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The role of IAA and its transport in the complex streptophyte algae Chara braunii

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/advs.201901850openalex-snapshot
Mesostigma viride Genome and Transcriptome Provide Insights into the Origin and Evolution of Streptophyta
inferredcites →https://doi.org/10.1002/pro.3235openalex-snapshot
UCSF ChimeraX: Meeting modern challenges in visualization and analysis
inferredcites →https://doi.org/10.1007/bf00196251openalex-snapshot
Studies on the evolution of auxin carriers and phytotropin receptors: Transmembrane auxin transport in unicellular and multicellular Chlorophyta
inferredcites →https://doi.org/10.1007/bf00262639openalex-snapshot
Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells
inferredcites →https://doi.org/10.1007/s00299-016-1979-xopenalex-snapshot
PIN2-like proteins may contribute to the regulation of morphogenetic processes during spermatogenesis in Chara vulgaris
inferredcites →https://doi.org/10.1007/s00709-014-0742-9openalex-snapshot
Photosynthesis-dependent formation of convoluted plasma membrane domains in Chara internodal cells is independent of chloroplast position
inferredcites →https://doi.org/10.1007/s00709-023-01900-3openalex-snapshot
Rediscovering Chara as a model organism for molecular and evo-devo studies
inferredcites →https://doi.org/10.1016/0014-4827(68)90403-5openalex-snapshot
Nutrient requirements of suspension cultures of soybean root cells
inferredcites →https://doi.org/10.1016/0309-1651(89)90098-2openalex-snapshot
Assembly of purified brain tubulin at cortical and endoplasmic sites in perfused internodal cells of the alga Nitella tasmanica
inferredcites →https://doi.org/10.1016/j.bbamem.2017.01.017openalex-snapshot
Evolutionary plasticity of plasma membrane interaction in DREPP family proteins
inferredcites →https://doi.org/10.1016/j.cell.2017.09.030openalex-snapshot
Insights into Land Plant Evolution Garnered from the Marchantia polymorpha Genome
inferredcites →https://doi.org/10.1016/j.cell.2018.06.033openalex-snapshot
The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization
inferredcites →https://doi.org/10.1016/j.cell.2019.10.019openalex-snapshot
Genomes of Subaerial Zygnematophyceae Provide Insights into Land Plant Evolution
inferredcites →https://doi.org/10.1016/j.cell.2023.11.021openalex-snapshot
RAF-like protein kinases mediate a deeply conserved, rapid auxin response
inferredcites →https://doi.org/10.1016/j.cellbi.2007.11.005openalex-snapshot
Auxin and cytoskeletal organization in algae
inferredcites →https://doi.org/10.1016/j.cub.2021.07.038openalex-snapshot
The evolutionary emergence of land plants
inferredcites →https://doi.org/10.1016/j.jplph.2016.02.009openalex-snapshot
Auxin effects on ion transport in Chara corallina
inferredcites →https://doi.org/10.1016/j.jplph.2020.153305openalex-snapshot
Arabidopsis NHX5 and NHX6 regulate PIN6-mediated auxin homeostasis and growth
inferredcites →https://doi.org/10.1016/j.pbi.2017.06.012openalex-snapshot
Polar transport in plants mediated by membrane transporters: focus on mechanisms of polar auxin transport
inferredcites →https://doi.org/10.1016/j.softx.2015.06.001openalex-snapshot
GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
inferredcites →https://doi.org/10.1016/j.tibs.2023.07.006openalex-snapshot
Substrate recognition and transport mechanism of the PIN-FORMED auxin exporters
inferredcites →https://doi.org/10.1016/s0015-3796(80)80072-2openalex-snapshot
Auxin as a factor regulating initiation, of mitosis in antheridial filaments of Chara vulgaris L.
