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The endodermal passage cell – just another brick in the wall?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02730.xopenalex-snapshot
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1002/j.1537-2197.1991.tb14494.xopenalex-snapshot
CHANGES IN HYDRAULIC CONDUCTIVITY AND ANATOMY CAUSED BY DRYING AND REWETTING ROOTS OF AGAVE DESERTI (AGAVACEAE)
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Vegetative anatomy of subtribe Habenariinae (Orchidaceae)
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Isolation and Analysis of mRNAs from Specific Cell Types of Plants by Ribosome Immunopurification
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Physiologische Pflanzenanatomie
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Root structure and arbuscular mycorrhizal colonization of the palm Serenoa repens under field conditions
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The tertiary endodermis in barley roots: Fine structure in relation to radial transport of ions and water
inferredcites →https://doi.org/10.1007/bf01279377openalex-snapshot
Observations of the pattern of secondary wall development in the hypodermis of onion (Allium cepa) roots
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Impact of the exodermis on infection of roots byFusarium culmorum
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Studien zur Anatomie einiger Luftwurzeln
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Some aspects of the development of the endodermis and cortex ofTilia cordata andPicea sitchensis
inferredcites →https://doi.org/10.1007/s00344-003-0002-2openalex-snapshot
Root Endodermis and Exodermis: Structure, Function, and Responses to the Environment
inferredcites →https://doi.org/10.1007/s00425-012-1694-yopenalex-snapshot
Deciphering the route of Ralstonia solanacearum colonization in Arabidopsis thaliana roots during a compatible interaction: focus at the plant cell wall
inferredcites →https://doi.org/10.1007/s10310-004-0120-0openalex-snapshot
Life cycles of individual roots in fine root system of Chamaecyparis obtusa Sieb. et Zucc.
inferredcites →https://doi.org/10.1007/s11104-011-0719-9openalex-snapshot
Sites, pathways, and mechanism of absorption of Cu-EDDS complex in primary roots of maize (Zea Mays L.): anatomical, chemical and histochemical analysis
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Anatomical characteristics of individual roots within the fine‐root architecture of Chamaecyparis obtusa (Sieb. & Zucc.) in organic and mineral soil layers
inferredcites →https://doi.org/10.1016/0098-8472(95)00015-1openalex-snapshot
Salinity accelerates endodermal development and induces an exodermis in cotton seedling roots
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.cell.2016.02.028openalex-snapshot
Root Endophyte Colletotrichum tofieldiae Confers Plant Fitness Benefits that Are Phosphate Status Dependent
inferredcites →https://doi.org/10.1016/j.chom.2020.09.006openalex-snapshot
Root-Secreted Coumarins and the Microbiota Interact to Improve Iron Nutrition in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2015.01.015openalex-snapshot
Asymmetric Localizations of the ABC Transporter PaPDR1 Trace Paths of Directional Strigolactone Transport
inferredcites →https://doi.org/10.1016/j.cub.2017.01.030openalex-snapshot
Role of LOTR1 in Nutrient Transport through Organization of Spatial Distribution of Root Endodermal Barriers
inferredcites →https://doi.org/10.1016/j.cub.2020.11.070openalex-snapshot
Tissue-Autonomous Phenylpropanoid Production Is Essential for Establishment of Root Barriers
inferredcites →https://doi.org/10.1016/j.flora.2014.01.001openalex-snapshot
Exodermis structure controls fungal invasion in the leafless epiphytic orchid Dendrophylax lindenii (Lindl.) Benth. ex Rolfe
inferredcites →https://doi.org/10.1016/j.gloenvcha.2008.10.009openalex-snapshot
The story of phosphorus: Global food security and food for thought
inferredcites →https://doi.org/10.1016/j.isci.2019.06.024openalex-snapshot
Strigolactones Play an Important Role in Shaping Exodermal Morphology via a KAI2-Dependent Pathway
inferredcites →https://doi.org/10.1016/j.jplph.2018.02.002openalex-snapshot
Suberized transport barriers in Arabidopsis, barley and rice roots: From the model plant to crop species
inferredcites →https://doi.org/10.1016/j.molp.2019.04.004openalex-snapshot
A Single-Cell RNA Sequencing Profiles the Developmental Landscape of Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.pbi.2017.06.010openalex-snapshot
The endodermis, a tightly controlled barrier for nutrients
inferredcites →https://doi.org/10.1016/j.pbi.2019.05.010openalex-snapshot
Polarized transport across root epithelia
inferredcites →https://doi.org/10.1016/j.tplants.2017.09.003openalex-snapshot
Feed Your Friends: Do Plant Exudates Shape the Root Microbiome?
