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Nuclear DNA Content Estimates in Multicellular Green, Red and Brown Algae: Phylogenetic Considerations
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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.1537-2197.1964.tb06618.xopenalex-snapshot
CULTURE AND DEVELOPMENTAL MORPHOLOGY OF COMPSOPOGON COERULEUS
inferredcites →https://doi.org/10.1002/j.1537-2197.1985.tb08345.xopenalex-snapshot
PLOIDAL CHANGES IN CLONAL CULTURES OF SPIROGYRA COMMUNIS AND IMPLICATIONS FOR SPECIES DEFINITION
inferredcites →https://doi.org/10.1007/978-94-009-2049-1_16openalex-snapshot
Recent approaches to the taxonomy of the Gracilariaceae (Gracilariales, Rhodophyta) and the Gracilaria verrucosa problem
inferredcites →https://doi.org/10.1007/978-94-009-2049-1_61openalex-snapshot
Notes on the life histories of Boergesenia and Valonia (Siphonocladales, Chlorophyta)
inferredcites →https://doi.org/10.1007/978-94-011-1998-6_92openalex-snapshot
Quantification and characterization of nuclear genomes in commercial red seaweeds: Gracilariales and Gelidiales
inferredcites →https://doi.org/10.1007/bf00003792openalex-snapshot
Agar Analysis, nuclear genome quantification and characterization of four agarophytes (Gracilaria) from the Mexican Gulf Coast
inferredcites →https://doi.org/10.1007/bf00380838openalex-snapshot
Generationswechsel, Kernphasenwechsel und Sexualit�t der Braunalge Ectocarpus siliculosus im Kulturversuch
inferredcites →https://doi.org/10.1007/bf00428482openalex-snapshot
Molecular divergence between North Atlantic and Indo-West Pacific Cladophora albida (Cladophorales: Chlorophyta) isolates as indicated by DNA-DNA hybridization
inferredcites →https://doi.org/10.1007/bf00640589openalex-snapshot
Der Ort der Meiosis und die Sporenbildung bei der siphonalen Gr�nalgeDerbesia marina
inferredcites →https://doi.org/10.1007/bf00942143openalex-snapshot
Cell cycle duration in antheridial filaments ofChara spp. (Characeae) with different genome size and heterochromatin content
inferredcites →https://doi.org/10.1007/bf01379001openalex-snapshot
Quantification of nuclear DNA and G-C content in marine macroalgae by flow cytometry of isolated nuclei
inferredcites →https://doi.org/10.1007/bf02182427openalex-snapshot
Nuclear genome characterization and carrageenan analysis ofGymnogongrus griffithsiae (Rhodophyta) from North Carolina
inferredcites →https://doi.org/10.1007/bf02185897openalex-snapshot
Nuclear genome characterization of the carrageenophyteHypnea musciformis (Rhodophyta)
inferredcites →https://doi.org/10.1007/bf02186315openalex-snapshot
Quantification and characterization of nuclear genomes in commercial red seaweeds (Gracilariales) from the Philippines
inferredcites →https://doi.org/10.1007/bf02365520openalex-snapshot
Karyology and nuclear DNA quantification of four species ofChaetomorpha (Cladophorales, Chlorophyta) from the western Atlantic
inferredcites →https://doi.org/10.1007/bf02366200openalex-snapshot
scDNA-DNA hybridization studies in Pacific and Caribbean isolates ofDictyosphaeria cavernosa (Chlorophyta) indicate a long divergence
inferredcites →https://doi.org/10.1007/bf02442461openalex-snapshot
Nuclear genome characterization of the carrageenophyteAgardhiella subulata (Rhodophyta)
inferredcites →https://doi.org/10.1016/0014-4827(78)90054-xopenalex-snapshot
DNA contents and numbers of nucleoli and pre-rRNA-genes in nuclei of gametes and vegetative cells of Acetabularia Mediterranea
