On the public citation graph

Quantitative proteomic analysis of auxin signaling during seedling development

0 signed · 75 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/s004250050493openalex-snapshot

The MSG1 and AXR1 genes of Arabidopsis are likely to act independently in growth-curvature responses of hypocotyls

inferredcites →https://doi.org/10.1016/j.cell.2006.05.050openalex-snapshot

Different Plant Hormones Regulate Similar Processes through Largely Nonoverlapping Transcriptional Responses

inferredcites →https://doi.org/10.1016/j.cpb.2016.12.001openalex-snapshot

The Bio-Analytic Resource: Data visualization and analytic tools for multiple levels of plant biology

inferredcites →https://doi.org/10.1016/j.cub.2011.08.057openalex-snapshot

Pectin-Induced Changes in Cell Wall Mechanics Underlie Organ Initiation in Arabidopsis

inferredcites →https://doi.org/10.1016/j.devcel.2013.02.007openalex-snapshot

CLASP Interacts with Sorting Nexin 1 to Link Microtubules and Auxin Transport via PIN2 Recycling in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/j.pbi.2016.04.004openalex-snapshot

Auxin perception and downstream events

inferredcites →https://doi.org/10.1016/j.plantsci.2012.04.008openalex-snapshot

Ribosomes and translation in plant developmental control

inferredcites →https://doi.org/10.1016/j.tplants.2005.02.009openalex-snapshot

The PIN auxin efflux facilitators: evolutionary and functional perspectives

inferredcites →https://doi.org/10.1016/j.ydbio.2012.05.039openalex-snapshot

AUXOLOGY: When auxin meets plant evo-devo

inferredcites →https://doi.org/10.1021/pr400697sopenalex-snapshot

Proteomics in Deciphering the Auxin Commitment in the Arabidopsis thaliana Root Growth

inferredcites →https://doi.org/10.1023/a:1011825114301openalex-snapshot

Gene isolation and characterization of two acyl CoA oxidases from soybean with broad substrate specificities and enhanced expression in the growing seedling axis

inferredcites →https://doi.org/10.1038/415806aopenalex-snapshot

Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis

inferredcites →https://doi.org/10.1038/msb.2010.59openalex-snapshot

Sequence signatures and mRNA concentration can explain two‐thirds of protein abundance variation in a human cell line

inferredcites →https://doi.org/10.1038/msb.2013.40openalex-snapshot

A map of cell type‐specific auxin responses

inferredcites →https://doi.org/10.1038/nature02046openalex-snapshot

Global analysis of protein expression in yeast

inferredcites →https://doi.org/10.1038/nature05046openalex-snapshot

AtSNX1 defines an endosome for auxin-carrier trafficking in Arabidopsis

inferredcites →https://doi.org/10.1038/nature10098openalex-snapshot

Global quantification of mammalian gene expression control

inferredcites →https://doi.org/10.1073/pnas.0634629100openalex-snapshot

Protein pathway and complex clustering of correlated mRNA and protein expression analyses in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1073/pnas.1214774109openalex-snapshot

Arabidopsis ribosomal proteins control developmental programs through translational regulation of auxin response factors

inferredcites →https://doi.org/10.1073/pnas.1319113110openalex-snapshot

Reconstruction of protein networks from an atlas of maize seed proteotypes

inferredcites →https://doi.org/10.1073/pnas.1504828112openalex-snapshot

Plastid-produced interorgannellar stress signal MEcPP potentiates induction of the unfolded protein response in endoplasmic reticulum

inferredcites →https://doi.org/10.1073/pnas.1618782114openalex-snapshot

Differential TOR activation and cell proliferation in Arabidopsis root and shoot apexes

inferredcites →https://doi.org/10.1074/mcp.m112.021220openalex-snapshot

Quantitative Phosphoproteomics after Auxin-stimulated Lateral Root Induction Identifies an SNX1 Protein Phosphorylation Site Required for Growth

inferredcites →https://doi.org/10.1080/15592324.2017.1363946openalex-snapshot

COP1 integrates light signals to ROP2 for cell cycle activation

inferredcites →https://doi.org/10.1093/abbs/gms057openalex-snapshot

A proteomics study of auxin effects in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/aob/mcp287openalex-snapshot

The AUX1 LAX family of auxin influx carriers is required for the establishment of embryonic root cell organization in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/emboj/cdg190openalex-snapshot

