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Understanding “green” multicellularity: do seaweeds hold the key?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Redox control and the evolution of multicellularity
inferredcites →https://doi.org/10.1007/bf00333718openalex-snapshot
Zooplankton-induced unicell-colony transformation in Scenedesmus acutus and its effect on growth of herbivore Daphnia
inferredcites →https://doi.org/10.1007/s00248-006-9060-xopenalex-snapshot
Effect of Marine Bacterial Isolates on the Growth and Morphology of Axenic Plantlets of the Green Alga Ulva linza
inferredcites →https://doi.org/10.1016/j.cell.2008.04.028openalex-snapshot
Early Sexual Origins of Homeoprotein Heterodimerization and Evolution of the Plant KNOX/BELL Family
inferredcites →https://doi.org/10.1016/j.cub.2010.09.014openalex-snapshot
Multicellular development in a choanoflagellate
inferredcites →https://doi.org/10.1016/j.devcel.2004.08.010openalex-snapshot
The Unicellular Ancestry of Animal Development
inferredcites →https://doi.org/10.1016/j.limno.2007.01.001openalex-snapshot
Direct effects of Daphnia-grazing, not infochemicals, mediate a shift towards large inedible colonies of the gelatinous green alga Sphaerocystis schroeteri
inferredcites →https://doi.org/10.1016/j.pbi.2013.09.004openalex-snapshot
Evolution and regulation of complex life cycles: a brown algal perspective
inferredcites →https://doi.org/10.1016/j.ydbio.2011.06.003openalex-snapshot
Cell differentiation and morphogenesis in the colony-forming choanoflagellate Salpingoeca rosetta
inferredcites →https://doi.org/10.1016/j.ydbio.2013.01.009openalex-snapshot
Development of ichthyosporeans sheds light on the origin of metazoan multicellularity
inferredcites →https://doi.org/10.1016/s0169-5347(97)01313-xopenalex-snapshot
One cell, two cell, red cell, blue cell: The persistence of a unicellular stage in multicellular life histories
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The protein kinases of budding yeast: six score and more
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Intracellular accommodation of microbes by plants: a common developmental program for symbiosis and disease?
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Phagotrophy by a flagellate selects for colonial prey: A possible origin of multicellularity
inferredcites →https://doi.org/10.1038/nature06617openalex-snapshot
The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans
inferredcites →https://doi.org/10.1038/nature09016openalex-snapshot
The Ectocarpus genome and the independent evolution of multicellularity in brown algae
inferredcites →https://doi.org/10.1038/nature12860openalex-snapshot
Green and golden seaweed tides on the rise
inferredcites →https://doi.org/10.1038/ncomms1251openalex-snapshot
Trends in the development of environmentally friendly fouling-resistant marine coatings
inferredcites →https://doi.org/10.1038/ncomms3325openalex-snapshot
The Capsaspora genome reveals a complex unicellular prehistory of animals
inferredcites →https://doi.org/10.1038/ncomms3742openalex-snapshot
Experimental evolution of an alternating uni- and multicellular life cycle in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1038/nrmicro3178openalex-snapshot
Bacterial solutions to multicellularity: a tale of biofilms, filaments and fruiting bodies
inferredcites →https://doi.org/10.1051/limn/2003014openalex-snapshot
Phenotypic plasticity in the green algae Desmodesmus and Scenedesmus with special reference to the induction of defensive morphology
inferredcites →https://doi.org/10.1051/limn/2006010openalex-snapshot
Palmelloids formation in Chlamydomonas reinhardtii : defence against rotifer predators?
