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A molecular framework to study periderm formation in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Polymer Thermosets from Multifunctional Polyester Resins Based on Renewable Monomers
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The Importance of Phellogen Cells and their Structural Characteristics in Susceptibility and Resistance to Excoriation in Immature and Mature Potato Tuber (Solanum tuberosum L.) Periderm
inferredcites →https://doi.org/10.1006/pmpp.1998.0179openalex-snapshot
Differential deposition of suberin phenolic and aliphatic domains and their roles in resistance to infection during potato tuber (Solanum tuberosumL.) wound-healing
inferredcites →https://doi.org/10.1007/978-1-4939-6722-3_10openalex-snapshot
Vascular Morphodynamics During Secondary Growth
inferredcites →https://doi.org/10.1007/bf00386015openalex-snapshot
Chemical composition and variability of cork from Quercus suber L.
inferredcites →https://doi.org/10.1007/bf02357889openalex-snapshot
Potato leafroll virus distribution in potato meristem tips and production of virus-free plants
inferredcites →https://doi.org/10.1007/s00299-014-1727-zopenalex-snapshot
Suberin: biosynthesis, regulation, and polymer assembly of a protective extracellular barrier
inferredcites →https://doi.org/10.1007/s00425-002-0811-8openalex-snapshot
Water and oxygen permeance of phellems isolated from trees: the role of waxes and lenticels
inferredcites →https://doi.org/10.1007/s00425-004-1364-9openalex-snapshot
Wax and suberin development of native and wound periderm of potato (Solanum tuberosum L.) and its relation to peridermal transpiration
inferredcites →https://doi.org/10.1007/s00425-011-1350-yopenalex-snapshot
A potato skin SSH library yields new candidate genes for suberin biosynthesis and periderm formation
inferredcites →https://doi.org/10.1007/s00709-011-0266-5openalex-snapshot
Rays, intrusive growth, and storied cambium in the inflorescence stems of Arabidopsis thaliana (L.) Heynh
inferredcites →https://doi.org/10.1007/s11103-017-0619-3openalex-snapshot
Identification of genes related to skin development in potato
inferredcites →https://doi.org/10.1016/j.cell.2015.12.021openalex-snapshot
Adaptation of Root Function by Nutrient-Induced Plasticity of Endodermal Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2008.02.070openalex-snapshot
Flowering as a Condition for Xylem Expansion in Arabidopsis Hypocotyl and Root
inferredcites →https://doi.org/10.1016/j.cub.2014.03.025openalex-snapshot
Programmed Cell Death Controlled by ANAC033/SOMBRERO Determines Root Cap Organ Size in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2015.02.023openalex-snapshot
Wood Formation in Trees Is Increased by Manipulating PXY-Regulated Cell Division
inferredcites →https://doi.org/10.1016/j.indcrop.2008.04.015openalex-snapshot
Quercus suber and Betula pendula outer barks as renewable sources of oleochemicals: A comparative study
inferredcites →https://doi.org/10.1016/j.jaap.2012.12.001openalex-snapshot
Lignin monomeric composition of corks from the barks of Betula pendula, Quercus suber and Quercus cerris determined by Py–GC–MS/FID
inferredcites →https://doi.org/10.1016/j.jplph.2011.12.010openalex-snapshot
Wounding coordinately induces cell wall protein, cell cycle and pectin methyl esterase genes involved in tuber closing layer and wound periderm development
inferredcites →https://doi.org/10.1016/j.jplph.2012.08.023openalex-snapshot
Molecular characterization of Quercus suber MYB1, a transcription factor up-regulated in cork tissues
inferredcites →https://doi.org/10.1016/j.jplph.2012.10.008openalex-snapshot
Molecular and cytological aspects of native periderm maturation in potato tubers
inferredcites →https://doi.org/10.1016/j.pbi.2010.03.002openalex-snapshot
Regulation of plant biomass production
inferredcites →https://doi.org/10.1016/j.pbi.2016.12.002openalex-snapshot
Secondary development in the stem: when Arabidopsis and trees are closer than it seems
inferredcites →https://doi.org/10.1016/j.phytochem.2015.06.011openalex-snapshot
Analysis of aliphatic waxes associated with root periderm or exodermis from eleven plant species
inferredcites →https://doi.org/10.1016/j.plantsci.2004.06.014openalex-snapshot
Arabidopsis MYB68 in development and responses to environmental cues
inferredcites →https://doi.org/10.1016/j.plaphy.2013.10.007openalex-snapshot
QsMYB1 expression is modulated in response to heat and drought stresses and during plant recovery in Quercus suber
inferredcites →https://doi.org/10.1016/s0092-8674(00)80115-4openalex-snapshot
The SCARECROW Gene Regulates an Asymmetric Cell Division That Is Essential for Generating the Radial Organization of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/s0367-2530(17)30892-7openalex-snapshot
The formation of a ligno-suberised layer and necrophylactic periderm in beech bark (Fagus sylvatica L.)
