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The cytological basis of the plastid inheritance in angiosperms
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1939.tb09353.xopenalex-snapshot
CYTOPLASMIC INCLUSIONS IN THE MALE GAMETES OF LILIUM
inferredcites →https://doi.org/10.1002/j.1537-2197.1965.tb06769.xopenalex-snapshot
FINE‐STRUCTURAL CHANGES IN THE CYTOPLASM OF GERMINATING POLLEN
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THE NATURE OF THE WALL BETWEEN GENERATIVE AND VEGETATIVE NUCLEI IN THE POLLEN GRAIN OF TRADESCANTIA PALUDOSA
inferredcites →https://doi.org/10.1002/j.1537-2197.1969.tb07545.xopenalex-snapshot
ULTRASTRUCTURE OF BETA POLLEN. I. CYTOPLASMIC CONSTITUENTS
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CHANGES IN PLASTID AND MITOCHONDRION CONTENT DURING MATURATION OF GENERATIVE CELLS OF SOLANUM (SOLANACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1981.tb06386.xopenalex-snapshot
ULTRASTRUCTURAL INVESTIGATIONS ON THE TWO‐NUCLEATE POLLEN GRAIN OF TILLANDSIA CAPUT‐MEDUSAE MORR. (BROMELIACEAE)
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AN ULTRASTRUCTURAL AND STEREOLOGICAL ANALYSIS OF POLLEN GRAINS OF HYOSCYAMUS NIGER DURING NORMAL ONTOGENY AND INDUCED EMBRYOGENIC DEVELOPMENT
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ULTRASTRUCTURE OF NICOTIANA ALATA POLLEN, ITS GERMINATION AND EARLY TUBE FORMATION
inferredcites →https://doi.org/10.1007/978-3-642-73271-3_79openalex-snapshot
The Development and Ultrastructure of Pollen in Frittillaria thunbergii MIQ
inferredcites →https://doi.org/10.1007/978-3-642-87137-5openalex-snapshot
Introduction to the Fine Structure of Plant Cells
inferredcites →https://doi.org/10.1007/bf00266555openalex-snapshot
Ultrastructural studies on plastids of generative and vegetative cells in Liliaceae
inferredcites →https://doi.org/10.1007/bf00267882openalex-snapshot
Unequal distribution of plastids during generative cell formation in Impatiens
inferredcites →https://doi.org/10.1007/bf00333187openalex-snapshot
Übertragung von Plastiden durch den Pollen bei Antirrhinum majus
inferredcites →https://doi.org/10.1007/bf00384700openalex-snapshot
Cytoplasmic inheritance and ultrastructure of the male generative cell of higher plants
inferredcites →https://doi.org/10.1007/bf00385991openalex-snapshot
Germination and early tube development in vitro of Lycopersicum peruvianum pollen: Ultrastructural features
inferredcites →https://doi.org/10.1007/bf00388107openalex-snapshot
Orchid embryology: Pollen tetrads of Epidendrum scutella in the anther and on the stigma
inferredcites →https://doi.org/10.1007/bf00392205openalex-snapshot
Structure and function of the microtubular cytoskeleton during pollen development in Gasteria verrucosa (Mill.) H. Duval
inferredcites →https://doi.org/10.1007/bf00393450openalex-snapshot
Ultrastructure of the sperm of Plumbago zeylanica
inferredcites →https://doi.org/10.1007/bf01247908openalex-snapshot
Fine structure of sperm cells in pollen grains ofBeta
inferredcites →https://doi.org/10.1007/bf01273229openalex-snapshot
Quantitative ultrastructural analysis of barley sperm
inferredcites →https://doi.org/10.1007/bf01273701openalex-snapshot
Computer-assisted reconstruction of the male germ unit in pollen ofBrassica campestris
inferredcites →https://doi.org/10.1007/bf01275703openalex-snapshot
Juxtaposition of the generative cell and vegetative nucleus in the mature pollen grain of amaryllis (Hippeastrum vitatum)
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/bf01373376openalex-snapshot
Elektronenmikroskopische Analyse der Pollenentwicklung vonHeleocharis palustris
inferredcites →https://doi.org/10.1007/bf02907773openalex-snapshot
Double fertilization in barley and the cytological explanation for haploid embryo formation, embryoless caryopses, and ovule abortion
inferredcites →https://doi.org/10.1016/0034-6667(77)90058-6openalex-snapshot
Fertilization in Higher Plants