inferredcites →https://doi.org/10.1016/s0092-8674(00)81606-2openalex-snapshot
Identification and Disruption of a Plant Shaker-like Outward Channel Involved in K+ Release into the Xylem Sap
inferredcites →https://doi.org/10.1016/s0953-7562(09)80415-2openalex-snapshot
Involvement of exodermal passage cells in mycorrhizal infection of some orchids
inferredcites →https://doi.org/10.1023/a:1004576001334openalex-snapshot
Root structure and arbuscular mycorrhizal colonization of the palm Serenoa repens under field conditions
inferredcites →https://doi.org/10.1034/j.1399-3054.1996.970323.xopenalex-snapshot
Functions of passage cells in the endodermis and exodermis of roots
inferredcites →https://doi.org/10.1038/nature10873openalex-snapshot
A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching
inferredcites →https://doi.org/10.1038/nature25976openalex-snapshot
Diffusible repression of cytokinin signalling produces endodermal symmetry and passage cells
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00342.xopenalex-snapshot
Anatomical characteristics of roots of citrus rootstocks that vary in specific root length
inferredcites →https://doi.org/10.1080/15592324.2020.1719749openalex-snapshot
Groups of multi-cellular passage cells in the root exodermis of Echinochloa crus-galli varieties lack not only suberin lamellae but also lignin deposits
inferredcites →https://doi.org/10.1093/aob/mcr005openalex-snapshot
Three-dimensional distribution of vessels, passage cells and lateral roots along the root axis of winter wheat (Triticum aestivum)
inferredcites →https://doi.org/10.1093/aob/mcs266openalex-snapshot
Anatomical aspects of angiosperm root evolution
inferredcites →https://doi.org/10.1093/aob/mcx047openalex-snapshot
Casparian bands and suberin lamellae in exodermis of lateral roots: an important trait of roots system response to abiotic stress factors
inferredcites →https://doi.org/10.1093/jexbot/52.365.2245openalex-snapshot
The exodermis: a variable apoplastic barrier
inferredcites →https://doi.org/10.1093/jxb/35.10.1481openalex-snapshot
Anatomy, Ultrastructure and Assimilate Concentrations of Roots of Citrus Genotypes Differing in Ability for Salt Exclusion
inferredcites →https://doi.org/10.1093/jxb/38.11.1769openalex-snapshot
Some Effects of Root Anatomy on K, Na and Cl Loading of Citrus Roots and Leaves
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a087413openalex-snapshot
Distribution of the Dimorphic Hypodermis of Roots in Angiosperm Families
inferredcites →https://doi.org/10.1093/pcp/pcaa170openalex-snapshot
A Novel Signaling Pathway Required for Arabidopsis Endodermal Root Organization Shapes the Rhizosphere Microbiome
inferredcites →https://doi.org/10.1093/pcp/pci081openalex-snapshot
A Putative Function for the Arabidopsis Fe–Phytosiderophore Transporter Homolog AtYSL2 in Fe and Zn Homeostasis
inferredcites →https://doi.org/10.1101/2020.06.29.178863openalex-snapshot
A single cell Arabidopsis root atlas reveals developmental trajectories in wild type and cell identity mutants
inferredcites →https://doi.org/10.1104/pp.106.091090openalex-snapshot
Soybean Root Suberin: Anatomical Distribution, Chemical Composition, and Relationship to Partial Resistance to Phytophthora sojae
inferredcites →https://doi.org/10.1104/pp.114.246124openalex-snapshot
Radial Transport of Nutrients: The Plant Root as a Polarized Epithelium
inferredcites →https://doi.org/10.1104/pp.17.00832openalex-snapshot
Cytokinin Biosynthesis Promotes Cortical Cell Responses during Nodule Development
inferredcites →https://doi.org/10.1104/pp.18.01482openalex-snapshot
Single-Cell RNA Sequencing Resolves Molecular Relationships Among Individual Plant Cells
inferredcites →https://doi.org/10.1105/tpc.000745openalex-snapshot
Identification and Characterization of the Arabidopsis PHO1 Gene Involved in Phosphate Loading to the Xylem
inferredcites →https://doi.org/10.1111/j.0031-9317.2004.0275.xopenalex-snapshot
Differences in structure of adventitious roots in Salix clones with contrasting characteristics of cadmium accumulation and sensitivity
inferredcites →https://doi.org/10.1111/j.1095-8339.1990.tb00177.xopenalex-snapshot
A survey of angiosperm species to detect hypodermal Casparian bands. II. Roots with a multiseriate hypodermis or epidermis
inferredcites →https://doi.org/10.1111/j.1438-8677.1995.tb00842.xopenalex-snapshot
Root Browning in Pinus banksiana Lamb. and Eucalyptus pilularis Sm. 1. Anatomy and Permeability of the White and Tannin Zones
inferredcites →https://doi.org/10.1111/j.1438-8677.1997.tb00628.xopenalex-snapshot
Modifications of Cortical Cell Walls in Roots of Seedless Vascular Plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02600.xopenalex-snapshot
Can hypodermal passage cell distribution limit root penetration by mycorrhizal fungi?