inferredcites →https://doi.org/10.1021/ci200227uopenalex-snapshot
LigPlot+: Multiple Ligand–Protein Interaction Diagrams for Drug Discovery
inferredcites →https://doi.org/10.1021/ct300400xopenalex-snapshot
Optimization of the Additive CHARMM All-Atom Protein Force Field Targeting Improved Sampling of the Backbone ϕ, ψ and Side-Chain χ 1 and χ 2 Dihedral Angles
inferredcites →https://doi.org/10.1038/ncomms4978openalex-snapshot
Klebsormidium flaccidum genome reveals primary factors for plant terrestrial adaptation
inferredcites →https://doi.org/10.1038/s41467-019-11471-8openalex-snapshot
Evolution of fast root gravitropism in seed plants
inferredcites →https://doi.org/10.1038/s41467-024-47753-zopenalex-snapshot
Phytohormone profiling in an evolutionary framework
inferredcites →https://doi.org/10.1038/s41467-024-55278-8openalex-snapshot
Evolutionary origins and functional diversification of Auxin Response Factors
inferredcites →https://doi.org/10.1038/s41477-019-0542-5openalex-snapshot
PIN-driven auxin transport emerged early in streptophyte evolution
inferredcites →https://doi.org/10.1038/s41477-022-01283-yopenalex-snapshot
The origin of a land flora
inferredcites →https://doi.org/10.1038/s41586-021-03819-2openalex-snapshot
Highly accurate protein structure prediction with AlphaFold
inferredcites →https://doi.org/10.1038/s41586-022-04883-yopenalex-snapshot
Structures and mechanism of the plant PIN-FORMED auxin transporter
inferredcites →https://doi.org/10.1038/s41586-022-05142-wopenalex-snapshot
Structures and mechanisms of the Arabidopsis auxin transporter PIN3
inferredcites →https://doi.org/10.1038/s41586-022-05143-9openalex-snapshot
Structural insights into auxin recognition and efflux by Arabidopsis PIN1
inferredcites →https://doi.org/10.1038/s41586-022-05187-xopenalex-snapshot
ABP1–TMK auxin perception for global phosphorylation and auxin canalization
inferredcites →https://doi.org/10.1038/s41588-024-01737-3openalex-snapshot
Genomes of multicellular algal sisters to land plants illuminate signaling network evolution
inferredcites →https://doi.org/10.1038/s41592-022-01488-1openalex-snapshot
ColabFold: making protein folding accessible to all
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00868.xopenalex-snapshot
An estrogen receptor‐based transactivator XVE mediates highly inducible gene expression in transgenic plants
inferredcites →https://doi.org/10.1071/pp9940113openalex-snapshot
Distribution of Charasomes in Chara : Re-establishment and Loss in Darkness and Correlation with Banding and Inorganic Carbon Uptake
inferredcites →https://doi.org/10.1073/pnas.1614380114openalex-snapshot
Dynamic PIN-FORMED auxin efflux carrier phosphorylation at the plasma membrane controls auxin efflux-dependent growth
inferredcites →https://doi.org/10.1080/00031305.1980.10483031openalex-snapshot
Population Marginal Means in the Linear Model: An Alternative to Least Squares Means
inferredcites →https://doi.org/10.1080/15592324.2015.1082697openalex-snapshot
Circadian changes in endogenous concentrations of indole-3-acetic acid, melatonin, serotonin, abscisic acid and jasmonic acid in Characeae (Chara australis Brown)
inferredcites →https://doi.org/10.1086/317566openalex-snapshot
Evolutionary Patterns in the Auxin Metabolism of Green Plants
inferredcites →https://doi.org/10.1091/mbc.e15-06-0404openalex-snapshot
KymographClear and KymographDirect: two tools for the automated quantitative analysis of molecular and cellular dynamics using kymographs
inferredcites →https://doi.org/10.1093/aob/mcae091openalex-snapshot
Phylogeny and evolution of streptophyte algae
inferredcites →https://doi.org/10.1093/aob/mcp044openalex-snapshot
Streptophyte algae and the origin of embryophytes
inferredcites →https://doi.org/10.1093/bioinformatics/btl481openalex-snapshot
Hierarchical and multi-resolution representation of protein flexibility
inferredcites →https://doi.org/10.1093/jxb/eraa169openalex-snapshot
The evolutionary origins of auxin transport: what we know and what we need to know
inferredcites →https://doi.org/10.1093/jxb/eraa181openalex-snapshot
Into another dimension: how streptophyte algae gained morphological complexity
inferredcites →https://doi.org/10.1093/jxb/ers106openalex-snapshot
Polar auxin transport: an early invention
inferredcites →https://doi.org/10.1093/molbev/msu147openalex-snapshot
Paralogous Radiations of PIN Proteins with Multiple Origins of Noncanonical PIN Structure
inferredcites →https://doi.org/10.1093/mp/ssn069openalex-snapshot
Cell Polarity Signaling: Focus on Polar Auxin Transport
inferredcites →https://doi.org/10.1093/pcp/pcn085openalex-snapshot
Agrobacterium-Mediated Transformation of the Haploid Liverwort Marchantia polymorpha L., an Emerging Model for Plant Biology
inferredcites →https://doi.org/10.1093/pcp/pcr074openalex-snapshot
Plasma Membrane Domains Participate in pH Banding of Chara Internodal Cells
inferredcites →https://doi.org/10.1098/rstb.2015.0490openalex-snapshot
Development and genetics in the evolution of land plant body plans
inferredcites →https://doi.org/10.1101/2022.04.08.487609openalex-snapshot
DeepTMHMM predicts alpha and beta transmembrane proteins using deep neural networks
inferredcites →https://doi.org/10.1101/cshperspect.a040048openalex-snapshot
On the Evolutionary Origins of Land Plant Auxin Biology
inferredcites →https://doi.org/10.1104/pp.012740openalex-snapshot
Do Phytotropins Inhibit Auxin Efflux by Impairing Vesicle Traffic?