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/10.1016/0968-0004(77)90447-9openalex-snapshot
Genetics and biogenesis of chloroplasts and mitochondria
inferredcites →https://doi.org/10.1016/s0022-5320(68)90028-2openalex-snapshot
Capsella embryogenesis: The early embryo
inferredcites →https://doi.org/10.1016/s0065-2660(08)60247-3openalex-snapshot
Genetic Analysis of Chloroplast Dna in Chlamydomonas
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/10.1073/pnas.80.10.3025openalex-snapshot
Differential methylation of chloroplast DNA regulates maternal inheritance in a methylated mutant of Chlamydomonas
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/10.1080/00087114.1984.10797684openalex-snapshot
The Ultrastructure of Pollen Grain Development inLycopersicum Peruvianum
inferredcites →https://doi.org/10.1080/00087114.1987.10797824openalex-snapshot
Ultrastructure of the Tricellular Pollen Grains of DiploidEuphorbia Dulcis
inferredcites →https://doi.org/10.1080/11263506809426473openalex-snapshot
Ultrastructure of the Pollen Grain and Taxonomy
inferredcites →https://doi.org/10.1086/336754openalex-snapshot
Ultrastructural Studies of the Pollen of Subtribe Castilleiinae, Family Scrophulariaceae
inferredcites →https://doi.org/10.1111/j.1438-8677.1924.tb00769.xopenalex-snapshot
1. W. Ruhland und K. Wetzel: Der Nachweis von Chloroplasten in den generativen Zellen von Pollenschläuchen
inferredcites →https://doi.org/10.1111/j.1438-8677.1964.tb00150.xopenalex-snapshot
FINE STRUCTURE OF PETUNIA POLLEN GRAIN AND POLLEN TUBE
inferredcites →https://doi.org/10.1111/j.1438-8677.1970.tb00672.xopenalex-snapshot
THE ULTRASTRUCTURE OF THE FERTILIZED EMBRYO SAC OF PETUNIA
inferredcites →https://doi.org/10.1111/j.1438-8677.1974.tb03152.xopenalex-snapshot
Das Zahlenverhältnis von mütterlichen und väterlichen Piastiden in den Zygoten von Oenothera erythrosepala Borbas (syn. Oe. lamarckiana )
inferredcites →https://doi.org/10.1111/j.1438-8677.1981.tb00390.xopenalex-snapshot
POLLEN TUBE PENETRATION AND FERTILIZATION IN SPINACH
inferredcites →https://doi.org/10.1111/j.1438-8677.1986.tb00480.xopenalex-snapshot
ULTRASTRUCTURE OF POLLEN DEVELOPMENT IN EUPHORBIA DULCIS L. 1. DIPLOID PLANTS
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb01033.xopenalex-snapshot
GAMETE COMPETITION IN PLANTS AND ANIMALS
inferredcites →https://doi.org/10.1126/science.208.4440.196openalex-snapshot
Organelle Alteration as a Mechanism for Maternal Inheritance
inferredcites →https://doi.org/10.1242/jcs.3.4.573openalex-snapshot
The formation of the generative cell in the pollen grain of Endymion non-scriptus (l)
inferredcites →https://doi.org/10.1242/jcs.8.2.289openalex-snapshot
Fine structure study of pollen development in Haemanthus katherinae baker: I. formation of vegetative and generative cells
inferredcites →https://doi.org/10.1515/znb-1960-0205openalex-snapshot
Elektronenmikroskopische Untersuchungen an Pollenschläuchen zweier Liliaceen
inferredcites →https://doi.org/10.1515/znb-1963-0712openalex-snapshot
Elektronenmikroskopische Beobachtungen an der generativen Zelle von Oenothera hookeri Torr. et Gray
inferredcites →https://doi.org/10.2135/cropsci1966.0011183x000600010013xopenalex-snapshot
Inheritance of a Variegated Leaf Pattern in Hexaploid Wheat1
inferredcites →https://doi.org/10.2307/2440229openalex-snapshot
Fine-Structural Changes in the Cytoplasm of Germinating Pollen
inferredcites →https://doi.org/10.5586/asbp.1981.042openalex-snapshot
Structural and physiological relationships between embryo and endosperm at the early stages of development
inferredcites →https://doi.org/10.5586/asbp.1981.052openalex-snapshot
Unequal plastid distribution during the development of the male gametophyte of angiosperms
inferredcites →https://doi.org/10.5860/choice.26-4486openalex-snapshot
Plant sperm cells as tools for biotechnology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.268.1.1zenodo-depositor-declared