inferredcites →https://doi.org/10.1016/s0926-6690(98)00029-6openalex-snapshot
Urethanes and polyurethanes from suberin 2: synthesis and characterization
inferredcites →https://doi.org/10.1038/nature10070openalex-snapshot
A novel protein family mediates Casparian strip formation in the endodermis
inferredcites →https://doi.org/10.1038/ng.253openalex-snapshot
Flowering-time genes modulate meristem determinacy and growth form in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1039/b9py00360fopenalex-snapshot
Performance polymers from renewable monomers: high molecular weight poly(pentadecalactone) for fiber applications
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00188.xopenalex-snapshot
Development of the vascular system in the inflorescence stem of Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0910772107openalex-snapshot
A developmental framework for endodermal differentiation and polarity
inferredcites →https://doi.org/10.1073/pnas.1205726109openalex-snapshot
Casparian strip diffusion barrier in Arabidopsis is made of a lignin polymer without suberin
inferredcites →https://doi.org/10.1073/pnas.1308412110openalex-snapshot
Dirigent domain-containing protein is part of the machinery required for formation of the lignin-based Casparian strip in the root
inferredcites →https://doi.org/10.1073/pnas.1515576112openalex-snapshot
MYB36 regulates the transition from proliferation to differentiation in the Arabidopsis root
inferredcites →https://doi.org/10.1093/aob/mcf147openalex-snapshot
Histological Analysis of the Maturation of Native and Wound Periderm in Potato (Solanum tuberosum L.) Tuber
inferredcites →https://doi.org/10.1093/aobpla/pls048openalex-snapshot
Russeting in apple and pear: a plastic periderm replaces a stiff cuticle
inferredcites →https://doi.org/10.1093/jxb/erl014openalex-snapshot
Survival strategies of plants during secondary growth: barrier properties of phellems and lenticels towards water, oxygen, and carbon dioxide
inferredcites →https://doi.org/10.1093/jxb/ern101openalex-snapshot
The Arabidopsis cytochrome P450 CYP86A1 encodes a fatty acid ω-hydroxylase involved in suberin monomer biosynthesis
inferredcites →https://doi.org/10.1093/jxb/ern314openalex-snapshot
Silencing of StKCS6 in potato periderm leads to reduced chain lengths of suberin and wax compounds and increased peridermal transpiration
inferredcites →https://doi.org/10.1093/jxb/erp281openalex-snapshot
Transcriptomic profiling of heat-stress response in potato periderm
inferredcites →https://doi.org/10.1093/jxb/erv547openalex-snapshot
TheSHORT-ROOT-like genePtSHR2Bis involved inPopulusphellogen activity
inferredcites →https://doi.org/10.1093/treephys/1.1.1openalex-snapshot
Boron and ectomycorrhizal influences on indole-3-acetic acid levels and indole-3-acetic acid oxidase and peroxidase activities of Pinus echinata Mill. roots
inferredcites →https://doi.org/10.1093/treephys/20.13.893openalex-snapshot
Influence of weather on cork-ring width
inferredcites →https://doi.org/10.1093/treephys/tpx060openalex-snapshot
Reconstructing the suberin pathway in poplar by chemical and transcriptomic analysis of bark tissues
inferredcites →https://doi.org/10.1094/phyto-08-15-0191-ropenalex-snapshot
Toughing It Out—Disease-Resistant Potato Mutants Have Enhanced Tuber Skin Defenses
inferredcites →https://doi.org/10.1097/00010694-196008000-00031openalex-snapshot
Anatomy of Seed Plants
inferredcites →https://doi.org/10.1104/pp.106.094227openalex-snapshot
A Genomic Approach to Suberin Biosynthesis and Cork Differentiation
inferredcites →https://doi.org/10.1104/pp.108.127183openalex-snapshot
CYP86A33 -Targeted Gene Silencing in Potato Tuber Alters Suberin Composition, Distorts Suberin Lamellae, and Impairs the Periderm's Water Barrier Function
inferredcites →https://doi.org/10.1104/pp.109.141408openalex-snapshot
CYP86B1 Is Required for Very Long Chainω-Hydroxyacid andα,ω-Dicarboxylic Acid Synthesis in Root and Seed Suberin Polyester
