On the public citation graph

The Arabidopsis organelle-localized glycyl-tRNA synthetase encoded by EMBRYO DEFECTIVE DEVELOPMENT1 is required for organ patterning

https://doi.org/10.1093/jxb/ers184
0 signed · 95 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00794.xopenalex-snapshot
DAG, a gene required for chloroplast differentiation and palisade development in Antirrhinum majus.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00795.xopenalex-snapshot
The DCL gene of tomato is required for chloroplast development and palisade cell morphogenesis in leaves.
inferredcites →https://doi.org/10.1006/dbio.1999.9443openalex-snapshot
Cell Cycling and Cell Enlargement in Developing Leaves of Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-004-1295-5openalex-snapshot
Altered expression of the Arabidopsis ortholog of DCL affects normal plant development
inferredcites →https://doi.org/10.1007/s11103-005-5992-7openalex-snapshot
Characterizations of a Hypomorphic Argonaute1 Mutant Reveal Novel AGO1 Functions in Arabidopsis Lateral Organ Development
inferredcites →https://doi.org/10.1016/j.cub.2003.09.035openalex-snapshot
Radial Patterning of Arabidopsis Shoots by Class III HD-ZIP and KANADI Genes
inferredcites →https://doi.org/10.1016/j.cub.2006.03.064openalex-snapshot
Specification of Leaf Polarity in Arabidopsis via the trans-Acting siRNA Pathway
inferredcites →https://doi.org/10.1016/j.devcel.2011.11.011openalex-snapshot
Exit from Proliferation during Leaf Development in Arabidopsis thaliana: A Not-So-Gradual Process
inferredcites →https://doi.org/10.1016/j.pbi.2011.10.009openalex-snapshot
Making leaves
inferredcites →https://doi.org/10.1016/s0021-9258(19)40150-6openalex-snapshot
A mutation in the small (alpha) subunit of glycyl-tRNA synthetase affects amino acid activation and subunit association parameters.
inferredcites →https://doi.org/10.1016/s0092-8674(00)81439-7openalex-snapshot
The PHANTASTICA Gene Encodes a MYB Transcription Factor Involved in Growth and Dorsoventrality of Lateral Organs in Antirrhinum
inferredcites →https://doi.org/10.1016/s0960-9822(01)00392-xopenalex-snapshot
Establishment of polarity in lateral organs of plants
inferredcites →https://doi.org/10.1023/b:plan.0000019061.79773.06openalex-snapshot
DCL is a plant-specific protein required for plastid ribosomal RNA processing and embryo development
inferredcites →https://doi.org/10.1038/35050091openalex-snapshot
Asymmetric leaves1 mediates leaf patterning and stem cell function in Arabidopsis
inferredcites →https://doi.org/10.1038/35079629openalex-snapshot
KANADI regulates organ polarity in Arabidopsis
inferredcites →https://doi.org/10.1038/35079635openalex-snapshot
Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots
inferredcites →https://doi.org/10.1038/379066a0openalex-snapshot
A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis
inferredcites →https://doi.org/10.1038/nature02366openalex-snapshot
Spatially restricted microRNA directs leaf polarity through ARGONAUTE1
inferredcites →https://doi.org/10.1042/bj2390249openalex-snapshot
Multienzyme complex of aminoacyl-tRNA synthetases: an essence of being eukaryotic
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00959.xopenalex-snapshot
REVOLUTA regulates meristem initiation at lateral positions
inferredcites →https://doi.org/10.1073/pnas.0803997105openalex-snapshot
KANADI1 regulates adaxial–abaxial polarity in Arabidopsis by directly repressing the transcription of ASYMMETRIC LEAVES2
inferredcites →https://doi.org/10.1073/pnas.1015162108openalex-snapshot
Model for the regulation of Arabidopsis thaliana leaf margin development
inferredcites →https://doi.org/10.1074/jbc.m011525200openalex-snapshot
Overlapping Destinations for Two Dual Targeted Glycyl-tRNA Synthetases in Arabidopsis thaliana and Phaseolus vulgaris
inferredcites →https://doi.org/10.1093/emboj/16.13.4041openalex-snapshot
The two RNA polymerases encoded by the nuclear and the plastid compartments transcribe distinct groups of genes in tobacco plastids
inferredcites →https://doi.org/10.1093/nar/12.10.4377openalex-snapshot