inferredcites →https://doi.org/10.1016/0022-0981(93)90221-9openalex-snapshot
Cytophotometric estimation of inter- and intraspecific variation in nuclear DNA content in ten taxa of the Gelidiales (Rhodophyta)
inferredcites →https://doi.org/10.1016/0022-5193(72)90007-0openalex-snapshot
The origin and evolution of gamete dimorphism and the male-female phenomenon
inferredcites →https://doi.org/10.1016/0167-4781(88)90079-6openalex-snapshot
Assignment of DNA binding sites for 4′,6-diamidine-2-phenylindole and bisbenzimide (Hoechst 33258). A comparative footprinting study
inferredcites →https://doi.org/10.1016/s0022-2836(62)80066-7openalex-snapshot
Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature
inferredcites →https://doi.org/10.1016/s0169-5347(98)01382-2openalex-snapshot
Reconstructing ancestral character states: a critical reappraisal
inferredcites →https://doi.org/10.1016/s0764-4469(01)01306-3openalex-snapshot
A comprehensive phylogeny of the Phaeophyceae based on nrDNA sequences resolves the earliest divergences
inferredcites →https://doi.org/10.1016/s1360-1385(98)01361-2openalex-snapshot
Phylogeny of early land plants: insights from genes and genomes
inferredcites →https://doi.org/10.1017/s0025315400026187openalex-snapshot
Chromosome numbers of Gracilaria foliifera and Gracilaria sp. (Rhodophyta) and attempted hybridizations
inferredcites →https://doi.org/10.1017/s0025315400057386openalex-snapshot
A Comment on Gracilaria verrucosa (Huds.) Papenf. (Rhodophyta: Gigartinales)
inferredcites →https://doi.org/10.1017/s1464793100005595openalex-snapshot
Coincidence, coevolution, or causation? DNA content, cell size, and the C-value enigma
inferredcites →https://doi.org/10.1023/a:1003701925110openalex-snapshot
The skeletal function of non‐genic nuclear DNA: new evidence from ancient cell chimaeras
inferredcites →https://doi.org/10.1023/a:1016015913350openalex-snapshot
Mechanisms and rates of genome expansion and contraction in flowering plants
inferredcites →https://doi.org/10.1023/a:1016020030189openalex-snapshot
Feast and famine in plant genomes
inferredcites →https://doi.org/10.1038/178370b0openalex-snapshot
Chromosome Counts in the Rhodophyceae
inferredcites →https://doi.org/10.1038/35001059openalex-snapshot
Ancestral chloroplast genome in Mesostigma viride reveals an early branch of green plant evolution
inferredcites →https://doi.org/10.1038/351315a0openalex-snapshot
Transition from haploidy to diploidy
inferredcites →https://doi.org/10.1046/j.1529-8817.2000.99106.xopenalex-snapshot
PHYLOGENY OF THE CONJUGATING GREEN ALGAE (ZYGNEMOPHYCEAE) BASED ON rbc L SEQUENCES
inferredcites →https://doi.org/10.1046/j.1529-8817.2000.99134.xopenalex-snapshot
TAXONOMY OF THE NEW ZEALAND‐ENDEMIC GENUSPLEUROSTICHIDIUM(RHODOMELACEAE, RHODOPHYTA)
inferredcites →https://doi.org/10.1073/pnas.162203299openalex-snapshot
The chloroplast and mitochondrial genome sequences of the charophyte Chaetosphaeridium globosum : Insights into the timing of the events that restructured organelle DNAs within the green algal lineage that led to land plants
inferredcites →https://doi.org/10.1073/pnas.91.15.7276openalex-snapshot
A molecular phylogeny of the marine red algae (Rhodophyta) based on the nuclear small-subunit rRNA gene.
inferredcites →https://doi.org/10.1073/pnas.91.15.7281openalex-snapshot
A gene phylogeny of the red algae (Rhodophyta) based on plastid rbcL.