inferredcites →https://doi.org/10.1073/pnas.0811205106openalex-snapshot
Triassic origin and early radiation of multicellular volvocine algae
inferredcites →https://doi.org/10.1073/pnas.1003391107openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.1115323109openalex-snapshot
Experimental evolution of multicellularity
inferredcites →https://doi.org/10.1073/pnas.1209927110openalex-snapshot
Evolution of multicellularity coincided with increased diversification of cyanobacteria and the Great Oxidation Event
inferredcites →https://doi.org/10.1073/pnas.1221259110openalex-snapshot
Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida
inferredcites →https://doi.org/10.1073/pnas.181141598openalex-snapshot
Receptor-like kinases from Arabidopsis form a monophyletic gene family related to animal receptor kinases
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Relationships between growth, development and photosynthetic activity during the cell cycle ofDesmodesmus armatus(Chlorophyta) in synchronous cultures
inferredcites →https://doi.org/10.1093/genetics/144.3.967openalex-snapshot
Saccharomyces cerevisiae S288C Has a Mutation in FL08, a Gene Required for Filamentous Growth
inferredcites →https://doi.org/10.1093/molbev/msp185openalex-snapshot
Phylogeny of the "Forgotten" Cellular Slime Mold, Fonticula alba, Reveals a Key Evolutionary Branch within Opisthokonta
inferredcites →https://doi.org/10.1093/molbev/msq309openalex-snapshot
Unexpected Repertoire of Metazoan Transcription Factors in the Unicellular Holozoan Capsaspora owczarzaki
inferredcites →https://doi.org/10.1093/molbev/mst241openalex-snapshot
Earliest Holozoan Expansion of Phosphotyrosine Signaling
inferredcites →https://doi.org/10.1098/rspb.2010.1459openalex-snapshot
Trade-offs limiting the evolution of coloniality: ecological displacement rates used to measure small costs
inferredcites →https://doi.org/10.1104/pp.109.149708openalex-snapshot
Auxin Metabolism and Function in the Multicellular Brown Alga Ectocarpus siliculosus
inferredcites →https://doi.org/10.1105/tpc.110.081919openalex-snapshot
ETOILERegulates Developmental Patterning in the Filamentous Brown AlgaEctocarpus siliculosus
inferredcites →https://doi.org/10.1111/j.0022-3646.1974.00028.xopenalex-snapshot
SCENEDESMUS MORPHOGENESIS. COLONY CONTROL IN DILUTE MEDIA1
inferredcites →https://doi.org/10.1111/j.1462-2920.2008.01569.xopenalex-snapshot
Colony induction and growth inhibition in Desmodesmus quadrispina ( Chlorococcales ) by allelochemicals released from the filamentous alga Uronema confervicolum ( Ulotrichales )
inferredcites →https://doi.org/10.1111/j.1529-8817.1974.tb02673.xopenalex-snapshot
SCENEDESMUS MORPHOGENESIS. COLONY CONTROL IN DILUTE MEDIA1
inferredcites →https://doi.org/10.1111/j.1529-8817.2010.00816.xopenalex-snapshot
GAMETOGENESIS AND GAMETE RELEASE OFULVA MUTABILISANDULVA LACTUCA(CHLOROPHYTA): REGULATORY EFFECTS AND CHEMICAL CHARACTERIZATION OF THE “SWARMING INHIBITOR”
inferredcites →https://doi.org/10.1111/j.1529-8817.2012.01231.xopenalex-snapshot
Growth and Thallus Morphogenesis of Ulva mutabilis (Chlorophyta) Depends on A Combination of Two Bacterial Species Excreting Regulatory Factors
inferredcites →https://doi.org/10.1126/science.1105486openalex-snapshot
Isolation of an Algal Morphogenesis Inducer from a Marine Bacterium
inferredcites →https://doi.org/10.1126/science.1143609openalex-snapshot
The Chlamydomonas Genome Reveals the Evolution of Key Animal and Plant Functions
inferredcites →https://doi.org/10.1126/science.1151084openalex-snapshot
The Premetazoan Ancestry of Cadherins
inferredcites →https://doi.org/10.1126/science.1188800openalex-snapshot
Genomic Analysis of Organismal Complexity in the Multicellular Green Alga Volvox carteri
inferredcites →https://doi.org/10.1127/archiv-hydrobiol/127/1993/129openalex-snapshot
Morphological changes in Scenedesmus induced by substances released from Daphnia
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102403.114735openalex-snapshot
The Evolution of Multicellularity: A Minor Major Transition?