inferredcites →https://doi.org/10.1104/pp.79.2.568openalex-snapshot
High Efficiency Transformation of Cultured Tobacco Cells
inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot
PIN-Dependent Auxin Transport: Action, Regulation, and Evolution
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1983.tb04234.xopenalex-snapshot
Ethylene, indoleacetic acid and apical dominance in peas: A reappraisal
inferredcites →https://doi.org/10.1111/j.1399-3054.1992.tb05823.xopenalex-snapshot
Auxin dependent growth of rhizoids of Chara globularis
inferredcites →https://doi.org/10.1111/nph.15625openalex-snapshot
Loop assembly: a simple and open system for recursive fabrication of DNA circuits
inferredcites →https://doi.org/10.1111/nph.18854openalex-snapshot
PIN‐FORMED is required for shoot phototropism/gravitropism and facilitates meristem formation in Marchantia polymorpha
inferredcites →https://doi.org/10.1111/ppl.14025openalex-snapshot
Insight into the nodal cells transcriptome of the streptophyte green alga Chara braunii S276
inferredcites →https://doi.org/10.1111/tpj.14474openalex-snapshot
Transcription of specific auxin efflux and influx carriers drives auxin homeostasis in tobacco cells
inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot
PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
inferredcites →https://doi.org/10.1186/s12870-023-04253-4openalex-snapshot
Different evolutionary patterns of TIR1/AFBs and AUX/IAAs and their implications for the morphogenesis of land plants
inferredcites →https://doi.org/10.1242/dev.02027openalex-snapshot
Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression
inferredcites →https://doi.org/10.1242/dev.168088openalex-snapshot
PIN-FORMED and PIN-LIKES auxin transport facilitators
inferredcites →https://doi.org/10.1371/journal.pcbi.1004586openalex-snapshot
AutoDockFR: Advances in Protein-Ligand Docking with Explicitly Specified Binding Site Flexibility
inferredcites →https://doi.org/10.1371/journal.pgen.1005207openalex-snapshot
A Simple Auxin Transcriptional Response System Regulates Multiple Morphogenetic Processes in the Liverwort Marchantia polymorpha
inferredcites →https://doi.org/10.1371/journal.pone.0138876openalex-snapshot
Development of Gateway Binary Vector Series with Four Different Selection Markers for the Liverwort Marchantia polymorpha
inferredcites →https://doi.org/10.15252/embj.2022113018openalex-snapshot
The birth of a giant: evolutionary insights into the origin of auxin responses in plants
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.3389/fpls.2021.650171openalex-snapshot
A Comprehensive Phylogenetic Analysis of the MAP4K Family in the Green Lineage
inferredcites →https://doi.org/10.3389/fpls.2022.987741openalex-snapshot
Establishment and optimization of a new model organism to study early land plant evolution: Germination, cultivation and oospore variation of Chara braunii Gmelin, 1826
inferredcites →https://doi.org/10.4161/psb.28457openalex-snapshot
Heterotrimeric G-proteins in green algae
inferredcites →https://doi.org/10.7554/elife.33399openalex-snapshot
Origin and evolution of the nuclear auxin response system
inferredcites →https://doi.org/10.7554/elife.42288openalex-snapshot
KymoButler, a deep learning software for automated kymograph analysis

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.cub.2025.03.037openalex-snapshot
Auxin and tryptophan trigger common responses in the streptophyte alga Penium margaritaceum
inferred← citeshttps://doi.org/10.1101/2024.12.06.627236openalex-snapshot
Auxin and tryptophan trigger common responses in the streptophyte alga Penium margaritaceum
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