The β subunit ofE. coilglycyl-tRNA synthetase plays a major role in tRNA recognition
inferredcites →https://doi.org/10.1093/pcp/pcf077openalex-snapshot
The ASYMMETRIC LEAVES2 Gene of Arabidopsis thaliana, Required for Formation of a Symmetric Flat Leaf Lamina, Encodes a Member of a Novel Family of Proteins Characterized by Cysteine Repeats and a Leucine Zipper
inferredcites →https://doi.org/10.1093/pcp/pch051openalex-snapshot
amphivasal vascular bundle 1, a Gain-of-Function Mutation of the IFL1/REV Gene, Is Associated with Alterations in the Polarity of Leaves, Stems and Carpels
inferredcites →https://doi.org/10.1093/pcp/pcr083openalex-snapshot
ASYMMETRIC LEAVES2 and Elongator, a Histone Acetyltransferase Complex, Mediate the Establishment of Polarity in Leaves of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.103.027979openalex-snapshot
A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta
inferredcites →https://doi.org/10.1104/pp.106.080069openalex-snapshot
The SCABRA3 Nuclear Gene Encodes the Plastid RpoTp RNA Polymerase, Which Is Required for Chloroplast Biogenesis and Mesophyll Cell Proliferation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.124.4.1477openalex-snapshot
Seed and Molecular Resources for Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.014969openalex-snapshot
The Arabidopsis LATERAL ORGAN BOUNDARIES-Domain Gene ASYMMETRIC LEAVES2 Functions in the Repression of KNOX Gene Expression and in Adaxial-Abaxial Patterning
inferredcites →https://doi.org/10.1105/tpc.019307openalex-snapshot
PHANTASTICA Regulates Development of the Adaxial Mesophyll in Nicotiana Leaves
inferredcites →https://doi.org/10.1105/tpc.10.8.1277openalex-snapshot
Inactivation of a Glycyl-tRNA Synthetase Leads to an Arrest in Plant Embryo Development
inferredcites →https://doi.org/10.1105/tpc.104.026161openalex-snapshot
Class III Homeodomain-Leucine Zipper Gene Family Members Have Overlapping, Antagonistic, and Distinct Roles in Arabidopsis Development
inferredcites →https://doi.org/10.1105/tpc.104.029447openalex-snapshot
The MutantcrispaReveals Multiple Roles forPHANTASTICAin Pea Compound Leaf Development
inferredcites →https://doi.org/10.1105/tpc.105.033449openalex-snapshot
The Putative RNA-Dependent RNA Polymerase RDR6 Acts Synergistically with ASYMMETRIC LEAVES1 and 2 to Repress BREVIPEDICELLUS and MicroRNA165/166 in Arabidopsis Leaf Development
inferredcites →https://doi.org/10.1105/tpc.105.034876openalex-snapshot
Auxin Response Factors Mediate Arabidopsis Organ Asymmetry via Modulation of KANADI Activity
inferredcites →https://doi.org/10.1105/tpc.106.042325openalex-snapshot
Histone Deacetylases and ASYMMETRIC LEAVES2 Are Involved in the Establishment of Polarity in Leaves ofArabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.045013openalex-snapshot
The Proteolytic Function of theArabidopsis26S Proteasome Is Required for Specifying Leaf Adaxial Identity
inferredcites →https://doi.org/10.1105/tpc.11.1.69openalex-snapshot
FILAMENTOUS FLOWER Controls the Formation and Development of Arabidopsis Inflorescences and Floral Meristems
inferredcites →https://doi.org/10.1105/tpc.11.11.2139openalex-snapshot
IFL1, a Gene Regulating Interfascicular Fiber Differentiation in Arabidopsis, Encodes a Homeodomain-Leucine Zipper Protein
inferredcites →https://doi.org/10.1105/tpc.110.081448openalex-snapshot
Evolution and Diverse Roles of theCUP-SHAPED COTYLEDONGenes inArabidopsisLeaf Development
inferredcites →https://doi.org/10.1105/tpc.111.088906openalex-snapshot
Nonessential Plastid-Encoded Ribosomal Proteins in Tobacco: A Developmental Role for Plastid Translation and Implications for Reductive Genome Evolution
inferredcites →https://doi.org/10.1105/tpc.12.11.2129openalex-snapshot
Tobacco VDL Gene Encodes a Plastid DEAD Box RNA Helicase and Is Involved in Chloroplast Differentiation and Plant Morphogenesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02057.xopenalex-snapshot
A mutation of the CRUMPLED LEAF gene that encodes a protein localized in the outer envelope membrane of plastids affects the pattern of cell division, cell differentiation, and plastid division in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02580.xopenalex-snapshot