A broadly sampled 3-loci plastid phylogeny of Atraphaxis (Polygoneae, Polygonoideae, Polygonaceae) reveals new taxa: I. Atraphaxis kamelinii spec. nov. from Mongolia
inferred← citeshttps://doi.org/10.1002/9781118373781.ch5openalex-snapshot
Biological Containment Strategies for Transgenic Crops
inferred← citeshttps://doi.org/10.1002/ajb2.70272openalex-snapshot
Evolutionary relationship between organellar DNA inheritance patterns and traits of seed plants
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1993.tb15301.xopenalex-snapshot
GENETIC EVIDENCE FOR TRACE PATERNAL TRANSMISSION OF PLASTIDS IN LIRIODENDRON AND MAGNOLIA (MAGNOLIACEAE)
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1993.tb15335.xopenalex-snapshot
Evidence for introgression in azaleas (Rhododendron; Ericaceae): Chloroplast DNA and morphological variation in a hybrid swarm on Stone Mountain, Georgia
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1994.tb11476.xopenalex-snapshot
I nheritance of plastid DNA in the T urnera ulmifolia complex (T urneraceae )
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1996.tb12718.xopenalex-snapshot
INVITED SPECIAL PAPER: The hows and whys of cytoplasmic inheritance in seed plants
inferred← citeshttps://doi.org/10.1007/1-4020-4904-8_2openalex-snapshot
Plant phylogeography based on organelle genes: an introduction
inferred← citeshttps://doi.org/10.1007/4735_2007_0223openalex-snapshot
Structure, function, and inheritance of plastid genomes
inferred← citeshttps://doi.org/10.1007/978-1-4020-3166-3_4openalex-snapshot
The Sexual Inheritance of Plant Organelles
inferred← citeshttps://doi.org/10.1007/978-1-4612-2958-2_40openalex-snapshot
Cytological Studies on Plastid Inheritance in Alfalfa (Medicago sativa)
inferred← citeshttps://doi.org/10.1007/978-1-4612-2958-2_8openalex-snapshot
Plastid Developmental Pathways in Some Angiosperm Reproductive Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-50133-3_11openalex-snapshot
Reproductive Biology of Angiosperms
inferred← citeshttps://doi.org/10.1007/978-3-642-56276-1_1openalex-snapshot
Milestones in Plastid Genetics of Higher Plants
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/10.1007/978-3-642-76293-2_3openalex-snapshot
Cytology and Morphogenesis of Pollen and Spores
inferred← citeshttps://doi.org/10.1007/978-3-7091-9138-5_2openalex-snapshot
Plastid Genetics in Higher Plants
inferred← citeshttps://doi.org/10.1007/978-94-017-1203-3_21openalex-snapshot
Inheritance of Cytoplasmic Traits — Embryological Perspectives
inferred← citeshttps://doi.org/10.1007/978-94-017-1669-7_14openalex-snapshot
Cell biology of anther and pollen development
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/bf00200550openalex-snapshot
Ultrastructural investigations of mature embryo sacs of Daaucus carota, D. aureus and D. muricatus ? possible cytological explanations of paternal plastid inheritance
inferred← citeshttps://doi.org/10.1007/bf00219445openalex-snapshot
Plastid DNA diversity in natural populations of Beta maritima showing additional variation in sexual phenotype and mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/bf00222876openalex-snapshot
Complementary genes control biparental plastid inheritance in Pelargonium
inferred← citeshttps://doi.org/10.1007/bf00226107openalex-snapshot
Quantitative cytology of the alfalfa generative cell and its relation to male plastid inheritance patterns in three genotypes
inferred← citeshttps://doi.org/10.1007/bf00228491openalex-snapshot
An intermediate-voltage electron microscopic study of freeze-substituted generative cell in pear (Pyrus communis L.): features with relevance to cell-cell communication between the two cells of a germinating pollen
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/bf00417958openalex-snapshot
Inheritance and restriction fragment length polymorphism of chloroplast DNA in the genus Coffea L.
