On the public citation graph
Histone Lysine Methyltransferase SDG26 Is Involved in Leaf-size Control through Regulation of Cytokinins Related Genes Expression in Arabidopsis thaliana
0 signed · 70 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/s00425-026-04974-4openalex-snapshot
Cytokinin response factor 1 acts as a negative regulator of cytokinin-mediated developmental pathways in Arabidopsis
inferredcites →https://doi.org/10.1007/s10265-005-0234-2openalex-snapshot
The Arabidopsis leaf as a model system for investigating the role of cell cycle regulation in organ growth
inferredcites →https://doi.org/10.1007/s10265-012-0485-7openalex-snapshot
The Arabidopsis thaliana SET-domain-containing protein ASHH1/SDG26 interacts with itself and with distinct histone lysine methyltransferases
inferredcites →https://doi.org/10.1016/bs.ctdb.2018.11.006openalex-snapshot
Leaf development and evolution
inferredcites →https://doi.org/10.1016/j.bbagrm.2016.02.003openalex-snapshot
Interplay of the histone methyltransferases SDG8 and SDG26 in the regulation of transcription and plant flowering and development
inferredcites →https://doi.org/10.1016/j.bbrc.2016.07.065openalex-snapshot
OaMAX2 of Orobanche aegyptiaca and Arabidopsis AtMAX2 share conserved functions in both development and drought responses
inferredcites →https://doi.org/10.1016/j.bbrc.2019.02.038openalex-snapshot
Crosstalk between the cytokinin and MAX2 signaling pathways in growth and callus formation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cell.2019.05.011openalex-snapshot
A Growth-Based Framework for Leaf Shape Development and Diversity
inferredcites →https://doi.org/10.1016/j.devcel.2024.08.010openalex-snapshot
DRMY1 promotes robust morphogenesis in Arabidopsis by sustaining the translation of cytokinin-signaling inhibitor proteins
inferredcites →https://doi.org/10.1016/j.devcel.2025.03.001openalex-snapshot
VRN2-PRC2 facilitates light-triggered repression of PIF signaling to coordinate growth in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2018.06.006openalex-snapshot
Molecular Mechanisms of Leaf Morphogenesis
inferredcites →https://doi.org/10.1016/j.pbi.2013.11.005openalex-snapshot
Regulation of plant lateral-organ growth by modulating cell number and size
inferredcites →https://doi.org/10.1016/j.pbi.2013.11.012openalex-snapshot
Comparative leaf development in angiosperms
inferredcites →https://doi.org/10.1016/j.plaphy.2023.02.026openalex-snapshot
PeGRF6-PeGIF1 complex regulates cell proliferation in the leaf of Phalaenopsis equestris
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.003openalex-snapshot
Leaf size control: complex coordination of cell division and expansion
inferredcites →https://doi.org/10.1016/j.ydbio.2009.11.029openalex-snapshot
Twenty years on: The inner workings of the shoot apical meristem, a developmental dynamo
inferredcites →https://doi.org/10.1016/s0070-2153(10)91007-7openalex-snapshot
Control of Tissue and Organ Growth in Plants
inferredcites →https://doi.org/10.1021/acs.est.2c03828openalex-snapshot
Elucidating the Differences in Metal Toxicity by Quantitative Adverse Outcome Pathways
inferredcites →https://doi.org/10.1038/ncb1329openalex-snapshot
Prevention of early flowering by expression of FLOWERING LOCUS C requires methylation of histone H3 K36
inferredcites →https://doi.org/10.1038/s41477-021-01021-wopenalex-snapshot
Plant cell polarity as the nexus of tissue mechanics and morphogenesis
inferredcites →https://doi.org/10.1039/b802262nopenalex-snapshot
Photosynthetic energy conversion: natural and artificial
inferredcites →https://doi.org/10.1039/c0pp00252fopenalex-snapshot
Balancing forces in the photoperiodic control of flowering
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/10.1073/pnas.0402887101openalex-snapshot
In planta functions of the Arabidopsis cytokinin receptor family
inferredcites →https://doi.org/10.1073/pnas.0603522103openalex-snapshot
Roles of Arabidopsis ATP/ADP isopentenyltransferases and tRNA isopentenyltransferases in cytokinin biosynthesis
inferredcites →https://doi.org/10.1073/pnas.0704166104openalex-snapshot
Arabidopsis CYCD3 D-type cyclins link cell proliferation and endocycles and are rate-limiting for cytokinin responses
inferredcites →https://doi.org/10.1074/jbc.m102130200openalex-snapshot
Identification of Genes Encoding Adenylate Isopentenyltransferase, a Cytokinin Biosynthesis Enzyme, inArabidopsis thaliana
inferredcites →https://doi.org/10.1093/emboj/cdf614openalex-snapshot
Cell numbers and leaf development in Arabidopsis: a functional analysis of the STRUWWELPETER gene
inferredcites →https://doi.org/10.1093/jxb/erae348openalex-snapshot
Five unaddressed questions about cytokinin biosynthesis
inferredcites →https://doi.org/10.1093/jxb/eraf449openalex-snapshot
H3K27me3 epigenetic mark crucial for Arabidopsis callus cellular identity and regeneration capacity
inferredcites →https://doi.org/10.1093/jxb/erq457openalex-snapshot
Distribution, biological activities, metabolism, and the conceivable function of cis-zeatin-type cytokinins in plants
inferredcites →https://doi.org/10.1093/jxb/ert354openalex-snapshot
Interplay between cell growth and cell cycle in plants
inferredcites →https://doi.org/10.1093/jxb/eru142openalex-snapshot
Isopentenyltransferase-1 (IPT1) knockout in Physcomitrella together with phylogenetic analyses of IPTs provide insights into evolution of plant cytokinin biosynthesis
inferredcites →https://doi.org/10.1093/jxb/erz522openalex-snapshot
Molecular networks regulating cell division during Arabidopsis leaf growth
inferredcites →https://doi.org/10.1093/nar/gkac551openalex-snapshot