inferredcites →https://doi.org/10.1073/pnas.91.21.9916openalex-snapshot
Group I introns are inherited through common ancestry in the nuclear-encoded rRNA of Zygnematales (Charophyceae).
inferredcites →https://doi.org/10.1073/pnas.91.9.3690openalex-snapshot
Evidence that an amoeba acquired a chloroplast by retaining part of an engulfed eukaryotic alga.
inferredcites →https://doi.org/10.1073/pnas.93.15.7732openalex-snapshot
Substitution rate calibration of small subunit ribosomal RNA identifies chlorarachniophyte endosymbionts as remnants of green algae.
inferredcites →https://doi.org/10.1080/00071616500650061openalex-snapshot
Some new chromosome counts in the desmids
inferredcites →https://doi.org/10.1080/09670269300650371openalex-snapshot
Karyology and cytophotometric estimation of nuclear DNA content variation inGracilaria, GracilariopsisandHydropuntia(Gracilariales, Rhodophyta)
inferredcites →https://doi.org/10.1080/11263508709431642openalex-snapshot
Karyological studies of four Cladophora (Cladophorales, Chlorophyta) species from coastal North Carolina
inferredcites →https://doi.org/10.1083/jcb.104.3.739openalex-snapshot
The solution to the cytological paradox of isomorphy.
inferredcites →https://doi.org/10.1083/jcb.115.4.941openalex-snapshot
Cellular dimensions affecting the nucleocytoplasmic volume ratio.
inferredcites →https://doi.org/10.1086/406830openalex-snapshot
Repetitive and Non-Repetitive DNA Sequences and a Speculation on the Origins of Evolutionary Novelty
inferredcites →https://doi.org/10.1093/aob/mcg057openalex-snapshot
Comparisons with Caenorhabditis (100 Mb) and Drosophila (175 Mb) Using Flow Cytometry Show Genome Size in Arabidopsis to be 157 Mb and thus 25 % Larger than the Arabidopsis Genome Initiative Estimate of 125 Mb
inferredcites →https://doi.org/10.1093/aob/mci010openalex-snapshot
Economy, Speed and Size Matter: Evolutionary Forces Driving Nuclear Genome Miniaturization and Expansion
inferredcites →https://doi.org/10.1093/aob/mci014openalex-snapshot
Evolution of DNA Amounts Across Land Plants (Embryophyta)
inferredcites →https://doi.org/10.1093/nar/19.22.6191openalex-snapshot
Electrophoretic karyotyping and chromosomal gene mapping ofChlorella
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003979openalex-snapshot
The Complete Mitochondrial DNA Sequence of Mesostigma viride Identifies This Green Alga as the Earliest Green Plant Divergence and Predicts a Highly Compact Mitochondrial Genome in the Ancestor of All Green Plants
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026089openalex-snapshot
The phylogeny of land plants inferred from 18S rDNA sequences: pushing the limits of rDNA signal?
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026190openalex-snapshot
Molecular phylogenetic evidence for a reversible morphogenetic switch controlling the gross morphology of two common genera of green seaweeds, Ulva and Enteromorpha
inferredcites →https://doi.org/10.1098/rspb.1972.0042openalex-snapshot
Nuclear DNA content and minimum generation time in herbaceous plants
inferredcites →https://doi.org/10.1098/rstb.1976.0044openalex-snapshot
Nuclear DNA amounts in angiosperms
inferredcites →https://doi.org/10.1105/tpc.9.9.1509openalex-snapshot
Do Plants Have a One-Way Ticket to Genomic Obesity?
