial DNA in male reproductive cells as evidence for cytoplasmic inheritance in Turnera ulmifolia and Zantedeschia aethiopica
inferred← citeshttps://doi.org/10.1007/s00709-005-0088-4openalex-snapshot
Paternal cytoplasmic transmission in Chinese pine (Pinus tabulaeformis)
inferred← citeshttps://doi.org/10.1007/s00709-015-0935-xopenalex-snapshot
Visualisation of plastid degradation in sperm cells of wheat pollen
inferred← citeshttps://doi.org/10.1007/s00709-019-01363-5openalex-snapshot
Distribution of plastids and mitochondria during male gametophyte formation in Tinantia erecta (Jacq.) Fenzl
inferred← citeshttps://doi.org/10.1007/s10265-009-0291-zopenalex-snapshot
Why does biparental plastid inheritance revive in angiosperms?
inferred← citeshttps://doi.org/10.1007/s10265-009-0293-xopenalex-snapshot
Mechanisms for independent cytoplasmic inheritance of mitochondria and plastids in angiosperms
inferred← citeshttps://doi.org/10.1007/s10265-010-0309-6openalex-snapshot
Cytoplasmic inheritance in green algae: patterns, mechanisms and relation to sex type
inferred← citeshttps://doi.org/10.1007/s10265-010-0313-xopenalex-snapshot
Cytoplasmic inheritance of organelles in brown algae
inferred← citeshttps://doi.org/10.1007/s10265-014-0646-yopenalex-snapshot
Outcrossing rates and organelle inheritance estimated from two natural populations of the Japanese endemic conifer Sciadopitys verticillata
inferred← citeshttps://doi.org/10.1007/s10265-017-0934-4openalex-snapshot
Autophagy, programmed cell death and reactive oxygen species in sexual reproduction in plants
inferred← citeshttps://doi.org/10.1007/s10265-017-0992-7openalex-snapshot
The origin of wild populations of Toxicodendron succedaneum on mainland Japan revealed by genetic variation in chloroplast and nuclear DNA
inferred← citeshttps://doi.org/10.1007/s10265-021-01301-8openalex-snapshot
Phylogenetic origin of two Japanese Torreya taxa found in two regions with strongly contrasting snow depth
inferred← citeshttps://doi.org/10.1007/s10310-012-0368-8openalex-snapshot
Indigenous genetic lineages ofFagus crenatafound in the Izu Peninsula suggest that there was one of refugia for the species during the last glacial maximum
inferred← citeshttps://doi.org/10.1007/s10310-012-0384-8openalex-snapshot
Genetic evidence for paternal inheritance of the chloroplast in four Australian Callitris species (Cupressaceae)
inferred← citeshttps://doi.org/10.1007/s10342-012-0602-0openalex-snapshot
Validation of DNA barcoding as an efficient tool for taxon identification and detection of species diversity in Italian conifers
inferred← citeshttps://doi.org/10.1007/s10342-019-01254-7openalex-snapshot
What does a mixed population of Pinus sibirica and P. pumila from the southern Baikal region suggest about the structure of their hybrid zone?
inferred← citeshttps://doi.org/10.1007/s10528-013-9638-1openalex-snapshot
Genetic Diversity and Conservation Implications of Four Cupressus Species in China as Revealed by Microsatellite Markers
inferred← citeshttps://doi.org/10.1007/s10577-013-9349-9openalex-snapshot
DNA abandonment and the mechanisms of uniparental inheritance of mitochondria and chloroplasts
inferred← citeshttps://doi.org/10.1007/s10592-011-0277-yopenalex-snapshot
Distinctiveness, rarity and conservation in a subtropical highland conifer
inferred← citeshttps://doi.org/10.1007/s10592-016-0849-yopenalex-snapshot
Bruguiera hainesii, a critically endangered mangrove species, is a hybrid between B. cylindrica and B. gymnorhiza (Rhizophoraceae)
inferred← citeshttps://doi.org/10.1007/s10681-005-3156-0openalex-snapshot
Maternal inheritance of cytoplasmic organelles in intergeneric hybrids of Carica papaya L. and Vasconcellea spp. (Caricaceae Dumort., Brassicales)
inferred← citeshttps://doi.org/10.1007/s10681-007-9458-7openalex-snapshot
Attaining inter-subgeneric hybrids in fragrant azalea breeding and the inheritance of organelle DNA
inferred← citeshttps://doi.org/10.1007/s10681-009-9900-0openalex-snapshot
Genetic analysis of Jatropha species and interspecific hybrids of Jatropha curcas using nuclear and organelle specific markers
inferred← citeshttps://doi.org/10.1007/s10681-013-0889-zopenalex-snapshot
Chimeric inheritance of organelle DNA in variegated leaf seedlings from inter-subgeneric crossing of azalea
inferred← citeshttps://doi.org/10.1007/s10709-006-7542-xopenalex-snapshot