inferredcites →https://doi.org/10.1104/pp.109.144907openalex-snapshot
Identification of an Arabidopsis Feruloyl-Coenzyme A Transferase Required for Suberin Synthesis
inferredcites →https://doi.org/10.1104/pp.110.158238openalex-snapshot
Three Arabidopsis Fatty Acyl-Coenzyme A Reductases, FAR1, FAR4, and FAR5, Generate Primary Fatty Alcohols Associated with Suberin Deposition
inferredcites →https://doi.org/10.1104/pp.112.201822openalex-snapshot
Identification of an Arabidopsis Fatty Alcohol:Caffeoyl-Coenzyme A Acyltransferase Required for the Synthesis of Alkyl Hydroxycinnamates in Root Waxes1
inferredcites →https://doi.org/10.1104/pp.113.224410openalex-snapshot
Suberin-Associated Fatty Alcohols in Arabidopsis: Distributions in Roots and Contributions to Seed Coat Barrier Properties
inferredcites →https://doi.org/10.1104/pp.15.00769openalex-snapshot
A conserved core of PCD indicator genes discriminates developmentally and environmentally induced programmed cell death in plants
inferredcites →https://doi.org/10.1105/tpc.105.038745openalex-snapshot
Blind Homologous R2R3 Myb Genes Control the Pattern of Lateral Meristem Initiation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.048033openalex-snapshot
The Acyltransferase GPAT5 Is Required for the Synthesis of Suberin in Seed Coat and Root of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03851.xopenalex-snapshot
Rapid, combinatorial analysis of membrane compartments in intact plants with a multicolor marker set
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04144.xopenalex-snapshot
A feruloyl transferase involved in the biosynthesis of suberin and suberin-associated wax is required for maturation and sealing properties of potato periderm
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03236.xopenalex-snapshot
Evolution of development of vascular cambia and secondary growth
inferredcites →https://doi.org/10.1111/nph.14631openalex-snapshot
WUSCHEL ‐ RELATED HOMEOBOX 4 ( WOX 4)‐like genes regulate cambial cell division activity and secondary growth inPopulustrees
inferredcites →https://doi.org/10.1111/tpj.13099openalex-snapshot
A versatile Multisite Gateway‐compatible promoter and transgenic line collection for cell type‐specific functional genomics in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13157openalex-snapshot
Functional network analysis of genes differentially expressed during xylogenesis insoc1fulwoody Arabidopsis plants
inferredcites →https://doi.org/10.1126/science.1245871openalex-snapshot
A Spatial Accommodation by Neighboring Cells Is Required for Organ Initiation in Arabidopsis
inferredcites →https://doi.org/10.1139/b75-164openalex-snapshot
Wound regeneration in the lamina of magnoliaceous leaves
inferredcites →https://doi.org/10.1139/b95-156openalex-snapshot
Wound healing in whole potato tubers: a cytochemical, fluorescence, and ultrastructural analysis of cut and bruise wounds
inferredcites →https://doi.org/10.1179/174328005x41168openalex-snapshot
Cork: properties, capabilities and applications
inferredcites →https://doi.org/10.1371/journal.pgen.1001312openalex-snapshot
Characterization of Transcriptome Remodeling during Cambium Formation Identifies MOL1 and RUL1 As Opposing Regulators of Secondary Growth
inferredcites →https://doi.org/10.1371/journal.pone.0083043openalex-snapshot
GreenGate - A Novel, Versatile, and Efficient Cloning System for Plant Transgenesis
inferredcites →https://doi.org/10.21273/jashs.130.6.936openalex-snapshot
Immunocytological Analysis of Potato Tuber Periderm and Changes in Pectin and Extensin Epitopes Associated with Periderm Maturation
inferredcites →https://doi.org/10.3389/fpls.2015.01048openalex-snapshot
A Role of TDIF Peptide Signaling in Vascular Cell Differentiation is Conserved Among Euphyllophytes
inferredcites →https://doi.org/10.3389/fpls.2016.01612openalex-snapshot
Lignin Composition and Structure Differs between Xylem, Phloem and Phellem in Quercus suber L.
