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Cellular organisation of the Arabidopsis thaliana root
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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DEMONSTRATION OF THE THREE GERM LAYERS IN THE SHOOT APEX OF DATURA BY MEANS OF INDUCED POLYPLOIDY IN PERICLINAL CHIMERAS
inferredcites →https://doi.org/10.1002/j.1537-2197.1943.tb14737.xopenalex-snapshot
CELL‐LINEAGE STUDIES IN ROOT MERISTEMS BY MEANS OF CHROMOSOME REARRANGEMENTS INDUCED BY X‐RAYS
inferredcites →https://doi.org/10.1002/j.1537-2197.1955.tb11110.xopenalex-snapshot
ON THE DETERMINATION OF VASCULAR PATTERNS DURING TISSUE DIFFERENTIATION IN EXCISED PEA ROOTS
inferredcites →https://doi.org/10.1002/j.1537-2197.1955.tb11118.xopenalex-snapshot
ZONATION OF PRIMARY AND LATERAL ROOT APICES OF PISUM SATIVUM
inferredcites →https://doi.org/10.1002/j.1537-2197.1955.tb11157.xopenalex-snapshot
LEVELS OF TISSUE DIFFERENTIATION IN PRIMARY ROOTS OF PISUM SATIVUM
inferredcites →https://doi.org/10.1002/j.1537-2197.1976.tb11804.xopenalex-snapshot
ONTOGENETIC REORGANIZATION OF THE ROOT MERISTEM IN THE COMPOSITAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08679.xopenalex-snapshot
CLONAL ANALYSIS OF CELL LINEAGE PATTERNS IN PLANT DEVELOPMENT
inferredcites →https://doi.org/10.1007/bf00193004openalex-snapshot
Pectin esterification is spatially regulated both within cell walls and between developing tissues of root apices
inferredcites →https://doi.org/10.1007/bf01910114openalex-snapshot
Über die Differenzierungsvorgänge in der Cruciferenwurzel
inferredcites →https://doi.org/10.1007/bf01916742openalex-snapshot
Studien über die Entwicklung des Wurzelvegetationspunktes der Dikotyledonen
inferredcites →https://doi.org/10.1007/bf01963405openalex-snapshot
Studien über die Entwicklung des Wurzelvegetationspunktes der Dikotyledonen. II
inferredcites →https://doi.org/10.1016/0012-1606(76)90150-0openalex-snapshot
Clonal analysis of primordial disc cells in the early embryo of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0012-1606(83)90201-4openalex-snapshot
The embryonic cell lineage of the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0014-5793(85)81194-7openalex-snapshot
Positional controls in plant development
inferredcites →https://doi.org/10.1016/0092-8674(89)90900-8openalex-snapshot
Arabidopsis, a useful weed
inferredcites →https://doi.org/10.1038/335025a0openalex-snapshot
The molecular genetics of embryonic pattern formation in Drosophila
inferredcites →https://doi.org/10.1038/351535a0openalex-snapshot
Multiple intercellular signalling systems control the development of the Caenorhabditis elegans vulva
inferredcites →https://doi.org/10.1038/353402a0openalex-snapshot
Mutations affecting body organization in the Arabidopsis embryo
inferredcites →https://doi.org/10.1083/jcb.11.3.736openalex-snapshot
A MODIFIED PROCEDURE FOR LEAD STAINING OF THIN SECTIONS
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a086183openalex-snapshot
The Difference Between Open and Closed Meristems
inferredcites →https://doi.org/10.1111/j.1095-8339.1965.tb00057.xopenalex-snapshot
Pattern in the meristems of vascular plants: III. Pursuing the patterns in the apical meristem where no cell is a permanent cell*
inferredcites →https://doi.org/10.1111/j.1469-8137.1950.tb07506.xopenalex-snapshot
ROOT APICAL MERISTEMS OF FAGUS SYLVATICA
inferredcites →https://doi.org/10.1111/j.1469-8137.1953.tb05204.xopenalex-snapshot
THE CYTOGENERATIVE CENTRE IN ROOTS WITH BROAD COLUMELLAS
inferredcites →https://doi.org/10.1139/b67-030openalex-snapshot
DIFFERENTIATION AND MATURATION OF PRIMARY TISSUES IN WHITE MUSTARD ROOT TIPS
inferredcites →https://doi.org/10.1139/b91-063openalex-snapshot
Early embryogenesis in Arabidopsis thaliana. II. The developing embryo
inferredcites →https://doi.org/10.1146/annurev.ge.18.120184.002421openalex-snapshot