High RAPD but no cpDNA sequence variation in the endemic and endangered plant, Heptacodium miconioides Rehd. (Caprifoliaceae)
inferred← citeshttps://doi.org/10.1007/s10709-006-7726-4openalex-snapshot
Differential organellar inheritance in Passiflora’s (Passifloraceae) subgenera
inferred← citeshttps://doi.org/10.1007/s10722-008-9379-xopenalex-snapshot
Relationships among Avena species as revealed by consensus chloroplast simple sequence repeat (ccSSR) markers
inferred← citeshttps://doi.org/10.1007/s10811-015-0687-1openalex-snapshot
Maternal inheritance of organellar DNA demonstrated with DNA markers in crosses of Saccharina japonica (Laminariales, Phaeophyta)
inferred← citeshttps://doi.org/10.1007/s11032-005-0236-8openalex-snapshot
Maternal Inheritance of Chloroplasts between Brassica rapa and F1-hybrids Demonstrated by cpDNA Markers Specific to Oilseed Rape and B. rapa
inferred← citeshttps://doi.org/10.1007/s11103-004-0192-4openalex-snapshot
Generation of fertile transplastomic soybean
inferred← citeshttps://doi.org/10.1007/s11248-005-5262-0openalex-snapshot
Stability of Soybean Recombinant Plastome Over Six Generations
inferred← citeshttps://doi.org/10.1007/s11248-014-9842-8openalex-snapshot
Low frequency paternal transmission of plastid genes in Brassicaceae
inferred← citeshttps://doi.org/10.1007/s11295-005-0007-zopenalex-snapshot
Species-diagnostic markers in Larix spp. based on RAPDs and nuclear, cpDNA, and mtDNA gene sequences, and their phylogenetic implications
inferred← citeshttps://doi.org/10.1007/s11295-010-0349-zopenalex-snapshot
Discordant mtDNA and cpDNA phylogenies indicate geographic speciation and reticulation as driving factors for the diversification of the genus Picea
inferred← citeshttps://doi.org/10.1007/s11295-011-0392-4openalex-snapshot
Range-wide chloroplast and mitochondrial DNA imprints reveal multiple lineages and complex biogeographic history for Douglas-fir
inferred← citeshttps://doi.org/10.1007/s11295-013-0601-4openalex-snapshot
Complex origin of Trinitario-type Theobroma cacao (Malvaceae) from Trinidad and Tobago revealed using plastid genomics
inferred← citeshttps://doi.org/10.1007/s11295-013-0619-7openalex-snapshot
Molecular identification of natural mangrove hybrids of Rhizophora in Peninsular Malaysia
inferred← citeshttps://doi.org/10.1007/s11295-017-1112-5openalex-snapshot
Differential landscape effects on the fine-scale genetic structure of populations of a montane conifer from central Mexico
inferred← citeshttps://doi.org/10.1007/s11295-018-1250-4openalex-snapshot
Phylogeography of Brazilian pine (Araucaria angustifolia): integrative evidence for pre-Columbian anthropogenic dispersal
inferred← citeshttps://doi.org/10.1007/s11295-020-01434-2openalex-snapshot
Phylogeography and species distribution modeling reveal a historic disjunction for the conifer Podocarpus lambertii
inferred← citeshttps://doi.org/10.1007/s11295-021-01519-6openalex-snapshot
Parent–offspring variation transmission in full-sib families revealed predominantly paternal inheritance of chloroplast DNA in Pinus massoniana (Pinaceae)
inferred← citeshttps://doi.org/10.1007/s11295-023-01617-7openalex-snapshot
Range shift and introgression of three Japanese Abies species: insights from population genetic data and species distribution modeling
inferred← citeshttps://doi.org/10.1007/s11515-008-0076-0openalex-snapshot
Confirmation of natural hybrids between Gentiana straminea and G. siphonantha (Gentianaceae) based on molecular evidence
inferred← citeshttps://doi.org/10.1007/s12041-010-0015-0openalex-snapshot
AFLP studies on downy-mildew-resistant and downy-mildew-susceptible genotypes of opium poppy
inferred← citeshttps://doi.org/10.1007/s12064-003-0061-8openalex-snapshot
Maintaining heritable variation via sex-limited temporally fluctuating selection: a phenotypic model accommodating non-Mendelian epigenetic effects
inferred← citeshttps://doi.org/10.1007/s13258-010-0630-4openalex-snapshot
Sequence diversification of 45S rRNA ITS, trnH-psbA spacer, and matK genic regions in several Allium species
inferred← citeshttps://doi.org/10.1007/s13258-012-0057-1openalex-snapshot
Molecular and cytological evidences for the natural wheatgrass hybrids occurrence and origin in west China
inferred← citeshttps://doi.org/10.1007/s13595-020-00967-9openalex-snapshot