inferred← citeshttps://doi.org/10.1007/bf00588602openalex-snapshot
Inheritance of chloroplast DNA inPopulus
inferred← citeshttps://doi.org/10.1007/bf00714556openalex-snapshot
Calcium in the synergid cells and other regions of pearl millet ovaries
inferred← citeshttps://doi.org/10.1007/bf01240926openalex-snapshot
Chloroplast DNA inheritance in theStellaria longipes complex (Caryophyllaceae)
inferred← citeshttps://doi.org/10.1007/bf01280507openalex-snapshot
Unique positioning of mitochondria in developing microspores and pollen grains inPharbitis nil: mitochondria cover the nuclear surface at specific developmental stages
inferred← citeshttps://doi.org/10.1007/bf01281330openalex-snapshot
Cytological evidence of biparental inheritance of plastids and mitochondria inPelargonium
inferred← citeshttps://doi.org/10.1007/bf01666263openalex-snapshot
Sperm cells in pollen tubes ofNicotians tabacum L.: three-dimensional reconstruction, cytoplasmic diminution, and quantitative cytology
inferred← citeshttps://doi.org/10.1007/bf02344239openalex-snapshot
Chloroplast DNA typing by PCR-SSCP in thePinus pumila-P. parviflora var.pentaphylla complex (Pinaceae)
inferred← citeshttps://doi.org/10.1007/bf02344373openalex-snapshot
Development of male gametes in flowering plants
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/s001220051217openalex-snapshot
Chloroplast-DNA variation in cultivated and wild olive (Olea europaea L.)
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/s00425-017-2706-8openalex-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/s004970050126openalex-snapshot
Potential for biparental cytoplasmic inheritance in Jasminum officinale and Jasminum nudiflorum
inferred← citeshttps://doi.org/10.1007/s004970050155openalex-snapshot
Ultrastructural and molecular study of plastid inheritance in Abies alba and some Abies hybrids
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/s00709-015-0935-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/s10265-004-0160-8openalex-snapshot
Geographical distribution of two haplotypes of chloroplast DNA in four oak species (Quercus) in Japan
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/s10265-009-0306-9openalex-snapshot
Review of cytological studies on cellular and molecular mechanisms of uniparental (maternal or paternal) inheritance of plastid and mitochondrial genomes induced by active digestion of organelle nuclei (nucleoids)
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/s11295-007-0121-1openalex-snapshot
The effect of volcanism on postglacial migration and seed dispersal. A case study in southern South America
inferred← citeshttps://doi.org/10.1007/s11295-017-1152-xopenalex-snapshot
Field-based artificial crossings indicate partial compatibility of reciprocal crosses between Pinus sylvestris and Pinus mugo and unexpected chloroplast DNA inheritance
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/10.1016/b978-1-891127-79-3.50002-0openalex-snapshot
Barley Grain: Development and Structure
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.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.tig.2023.03.002openalex-snapshot
Maternal plastid inheritance: two abating factors identified
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61095-5openalex-snapshot
The Male Germ Unit: Concept, Composition, and Significance
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61109-2openalex-snapshot
Plant Reproductive Biology: Trends
inferred← citeshttps://doi.org/10.1023/a:1017914219789openalex-snapshot
Maternal Inheritance of Chloroplast DNA in Interspecific Crosses of Bromus
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Effect of geographical discontinuity on genetic variation in Quercus ilex L. (holm oak). Evidence from enzyme polymorphism
inferred← citeshttps://doi.org/10.1038/nbt0602-581openalex-snapshot
Molecular strategies for gene containment in transgenic crops
inferred← citeshttps://doi.org/10.1038/s41477-022-01323-7openalex-snapshot
Control of plastid inheritance by environmental and genetic factors
inferred← citeshttps://doi.org/10.1046/j.1365-2745.2003.00801.xopenalex-snapshot
Spatial patterns of maternal lineages and clones of Galium odoratum in a large ancient woodland: inferences about seedling recruitment
inferred← citeshttps://doi.org/10.1073/pnas.0700008104openalex-snapshot
Determining the transgene containment level provided by chloroplast transformation
inferred← citeshttps://doi.org/10.1080/03746600508684790openalex-snapshot
The components of the sexual reproduction process and the pathway toin Vivofertilization in higher plants
inferred← citeshttps://doi.org/10.1080/07352680903133252openalex-snapshot
Albinism in Plants: A Major Bottleneck in Wide Hybridization, Androgenesis and Doubled Haploid Culture
inferred← citeshttps://doi.org/10.1080/11263504.2024.2375333openalex-snapshot
Transition dynamics in plastid interconversion in land plants
inferred← citeshttps://doi.org/10.1080/11263509409430310openalex-snapshot
Morphological and molecular characterization of xOrchiaceras bergonii (Nanteuil) E.G. Cam
inferred← citeshttps://doi.org/10.1080/23802359.2020.1866450openalex-snapshot
Inheritance of Solanum chloroplast genomic DNA in interspecific hybrids
inferred← citeshttps://doi.org/10.1080/28347056.2023.2261790openalex-snapshot
Organelle inheritance: understanding the basis of plastid transmission for transgenic engineering
inferred← citeshttps://doi.org/10.1093/genetics/130.3.677openalex-snapshot
Biased gene conversion, copy number, and apparent mutation rate differences within chloroplast and bacterial genomes.