inferredcites →https://doi.org/10.3390/plants4020183openalex-snapshot
Determining the Composition of Lignins in Different Tissues of Silver Birch
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.4846400openalex-extracted
MYB68 Regulates Suberin Patterning and Radially Distinct Endodermal Differentiation
inferred← citeshttps://doi.org/10.1002/advs.202511837openalex-snapshot
Root Meristem Maintenance Mechanisms are Key to Plant Defense Against Nanoplastics
inferred← citeshttps://doi.org/10.1007/978-3-030-35772-6_8openalex-snapshot
microRNA-Mediated Regulation of Plant Vascular Development and Secondary Growth
inferred← citeshttps://doi.org/10.1007/978-981-97-9819-3_12openalex-snapshot
Mangroves: Biodiversity and Omics Insights
inferred← citeshttps://doi.org/10.1007/s00468-023-02398-1openalex-snapshot
Periderm differentiation: a cellular and molecular approach to cork oak
inferred← citeshttps://doi.org/10.1007/s00468-026-02832-0openalex-snapshot
Contrasting phellem patterns associated with phellogen longevity in Quercus suber and Quercus rotundifolia (Fagaceae)
inferred← citeshttps://doi.org/10.1007/s11540-020-09468-8openalex-snapshot
Potato Periderm is the First Layer of Defence against Biotic and Abiotic Stresses: a Review
inferred← citeshttps://doi.org/10.1007/s11676-023-01641-2openalex-snapshot
Development, differentiation, and material distribution of secondary phloem in Pinus massoniana
inferred← citeshttps://doi.org/10.1016/j.cdev.2023.203842openalex-snapshot
Deep machine learning for cell segmentation and quantitative analysis of radial plant growth
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115794openalex-snapshot
MYB68 regulates radial endodermal differentiation and suberin patterning
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116048openalex-snapshot
Members of the MYB68 subclade orchestrate cork differentiation by regulating stem cell proliferation and suberin deposition
inferred← citeshttps://doi.org/10.1016/j.copbio.2018.10.004openalex-snapshot
The Casparian strip—one ring to bring cell biology to lignification?
inferred← citeshttps://doi.org/10.1016/j.cub.2020.08.053openalex-snapshot
Pluripotent Pericycle Cells Trigger Different Growth Outputs by Integrating Developmental Cues into Distinct Regulatory Modules
inferred← citeshttps://doi.org/10.1016/j.cub.2020.11.070openalex-snapshot
Tissue-Autonomous Phenylpropanoid Production Is Essential for Establishment of Root Barriers
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.12.025openalex-snapshot
A single-nuclei transcriptome census of the Arabidopsis maturing root identifies that MYB67 controls phellem cell maturation
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105785openalex-snapshot
The impact of drought on phellem development: Identification of novel gene regulators and evidence of photosynthetic activity in cork oak stems
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101978openalex-snapshot
Highlighting reactive oxygen species as multitaskers in root development
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.03.009openalex-snapshot
More than cell wall hydrolysis: orchestration of cellular dynamics for organ separation
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.08.008openalex-snapshot
The development of the periderm: the final frontier between a plant and its environment
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102369openalex-snapshot
Spatiotemporal control of root immune responses during microbial colonization
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102404openalex-snapshot
From procambium patterning to cambium activation and maintenance in the Arabidopsis root
inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102647openalex-snapshot
Diversity and development of domatia: Symbiotic plant structures to host mutualistic ants or mites
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102933openalex-snapshot
The life and legacy of the root endodermis: A spatiotemporal view of function and development