THE GENETIC CONTROL OF CELL LINEAGE DURING NEMATODE DEVELOPMENT
inferredcites →https://doi.org/10.1242/dev.115.3.745openalex-snapshot
A fate map of the Arabidopsis embryonic shoot apical meristem
inferredcites →https://doi.org/10.1242/dev.115.3.755openalex-snapshot
Cell fate in the shoot apical meristem of Arabidopsis thaliana
inferredcites →https://doi.org/10.5586/asbp.1979.033openalex-snapshot
Rape embryogenesis. II. Development of embryo proper
inferredcites →https://doi.org/10.5586/asbp.1980.034openalex-snapshot
Activation of embryo during rape (Brassica napus L.) seed germination II. Transversal organisation of radicle apical meristem
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/bf01306609openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf01587592openalex-snapshot
Structure and function at the root apex - phylogenetic and ontogenetic perspectives on apical cells and quiescent centres
inferred← citeshttps://doi.org/10.1007/bf02512190openalex-snapshot
Regulatory systems of root patterning
inferred← citeshttps://doi.org/10.1007/bf02637253openalex-snapshot
The inflorescence stem fibers ofArabidopsis thaliana revoluta (ifl1) mutant
inferred← citeshttps://doi.org/10.1007/bf02680127openalex-snapshot
Primary and secondary plasmodesmata: structure, origin, and functioning
inferred← citeshttps://doi.org/10.1007/bf02919467openalex-snapshot
The “root” experiment of the “cervantes” spanish soyuz mission: Cell proliferation and nucleolar activity alterations in arabidopsis roots germinated in real or simulated microgravity
inferred← citeshttps://doi.org/10.1007/bf03030384openalex-snapshot
Expression of root-specific genes inPhaseolus vulgaris L.
inferred← citeshttps://doi.org/10.1007/bf03030659openalex-snapshot
Root development inarabidopsis thaliana: attraction from underground
inferred← citeshttps://doi.org/10.1007/bf03036062openalex-snapshot
An ArabidopsisSUPERMAN-like gene,AtZFP12, Expressed at Shoot Organ Boundaries Suppresses cell Growth.
inferred← citeshttps://doi.org/10.1007/pl00009745openalex-snapshot
Cambium: old challenges – new opportunities
inferred← citeshttps://doi.org/10.1007/pl00013864openalex-snapshot
Low pH-Induced Root Hair Formation in Lettuce (Lactuca sativa L. cv. Grand Rapids) Seedlings: Determination of Root Hair-Forming Site
inferred← citeshttps://doi.org/10.1007/pl00013974openalex-snapshot
Differential Hypocotyl and Root Development of Arabidopsis Auxin-Insensitive Mutants
inferred← citeshttps://doi.org/10.1007/s00018-018-2980-zopenalex-snapshot
Stem cells within the shoot apical meristem: identity, arrangement and communication
inferred← citeshttps://doi.org/10.1007/s00018-020-03496-wopenalex-snapshot
Plant vascular development: mechanisms and environmental regulation
inferred← citeshttps://doi.org/10.1007/s00114-012-0988-zopenalex-snapshot
Cell-to-cell communication in plants, animals, and fungi: a comparative review
inferred← citeshttps://doi.org/10.1007/s002850000075openalex-snapshot
A mathematical model of plant nutrient uptake
inferred← citeshttps://doi.org/10.1007/s00299-014-1575-xopenalex-snapshot
The key players of the primary root growth and development also function in lateral roots in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-014-1591-xopenalex-snapshot
The Arabidopsis thaliana hypocotyl, a model to identify and study control mechanisms of cellular expansion
inferred← citeshttps://doi.org/10.1007/s00299-024-03274-zopenalex-snapshot
BIG coordinates auxin and SHORT ROOT to promote asymmetric stem cell divisions in Arabidopsis roots
inferred← citeshttps://doi.org/10.1007/s00299-025-03649-wopenalex-snapshot
Single-cell transcriptional decoding of iron deficiency responses in maize root tips
inferred← citeshttps://doi.org/10.1007/s00344-002-0037-9openalex-snapshot
Root Meristem Establishment and Maintenance: The Role of Auxin
