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Ancient trans -acting siRNAs Confer Robustness and Sensitivity onto the Auxin Response
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Outgoing claims: the papers this work cites, builds on, or argues with.
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The Hormonal Regulation of Morphogenesis in Mosses
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Plant small RNAs as morphogens
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Cilia functions in development
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The Arabidopsis Heterochronic Gene ZIPPY Is an ARGONAUTE Family Member
inferredcites →https://doi.org/10.1016/j.cub.2010.08.050openalex-snapshot
Physcomitrella patens Auxin-Resistant Mutants Affect Conserved Elements of an Auxin-Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cub.2014.09.054openalex-snapshot
Plasma Membrane-Targeted PIN Proteins Drive Shoot Development in a Moss
inferredcites →https://doi.org/10.1016/j.cub.2014.09.056openalex-snapshot
Directional Auxin Transport Mechanisms in Early Diverging Land Plants
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Transcriptional regulation by the numbers: applications
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Transcriptional regulation by the numbers: models
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Developmental patterning by gradients of mobile small RNAs
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AUXOLOGY: When auxin meets plant evo-devo
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The origin and early evolution of plants on land
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The auxin signalling network translates dynamic input into robust patterning at the shoot apex
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Summing up the noise in gene networks
inferredcites →https://doi.org/10.1038/nature09158openalex-snapshot
Phenotypic robustness conferred by apparently redundant transcriptional enhancers
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Selection on noise constrains variation in a eukaryotic promoter
inferredcites →https://doi.org/10.1038/nrg2102openalex-snapshot
Network motifs: theory and experimental approaches
inferredcites →https://doi.org/10.1038/nrg2179openalex-snapshot
Specialization and evolution of endogenous small RNA pathways
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The evolution of hierarchical gene regulatory networks
inferredcites →https://doi.org/10.1073/pnas.0704339104openalex-snapshot
The small interfering RNA production pathway is required for shoot meristem initiation in rice
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Cell-specific nitrogen responses mediate developmental plasticity
inferredcites →https://doi.org/10.1073/pnas.1100059108openalex-snapshot
Impact of gene expression noise on organismal fitness and the efficacy of natural selection
inferredcites →https://doi.org/10.1073/pnas.1305457110openalex-snapshot
Recruitment and remodeling of an ancient gene regulatory network during land plant evolution
inferredcites →https://doi.org/10.1093/jxb/erm047openalex-snapshot
Both chloronemal and caulonemal cells expand by tip growth in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1093/molbev/mss220openalex-snapshot
Evolution of the ARF Gene Family in Land Plants: Old Domains, New Tricks
inferredcites →https://doi.org/10.1093/mp/ssm021openalex-snapshot
Comprehensive Transcriptome Analysis of Auxin Responses in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/sss036openalex-snapshot
DICER-LIKE3 Activity in Physcomitrella patens DICER-LIKE4 Mutants Causes Severe Developmental Dysfunction and Sterility
inferredcites →https://doi.org/10.1093/nar/gkp1128openalex-snapshot
Auxin regulation of the microRNA390-dependent transacting small interfering RNA pathway in Arabidopsis lateral root development
inferredcites →https://doi.org/10.1101/gad.1528607openalex-snapshot
Two small regulatory RNAs establish opposing fates of a developmental axis
inferredcites →https://doi.org/10.1101/gad.1678608openalex-snapshot
A C. elegans genome-scale microRNA network contains composite feedback motifs with high flux capacity
inferredcites →https://doi.org/10.1101/gad.1770009openalex-snapshot
Pattern formation via small RNA mobility
inferredcites →https://doi.org/10.1101/pdb.prot5136openalex-snapshot
Culturing the Moss Physcomitrella patens: Figure 1.
inferredcites →https://doi.org/10.1101/pdb.prot5143openalex-snapshot
Transformation of the Moss Physcomitrella patens Using Direct DNA Uptake by Protoplasts
inferredcites →https://doi.org/10.1101/sqb.2013.77.014878openalex-snapshot
Small RNA-Regulated Networks and the Evolution of Novel Structures in Plants
inferredcites →https://doi.org/10.1104/pp.109.140947openalex-snapshot
TheREDUCED LEAFLETGenes Encode Key Components of the trans-Acting Small Interfering RNA Pathway and Regulate Compound Leaf and Flower Development inLotus japonicus
inferredcites →https://doi.org/10.1105/tpc.105.032185openalex-snapshot
Antiquity of MicroRNAs and Their Targets in Land Plants
inferredcites →https://doi.org/10.1105/tpc.105.035493openalex-snapshot
Cell Cycle Progression in the Pericycle Is Not Sufficient for SOLITARY ROOT/IAA14-Mediated Lateral Root Initiation inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.107.051706openalex-snapshot
Common Functions for Diverse Small RNAs of Land Plants
inferredcites →https://doi.org/10.1105/tpc.107.055046openalex-snapshot