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101576openalex-snapshot
Gaseous cues regenerate the periderm
inferred← citeshttps://doi.org/10.1017/qpb.2021.13openalex-snapshot
Dynamic cytokinin signalling landscapes during lateral root formation in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41438-020-0242-3openalex-snapshot
Proteome and transcriptome profile analysis reveals regulatory and stress-responsive networks in the russet fruit skin of sand pear
inferred← citeshttps://doi.org/10.1038/s41467-025-59072-yopenalex-snapshot
Strigolactones optimise plant water usage by modulating vessel formation
inferred← citeshttps://doi.org/10.1038/s41477-023-01391-3openalex-snapshot
Gibberellin and abscisic acid transporters facilitate endodermal suberin formation in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-026-02279-8openalex-snapshot
Root hair lifespan is antagonistically controlled by autophagy and programmed cell death
inferred← citeshttps://doi.org/10.1038/s41586-018-0837-0openalex-snapshot
High levels of auxin signalling define the stem-cell organizer of the vascular cambium
inferred← citeshttps://doi.org/10.1038/s41586-025-09223-4openalex-snapshot
Plants monitor the integrity of their barrier by sensing gas diffusion
inferred← citeshttps://doi.org/10.1038/s41592-025-02677-4openalex-snapshot
CarboTag: a modular approach for live and functional imaging of plant cell walls
inferred← citeshttps://doi.org/10.1038/s41598-019-46681-zopenalex-snapshot
The transcriptome of potato tuber phellogen reveals cellular functions of cork cambium and genes involved in periderm formation and maturation
inferred← citeshttps://doi.org/10.1071/fp19135openalex-snapshot
A review of current knowledge about the formation of native peridermal exocarp in fruit
inferred← citeshttps://doi.org/10.1073/pnas.2012728117openalex-snapshot
High-order mutants reveal an essential requirement for peroxidases but not laccases in Casparian strip lignification
inferred← citeshttps://doi.org/10.1073/pnas.2510538122openalex-snapshot
An AINTEGUMENTA phosphoswitch controls bilateral stem cell activity during secondary growth
inferred← citeshttps://doi.org/10.1093/hr/uhab061openalex-snapshot
An ARF1-binding factor triggering programmed cell death and periderm development in pear russet fruit skin
inferred← citeshttps://doi.org/10.1093/jxb/erab009openalex-snapshot
The production of auxin by dying cells
inferred← citeshttps://doi.org/10.1093/jxb/erab089openalex-snapshot
Auxin and gibberellin signaling cross-talk promotes hypocotyl xylem expansion and cambium homeostasis
inferred← citeshttps://doi.org/10.1093/jxb/erab455openalex-snapshot
Laying it on thick: a study in secondary growth
inferred← citeshttps://doi.org/10.1093/jxb/eraf207openalex-snapshot
Age-dependent differential iron deficiency responses of rosette leaves during reproductive stages in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/plcell/koag160openalex-snapshot
Loss of PMR4 callose synthase triggers jasmonic acid–dependent resistance to the clubroot disease in Arabidopsis and Brassica napus
inferred← citeshttps://doi.org/10.1093/plphys/kiab392openalex-snapshot
Root plasticity under abiotic stress
inferred← citeshttps://doi.org/10.1093/treephys/tpab031openalex-snapshot
Cork cells in cork oak periderms undergo programmed cell death and proanthocyanidin deposition
inferred← citeshttps://doi.org/10.1093/treephys/tpab176openalex-snapshot
Spatiotemporal development of suberized barriers in cork oak taproots
inferred← citeshttps://doi.org/10.1093/treephys/tpz118openalex-snapshot
Phellem versus xylem: genome-wide transcriptomic analysis reveals novel regulators of cork formation in cork oak
inferred← citeshttps://doi.org/10.1101/2020.11.13.381558openalex-snapshot
AUXIN RESPONSE FACTOR 6 ( ARF6) and ARF8 promote Gibberellin-mediated hypocotyl xylem expansion and cambium homeostasis
inferred← citeshttps://doi.org/10.1101/2021.06.02.446769openalex-snapshot
Regulation of suberin biosynthesis and Casparian strip development in the root endodermis by two plant auxins
