On the public citation graph

PIN-LIKES coordinate brassinosteroid signalling with nuclear auxin input in Arabidopsis thaliana

0 signed · 46 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/978-1-4939-6469-7_8openalex-snapshot
Histochemical Staining of β-Glucuronidase and Its Spatial Quantification
inferredcites →https://doi.org/10.1007/s11538-009-9497-4openalex-snapshot
Mathematical Modelling of the Aux/IAA Negative Feedback Loop
inferredcites →https://doi.org/10.1016/j.cell.2009.03.009openalex-snapshot
SnapShot: Auxin Signaling and Transport
inferredcites →https://doi.org/10.1016/j.cub.2015.02.046openalex-snapshot
Spatiotemporal Brassinosteroid Signaling and Antagonism with Auxin Pattern Stem Cell Dynamics in Arabidopsis Roots
inferredcites →https://doi.org/10.1016/j.jtbi.2017.08.013openalex-snapshot
Mathematical modelling and analysis of the brassinosteroid and gibberellin signalling pathways and their interactions
inferredcites →https://doi.org/10.1016/j.phytochem.2007.04.030openalex-snapshot
Three oxidative metabolites of indole-3-acetic acid from Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1016/s1534-5807(02)00153-3openalex-snapshot
Nuclear-Localized BZR1 Mediates Brassinosteroid-Induced Growth and Feedback Suppression of Brassinosteroid Biosynthesis
inferredcites →https://doi.org/10.1038/nature03542openalex-snapshot
The Arabidopsis F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature03543openalex-snapshot
The F-box protein TIR1 is an auxin receptor
inferredcites →https://doi.org/10.1038/nature05130openalex-snapshot
BRX mediates feedback between brassinosteroid levels and auxin signalling in root growth
inferredcites →https://doi.org/10.1038/nature08066openalex-snapshot
Subcellular homeostasis of phytohormone auxin is mediated by the ER-localized PIN5 transporter
inferredcites →https://doi.org/10.1038/nature11001openalex-snapshot
A novel putative auxin carrier family regulates intracellular auxin homeostasis in plants
inferredcites →https://doi.org/10.1038/nbt.1957openalex-snapshot
Astrocytes from familial and sporadic ALS patients are toxic to motor neurons
inferredcites →https://doi.org/10.1038/ncb2893openalex-snapshot
A secreted peptide acts on BIN2-mediated phosphorylation of ARFs to potentiate auxin response during lateral root development
inferredcites →https://doi.org/10.1038/ncomms1941openalex-snapshot
ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1038/nplants.2017.105openalex-snapshot
Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition
inferredcites →https://doi.org/10.1038/s41467-017-00355-4openalex-snapshot
Brassinosteroid signaling-dependent root responses to prolonged elevated ambient temperature
inferredcites →https://doi.org/10.1038/s41477-018-0190-1openalex-snapshot
Rapid and reversible root growth inhibition by TIR1 auxin signalling
inferredcites →https://doi.org/10.1073/pnas.0803996105openalex-snapshot
Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1108436108openalex-snapshot
Conversion of tryptophan to indole-3-acetic acid by TRYPTOPHAN AMINOTRANSFERASES OF ARABIDOPSIS and YUCCAs in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1814015116openalex-snapshot
PILS6 is a temperature-sensitive regulator of nuclear auxin input and organ growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/erp306openalex-snapshot
Aluminium-induced inhibition of root elongation in Arabidopsis is mediated by ethylene and auxin
inferredcites →https://doi.org/10.1093/jxb/ert139openalex-snapshot
Auxin: simply complicated
inferredcites →https://doi.org/10.1093/mp/ssr034openalex-snapshot
Seven Things We Think We Know about Auxin Transport
inferredcites →https://doi.org/10.1104/pp.109.138529openalex-snapshot
The Tryptophan Conjugates of Jasmonic and Indole-3-Acetic Acids Are Endogenous Auxin Inhibitors
inferredcites →https://doi.org/10.1104/pp.118.1.285openalex-snapshot
Metabolism of Indole-3-Acetic Acid in Arabidopsis1
inferredcites →https://doi.org/10.1104/pp.121.3.743openalex-snapshot
Brassinosteroid-Insensitive Dwarf Mutants of Arabidopsis Accumulate Brassinosteroids
inferredcites →https://doi.org/10.1104/pp.123.4.1247openalex-snapshot
Brassinosteroid-Insensitive-1 Is a Ubiquitously Expressed Leucine-Rich Repeat Receptor Serine/Threonine Kinase
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.113.114421openalex-snapshot
Regulation of Auxin Homeostasis and Gradients in Arabidopsis Roots through the Formation of the Indole-3-Acetic Acid Catabolite 2-Oxindole-3-Acetic Acid
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05037.xopenalex-snapshot
The endoplasmic reticulum localized PIN8 is a pollen‐specific auxin carrier involved in intracellular auxin homeostasis
inferredcites →https://doi.org/10.1126/science.1107580openalex-snapshot
BZR1 Is a Transcriptional Repressor with Dual Roles in Brassinosteroid Homeostasis and Growth Responses
inferredcites →https://doi.org/10.1126/science.1121356openalex-snapshot
Polar PIN Localization Directs Auxin Flow in Plants
inferredcites →https://doi.org/10.1242/dev.057331openalex-snapshot
Brassinosteroids control meristem size by promoting cell cycle progression in Arabidopsis roots
inferredcites →https://doi.org/10.1242/dev.061804openalex-snapshot
Brassinosteroid perception in the epidermis controls root meristem size
inferredcites →https://doi.org/10.1371/journal.pbio.0020258openalex-snapshot
Interdependency of Brassinosteroid and Auxin Signaling in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1003294openalex-snapshot
Patterning of Leaf Vein Networks by Convergent Auxin Transport Pathways
inferredcites →https://doi.org/10.3389/fpls.2012.00227openalex-snapshot
Evolution and structural diversification of PILS putative auxin carriers in plants
inferredcites →https://doi.org/10.3389/fpls.2017.02256openalex-snapshot
Auxin-BR Interaction Regulates Plant Growth and Development
inferredcites →https://doi.org/10.7554/elife.03031openalex-snapshot
Cell elongation is regulated through a central circuit of interacting transcription factors in the Arabidopsis hypocotyl
inferredcites →https://doi.org/10.7554/elife.05868openalex-snapshot
Auxin regulates SNARE-dependent vacuolar morphology restricting cell size

What points at this work

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

inferred← citeshttps://doi.org/10.1093/jxb/eraa027openalex-snapshot
Same same, but different: growth responses of primary and lateral roots
inferred← citeshttps://doi.org/10.1242/dev.168088openalex-snapshot
PIN-FORMED and PIN-LIKES auxin transport facilitators
inferred← citeshttps://doi.org/10.3390/ijms21051561openalex-snapshot
Deviating from the Beaten Track: New Twists in Brassinosteroid Receptor 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.