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00042.xopenalex-snapshot
INDEPENDENT CONTRASTS SUCCEED WHERE ANCESTOR RECONSTRUCTION FAILS IN A KNOWN BACTERIOPHAGE PHYLOGENY
inferredcites →https://doi.org/10.1111/j.0022-3646.1991.00617.xopenalex-snapshot
EVOLUTIONARY RELATIONSHIPS BETWEEN FOUR SPECIES OF CLADOPHORA (CLADOPHORALES, CHLOROPHYTA) BASED ON DNA–DNA HYBRIDIZATION1
inferredcites →https://doi.org/10.1111/j.1469-8137.1960.tb06203.xopenalex-snapshot
THE CYTOLOGY OF THE DESMIDS: THE CHROMOSOMES*
inferredcites →https://doi.org/10.1111/j.1529-8817.1971.tb01518.xopenalex-snapshot
THE NUCLEAR CYTOLOGY OF SIROGONIUM1,2
inferredcites →https://doi.org/10.1111/j.1529-8817.1980.tb03053.xopenalex-snapshot
DISTRIBUTION AND SALINITY ADAPTATIONS OF BANGIA ATROPURPUREA (RHODOPHYTA), A PUTATIVE MIGRANT INTO THE LAURENTIAN GREAT LAKES1
inferredcites →https://doi.org/10.1126/science.1065156openalex-snapshot
The Closest Living Relatives of Land Plants
inferredcites →https://doi.org/10.1126/science.163.3862.87openalex-snapshot
Algae: Amounts of DNA and Organic Carbon in Single Cells
inferredcites →https://doi.org/10.1126/science.213.4510.907openalex-snapshot
Disease Resistance: Incorporation into Sexually Incompatible Somatic Hybrids of the Genus Nicotiana
inferredcites →https://doi.org/10.1126/science.290.5499.2105openalex-snapshot
Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes
inferredcites →https://doi.org/10.1139/b76-312openalex-snapshot
A contribution towards elucidating the life history of Palmaria palmate (=Rhodymenia palmata)
inferredcites →https://doi.org/10.1146/annurev.ge.05.120171.001321openalex-snapshot
THE GENETIC ORGANIZATION OF CHROMOSOMES
inferredcites →https://doi.org/10.1177/29.8.6168681openalex-snapshot
Mithramycin- and 4'-6-diamidino-2-phenylindole (DAPI)-DNA staining for fluorescence microspectrophotometric measurement of DNA in nuclei, plastids, and virus particles.
inferredcites →https://doi.org/10.1242/jcs.34.1.247openalex-snapshot
Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the DNA C-value paradox
inferredcites →https://doi.org/10.1508/cytologia.31.375openalex-snapshot
Cytological Studies in the Genus Zygnema
inferredcites →https://doi.org/10.1515/botm.1991.34.2.139openalex-snapshot
Cytophotometric Estimation of Inter- and Intraspecific Nuclear DNA Content Variation in Gracilaria and Gracilariopsis (Gracilariales, Rhodophyta)
inferredcites →https://doi.org/10.1515/botm.1992.35.4.329openalex-snapshot
Biogeography of Cladophoropsis membranacea (Siphonocladales, Chlorophyta) as Revealed by Single Copy DNA Distances
inferredcites →https://doi.org/10.1515/botm.1993.36.6.507openalex-snapshot
Karyology and Cytophotometric Estimation of Nuclear DNA Variation in Several Species of Polysiphonia (Rhodophyta, Ceramiales)
inferredcites →https://doi.org/10.15281/jplantres1887.83.270openalex-snapshot
On the Life-History of Anadyomene wrightii with Special Reference to the Reproduction, Development, and Cytological Sequences
inferredcites →https://doi.org/10.2216/i0031-8884-23-1-21.1openalex-snapshot
Growth experiments on autopolyploids of Gracilaria tikvahiae (Rhodophyceae)
inferredcites →https://doi.org/10.2216/i0031-8884-26-1-82.1openalex-snapshot
Karyological studies of five species of Porphyra (Bangiales, Rhodophyta) from the North Atlantic and Mediterranean
inferredcites →https://doi.org/10.2216/i0031-8884-26-2-228.1openalex-snapshot
Karyological studies of three species of Codium (Codiales, Chlorophyta) from coastal North Carolina
inferredcites →https://doi.org/10.2216/i0031-8884-28-2-159.1openalex-snapshot
Biogeographic and phylogenetic studies in three North Atlantic species of Cladophora (Cladophorales, Chlorophyta) using DNA–DNA hybridization
inferredcites →https://doi.org/10.2216/i0031-8884-30-5-458.1openalex-snapshot
Karyology and cytophotometric estimation of inter- and intraspecific nuclear DNA variation in four species of Porphyra (Rhodophyta)