Requirement of aminoacyl‐tRNA synthetases for gametogenesis and embryo development in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03132.xopenalex-snapshot
Expression of the ASYMMETRIC LEAVES2 gene in the adaxial domain of Arabidopsis leaves represses cell proliferation in this domain and is critical for the development of properly expanded leaves
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03907.xopenalex-snapshot
The lack of mitochondrial AtFtsH4 protease alters Arabidopsis leaf morphology at the late stage of rosette development under short‐day photoperiod
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04156.xopenalex-snapshot
Mechanisms of leaf tooth formation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04422.xopenalex-snapshot
Ribosomal protein L27a is required for growth and patterning in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04457.xopenalex-snapshot
Differential contributions of ribosomal protein genes to Arabidopsis thaliana leaf development
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105310openalex-snapshot
PLASTID-TO-NUCLEUS RETROGRADE SIGNALING
inferredcites →https://doi.org/10.1242/dev.00622openalex-snapshot
Novelas1andas2defects in leaf adaxial-abaxial polarity reveal the requirement forASYMMETRIC LEAVES1and2andERECTAfunctions in specifying leaf adaxial identity
inferredcites →https://doi.org/10.1242/dev.00949openalex-snapshot
The role of JAGGED in shaping lateral organs
inferredcites →https://doi.org/10.1242/dev.00991openalex-snapshot
The Arabidopsis JAGGED gene encodes a zinc finger protein that promotes leaf tissue development
inferredcites →https://doi.org/10.1242/dev.01186openalex-snapshot
Asymmetric leaf development and blade expansion in Arabidopsis are mediated by KANADI and YABBY activities
inferredcites →https://doi.org/10.1242/dev.016469openalex-snapshot
ThreePIGGYBACKgenes that specifically influence leaf patterning encode ribosomal proteins
inferredcites →https://doi.org/10.1242/dev.017913openalex-snapshot
Ribosomal proteins promote leaf adaxial identity
inferredcites →https://doi.org/10.1242/dev.02335openalex-snapshot
NUBBINandJAGGEDdefine stamen and carpel shape inArabidopsis
inferredcites →https://doi.org/10.1242/dev.02416openalex-snapshot
NUBBIN and JAGGED define stamen and carpel shape in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.067918openalex-snapshot
ETTIN (ARF3) physically interacts with KANADI proteins to form a functional complex essential for integument development and polarity determination in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.121.7.2143openalex-snapshot
phantastica: a gene required for dorsoventrality of leaves in Antirrhinum majus
inferredcites →https://doi.org/10.1242/dev.121.9.2723openalex-snapshot
The REVOLUTA gene is necessary for apical meristem development and for limiting cell divisions in the leaves and stems of Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.126.18.4117openalex-snapshot
Members of the YABBY gene family specify abaxial cell fate in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.129.8.1957openalex-snapshot
ASYMMETRIC LEAVES1revealsknoxgene redundancy inArabidopsis

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4141086openalex-extracted
Are3, Encoding a Gly-Trna Synthetase, Genetically Interacts with Gogat to Regulate Nitrogen Metabolism in Rice
inferred← citeshttps://doi.org/10.1002/wdev.196openalex-snapshot
The complex of ASYMMETRIC LEAVES ( AS ) proteins plays a central role in antagonistic interactions of genes for leaf polarity specification in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2017.12.004openalex-snapshot
Regulation of tRNA biogenesis in plants and its link to plant growth and response to pathogens
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.11.003openalex-snapshot
Arabidopsis mTERF6 is required for leaf patterning
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.04.008openalex-snapshot