Genome-Wide Analysis of mRNA Decay Rates and Their Determinants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.109.066480openalex-snapshot
An Auxin Gradient and Maximum in the Arabidopsis Root Apex Shown by High-Resolution Cell-Specific Analysis of IAA Distribution and Synthesis
inferredcites →https://doi.org/10.1105/tpc.109.072553openalex-snapshot
miR390, Arabidopsis TAS3 tasiRNAs, and Their AUXIN RESPONSE FACTOR Targets Define an Autoregulatory Network Quantitatively Regulating Lateral Root Growth
inferredcites →https://doi.org/10.1105/tpc.110.082784openalex-snapshot
Evolution and Functional Diversification of MIRNA Genes
inferredcites →https://doi.org/10.1105/tpc.111.085852openalex-snapshot
Tissue-Autonomous Promotion of Palisade Cell Development by Phototropin 2 inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.100222openalex-snapshot
Failure of the Tomato Trans-Acting Short Interfering RNA Program to Regulate AUXIN RESPONSE FACTOR3 and ARF4 Underlies the Wiry Leaf Syndrome
inferredcites →https://doi.org/10.1105/tpc.112.101840openalex-snapshot
Modeling Regulatory Networks to Understand Plant Development: Small Is Beautiful
inferredcites →https://doi.org/10.1105/tpc.112.103176openalex-snapshot
miR156 and miR390 Regulate tasiRNA Accumulation and Developmental Timing in Physcomitrella patens
inferredcites →https://doi.org/10.1105/tpc.113.114652openalex-snapshot
Phased, Secondary, Small Interfering RNAs in Posttranscriptional Regulatory Networks
inferredcites →https://doi.org/10.1105/tpc.113.117788openalex-snapshot
TheTrans-Acting Short Interfering RNA3 Pathway and NO APICAL MERISTEM Antagonistically Regulate Leaf Margin Development and Lateral Organ Separation, as Revealed by Analysis of anargonaute7/lobed leaflet1Mutant inMedicago truncatula
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02895.xopenalex-snapshot
Identification of trans ‐acting siRNAs in moss and an RNA‐dependent RNA polymerase required for their biogenesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05001.xopenalex-snapshot
Rice RNA‐dependent RNA polymerase 6 acts in small RNA biogenesis and spikelet development
inferredcites →https://doi.org/10.1111/j.1438-8677.1998.tb00670.xopenalex-snapshot
Development, Genetics and Molecular Biology of Mosses
inferredcites →https://doi.org/10.1126/science.1105891openalex-snapshot
Noise in Gene Expression: Origins, Consequences, and Control
inferredcites →https://doi.org/10.1126/science.1142618openalex-snapshot
An Ancient Mechanism Controls the Development of Cells with a Rooting Function in Land Plants
inferredcites →https://doi.org/10.1126/science.1160631openalex-snapshot
Shadow Enhancers as a Source of Evolutionary Novelty
inferredcites →https://doi.org/10.1126/science.280.5365.895openalex-snapshot
The Biochemical Basis of an All-or-None Cell Fate Switch in Xenopus Oocytes
inferredcites →https://doi.org/10.1126/science.298.5594.824openalex-snapshot
Network Motifs: Simple Building Blocks of Complex Networks
inferredcites →https://doi.org/10.1126/science.aaa1738openalex-snapshot
MicroRNA control of protein expression noise
inferredcites →https://doi.org/10.1146/annurev-cellbio-100109-104113openalex-snapshot
Stochastic Mechanisms of Cell Fate Specification that Yield Random or Robust Outcomes
inferredcites →https://doi.org/10.1186/1471-2164-6-43openalex-snapshot
Protein encoding genes in an ancient plant: analysis of codon usage, retained genes and splice sites in a moss, Physcomitrella patens
inferredcites →https://doi.org/10.1186/1746-4811-3-12openalex-snapshot
Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs
inferredcites →https://doi.org/10.1186/1746-4811-3-3openalex-snapshot
Kinome profiling of Arabidopsis using arrays of kinase consensus substrates.
inferredcites →https://doi.org/10.1242/dev.02491openalex-snapshot
Trans-acting siRNA-mediated repression of ETTIN and ARF4 regulates heteroblasty in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.060582openalex-snapshot
RSL genes are sufficient for rhizoid system development in early diverging land plants
inferredcites →https://doi.org/10.1242/dev.076091openalex-snapshot
AP2-type transcription factors determine stem cell identity in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1371/journal.pcbi.0030233openalex-snapshot
Small Regulatory RNAs May Sharpen Spatial Expression Patterns
inferredcites →https://doi.org/10.1371/journal.pcbi.0040008openalex-snapshot
Noise Propagation and Signaling Sensitivity in Biological Networks: A Role for Positive Feedback
inferredcites →https://doi.org/10.1371/journal.pcbi.1003112openalex-snapshot
Dual Delayed Feedback Provides Sensitivity and Robustness to the NF-κB Signaling Module
inferredcites →https://doi.org/10.1371/journal.pgen.1000314openalex-snapshot
Physcomitrella patens DCL3 Is Required for 22–24 nt siRNA Accumulation, Suppression of Retrotransposon-Derived Transcripts, and Normal Development
inferredcites →https://doi.org/10.1371/journal.pgen.1004826openalex-snapshot
Genome-Wide Analysis of leafbladeless1-Regulated and Phased Small RNAs Underscores the Importance of the TAS3 ta-siRNA Pathway to Maize Development
inferredcites →https://doi.org/10.1371/journal.pone.0077356openalex-snapshot
System for Stable β-Estradiol-Inducible Gene Expression in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.2307/2806602openalex-snapshot
A Cladistic Approach to the Phylogeny of the "Bryophytes"
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