inferredcites →https://doi.org/10.2216/i0031-8884-32-1-1.1openalex-snapshot
Karyology of marine green algae
inferredcites →https://doi.org/10.2216/i0031-8884-33-1-42.1openalex-snapshot
Karyology, nuclear DNA quantification and nucleus-cytoplasmic domain variations in some multinucleate green algae (Siphonocladales, Chlorophyta)
inferredcites →https://doi.org/10.2216/i0031-8884-37-3-176.1openalex-snapshot
Evolution of genome size in the Dasycladales (Chlorophyta) as determined by DAPI cytophotometry
inferredcites →https://doi.org/10.2216/i0031-8884-41-5-507.1openalex-snapshot
Relationship of nuclear genome size to some reproductive cell parameters in the Florideophycidae (Rhodophyta)
inferredcites →https://doi.org/10.2307/2656569openalex-snapshot
Reference standards for determination of DNA content of plant nuclei
inferredcites →https://doi.org/10.2307/3558445openalex-snapshot
Ribosomal DNA phylogeny of the Bangiophycidae (Rhodophyta) and the origin of secondary plastids
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s13127-018-0365-7zenodo-depositor-declared
Genome size of chrysophytes varies with cell size and nutritional mode
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inferred← citeshttps://doi.org/10.1002/9780470015902.a0002018.pub3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.330openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-37843-3_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-28451-9_12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-017-9642-2_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-017-9642-2_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-97-9427-0_15openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00227-023-04173-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00232-006-0860-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-010-0869-xopenalex-snapshot
Inter- and intrachromosomal asynchrony of cell division cycle events in root meristem cells of Allium cepa: possible connection with gradient of cyclin B-like proteins
inferred← citeshttps://doi.org/10.1007/s00300-020-02708-0openalex-snapshot
Nuclear DNA content estimations and nuclear development patterns in Antarctic macroalgae
inferred← citeshttps://doi.org/10.1007/s10126-022-10137-9openalex-snapshot
Nuclear DNA Content Variation in Different Life Cycle Stages of Sugar Kelp, Saccharina latissima
inferred← citeshttps://doi.org/10.1007/s10722-018-0648-zopenalex-snapshot
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Multiplex PCR methods for the species-specific detection and quantification of Prymnesium parvum (Haptophyta)
inferred← citeshttps://doi.org/10.1007/s10811-010-9586-7openalex-snapshot
Genome size and phylogenetic analysis of the A and L races of Botryococcus braunii
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Ploidy determination of three Kappaphycus alvarezii strains (Rhodophyta, Gigartinales) by confocal fluorescence microscopy
inferred← citeshttps://doi.org/10.1007/s10811-020-02121-4openalex-snapshot
Concise review of the genus Dictyota J.V. Lamouroux
inferred← citeshttps://doi.org/10.1007/s10811-020-02222-0openalex-snapshot
Concise review of the genus Alaria Greville, 1830
inferred← citeshttps://doi.org/10.1007/s10811-021-02433-zopenalex-snapshot
Nuclei isolation protocols for flow cytometry allowing nuclear DNA content estimation in problematic microalgal groups
inferred← citeshttps://doi.org/10.1007/s40415-020-00619-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-385536-7.00002-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-012301463-4/50004-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2018.08.030openalex-snapshot
Development of potential yield loss indicators to assess the effect of seaweed farming on fish landings
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Quantitative assessment of extraction methods for bound extracellular polymeric substances (B-EPSs) produced by Microcystis sp. and Scenedesmus sp.