The RUB/Nedd8 conjugation pathway is required for early development in Arabidopsis

inferredcites →https://doi.org/10.1093/nar/gks1094openalex-snapshot

STRING v9.1: protein-protein interaction networks, with increased coverage and integration

inferredcites →https://doi.org/10.1093/nar/gku1003openalex-snapshot

STRING v10: protein–protein interaction networks, integrated over the tree of life

inferredcites →https://doi.org/10.1093/nar/gkw937openalex-snapshot

The STRING database in 2017: quality-controlled protein–protein association networks, made broadly accessible

inferredcites →https://doi.org/10.1093/pcp/pcj043openalex-snapshot

Expression Profiling of Auxin-treated Arabidopsis Roots: Toward a Molecular Analysis of Lateral Root Emergence

inferredcites →https://doi.org/10.1094/mpmi-01-15-0005-ropenalex-snapshot

Mitogen-Activated Protein Kinase 6 and Ethylene and Auxin Signaling Pathways Are Involved in Arabidopsis Root-System Architecture Alterations by Trichoderma atroviride

inferredcites →https://doi.org/10.1104/pp.103.021261openalex-snapshot

Gene Expression Phenotypes of Arabidopsis Associated with Sensitivity to Low Temperatures

inferredcites →https://doi.org/10.1104/pp.112.207779openalex-snapshot

incurvata13, a Novel Allele of AUXIN RESISTANT6, Reveals a Specific Role for Auxin and the SCF Complex in Arabidopsis Embryogenesis, Vascular Specification, and Leaf Flatness

inferredcites →https://doi.org/10.1104/pp.114.238378openalex-snapshot

The Arabidopsis Endosomal Sorting Complex Required for Transport III Regulates Internal Vesicle Formation of the Prevacuolar Compartment and Is Required for Plant Development

inferredcites →https://doi.org/10.1105/tpc.010282openalex-snapshot

AXR1-ECR1–Dependent Conjugation of RUB1 to the Arabidopsis Cullin AtCUL1 Is Required for Auxin Response

inferredcites →https://doi.org/10.1105/tpc.104.024737openalex-snapshot

Structure-Function Analysis of the Presumptive Arabidopsis Auxin Permease AUX1[W]

inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot

Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid

inferredcites →https://doi.org/10.1105/tpc.105.036533openalex-snapshot

The Arabidopsis STV1 Protein, Responsible for Translation Reinitiation, Is Required for Auxin-Mediated Gynoecium Patterning

inferredcites →https://doi.org/10.1105/tpc.105.036723openalex-snapshot

Functional Genomic Analysis of the AUXIN/INDOLE-3-ACETIC ACID Gene Family Members in Arabidopsis thaliana [W]

inferredcites →https://doi.org/10.1105/tpc.106.047571openalex-snapshot

Role of the MPN Subunits in COP9 Signalosome Assembly and Activity, and Their Regulatory Interaction with Arabidopsis Cullin3-Based E3 Ligases

inferredcites →https://doi.org/10.1105/tpc.107.052068openalex-snapshot

Multilevel Interactions between Ethylene and Auxin in Arabidopsis Roots

inferredcites →https://doi.org/10.1105/tpc.111.087999openalex-snapshot

Modulation of Phototropic Responsiveness in Arabidopsis through Ubiquitination of Phototropin 1 by the CUL3-Ring E3 Ubiquitin Ligase CRL3NPH3

inferredcites →https://doi.org/10.1105/tpc.111.095190openalex-snapshot

The Conjugated Auxin Indole-3-Acetic Acid–Aspartic Acid Promotes Plant Disease Development

inferredcites →https://doi.org/10.1105/tpc.112.098905openalex-snapshot

A PP6-Type Phosphatase Holoenzyme Directly Regulates PIN Phosphorylation and Auxin Efflux in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.114868openalex-snapshot

A Kinetic Analysis of the Auxin Transcriptome Reveals Cell Wall Remodeling Proteins That Modulate Lateral Root Development in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.115881openalex-snapshot

Cellular Auxin Homeostasis under High Temperature Is Regulated through a SORTING NEXIN1–Dependent Endosomal Trafficking Pathway

inferredcites →https://doi.org/10.1105/tpc.12.5.757openalex-snapshot

The NPH4 Locus Encodes the Auxin Response Factor ARF7, a Conditional Regulator of Differential Growth in Aerial Arabidopsis Tissue

inferredcites →https://doi.org/10.1109/tnb.2016.2516950openalex-snapshot

Genome-Wide Search for Translated Upstream Open Reading Frames in Arabidopsis Thaliana

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02324.xopenalex-snapshot

Stress homeostasis – the redox and auxin perspective

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02220.xopenalex-snapshot

Disruption and overexpression of auxin response factor 8 gene of Arabidopsis affect hypocotyl elongation and root growth habit, indicating its possible involvement in auxin homeostasis in light condition