Characterization of an autonomous pathway complex that promotes flowering in Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029604openalex-snapshot
Differential Expression of Genes for Response Regulators in Response to Cytokinins and Nitrate in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcf173openalex-snapshot
Amyloplast Formation in Cultured Tobacco BY-2 Cells Requires a High Cytokinin Content
inferredcites →https://doi.org/10.1093/pcp/pcq138openalex-snapshot
ROTUNDIFOLIA4 Regulates Cell Proliferation Along the Body Axis in Arabidopsis Shoot
inferredcites →https://doi.org/10.1093/plphys/kiac374openalex-snapshot
Identification of growth regulators using cross-species network analysis in plants
inferredcites →https://doi.org/10.1101/gad.497009openalex-snapshot
Integration of transport-based models for phyllotaxis and midvein formation
inferredcites →https://doi.org/10.1104/pp.100.4.2090openalex-snapshot
Inhibition of Growth of Cultured Tobacco Cells at Low Concentrations of Lovastatin Is Reversed by Cytokinin
inferredcites →https://doi.org/10.1104/pp.102.013722openalex-snapshot
Comparative Analysis of SET Domain Proteins in Maize and Arabidopsis Reveals Multiple Duplications Preceding the Divergence of Monocots and Dicots
inferredcites →https://doi.org/10.1104/pp.104.046367openalex-snapshot
GENEVESTIGATOR. Arabidopsis Microarray Database and Analysis Toolbox
inferredcites →https://doi.org/10.1104/pp.113.217026openalex-snapshot
Identification of Cytokinin-Responsive Genes Using Microarray Meta-Analysis and RNA-Seq in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.124.4.1706openalex-snapshot
Characterization of the Response of the Arabidopsis Response Regulator Gene Family to Cytokinin
inferredcites →https://doi.org/10.1105/tpc.010087openalex-snapshot
Functional Analysis of Cyclin-Dependent Kinase Inhibitors of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.014928openalex-snapshot
Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity
inferredcites →https://doi.org/10.1105/tpc.106.045674openalex-snapshot
The Arabidopsis Histidine Phosphotransfer Proteins Are Redundant Positive Regulators of Cytokinin Signaling
inferredcites →https://doi.org/10.1111/j.1365-313x.2000.00909.xopenalex-snapshot
Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04033.xopenalex-snapshot
Genetic networks regulated by ASYMMETRIC LEAVES1 ( AS1 ) and AS2 in leaf development in Arabidopsis thaliana : KNOX genes control five morphological events
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00556.xopenalex-snapshot
Assessment of lovastatin application as tool in probing cytokinin‐mediated cell cycle regulation
inferredcites →https://doi.org/10.1111/j.1462-5822.2012.01785.xopenalex-snapshot
Chromatin modification and remodelling: a regulatory landscape for the control of Arabidopsis defence responses upon pathogen attack
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00898.xopenalex-snapshot
Metabolism and Long‐distance Translocation of Cytokinins
inferredcites →https://doi.org/10.1111/jipb.13084openalex-snapshot
From genes to networks: The genetic control of leaf development
inferredcites →https://doi.org/10.1111/nph.12493openalex-snapshot
Combinatorial functions of diverse histone methylations in Arabidopsis thaliana flowering time regulation.
inferredcites →https://doi.org/10.1111/nph.15371openalex-snapshot
On the mechanisms of development in monocot and eudicot leaves
inferredcites →https://doi.org/10.1111/ppl.70416openalex-snapshot
Transcription Factor ClTCP4 Regulates Leaf Size and Wavy Margin in Leaf Morphogenesis of Citrullus lanatus
inferredcites →https://doi.org/10.1111/tpj.12729openalex-snapshot
The trx G family histone methyltransferase SET DOMAIN GROUP 26 promotes flowering via a distinctive genetic pathway
inferredcites →https://doi.org/10.1111/tpj.13097openalex-snapshot
The cytokinin response factors modulate root and shoot growth and promote leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.16558openalex-snapshot
Leaf growth – complex regulation of a seemingly simple process
inferredcites →https://doi.org/10.1126/science.283.5407.1541openalex-snapshot
Cytokinin Activation of Arabidopsis Cell Division Through a D-Type Cyclin
inferredcites →https://doi.org/10.1128/mcb.01607-07openalex-snapshot
Di- and Tri- but Not Monomethylation on Histone H3 Lysine 36 Marks Active Transcription of Genes Involved in Flowering Time Regulation and Other Processes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112206openalex-snapshot
Improving Photosynthetic Efficiency for Greater Yield
inferredcites →https://doi.org/10.1146/annurev-arplant-080720-081920openalex-snapshot
Solving the Puzzle of Shape Regulation in Plant Epidermal Pavement Cells
inferredcites →https://doi.org/10.1242/dev.01261openalex-snapshot
Real-time lineage analysis reveals oriented cell divisions associated with morphogenesis at the shoot apex of Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.080523openalex-snapshot
Stomatal development: a plant's perspective on cell polarity, cell fate transitions and intercellular communication
inferredcites →https://doi.org/10.1242/dev.149344openalex-snapshot
Cytokinin signaling in plant development
inferredcites →https://doi.org/10.1371/journal.pbio.0060174openalex-snapshot
Controlling Size in Multicellular Organs: Focus on the Leaf
inferredcites →https://doi.org/10.1371/journal.pgen.1009674openalex-snapshot
An auxin signaling network translates low-sugar-state input into compensated cell enlargement in the fugu5 cotyledon
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.