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02766.xopenalex-snapshot
Arabidopsis IRT3 is a zinc‐regulated and plasma membrane localized zinc/iron transporter
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03598.xopenalex-snapshot
Contrasting the morphology, anatomy and fungal colonization of new pioneer and fibrous roots
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00777.xopenalex-snapshot
Interaction between a Dark Septate Endophytic Isolate from Dendrobium sp. and Roots of D. nobile Seedlings
inferredcites →https://doi.org/10.1111/pce.12586openalex-snapshot
The potassium transporter O s HAK 21 functions in the maintenance of ion homeostasis and tolerance to salt stress in rice
inferredcites →https://doi.org/10.1111/ppl.12267openalex-snapshot
Cloning and characterization of a novel Nicotiana tabacum ABC transporter involved in shoot branching
inferredcites →https://doi.org/10.1111/tpj.13720openalex-snapshot
3D analysis of mitosis distribution highlights the longitudinal zonation and diarch symmetry in proliferation activity of the Arabidopsis thaliana root meristem
inferredcites →https://doi.org/10.1111/tpj.13784openalex-snapshot
A protocol for combining fluorescent proteins with histological stains for diverse cell wall components
inferredcites →https://doi.org/10.1111/tpj.14459openalex-snapshot
Root endodermal barrier system contributes to defence against plant‐parasitic cyst and root‐knot nematodes
inferredcites →https://doi.org/10.1126/science.aay4970openalex-snapshot
Vascular transcription factors guide plant epidermal responses to limiting phosphate conditions
inferredcites →https://doi.org/10.1139/b03-042openalex-snapshot
Current insights into the development, structure, and chemistry of the endodermis and exodermis of roots
inferredcites →https://doi.org/10.1139/b09-105openalex-snapshot
Exploring the role of root anatomy in P-mediated control of colonization by arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1139/b79-129openalex-snapshot
The root endodermis in Ranunculus acris. I. Structure and ontogeny
inferredcites →https://doi.org/10.1139/b89-035openalex-snapshot
Zoospore encystment pattern and germination on onion roots, and the colonization of hypodermal cells by Pythium coloratum
inferredcites →https://doi.org/10.1139/b93-080openalex-snapshot
Effects of drought and subsequent rehydration on the structure, vitality, and permeability of Allium cepa adventitious roots
inferredcites →https://doi.org/10.1139/cjb-77-8-1159openalex-snapshot
Entry and colonization of Asparagus officinalis roots by arbuscular mycorrhizal fungi with emphasis on changes in host microtubules
inferredcites →https://doi.org/10.1146/annurev-genet-110410-132549openalex-snapshot
The Rules of Engagement in the Legume-Rhizobial Symbiosis
inferredcites →https://doi.org/10.1155/2012/769196openalex-snapshot
The Effects of Cation Ratios on Root Lamella Suberization in Rice (Oryza sativaL.) with Contrasting Salt Tolerance
inferredcites →https://doi.org/10.1186/2193-1801-2-587openalex-snapshot
Phosphate solubilizing microbes: sustainable approach for managing phosphorus deficiency in agricultural soils
inferredcites →https://doi.org/10.1242/dev.110775openalex-snapshot
Fate map of Medicago truncatula root nodules
inferredcites →https://doi.org/10.1242/dev.124.9.1781openalex-snapshot
Ethylene provides positional information on cortical cell division but is not involved in Nod factor-induced root hair tip growth in Rhizobium-legume interaction
inferredcites →https://doi.org/10.21273/hortsci.42.5.1103openalex-snapshot
Water Uptake by Older Roots: Evidence From Desert Succulents
inferredcites →https://doi.org/10.2139/ssrn.3475205openalex-snapshot
Two Receptor-Like Kinases Required for Arabidopsis Endodermal Root Organisation Shape the Rhizosphere Microbiome