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02343.xopenalex-snapshot

Mutations in Arabidopsis acyl‐CoA oxidase genes reveal distinct and overlapping roles in β‐oxidation

inferredcites →https://doi.org/10.1111/nph.12880openalex-snapshot

Involvement of YODA and mitogen activated protein kinase 6 in Arabidopsis post‐embryogenic root development through auxin up‐regulation and cell division plane orientation

inferredcites →https://doi.org/10.1111/pce.13021openalex-snapshot

Redox regulation at the site of primary growth: auxin, cytokinin and ROS crosstalk

inferredcites →https://doi.org/10.1111/tpj.12482openalex-snapshot

Correlation of mRNA and protein abundance in the developing maize leaf

inferredcites →https://doi.org/10.1111/tpj.13667openalex-snapshot

Regulatory‐associated protein of TOR ( RAPTOR ) alters the hormonal and metabolic composition of Arabidopsis seeds, controlling seed morphology, viability and germination potential

inferredcites →https://doi.org/10.1126/science.1157956openalex-snapshot

Genome-Scale Proteomics Reveals Arabidopsis thaliana Gene Models and Proteome Dynamics

inferredcites →https://doi.org/10.1126/science.280.5370.1760openalex-snapshot

The Ubiquitin-Related Protein RUB1 and Auxin Response in Arabidopsis

inferredcites →https://doi.org/10.1126/science.aag1125openalex-snapshot

Integration of omic networks in a developmental atlas of maize

inferredcites →https://doi.org/10.1146/annurev-arplant-043015-112122openalex-snapshot

Transcriptional Responses to the Auxin Hormone

inferredcites →https://doi.org/10.1186/1471-2105-10-48openalex-snapshot

GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists

inferredcites →https://doi.org/10.1186/1471-2229-10-193openalex-snapshot

Translation reinitiation and development are compromised in similar ways by mutations in translation initiation factor eIF3h and the ribosomal protein RPL24

inferredcites →https://doi.org/10.1371/journal.pgen.1001393openalex-snapshot

Comparative Analysis of Proteome and Transcriptome Variation in Mouse

inferredcites →https://doi.org/10.1371/journal.pone.0036210openalex-snapshot

Hypocotyl Transcriptome Reveals Auxin Regulation of Growth-Promoting Genes through GA-Dependent and -Independent Pathways

inferredcites →https://doi.org/10.1371/journal.pone.0057813openalex-snapshot

Mechano-Chemical Aspects of Organ Formation in Arabidopsis thaliana: The Relationship between Auxin and Pectin

inferredcites →https://doi.org/10.3389/fpls.2016.00291openalex-snapshot

Target of Rapamycin Is a Key Player for Auxin Signaling Transduction in Arabidopsis

inferredcites →https://doi.org/10.3389/fpls.2017.00036openalex-snapshot

Arabidopsis NITRILASE 1 Contributes to the Regulation of Root Growth and Development through Modulation of Auxin Biosynthesis in Seedlings

inferredcites →https://doi.org/10.3389/fpls.2017.01204openalex-snapshot

TOR-Dependent and -Independent Pathways Regulate Autophagy in Arabidopsis thaliana

inferredcites →https://doi.org/10.3390/proteomes5030016openalex-snapshot

Exogenous Auxin Elicits Changes in the Arabidopsis thaliana Root Proteome in a Time-Dependent Manner

inferredcites →https://doi.org/10.3732/ajb.1200436openalex-snapshot

GRAVITY PERSISTENT SIGNAL 1 (GPS1) Reveals Novel Cytochrome P450s Involved in Gravitropism

What points at this work

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

inferred← citeshttps://doi.org/10.1002/pld3.326openalex-snapshot

slim shady is a novel allele of PHYTOCHROME B present in the T‐DNA line SALK_015201

inferred← citeshttps://doi.org/10.1007/s00344-026-12312-xopenalex-snapshot

ARF Gene Family: Expression Dynamics, Signalling, and Importance in Seed Development

inferred← citeshttps://doi.org/10.1007/s10142-026-01907-yopenalex-snapshot

Role of GhMyoVIII2 in regulating the fruit branch angle revealed by integrated bioinformatic, expression, and VIGS analyses in upland cotton

inferred← citeshttps://doi.org/10.1101/2021.02.12.430994openalex-snapshot

slim shady is a novel allele of PHYTOCHROME B present in the T-DNA line SALK_015201

inferred← citeshttps://doi.org/10.1242/dev.201762openalex-snapshot

The class VIII myosin ATM1 is required for root apical meristem function

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.