Portuguese Pinus nigra J.F. Arnold populations: genetic diversity, structure and relationships inferred by SSR markers
inferred← citeshttps://doi.org/10.1016/b0-12-227050-9/00017-xopenalex-snapshot
FLOWERING AND REPRODUCTION | Fertilization
inferred← citeshttps://doi.org/10.1016/b978-0-12-394279-1.00005-3openalex-snapshot
Cytonuclear Adaptation in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-815396-3.00010-xopenalex-snapshot
Natural Mating Systems and Controlled Mating
inferred← citeshttps://doi.org/10.1016/j.aquabot.2011.03.001openalex-snapshot
Molecular confirmation of natural hybridization between Lumnitzera racemosa and Lumnitzera littorea
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.03.010openalex-snapshot
Maternal inheritance of mitochondrial DNA by diverse mechanisms to eliminate paternal mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2009.01.012openalex-snapshot
Gene duplication, transfer, and evolution in the chloroplast genome
inferred← citeshttps://doi.org/10.1016/j.bse.2009.09.009openalex-snapshot
Hybrid status of Tibouchina urvilleana Cogn. revealed by ITS sequences of nuclear ribosomal DNA
inferred← citeshttps://doi.org/10.1016/j.bse.2011.12.019openalex-snapshot
Genetic diversity and differentiation of Sinocalycanthus chinensis populations revealed by chloroplast microsatellite (cpSSRs) markers
inferred← citeshttps://doi.org/10.1016/j.bse.2015.09.005openalex-snapshot
Initial diversification, glacial survival, and continuous range expansion of Gentiana straminea (Gentianaceae) in the Qinghai–Tibet Plateau
inferred← citeshttps://doi.org/10.1016/j.bse.2015.11.011openalex-snapshot
Phylogenetic relationships and natural hybridization in Triadica inferred from nuclear and chloroplast DNA analyses
inferred← citeshttps://doi.org/10.1016/j.btre.2017.07.003openalex-snapshot
Evaluation of ITS2 for intraspecific identification of Paeonia lactiflora cultivars
inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.020openalex-snapshot
Selfish Mitonuclear Conflict
inferred← citeshttps://doi.org/10.1016/j.foreco.2007.02.012openalex-snapshot
Chloroplast DNA diversity in Castanopsis hystrix populations in south China
inferred← citeshttps://doi.org/10.1016/j.foreco.2021.119211openalex-snapshot
Targeted conservation management of white pines in China: Integrating phylogeographic structure, niche modeling, and conservation gap analyses
inferred← citeshttps://doi.org/10.1016/j.jsb.2005.07.011openalex-snapshot
Programmed cell death progressively models the development of anther sporophytic tissues from the tapetum and is triggered in pollen grains during maturation
inferred← citeshttps://doi.org/10.1016/j.micron.2011.10.012openalex-snapshot
Ultrastructural study on dynamics of plastids and mitochondria during microgametogenesis in watermelon
inferred← citeshttps://doi.org/10.1016/j.mito.2014.04.004openalex-snapshot
Mitochondrion role in molecular basis of cytoplasmic male sterility
inferred← citeshttps://doi.org/10.1016/j.molp.2018.11.002openalex-snapshot
Tension and Resolution: Dynamic, Evolving Populations of Organelle Genomes within Plant Cells
inferred← citeshttps://doi.org/10.1016/j.protis.2013.01.001openalex-snapshot
Inheritance of Mitochondrial DNA in the Pennate Diatom Haslea ostrearia (Naviculaceae) during Auxosporulation Suggests a Uniparental Transmission
inferred← citeshttps://doi.org/10.1016/j.recqb.2016.06.002openalex-snapshot
SPECIES DIVERSITY AND PLASTID DNA HAPLOTYPE DISTRIBUTIONS OF PINUS SUBSECTION AUSTRALES (PINACEAE) IN GUERRERO AND OAXACA
inferred← citeshttps://doi.org/10.1016/j.scienta.2012.05.004openalex-snapshot
Plastid trnL intron polymorphisms among Phalaenopsis species used for identifying the plastid genome type of Phalaenopsis hybrids
inferred← citeshttps://doi.org/10.1016/j.scienta.2017.02.031openalex-snapshot
Pollen and seed fertility differences of the backcross progenies between Solanum virginianum and eggplant with different inheritance pattern of chloroplast DNA
inferred← citeshttps://doi.org/10.1016/j.tree.2012.12.006openalex-snapshot
Evolutionary and ecological implications of sexual parasitism
inferred← citeshttps://doi.org/10.1016/j.virusres.2019.02.008openalex-snapshot
Beta vulgaris mitovirus 1 in diverse cultivars of beet and chard
inferred← citeshttps://doi.org/10.1016/j.ympev.2005.03.011openalex-snapshot