inferredcites →https://doi.org/10.3389/fpls.2015.01125openalex-snapshot
Differential Responses of Vanilla Accessions to Root Rot and Colonization by Fusarium oxysporum f. sp. radicis-vanillae
inferredcites →https://doi.org/10.3389/fpls.2020.00018openalex-snapshot
The Full-Size ABCG Transporter of Medicago truncatula Is Involved in Strigolactone Secretion, Affecting Arbuscular Mycorrhiza
inferredcites →https://doi.org/10.7554/elife.29107openalex-snapshot
Lipid transfer from plants to arbuscular mycorrhiza fungi
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/10.1007/s11104-025-07498-0openalex-snapshot
The root cortex of the Poaceae: a diverse, dynamic, and dispensable tissue
inferred← citeshttps://doi.org/10.1016/b978-0-12-819773-8.00018-6openalex-snapshot
Ion-uptake mechanisms of individual cells and roots: short-distance transport
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.isci.2021.103228openalex-snapshot
MYB70 modulates seed germination and root system development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154118openalex-snapshot
The exodermis: A forgotten but promising apoplastic barrier
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154840openalex-snapshot
Three-dimensional reconstruction reveals distinct endodermal network topology associated with root ion transport characteristics in balsa
inferred← citeshttps://doi.org/10.1016/j.pbi.2021.102153openalex-snapshot
Building and breaking of a barrier: Suberin plasticity and function in the endodermis
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.pld.2024.03.008openalex-snapshot
Comprehensive integration of single-cell transcriptomic data illuminates the regulatory network architecture of plant cell fate specification
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.06.003openalex-snapshot
Root cell types as an interface for biotic interactions
inferred← citeshttps://doi.org/10.1017/qpb.2025.10008openalex-snapshot
Chloride transport and homeostasis in plants
inferred← citeshttps://doi.org/10.1094/phyto-03-25-0090-ropenalex-snapshot
Glutathione Promotes Susceptibility to Meloidogyne incognita by Modulating Thiol Homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.12.20.521223openalex-snapshot
Endodermal suberin deposition restricts potassium leakage from roots
inferred← citeshttps://doi.org/10.1111/pce.14143openalex-snapshot
Convergent evolution of gene regulatory networks underlying plant adaptations to dry environments
inferred← citeshttps://doi.org/10.1111/ppl.13955openalex-snapshot
Diurnal changes in apoplast bypass flow of water and ions in salt‐stressed wheat (Triticum aestivum L.) and barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1111/ppl.14393openalex-snapshot
Endodermal suberin restricts root leakage of cesium: a suitable tracer for potassium
inferred← citeshttps://doi.org/10.1146/annurev-arplant-102820-112451openalex-snapshot
A Way to Interact with the World: Complex and Diverse Spatiotemporal Cell Wall Thickenings in Plant Roots
inferred← citeshttps://doi.org/10.1242/dev.199820openalex-snapshot
Visualizing polymeric components that define distinct root barriers across plant lineages
inferred← citeshttps://doi.org/10.1360/tb-2022-0971openalex-snapshot
Advances in the development and function of plant root endodermis
inferred← citeshttps://doi.org/10.3390/ijms26178748openalex-snapshot
Towards Understanding the Factors Shaping the Composition and Function of the Noccaea Microbiome in Metal-Contaminated Environments
inferred← citeshttps://doi.org/10.9734/arrb/2021/v36i1030443openalex-snapshot
Root Morphology, Anatomy, and Mycorrhiza of Peristylus goodyeroides (D.Don) Lindl. (Orchidaceae) in Different Life Stages: Ecological Significance and Implication for Conservation
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