inferred← citeshttps://doi.org/10.1007/s00344-003-0012-0openalex-snapshot
The Influence of Steep Slopes on Root System Development
inferred← citeshttps://doi.org/10.1007/s00344-004-0024-4openalex-snapshot
The Inflorescence Stem Fibers of Arabidopsis thaliana Revoluta (ifl1) Mutant
inferred← citeshttps://doi.org/10.1007/s00344-013-9386-9openalex-snapshot
Overexpression of Arabidopsis Wali7 Domain-Containing Protein ASR Produces Auxin-Mediated Short-Root Phenotype
inferred← citeshttps://doi.org/10.1007/s00425-003-0985-8openalex-snapshot
Elevated levels of N-lauroylethanolamine, an endogenous constituent of desiccated seeds, disrupt normal root development in Arabidopsis thaliana seedlings
inferred← citeshttps://doi.org/10.1007/s00425-003-0989-4openalex-snapshot
The root epidermis of Echium plantagineum L.: a novel type of pattern based on the distribution of short and long root hairs
inferred← citeshttps://doi.org/10.1007/s00425-004-1225-6openalex-snapshot
Developmental anatomy of the fifth shoot-borne root in young sporophytes of Ceratopteris richardii
inferred← citeshttps://doi.org/10.1007/s00425-004-1280-zopenalex-snapshot
Rescue of defective auxin-mediated gene expression and root meristem function by inhibition of ethylene signalling in sterol biosynthesis mutants of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-009-0912-8openalex-snapshot
The short-rooted vitamin B6-deficient mutant pdx1 has impaired local auxin biosynthesis
inferred← citeshttps://doi.org/10.1007/s00425-009-0988-1openalex-snapshot
The association of homeobox gene expression with stem cell formation and morphogenesis in cultured Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s00425-011-1454-4openalex-snapshot
Unique cell wall abnormalities in the putative phosphoinositide phosphatase mutant AtSAC9
inferred← citeshttps://doi.org/10.1007/s00425-011-1470-4openalex-snapshot
Apical meristem exhaustion during determinate primary root growth in the moots koom 1 mutant of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-012-1592-3openalex-snapshot
ARAD proteins associated with pectic Arabinan biosynthesis form complexes when transiently overexpressed in planta
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s00425-012-1707-xopenalex-snapshot
A method to determine the displacement velocity field in the apical region of the Arabidopsis root
inferred← citeshttps://doi.org/10.1007/s00425-013-1838-8openalex-snapshot
Formin homology 1 (OsFH1) regulates root-hair elongation in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s00425-017-2651-6openalex-snapshot
Regulation of seedling growth by ethylene and the ethylene–auxin crosstalk
inferred← citeshttps://doi.org/10.1007/s00425-017-2663-2openalex-snapshot
Repression of BLADE-ON-PETIOLE genes by KNOX homeodomain protein BREVIPEDICELLUS is essential for differentiation of secondary xylem in Arabidopsis root
inferred← citeshttps://doi.org/10.1007/s00425-019-03212-4openalex-snapshot
Mitogen-activated protein kinase 6 integrates phosphate and iron responses for indeterminate root growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-022-03911-5openalex-snapshot
AtFTCD-L, a trans-Golgi network localized protein, modulates root growth of Arabidopsis in high-concentration agar culture medium
inferred← citeshttps://doi.org/10.1007/s00425-023-04144-wopenalex-snapshot
The inhibition of maize (Zea mays L.) root stem cell regeneration by low oxygen is attenuated by Phytoglobin 1 (Pgb1) through changes in auxin and jasmonic acid
inferred← citeshttps://doi.org/10.1007/s00425-023-04239-4openalex-snapshot
Arabidopsis root apical meristem survival during waterlogging is determined by phytoglobin through nitric oxide and auxin
inferred← citeshttps://doi.org/10.1007/s00425-023-04246-5openalex-snapshot
Preserving root stem cell functionality under low oxygen stress: the role of nitric oxide and phytoglobins