The internal transcribed spacer of nuclear ribosomal DNA in the gymnosperm Gnetum
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.05.039openalex-snapshot
Molecular phylogeny and biogeography of Picea (Pinaceae): Implications for phylogeographical studies using cytoplasmic haplotypes
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.02.001openalex-snapshot
Reticulate evolution in Thuja inferred from multiple gene sequences: Implications for the study of biogeographical disjunction between eastern Asia and North America
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.05.003openalex-snapshot
Phylogeography of a living fossil: Pleistocene glaciations forced Ginkgo biloba L. (Ginkgoaceae) into two refuge areas in China with limited subsequent postglacial expansion
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.09.011openalex-snapshot
Fast evolution of the retroprocessed mitochondrial rps3 gene in Conifer II and further evidence for the phylogeny of gymnosperms
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.03.007openalex-snapshot
Molecular phylogeny and biogeography of Pseudotsuga (Pinaceae): Insights into the floristic relationship between Taiwan and its adjacent areas
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.05.007openalex-snapshot
Plant recolonization in the Himalaya from the southeastern Qinghai-Tibetan Plateau: Geographical isolation contributed to high population differentiation
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.01.012openalex-snapshot
Plant molecular phylogeography in China and adjacent regions: Tracing the genetic imprints of Quaternary climate and environmental change in the world’s most diverse temperate flora
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.02.032openalex-snapshot
Arnica (Asteraceae) phylogeny revisited using RPB2: Complex patterns and multiple d-paralogues
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.004openalex-snapshot
Three genome-based phylogeny of Cupressaceae s.l.: Further evidence for the evolution of gymnosperms and Southern Hemisphere biogeography
inferred← citeshttps://doi.org/10.1016/j.ympev.2013.07.004openalex-snapshot
A new phylogeny for the genus Picea from plastid, mitochondrial, and nuclear sequences
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.02.005openalex-snapshot
Evolution and biogeography of gymnosperms
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.11.003openalex-snapshot
Deep phylogenetic incongruence in the angiosperm clade Rosidae
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.03.013openalex-snapshot
Molecular phylogenetics and evolutionary history of sect. Quinquefoliae (Pinus): Implications for Northern Hemisphere biogeography
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.07.020openalex-snapshot
Mitochondrial introgression and complex biogeographic history of the genus Picea
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106610openalex-snapshot
Phylotranscriptomics resolves interspecific relationships and indicates multiple historical out-of-North America dispersals through the Bering Land Bridge for the genus Picea (Pinaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106903openalex-snapshot
Under the rug: Abandoning persistent misconceptions that obfuscate organelle evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.107022openalex-snapshot
Genome-wide RAD sequencing resolves the evolutionary history of serrate leaf Juniperus and reveals discordance with chloroplast phylogeny
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.107066openalex-snapshot
Phylotranscriptomics reveals the complex evolutionary and biogeographic history of the genus Tsuga with an East Asian-North American disjunct distribution
inferred← citeshttps://doi.org/10.1016/s0065-2296(08)60298-0openalex-snapshot
Gametes, Fertilization and Early Embryogenesis in Flowering Plants
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61780-5openalex-snapshot
Temporal and Spatial Coordination of Cells with Their Plastid Component
inferred← citeshttps://doi.org/10.1016/s0075-9511(00)80006-7openalex-snapshot
Phylogenetic variability in the pigment complement of aquatic tracheophytes
inferred← citeshttps://doi.org/10.1016/s0169-5347(00)01856-5openalex-snapshot
Human mitochondrial DNA recombination: can it be true?