Rice albino 1, encoding a glycyl-tRNA synthetase, is involved in chloroplast development and establishment of the plastidic ribosome system in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.07.029openalex-snapshot
Unveiling the functions of plastid ribosomal proteins in plant development and abiotic stress tolerance
inferred← citeshttps://doi.org/10.1038/srep15975openalex-snapshot
Plastid control of abaxial-adaxial patterning
inferred← citeshttps://doi.org/10.1080/15592324.2021.1913366openalex-snapshot
Mutation of the OsGlyRS3 gene affects heading date in rice
inferred← citeshttps://doi.org/10.1093/mp/ssu022openalex-snapshot
The Translational Apparatus of Plastids and Its Role in Plant Development
inferred← citeshttps://doi.org/10.1093/pcp/pcx004openalex-snapshot
The Pentratricopeptide Repeat Protein Pigment-Defective Mutant2 is Involved in the Regulation of Chloroplast Development and Chloroplast Gene Expression in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcz153openalex-snapshot
An Aminoacyl tRNA Synthetase, OKI1, Is Required for Proper Shoot Meristem Size in Arabidopsis
inferred← citeshttps://doi.org/10.1101/039115openalex-snapshot
Plastid Osmotic Stress influences cell differentiation at the Plant Shoot Apex
inferred← citeshttps://doi.org/10.1104/pp.16.01840openalex-snapshot
The Pentatricopeptide Repeat Protein EMB2654 Is Essential for Trans-Splicing of a Chloroplast Small Ribosomal Subunit Transcript
inferred← citeshttps://doi.org/10.1104/pp.17.00248openalex-snapshot
pTAC10, a Key Subunit of Plastid-Encoded RNA Polymerase, Promotes Chloroplast Development
inferred← citeshttps://doi.org/10.1111/pce.15330openalex-snapshot
Chloroplastic Aspartyl‐tRNA Synthetase Is Required for Chloroplast Development, Photosynthesis and Photorespiratory Metabolism
inferred← citeshttps://doi.org/10.1111/plb.13084openalex-snapshot
Functional analysis of mTERF5 and mTERF9 contribution to salt tolerance, plastid gene expression and retrograde signalling in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1201/b19543-7openalex-snapshot
Molecular biology of mitochondria: Genome, transcriptome, and proteome
inferred← citeshttps://doi.org/10.1242/bio.028175openalex-snapshot
Plastid translation is essential for lateral root stem-cell patterning in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1242/dev.136234openalex-snapshot
Plastid osmotic stress influences cell differentiation at the plant shoot apex
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003655openalex-snapshot
Pattern Dynamics in Adaxial-Abaxial Specific Gene Expression Are Modulated by a Plastid Retrograde Signal during Arabidopsis thaliana Leaf Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0091071openalex-snapshot
The Small Subunit 1 of the Arabidopsis Isopropylmalate Isomerase Is Required for Normal Growth and Development and the Early Stages of Glucosinolate Formation
inferred← citeshttps://doi.org/10.3389/fpls.2015.01148openalex-snapshot
RNA Sequencing Analysis of the msl2msl3, crl, and ggps1 Mutants Indicates that Diverse Sources of Plastid Dysfunction Do Not Alter Leaf Morphology Through a Common Signaling Pathway
inferred← citeshttps://doi.org/10.3389/fpls.2022.1009895openalex-snapshot
The Arabidopsis ATP-Binding Cassette E protein ABCE2 is a conserved component of the translation machinery
inferred← citeshttps://doi.org/10.3390/genes11091056openalex-snapshot
Plant-Specific Domains and Fragmented Sequences Imply Non-Canonical Functions in Plant Aminoacyl-tRNA Synthetases
inferred← citeshttps://doi.org/10.3390/ijms19082388openalex-snapshot
The Characterization of Arabidopsis mterf6 Mutants Reveals a New Role for mTERF6 in Tolerance to Abiotic Stress
inferred← citeshttps://doi.org/10.3390/plants2020174openalex-snapshot
The Leaf Adaxial-Abaxial Boundary and Lamina Growth
inferred← citeshttps://doi.org/10.3390/plants9070834openalex-snapshot
Arabidopsis Plastid-RNA Polymerase RPOTp Is Involved in Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.13.0513aopenalex-snapshot
ASYMMETRIC LEAVES2 and FASCIATA2 cooperatively regulate the formation of leaf adaxial-abaxial polarity in Arabidopsis thaliana
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.