inferred← citeshttps://doi.org/10.1101/2023.03.31.535027openalex-snapshot
Rhytidome- and cork-type barks of holm oak, cork oak and their hybrids highlight processes leading to cork formation
inferred← citeshttps://doi.org/10.1101/2024.03.06.583666openalex-snapshot
MYB68 orchestrates cork differentiation by regulating stem cell proliferation and suberin deposition
inferred← citeshttps://doi.org/10.1101/357244openalex-snapshot
Paralogues of the PXY and ER receptor kinases enforce radial patterning in plant vascular tissue
inferred← citeshttps://doi.org/10.1104/pp.20.01054openalex-snapshot
Regulation of a Cytochrome P450 Gene CYP94B1 by WRKY33 Transcription Factor Controls Apoplastic Barrier Formation in Roots to Confer Salt Tolerance
inferred← citeshttps://doi.org/10.1111/1365-2745.13908openalex-snapshot
Variations in bark structural properties affect both water loss and carbon economics in neotropical savanna trees in the Cerrado region of Brazil
inferred← citeshttps://doi.org/10.1111/brv.13064openalex-snapshot
Plant periderm as a continuum in structural organisation: a tracheophyte‐wide survey and hypotheses on evolution
inferred← citeshttps://doi.org/10.1111/jmi.13289openalex-snapshot
Imaging plant cell walls using fluorescent stains: The beauty is in the details
inferred← citeshttps://doi.org/10.1111/nph.15640openalex-snapshot
Mosaic modularity: an updated perspective and research agenda for the evolution of vascular cambial growth
inferred← citeshttps://doi.org/10.1111/nph.15725openalex-snapshot
Tissue‐specific study across the stem reveals the chemistry and transcriptome dynamics of birch bark
inferred← citeshttps://doi.org/10.1111/nph.71285openalex-snapshot
Cross‐stage single‐cell and spatial metabolome analyses reveal periderm specialization and tanshinone biosynthesis in Salvia miltiorrhiza roots
inferred← citeshttps://doi.org/10.1111/ppl.13371openalex-snapshot
WRKY9 transcription factor regulates cytochrome P450 genes CYP94B3 and CYP86B1 , leading to increased root suberin and salt tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.14459openalex-snapshot
Root endodermal barrier system contributes to defence against plant‐parasitic cyst and root‐knot nematodes
inferred← citeshttps://doi.org/10.1111/tpj.15691openalex-snapshot
Translational profile of developing phellem cells in Arabidopsis thaliana roots
inferred← citeshttps://doi.org/10.1146/annurev-arplant-050718-100402openalex-snapshot
The Dynamics of Cambial Stem Cell Activity
inferred← citeshttps://doi.org/10.1146/annurev-arplant-102720-031405openalex-snapshot
The Making of Plant Armor: The Periderm
inferred← citeshttps://doi.org/10.1186/s10086-022-02027-4openalex-snapshot
Sequent periderm formation and changes in the cellular contents of phloem parenchyma during rhytidome development in Cryptomeria japonica
inferred← citeshttps://doi.org/10.1186/s12870-021-03025-2openalex-snapshot
Peridermal fruit skin formation in Actinidia sp. (kiwifruit) is associated with genetic loci controlling russeting and cuticle formation
inferred← citeshttps://doi.org/10.1186/s12870-023-04483-6openalex-snapshot
Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.1186/s12870-025-07381-1openalex-snapshot
Comprehensive analysis of SDH genes in Populus and functional characterization of SDH4 in xylem and cambium development
inferred← citeshttps://doi.org/10.1186/s13059-025-03728-xopenalex-snapshot
Deep tissue profiling of Populus stem at single nucleus level reveals uncharacterized cell types and cell-specific gene regulatory networks
inferred← citeshttps://doi.org/10.1242/dev.177105openalex-snapshot
Organ-specific genetic interactions between paralogues of the PXY and ER receptor kinases enforce radial patterning in Arabidopsis vascular tissue
inferred← citeshttps://doi.org/10.1590/1677-941x-abb-2023-0019openalex-snapshot
Are the anatomical traits of stems and leaves good indicators of habitat specificity in closely related Myrtaceae species from Patagonia?