inferred← citeshttps://doi.org/10.1093/genetics/133.4.989openalex-snapshot
Plastome-genome interactions affect plastid transmission in Oenothera.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025860openalex-snapshot
Association between chloroplast and mitochondrial lineages in oaks
inferred← citeshttps://doi.org/10.1093/pcp/pcad104openalex-snapshot
Plastid Inheritance Revisited: Emerging Role of Organelle DNA Degradation in Angiosperms
inferred← citeshttps://doi.org/10.1093/pcp/pcg121openalex-snapshot
Examination of the Cytoplasmic DNA in Male Reproductive Cells to Determine the Potential for Cytoplasmic Inheritance in 295 Angiosperm Species
inferred← citeshttps://doi.org/10.1093/pcp/pci110openalex-snapshot
Potential Cytoplasmic Inheritance in Wisteria sinensis and Robinia pseudoacacia (Leguminosae)
inferred← citeshttps://doi.org/10.1093/pcp/pcm170openalex-snapshot
The Model Plant Medicago truncatula Exhibits Biparental Plastid Inheritance
inferred← citeshttps://doi.org/10.1093/pcp/pcn069openalex-snapshot
Occurrence of Plastids in the Sperm Cells of Caprifoliaceae: Biparental Plastid Inheritance in Angiosperms is Unilaterally Derived from Maternal Inheritance
inferred← citeshttps://doi.org/10.1093/pcp/pcy084openalex-snapshot
Chloroplast DNA Dynamics: Copy Number, Quality Control and Degradation
inferred← citeshttps://doi.org/10.1093/plphys/kiaf168openalex-snapshot
Cytoplasmic inheritance: The transmission of plastid and mitochondrial genomes across cells and generations
inferred← citeshttps://doi.org/10.1098/rspb.1992.0044openalex-snapshot
Intracellular symbionts and the evolution of uniparental cytoplasmic inheritance
inferred← citeshttps://doi.org/10.1101/gad.979902openalex-snapshot
An mt + gamete-specific nuclease that targets mt − chloroplasts during sexual reproduction in C. reinhardtii
inferred← citeshttps://doi.org/10.1104/pp.103.036657openalex-snapshot
Heterogeneous Pollen in Chlorophytum comosum, a Species with a Unique Mode of Plastid Inheritance Intermediate between the Maternal and Biparental Modes
inferred← citeshttps://doi.org/10.1104/pp.104.048298openalex-snapshot
Divergent Potentials for Cytoplasmic Inheritance within the Genus Syringa. A New Trait Associated with Speciogenesis
inferred← citeshttps://doi.org/10.1105/tpc.109.071902openalex-snapshot
The Levels of Male Gametic Mitochondrial DNA Are Highly Regulated in Angiosperms with Regard to Mitochondrial Inheritance
inferred← citeshttps://doi.org/10.1105/tpc.111.084012openalex-snapshot
A Conserved, Mg2+-Dependent Exonuclease Degrades Organelle DNA duringArabidopsisPollen Development
inferred← citeshttps://doi.org/10.1105/tpc.5.7.747openalex-snapshot
Karyogamy after Electrofusion of Single Egg and Sperm Cell Protoplasts from Maize: Cytological Evidence and Time Course.