inferred← citeshttps://doi.org/10.1016/s0171-9335(99)80057-0openalex-snapshot
Decrease in mitochondrial DNA and concurrent increase in plastid DNA in generative cells of Pharbitis nil during pollen development
inferred← citeshttps://doi.org/10.1016/s0764-4469(01)01325-7openalex-snapshot
Double fertilization in flowering plants: Discovery, study methods and mechanisms
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr1openalex-snapshot
Author comment: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR1
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr11openalex-snapshot
Decision: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R1/PR11
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr13openalex-snapshot
Recommendation: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R2/PR13
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr2openalex-snapshot
Review: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR2
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr3openalex-snapshot
Review: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR3
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr4openalex-snapshot
Review: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR4
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr5openalex-snapshot
Recommendation: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR5
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr6openalex-snapshot
Decision: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R0/PR6
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr7openalex-snapshot
Author comment: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R1/PR7
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr8openalex-snapshot
Review: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R1/PR8
inferred← citeshttps://doi.org/10.1017/qpb.2022.15.pr9openalex-snapshot
Review: Exchange on dynamic encounter networks allows plant mitochondria to collect complete sets of mitochondrial DNA products despite their incomplete genomes — R1/PR9
inferred← citeshttps://doi.org/10.1017/s0016672311000127openalex-snapshot
Mating system and the critical migration rate for swamping selection
inferred← citeshttps://doi.org/10.1017/s0960258518000417openalex-snapshot
How much influence does the paternal parent have on seed germination?
inferred← citeshttps://doi.org/10.1017/s0960428603000301openalex-snapshot
PLASTID INHERITANCE IN STREPTOCARPUS (GESNERIACEAE) AND AN INFERRED HYBRID ORIGIN FOR A POPULATION OF S. AFF. PRIMULIFOLIUS FROM IGODA RIVER, SOUTH AFRICA
inferred← citeshttps://doi.org/10.1017/s0967026202003682openalex-snapshot
Inheritance patterns of ITS1, chloroplasts and mitochondria in artificial hybrids of the seaweeds Fucus serratus and F. evanescens (Phaeophyceae)
inferred← citeshttps://doi.org/10.1023/a:1025812621775openalex-snapshot
Plastid ultrastructure and DNA related to albinism in androgenetic embryos of various barley (Hordeum vulgare L.) cultivars
inferred← citeshttps://doi.org/10.1038/hdy.1997.103openalex-snapshot
Genetic control of the rate of transmission of rye B chromosomes. III. Male meiosis and gametogenesis
inferred← citeshttps://doi.org/10.1038/hdy.2008.11openalex-snapshot
Detection of rare paternal chloroplast inheritance in controlled crosses of the endangered sunflower Helianthus verticillatus
inferred← citeshttps://doi.org/10.1038/hdy.2016.65openalex-snapshot
Relative strength of fine-scale spatial genetic structure in paternally vs biparentally inherited DNA in a dioecious plant depends on both sex proportions and pollen-to-seed dispersal ratio
inferred← citeshttps://doi.org/10.1038/hdy.2016.72openalex-snapshot
Importance of incomplete lineage sorting and introgression in the origin of shared genetic variation between two closely related pines with overlapping distributions
inferred← citeshttps://doi.org/10.1038/s41437-019-0218-yopenalex-snapshot
Phylogeography of the Neotropical epiphytic orchid, Brassavola nodosa: evidence for a secondary contact zone in northwestern Costa Rica
inferred← citeshttps://doi.org/10.1038/s41477-018-0291-xopenalex-snapshot
Organelle DNA degradation contributes to the efficient use of phosphate in seed plants
inferred← citeshttps://doi.org/10.1038/s41598-020-73397-2openalex-snapshot
Large-scale phylogenomics reveals ancient introgression in Asian Hepatica and new insights into the origin of the insular endemic Hepatica maxima
inferred← citeshttps://doi.org/10.1038/s41598-021-81988-wopenalex-snapshot
Inheritance of chloroplast and mitochondrial genomes in cucumber revealed by four reciprocal F1 hybrid combinations
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800616openalex-snapshot
Genetic variation of Ginkgo biloba L. (Ginkgoaceae) based on cpDNA PCR-RFLPs: inference of glacial refugia
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800676openalex-snapshot
Evidence for paternal transmission and heteroplasmy in the mitochondrial genome of Silene vulgaris, a gynodioecious plant
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800796openalex-snapshot
Competition affects gene flow from oilseed rape (♀) to Brassica rapa (♂)
inferred← citeshttps://doi.org/10.1042/bst0380598openalex-snapshot
Male gamete biology in flowering plants
inferred← citeshttps://doi.org/10.1042/bst20190238openalex-snapshot
Evolving mtDNA populations within cells
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