inferred← citeshttps://doi.org/10.1007/s004250000276openalex-snapshot
Three maize root-specific genes are not correctly expressed in regenerated caps in the absence of the quiescent center
inferred← citeshttps://doi.org/10.1007/s004250000284openalex-snapshot
Clonal analysis of the Arabidopsis root confirms that position, not lineage, determines cell fate
inferred← citeshttps://doi.org/10.1007/s004250000333openalex-snapshot
Developmental expression of the Arabidopsis thaliana CycA2;1 gene
inferred← citeshttps://doi.org/10.1007/s004250050265openalex-snapshot
Arabidopsis SKP1, a homologue of a cell cycle regulator gene, is predominantly expressed in meristematic cells
inferred← citeshttps://doi.org/10.1007/s004250050347openalex-snapshot
Cell fate and cell differentiation status in the Arabidopsis root
inferred← citeshttps://doi.org/10.1007/s004250050492openalex-snapshot
Cortical cell death, cell proliferation, macromolecular movements and rTip1 expression pattern in roots of rice ( Oryza sativa L.) under NaCl stress
inferred← citeshttps://doi.org/10.1007/s004250100637openalex-snapshot
MADS-box gene expression in lateral primordia, meristems and differentiated tissues of Arabidopsis thaliana roots
inferred← citeshttps://doi.org/10.1007/s00429-014-0861-2openalex-snapshot
Contralateral cerebello-thalamo-cortical pathways with prominent involvement of associative areas in humans in vivo
inferred← citeshttps://doi.org/10.1007/s00468-015-1278-0openalex-snapshot
Shoot organogenesis from roots of seabuckthorn (Hippophaë rhamnoides L.): structure, initiation and effects of phosphorus and auxin
inferred← citeshttps://doi.org/10.1007/s00709-010-0211-zopenalex-snapshot
The vascular cambium: molecular control of cellular structure
inferred← citeshttps://doi.org/10.1007/s00709-012-0452-0openalex-snapshot
On the genetic control of planar growth during tissue morphogenesis in plants
inferred← citeshttps://doi.org/10.1007/s00709-014-0620-5openalex-snapshot
Cellular events during interfascicular cambium ontogenesis in inflorescence stems of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00709-015-0886-2openalex-snapshot
Origin of the concept of the quiescent centre of plant roots
inferred← citeshttps://doi.org/10.1007/s00709-019-01362-6openalex-snapshot
Topological traits of a cellular pattern versus growth rate anisotropy in radish roots
inferred← citeshttps://doi.org/10.1007/s10059-010-0095-yopenalex-snapshot
Characterization of SHORT-ROOT Function in the Arabidopsis Root Vascular System
inferred← citeshttps://doi.org/10.1007/s10265-017-0999-0openalex-snapshot
Phloem differentiation: an integrative model for cell specification
inferred← citeshttps://doi.org/10.1007/s10265-024-01575-8openalex-snapshot
Physiological roles of Arabidopsis MCA1 and MCA2 based on their dynamic expression patterns
inferred← citeshttps://doi.org/10.1007/s10534-015-9838-8openalex-snapshot
Chromate induces adventitious root formation via auxin signalling and SOLITARY-ROOT/IAA14 gene function in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10628-005-0015-9openalex-snapshot
Phloem unloading and activity of enzymes hydrolyzing sucrose in the apex of the growing root
inferred← citeshttps://doi.org/10.1007/s10658-012-0119-xopenalex-snapshot
Histological analysis of spindle and spheroid root galls caused by Plasmodiophora brassicae
inferred← citeshttps://doi.org/10.1007/s10725-018-0425-1openalex-snapshot
Temporal root responses in Arabidopsis thaliana L. to chromate reveal structural and regulatory mechanisms involving the SOLITARY ROOT/IAA14 repressor for maintenance of identity meristem genes
inferred← citeshttps://doi.org/10.1007/s11033-012-1896-1openalex-snapshot
Cytoplasm localization of aminopeptidase M1 and its functional activity in root hair cells and BY-2 cells
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