inferred← citeshttps://doi.org/10.1016/j.algal.2024.103887openalex-snapshot
Draft genome of Palmaria palmata and intraspecific genetic variations in the North-East Atlantic
inferred← citeshttps://doi.org/10.1016/j.ecolind.2006.01.001openalex-snapshot
Application of specific exergy to macrophytes as an integrated index of environmental quality for coastal lagoons
inferred← citeshttps://doi.org/10.1016/j.flora.2023.152421openalex-snapshot
Genome size and DNA endoreplication pattern of non-generative cells in the antheridia of Chara connivens Salzmann ex A. Braun from Northern Morocco
inferred← citeshttps://doi.org/10.1016/j.gde.2005.09.003openalex-snapshot
Causes and effects of nuclear genome reduction
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Microsatellite markers in an invasive strain of Asparagopsis taxiformis (Bonnemaisoniales, Rhodophyta): Insights in ploidy level and sexual reproduction
inferred← citeshttps://doi.org/10.1016/j.tig.2014.09.011openalex-snapshot
Unreduced gametes: meiotic mishap or evolutionary mechanism?
inferred← citeshttps://doi.org/10.1051/ro/2015002openalex-snapshot
The use of the hyperbolic smoothing clustering algorithm in taxonomy of macroalgae
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Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida
inferred← citeshttps://doi.org/10.1073/pnas.2403222121openalex-snapshot
Genome of Halimeda opuntia reveals differentiation of subgenomes and molecular bases of multinucleation and calcification in algae
inferred← citeshttps://doi.org/10.1080/09670260902780782openalex-snapshot
Somatic meiosis in the life history ofBonnemaisonia asparagoidesandBonnemaisonia clavata(Bonnemaisoniales, Rhodophyta) from the Iberian peninsula
inferred← citeshttps://doi.org/10.1080/09670262.2017.1309688openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/09670262.2026.2618204openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mci001openalex-snapshot
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Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects
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First Nuclear DNA Amounts in more than 300 Angiosperms
inferred← citeshttps://doi.org/10.1093/aob/mcl294openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aobpla/plr001openalex-snapshot
Estimates of nuclear DNA content in 98 species of brown algae (Phaeophyta)
inferred← citeshttps://doi.org/10.1093/aobpla/pls005openalex-snapshot
Estimates of nuclear DNA content in red algal lineages
inferred← citeshttps://doi.org/10.1093/gbe/evq075openalex-snapshot
Red Algae Lose Key Mitochondrial Genes in Response to Becoming Parasitic
inferred← citeshttps://doi.org/10.1093/jhered/esaf077openalex-snapshot
The reference genome for the northeastern Pacific bull kelp, Nereocystis luetkeana
inferred← citeshttps://doi.org/10.1093/jmedent/44.6.1009openalex-snapshot
Body Lice and Head Lice (Anoplura: Pediculidae) Have the Smallest Genomes of Any Hemimetabolous Insect Reported to Date
inferred← citeshttps://doi.org/10.1093/molbev/msy081openalex-snapshot
Analysis of the Draft Genome of the Red Seaweed Gracilariopsis chorda Provides Insights into Genome Size Evolution in Rhodophyta
inferred← citeshttps://doi.org/10.1098/rstb.2019.0085openalex-snapshot
Combining morphology, behaviour and genomics to understand the evolution and ecology of microbial eukaryotes
inferred← citeshttps://doi.org/10.1101/2024.05.04.592553openalex-snapshot
