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Network analyses implicate a role for PHYTOCHROME-mediated light signaling in the regulation of cuticle development in plant leaves
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4020-2686-7_1openalex-snapshot
The Plant Hormones: Their Nature, Occurrence, and Functions
inferredcites →https://doi.org/10.1007/978-94-010-0377-3_10openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferredcites →https://doi.org/10.1007/s00425-016-2585-4openalex-snapshot
Lipid transfer proteins: classification, nomenclature, structure, and function
inferredcites →https://doi.org/10.1007/s11103-008-9339-zopenalex-snapshot
The VLCFA elongase gene family in Arabidopsis thaliana: phylogenetic analysis, 3D modelling and expression profiling
inferredcites →https://doi.org/10.1016/b978-012339552-8/50003-2openalex-snapshot
Physiological evolution of lower embryophytes
inferredcites →https://doi.org/10.1016/j.cub.2018.05.068openalex-snapshot
CLAVATA Was a Genetic Novelty for the Morphological Innovation of 3D Growth in Land Plants
inferredcites →https://doi.org/10.1016/j.pbi.2009.09.009openalex-snapshot
Plant cuticles shine: advances in wax biosynthesis and export
inferredcites →https://doi.org/10.1023/a:1015255030047openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferredcites →https://doi.org/10.1038/37918openalex-snapshot
The origin and early evolution of plants on land
inferredcites →https://doi.org/10.1038/nature25966openalex-snapshot
Dysregulation of expression correlates with rare-allele burden and fitness loss in maize
inferredcites →https://doi.org/10.1038/ncomms8852openalex-snapshot
Phytochrome diversity in green plants and the origin of canonical plant phytochromes
inferredcites →https://doi.org/10.1038/nmeth.3317openalex-snapshot
HISAT: a fast spliced aligner with low memory requirements
inferredcites →https://doi.org/10.1038/nrg1272openalex-snapshot
Network biology: understanding the cell's functional organization
inferredcites →https://doi.org/10.1073/pnas.0403140101openalex-snapshot
Targeted knockout in Physcomitrella reveals direct actions of phytochrome in the cytoplasm
inferredcites →https://doi.org/10.1073/pnas.1416751111openalex-snapshot
Marine algae and land plants share conserved phytochrome signaling systems
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/bioinformatics/btu638openalex-snapshot
HTSeq—a Python framework to work with high-throughput sequencing data
inferredcites →https://doi.org/10.1093/jxb/erl017openalex-snapshot
Water transport in plant cuticles: an update
inferredcites →https://doi.org/10.1093/mp/ssr019openalex-snapshot
Evolutionary History of the Non-Specific Lipid Transfer Proteins
inferredcites →https://doi.org/10.1093/nar/gks042openalex-snapshot
Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation
inferredcites →https://doi.org/10.1093/pcp/pcs083openalex-snapshot
Characterization of Glycosylphosphatidylinositol-Anchored Lipid Transfer Protein 2 (LTPG2) and Overlapping Function between LTPG/LTPG1 and LTPG2 in Cuticular Wax Export or Accumulation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcy033openalex-snapshot
DEWAX2 Transcription Factor Negatively Regulates Cuticular Wax Biosynthesis in Arabidopsis Leaves
inferredcites →https://doi.org/10.1098/rsfs.2011.0053openalex-snapshot
How to infer gene networks from expression profiles, revisited
inferredcites →https://doi.org/10.1101/087969428.27.579openalex-snapshot
22 Light Signal Transduction and the Control of Seedling Development
inferredcites →https://doi.org/10.1101/625343openalex-snapshot
Changes in lipid composition and ultrastructure associated with functional maturation of the cuticle during adult maize leaf development
inferredcites →https://doi.org/10.1104/pp.003707openalex-snapshot
Significance of the Expression of the CER6 Condensing Enzyme for Cuticular Wax Production in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.070805openalex-snapshot
Cuticular Lipid Composition, Surface Structure, and Gene Expression in Arabidopsis Stem Epidermis
inferredcites →https://doi.org/10.1104/pp.108.1.369openalex-snapshot
Leaf Epicuticular Waxes of the Eceriferum Mutants in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.136028openalex-snapshot
Unraveling Transcriptional Control in Arabidopsis Using cis-Regulatory Elements and Coexpression Networks
inferredcites →https://doi.org/10.1104/pp.109.137497openalex-snapshot
Functional Characterization of the Arabidopsis β -Ketoacyl-Coenzyme A Reductase Candidates of the Fatty Acid Elongase
inferredcites →https://doi.org/10.1104/pp.109.137745openalex-snapshot
Disruption of Glycosylphosphatidylinositol-Anchored Lipid Transfer Protein Gene Altered Cuticular Lipid Composition, Increased Plastoglobules, and Enhanced Susceptibility to Infection by the Fungal Pathogen Alternaria brassicicola