inferred← citeshttps://doi.org/10.17875/gup2022-2358openalex-snapshot
Jahrbuch der Niedersächsischen Akademie der Wissenschaften zu Göttingen. 2020/2021
inferred← citeshttps://doi.org/10.17875/gup2023-2358openalex-snapshot
Jahrbuch der Niedersächsischen Akademie der Wissenschaften zu Göttingen. 2020/2021
inferred← citeshttps://doi.org/10.22215/etd/2021-14501openalex-snapshot
Investigating the Role of BLADE-ON-PETIOLE Genes and Hydrophobic Cell-Wall Polymer Suberin in Arabidopsis thaliana Defense Against Bacterial and Fungal Pathogens
inferred← citeshttps://doi.org/10.3389/fpls.2018.01194openalex-snapshot
Cork Oak Young and Traumatic Periderms Show PCD Typical Chromatin Patterns but Different Chromatin-Modifying Genes Expression
inferred← citeshttps://doi.org/10.3389/fpls.2022.1006153openalex-snapshot
Solving the regulation puzzle of periderm development using advances in fruit skin
inferred← citeshttps://doi.org/10.3390/cells11152341openalex-snapshot
The Combined Effect of Heat and Osmotic Stress on Suberization of Arabidopsis Roots
inferred← citeshttps://doi.org/10.3390/f16010176openalex-snapshot
Seasonal Dynamics of Periderm Maintenance and Phellogen Re-Initiation in Aesculus hippocastanum
inferred← citeshttps://doi.org/10.3390/metabo11110735openalex-snapshot
Root Suberin Plays Important Roles in Reducing Water Loss and Sodium Uptake in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants11162099openalex-snapshot
Potato Periderm Development and Tuber Skin Quality
inferred← citeshttps://doi.org/10.3390/plants11202671openalex-snapshot
Cork Development: What Lies Within
inferred← citeshttps://doi.org/10.3390/plants12101985openalex-snapshot
Priorities for Bark Anatomical Research: Study Venues and Open Questions
inferred← citeshttps://doi.org/10.3390/plants12203661openalex-snapshot
Functional Modules in the Meristems: “Tinkering” in Action
inferred← citeshttps://doi.org/10.34133/plantphenomics.0156openalex-snapshot
PAT (Periderm Assessment Toolkit): A Quantitative and Large-Scale Screening Method for Periderm Measurements
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.21.1202aopenalex-snapshot
Pericycle cell division competence underlies various developmental programs
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984976openalex-snapshot
Additional file 1 of Peridermal fruit skin formation in Actinidia sp. (kiwifruit) is associated with genetic loci controlling russeting and cuticle formation
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984979openalex-snapshot
Additional file 2 of Peridermal fruit skin formation in Actinidia sp. (kiwifruit) is associated with genetic loci controlling russeting and cuticle formation
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984982openalex-snapshot
Additional file 3 of Peridermal fruit skin formation in Actinidia sp. (kiwifruit) is associated with genetic loci controlling russeting and cuticle formation
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621131openalex-snapshot
Additional file 1 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621134openalex-snapshot
Additional file 2 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621137openalex-snapshot
Additional file 3 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621140openalex-snapshot
Additional file 4 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621143openalex-snapshot
Additional file 5 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621146openalex-snapshot
Additional file 6 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621149openalex-snapshot
Additional file 7 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621152openalex-snapshot
Additional file 8 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621155openalex-snapshot
Additional file 9 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621158openalex-snapshot
Additional file 10 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621161openalex-snapshot
Additional file 11 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621164openalex-snapshot
Additional file 12 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621167openalex-snapshot
Additional file 13 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621170openalex-snapshot
Additional file 14 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621173openalex-snapshot
Additional file 15 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621176openalex-snapshot
Additional file 16 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621179openalex-snapshot
Additional file 17 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621182openalex-snapshot
Additional file 18 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621185openalex-snapshot
Additional file 19 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621188openalex-snapshot
Additional file 20 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621191openalex-snapshot
Additional file 21 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621194openalex-snapshot
Additional file 22 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621197openalex-snapshot
Additional file 23 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.6084/m9.figshare.26621200openalex-snapshot
Additional file 24 of Time course of changes in the transcriptome during russet induction in apple fruit
inferred← citeshttps://doi.org/10.64898/2026.02.06.704465openalex-snapshot
Every Cell Counts: Tomato Root Responses to Nitrogen at Single-Cell Resolution
inferred← citeshttps://doi.org/10.70675/e1acd2a8z6057z4186z8c06zbfc749fd00a4openalex-snapshot
Arabidopsis thaliana : a model to study thermal and saline adaptations of plants in the Pyrenees
inferred← citeshttps://doi.org/10.70675/f833dd10zd298z45bcz875eze0d3ff153ffbopenalex-snapshot
La mousse Physcomitrella patens, un modèle pour explorer l’évolution et l’ingénierie du métabolisme phénolique
inferred← citeshttps://doi.org/10.7554/elife.96266openalex-snapshot
Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.7554/elife.96266.1openalex-snapshot
Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.7554/elife.96266.2openalex-snapshot
Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.7554/elife.96266.3openalex-snapshot
Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana
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