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2009.00088.xopenalex-snapshot
Bridging the generation gap: flowering plant gametophytes and animal germlines reveal unexpected similarities
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1996.tb04471.xopenalex-snapshot
PARENTAL EFFECTS ON PROGENY PHENOTYPE IN PLANTS: DISTINGUISHING GENETIC AND ENVIRONMENTAL CAUSES
inferred← citeshttps://doi.org/10.1111/nph.70385openalex-snapshot
The Cpn20‐mediated plastid integrity is essential for growth and female gametophyte development in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pbi.13556openalex-snapshot
Green giant—a tiny chloroplast genome with mighty power to produce high‐value proteins: history and phylogeny
inferred← citeshttps://doi.org/10.1139/b94-047openalex-snapshot
Pollen development in Liriodendron tulipifera: some unusual features
inferred← citeshttps://doi.org/10.1146/annurev.arplant.42.1.189openalex-snapshot
Isolation And Characterization Of Sperm Cells In Flowering Plants
inferred← citeshttps://doi.org/10.1186/1754-6834-6-77openalex-snapshot
Advances in biotechnology and genomics of switchgrass
inferred← citeshttps://doi.org/10.1199/tab.0110openalex-snapshot
Chloroplast Biogenesis: Control of Plastid Development, Protein Import, Division and Inheritance
inferred← citeshttps://doi.org/10.1242/jcs.99.1.21openalex-snapshot
Microtubule-determined plastid distribution during microsporogenesis in Lilium longiflorum
inferred← citeshttps://doi.org/10.1508/cytologia.60.173openalex-snapshot
Maternal Cytoplasmic Inheritance and Pollen Nucleolytic Activities in Some Poaceae species.
inferred← citeshttps://doi.org/10.2307/1223218openalex-snapshot
Chloroplast DNA and biosystematics: The effects of intraspecific diversity and plastid transmission
inferred← citeshttps://doi.org/10.2307/2446324openalex-snapshot
Paternally biased cpDNA inheritance in Turnera ulmifolia (Turneraceae)
inferred← citeshttps://doi.org/10.2307/2656656openalex-snapshot
Occurrence of plastids in rye (Poaceae) sperm cells
inferred← citeshttps://doi.org/10.2307/2656871openalex-snapshot
Paternal inheritance of chloroplast DNA in interspecific hybrids in the genus Larrea (Zygophyllaceae)
inferred← citeshttps://doi.org/10.2478/fhort-2013-0138openalex-snapshot
Quantitative assessment of the morphogenetic efficiency in strawberry Fragaria × ananassa Duch
inferred← citeshttps://doi.org/10.2503/hortj.mi-004openalex-snapshot
Maternal Nuclear Genome Controls Paternal ptDNA Inheritance in Progeny from Interspecific Crosses of Rhododendron spp.
inferred← citeshttps://doi.org/10.25223/brad.n22.2004.a2openalex-snapshot
Resolving the phylogenetic placement of Blossfeldia liliputana (Cactaceae): reticulate evolution, chloroplast inheritance, and graft-chimeras
inferred← citeshttps://doi.org/10.3109/10520299909066476openalex-snapshot
Improved Sensitivity for High Resolution in Situ Hybridization Using Resin Extraction of Methyl Methacrylate Embedded Material
inferred← citeshttps://doi.org/10.3389/fpls.2021.697136openalex-snapshot
Sequence of the Mitochondrial Genome of Lactuca virosa Suggests an Unexpected Role in Lactuca sativa’s Evolution
inferred← citeshttps://doi.org/10.3390/ijms22052278openalex-snapshot
Clade-Specific Plastid Inheritance Patterns Including Frequent Biparental Inheritance in Passiflora Interspecific Crosses
inferred← citeshttps://doi.org/10.3390/life11010020openalex-snapshot
Haploid Embryogenesis in Isolated Microspore Culture of Carrots (Daucus carota L.)
inferred← citeshttps://doi.org/10.3410/f.4014956.3777054openalex-snapshot
Faculty Opinions recommendation of The levels of male gametic mitochondrial DNA are highly regulated in angiosperms with regard to mitochondrial inheritance.
inferred← citeshttps://doi.org/10.3732/ajb.91.6.976openalex-snapshot
Molecular genetic evidence for interspecific hybridization among endemic Hispaniolan Bursera (Burseraceae)
inferred← citeshttps://doi.org/10.5685/plmorphol.15.68openalex-snapshot
Differentiation of organelles during male gametophyte development in higher plants
inferred← citeshttps://doi.org/10.5685/plmorphol.23.25openalex-snapshot
Cytoplasmic inheritance in angiosperms
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