inferredcites →https://doi.org/10.1104/pp.113.222737openalex-snapshot
The Formation and Function of Plant Cuticles
inferredcites →https://doi.org/10.1104/pp.15.01699openalex-snapshot
Localization of the Transpiration Barrier in the Epi- and Intracuticular Waxes of Eight Plant Species: Water Transport Resistances Are Associated with Fatty Acyl Rather Than Alicyclic Components
inferredcites →https://doi.org/10.1104/pp.16.00462openalex-snapshot
Microalgae Synthesize Hydrocarbons from Long-Chain Fatty Acids via a Light-Dependent Pathway
inferredcites →https://doi.org/10.1105/tpc.108.061325openalex-snapshot
A Battery of Transcription Factors Involved in the Regulation of Secondary Cell Wall Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.064451openalex-snapshot
Arabidopsis LTPG Is a Glycosylphosphatidylinositol-Anchored Lipid Transfer Protein Required for Export of Lipids to the Plant Surface
inferredcites →https://doi.org/10.1105/tpc.110.077974openalex-snapshot
Arabidopsis ABCG Transporters, Which Are Required for Export of Diverse Cuticular Lipids, Dimerize in Different Combinations
inferredcites →https://doi.org/10.1105/tpc.111.083485openalex-snapshot
The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.126037openalex-snapshot
SAUR Inhibition of PP2C-D Phosphatases Activates Plasma Membrane H+-ATPases to Promote Cell Expansion in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.132688openalex-snapshot
Transcriptomic Analyses Indicate That Maize Ligule Development Recapitulates Gene Expression Patterns That Occur during Lateral Organ Initiation
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03252.xopenalex-snapshot
Characterization of Arabidopsis ABCG11/WBC11, an ATP binding cassette (ABC) transporter that is required for cuticular lipid secretion †
inferredcites →https://doi.org/10.1126/science.1102331openalex-snapshot
Plant Cuticular Lipid Export Requires an ABC Transporter
inferredcites →https://doi.org/10.1126/science.aan6349openalex-snapshot
An algal photoenzyme converts fatty acids to hydrocarbons
inferredcites →https://doi.org/10.1146/annurev.arplant.59.103006.093219openalex-snapshot
Sealing Plant Surfaces: Cuticular Wax Formation by Epidermal Cells
inferredcites →https://doi.org/10.1146/annurev.cellbio.13.1.203openalex-snapshot
LIGHT CONTROL OF PLANT DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.ecolsys.29.1.263openalex-snapshot
EARLY EVOLUTION OF LAND PLANTS: Phylogeny, Physiology, and Ecology of the Primary Terrestrial Radiation
inferredcites →https://doi.org/10.1146/annurev.pp.36.060185.003033openalex-snapshot
Light Regulation of Gene Expression in Higher Plants
inferredcites →https://doi.org/10.1186/1471-2105-9-559openalex-snapshot
WGCNA: an R package for weighted correlation network analysis
inferredcites →https://doi.org/10.1194/jlr.r083139openalex-snapshot
Plant lipid transfer proteins: are we finally closing in on the roles of these enigmatic proteins?
inferredcites →https://doi.org/10.1534/genetics.103.026096openalex-snapshot
Structure and Expression of Maize Phytochrome Family HomeologsSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession nos. AY234825, AY234826, AY234827, AY234828, AY234829, AY234830.
inferredcites →https://doi.org/10.18637/jss.v046.i11openalex-snapshot
Fast R Functions for Robust Correlations and Hierarchical Clustering
inferredcites →https://doi.org/10.25080/tcwv9851openalex-snapshot
Exploring Network Structure, Dynamics, and Function using NetworkX
inferredcites →https://doi.org/10.32607/20758251-2016-8-2-47-61openalex-snapshot
Lipid Transfer Proteins As Components of the Plant Innate Immune System: Structure, Functions, and Applications
inferredcites →https://doi.org/10.3390/plants7010006openalex-snapshot
Deciphering the Evolution and Development of the Cuticle by Studying Lipid Transfer Proteins in Mosses and Liverworts
inferredcites →https://doi.org/10.4161/psb.29463openalex-snapshot
DEWAX-mediated transcriptional repression of cuticular wax biosynthesis inArabidopsis thaliana
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-031-40173-2_11openalex-snapshot
Melatonin-Mediated Regulation of Biotic Stress Responses in Plants
inferred← citeshttps://doi.org/10.1101/2021.10.26.465975openalex-snapshot
Integration of GWAS and TWAS to elucidate the genetic architecture of natural variation for leaf cuticular conductance in maize
inferred← citeshttps://doi.org/10.1534/g3.119.400884openalex-snapshot
Genome-Wide Association Study for Maize Leaf Cuticular Conductance Identifies Candidate Genes Involved in the Regulation of Cuticle Development
inferred← citeshttps://doi.org/10.3389/fpls.2024.1433436openalex-snapshot
Comprehensive genetic diversity and genome-wide association studies revealed the genetic basis of avocado fruit quality traits
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