CLONALITY AND POLYPLOIDY CONTRIBUTE TO THE SPREAD OF AVRAINVILLEA LACERATA (BRYOPSIDALES, CHLOROPHYTA) IN HAWAIʻI
inferred← citeshttps://doi.org/10.1101/gr.279002.124openalex-snapshot
Genome-wide patterns of selection–drift variation strongly associate with organismal traits across the green plant lineage
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.04022.xopenalex-snapshot
High genetic diversity and connectivity in the polyploid invasive seaweedAsparagopsis taxiformis(Bonnemaisoniales) in the Mediterranean, explored with microsatellite alleles and multilocus genotypes
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2006.00182.xopenalex-snapshot
PROTEOMICS OF THE RED ALGA, GRACILARIA CHANGII (GRACILARIALES, RHODOPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2010.00820.xopenalex-snapshot
PHYLOGENETIC PLACEMENT, GENOME SIZE, AND GC CONTENT OF THE LIQUID‐HYDROCARBON‐PRODUCING GREEN MICROALGA BOTRYOCOCCUS BRAUNII STRAIN BERKELEY (SHOWA) (CHLOROPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2008.00357.xopenalex-snapshot
Nuclear Genome Sequence Survey of the Dinoflagellate Heterocapsa triquetra
inferred← citeshttps://doi.org/10.1111/jpy.13212openalex-snapshot
Whole‐genome sequencing reveals forgotten lineages and recurrent hybridizations within the kelp genus Alaria (Phaeophyceae)
inferred← citeshttps://doi.org/10.1111/jpy.13508openalex-snapshot
Clonality contributes to the spread of Avrainvillea lacerata (Bryopsidales, Chlorophyta) in Hawai‘i
inferred← citeshttps://doi.org/10.1111/mec.12000openalex-snapshot
Ecological and evolutionary genomics of marine photosynthetic organisms
inferred← citeshttps://doi.org/10.1111/mec.15993openalex-snapshot
Genotype–Environment mismatch of kelp forests under climate change
inferred← citeshttps://doi.org/10.1111/rec.13798openalex-snapshot
Land–sea linkages depend on macroalgal species, predator invasion history in a New Zealand archipelago
inferred← citeshttps://doi.org/10.1128/msphere.00094-17openalex-snapshot
Molecular Mechanisms for Microbe Recognition and Defense by the Red Seaweed Laurencia dendroidea
inferred← citeshttps://doi.org/10.1186/1471-2164-13-487openalex-snapshot
Transcriptomic analysis of the red seaweed Laurencia dendroidea (Florideophyceae, Rhodophyta) and its microbiome
inferred← citeshttps://doi.org/10.1186/s12862-017-0878-2openalex-snapshot
Cryptic diversity, geographical endemism and allopolyploidy in NE Pacific seaweeds
inferred← citeshttps://doi.org/10.13140/rg.2.2.16651.49446openalex-snapshot
Conceptual and Empirical Investigations of Eukaryotic Transposable Element Evolution
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004355openalex-snapshot
A Lack of Parasitic Reduction in the Obligate Parasitic Green Alga Helicosporidium
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004900openalex-snapshot
An Intracellular Transcriptomic Atlas of the Giant Coenocyte Caulerpa taxifolia
inferred← citeshttps://doi.org/10.1371/journal.pone.0047728openalex-snapshot
Mediterranean Species of Caulerpa Are Polyploid with Smaller Genomes in the Invasive Ones
inferred← citeshttps://doi.org/10.1371/journal.pone.0048784openalex-snapshot
Localization of a Female-Specific Marker on the Chromosomes of the Brown Seaweed Saccharina japonica Using Fluorescence In Situ Hybridization
inferred← citeshttps://doi.org/10.1371/journal.pone.0086006openalex-snapshot
Nuclear DNA Content Variation in Life History Phases of the Bonnemasoniaceae (Rhodophyta)