inferredcites →https://doi.org/10.1146/annurev.genet.35.102401.090145openalex-snapshot
Building a Multicellular Organism
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091513openalex-snapshot
The Origins of Multicellularity and the Early History of the Genetic Toolkit For Animal Development
inferredcites →https://doi.org/10.1186/gb-2010-11-3-r35openalex-snapshot
Conserved developmental transcriptomes in evolutionarily divergent species
inferredcites →https://doi.org/10.1186/gb-2013-14-2-r15openalex-snapshot
Premetazoan genome evolution and the regulation of cell differentiation in the choanoflagellate Salpingoeca rosetta
inferredcites →https://doi.org/10.1242/dev.048934openalex-snapshot
Evolutionary crossroads in developmental biology: Dictyostelium discoideum
inferredcites →https://doi.org/10.1242/jcs.114.24.4349openalex-snapshot
Cell-cell adhesion and signal transduction duringDictyosteliumdevelopment
inferredcites →https://doi.org/10.1371/journal.pone.0057122openalex-snapshot
The First Symbiont-Free Genome Sequence of Marine Red Alga, Susabi-nori (Pyropia yezoensis)
inferredcites →https://doi.org/10.1666/0094-8373(2005)031<0165:ppf>2.0.co;2openalex-snapshot
Probable Proterozoic fungi
inferredcites →https://doi.org/10.2216/i0031-8884-20-1-1.1openalex-snapshot
Morphological control and physiology of Scenedesmus strain 170
inferredcites →https://doi.org/10.3389/fpls.2015.00015openalex-snapshot
Regulation of gametogenesis and zoosporogenesis in Ulva linza (Chlorophyta): comparison with Ulva mutabilis and potential for laboratory culture
inferredcites →https://doi.org/10.3732/ajb.1300314openalex-snapshot
The evolutionary‐developmental origins of multicellularity
inferredcites →https://doi.org/10.4319/lo.1994.39.7.1543openalex-snapshot
Chemical induction of colony formation in a green alga (Scenedesmus acutus) by grazers (Daphnia)
inferredcites →https://doi.org/10.7554/elife.00013openalex-snapshot
A bacterial sulfonolipid triggers multicellular development in the closest living relatives of animals
inferredcites →https://doi.org/10.7554/elife.01287openalex-snapshot
Regulated aggregative multicellularity in a close unicellular relative of metazoa
inferredcites →https://doi.org/10.7554/elife.04070openalex-snapshot
The rosetteless gene controls development in the choanoflagellate S. rosetta
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Ancient reproductive modes and criteria of multicellularity
inferred← citeshttps://doi.org/10.1007/978-3-319-43669-2_14openalex-snapshot
Construction Kits for Biological Evolution
inferred← citeshttps://doi.org/10.1007/s00216-017-0430-7openalex-snapshot
In situ monitoring of molecular changes during cell differentiation processes in marine macroalgae through mass spectrometric imaging
inferred← citeshttps://doi.org/10.1007/s00606-018-1503-6openalex-snapshot
An insight into the evolution of introns in the gyrase A gene of plants
inferred← citeshttps://doi.org/10.1016/j.fbr.2020.07.002openalex-snapshot
Fungi took a unique evolutionary route to multicellularity: Seven key challenges for fungal multicellular life
inferred← citeshttps://doi.org/10.1038/s41467-019-12085-wopenalex-snapshot
Comparative genomics reveals the origin of fungal hyphae and multicellularity
inferred← citeshttps://doi.org/10.1073/pnas.1910060117openalex-snapshot
Neoproterozoic origin and multiple transitions to macroscopic growth in green seaweeds
inferred← citeshttps://doi.org/10.1093/biolinnean/blac005openalex-snapshot
Cellular and evolutionary perspectives on organismal cognition: from unicellular to multicellular organisms
inferred← citeshttps://doi.org/10.1093/dnares/dsz002openalex-snapshot
A siphonous macroalgal genome suggests convergent functions of homeobox genes in algae and land plants
inferred← citeshttps://doi.org/10.1093/jxb/eraa066openalex-snapshot
Macroalgal–bacterial interactions: identification and role of thallusin in morphogenesis of the seaweed Ulva (Chlorophyta)
inferred← citeshttps://doi.org/10.1093/jxb/erz547openalex-snapshot
The many roads to and from multicellularity
inferred← citeshttps://doi.org/10.1093/molbev/msaa077openalex-snapshot
Unmatched Level of Molecular Convergence among Deeply Divergent Complex Multicellular Fungi
inferred← citeshttps://doi.org/10.1101/283549openalex-snapshot
Genome-wide features of introns are evolutionary decoupled among themselves and from genome size throughout Eukarya
inferred← citeshttps://doi.org/10.1101/546531openalex-snapshot
Comparative genomics reveals the origin of fungal hyphae and multicellularity
inferred← citeshttps://doi.org/10.1101/668475openalex-snapshot
Neoproterozoic origin and multiple transitions to macroscopic growth in green seaweeds
inferred← citeshttps://doi.org/10.1266/ggs.19-00054openalex-snapshot
Construction of genomic marker sets based on the chloroplast genome of a green alga, Ulva pertusa (syn. Ulva australis), leads to simple detection of Ulva species
inferred← citeshttps://doi.org/10.1371/journal.pone.0214491openalex-snapshot
Dynamic metabolic profiles of the marine macroalga Ulva prolifera during fragmentation-induced proliferation
inferred← citeshttps://doi.org/10.31857/s0042132423060042openalex-snapshot
Reproductive Criteria of Multicellularity and Original Modes of Reproduction
inferred← citeshttps://doi.org/10.3389/fgeed.2024.1380682openalex-snapshot
Genome editing in macroalgae: advances and challenges
inferred← citeshttps://doi.org/10.3389/fpls.2015.00072openalex-snapshot
The green seaweed Ulva: a model system to study morphogenesis
inferred← citeshttps://doi.org/10.3389/fpls.2015.00086openalex-snapshot
Exploring bacteria-induced growth and morphogenesis in the green macroalga order Ulvales (Chlorophyta)
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