inferred← citeshttps://doi.org/10.1371/journal.pone.0086247openalex-snapshot
DNA Content Variation and Its Significance in the Evolution of the Genus Micrasterias (Desmidiales, Streptophyta)
inferred← citeshttps://doi.org/10.2174/1874401x00801010011openalex-snapshot
Application of Specific Eco-Exergy to FAO Fisheries Data
inferred← citeshttps://doi.org/10.2216/06-18.1openalex-snapshot
Nuclear DNA content variation in the freshwater red algal orders Batrachospermales and Thoreales (Florideophyceae, Nemaliophycidae)
inferred← citeshttps://doi.org/10.2216/09-14.1openalex-snapshot
Fucales (Phaeophyceae) from Spain characterized by large-scale discontinuous nuclear DNA contents consistent with ancestral cryptopolyploidy
inferred← citeshttps://doi.org/10.22201/ib.20078706e.2019.90.2679openalex-snapshot
Las especies del género Bryopsis (Chlorophyta) presentes en las costas del Atlántico mexicano. Una propuesta
inferred← citeshttps://doi.org/10.26686/wgtn.17136164openalex-snapshot
Speciation in the Cladophorales species flock of ancient Lake Baikal
inferred← citeshttps://doi.org/10.26686/wgtn.17136164.v1openalex-snapshot
Speciation in the Cladophorales species flock of ancient Lake Baikal
inferred← citeshttps://doi.org/10.2989/1814232x.2011.600339openalex-snapshot
Molecular evidence for three separate cryptic introductions of the red seaweedAsparagopsis(Bonnemaisoniales, Rhodophyta) in South Africa
inferred← citeshttps://doi.org/10.3389/fmars.2021.628183openalex-snapshot
Genomes Vary in Size and Spatial Patterns Within Chimeric Blades of Porphyra spp.
inferred← citeshttps://doi.org/10.3389/fpls.2021.610381openalex-snapshot
Characterization of Two Zygnema Strains (Zygnema circumcarinatum SAG 698-1a and SAG 698-1b) and a Rapid Method to Estimate Nuclear Genome Size of Zygnematophycean Green Algae
inferred← citeshttps://doi.org/10.3390/md13020879openalex-snapshot
New Insights on the Terpenome of the Red Seaweed Laurencia dendroidea (Florideophyceae, Rhodophyta)
inferred← citeshttps://doi.org/10.3390/plants15152320openalex-snapshot
Abiotic Stress Responses in Raphanus sativus L.: Insights into the Role of Endopolyploidization in Stress Adaptation
inferred← citeshttps://doi.org/10.3989/ajbm.2381openalex-snapshot
First record of Caulerpa cylindracea (Caulerpaceae, Chlorophyta) in Andalusia (Southern Spain)
inferred← citeshttps://doi.org/10.4236/ajps.2019.1010122openalex-snapshot
New Records of Marine Macroalgae on the Caribbean on Coast of Costa Rica
inferred← citeshttps://doi.org/10.5507/fot.2011.030openalex-snapshot
Quantification of DNA content in freshwater microalgae using flow cytometry: a modified protocol for selected green microalgae.
inferred← citeshttps://doi.org/10.5586/asbp.2014.039openalex-snapshot
Helicosporidia: a genomic snapshot of an early transition to parasitism
inferred← citeshttps://doi.org/10.70675/44c9f341z435cz48c8z9e8fz811c00a4ce39openalex-snapshot
Exploration génétique de la polyploïdie du genre Juniperus (Cupressaceae)
inferred← citeshttps://doi.org/10.70675/623f1e9cz015dz4ae3zacefzb980ab2f491dopenalex-snapshot
Connectivité et structure génétiques des populations d'Ericaria Zosteroides (Fucales) et Laminaria rodriguezii (Laminariales) des côtes françaises
inferred← citeshttps://doi.org/10.7872/crya.v32.iss2.2011.205openalex-snapshot
Nuclear Content Estimates Suggest a Synapomorphy betweenDictyotaand Six Other Genera of the Dictyotales (Phaeophyceae)
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