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Organogenetic capacity of leaves: The significance of marginal blastozones in angiosperms
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Schüepp, O.: Meristeme. Wachstum und Formbildung in den Teilungsgeweben höherer Pflanzen (Experientia Supplementum 11). Birkhäuser Verlag, Basel‐Stuttgart 1966. 253 S., 159 Abb
inferredcites →https://doi.org/10.1002/j.1537-2197.1933.tb08913.xopenalex-snapshot
STRUCTURE AND DEVELOPMENT OF THE TOBACCO LEAF
inferredcites →https://doi.org/10.1002/j.1537-2197.1960.tb10611.xopenalex-snapshot
DEVELOPMENT OF THE LAMINA IN XANTHIUM ITALICUM REPRESENTED BY THE PLASTOCHRON INDEX
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ONTOGENY AND PHYLLOTAXIS OF THE TERMINAL VEGETATIVE SHOOTS OF MICHELIA FUSCATA
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COMPARATIVE MORPHOGENESIS OF THE DIMORPHIC LEAVES OF CYAMOPSIS TETRAGONOLOBA
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ACTIVITY OF MARGINAL AND PLATE MERISTEMS DURING LEAF DEVELOPMENT OF XANTHIUM PENNSYLVANICUM
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LEAF DEVELOPMENT IN DOXANTHA UNGUIS‐CATI (BIGNONIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1975.tb14134.xopenalex-snapshot
FLEXIBILITY IN ONTOGENY AS SHOWN BY THE CONTRIBUTION OF THE SHOOT APICAL LAYERS TO LEAVES OF PERICLINAL CHIMERAS
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The cellular parameters of leaf development in tobacco: a clonal analysis
inferredcites →https://doi.org/10.1007/bf00992728openalex-snapshot
�ber die strittige Homologie sogenannter Stipulardr�sen bei einigenEuphorbia-Arten der SektionEuphorbium
inferredcites →https://doi.org/10.1007/bf01929609openalex-snapshot
Entwicklungsgeschichtliche Untersuchungen über das Zustandekommen unifazialer Blattstrukturen
inferredcites →https://doi.org/10.1007/bf01944396openalex-snapshot
Zur Entwicklungsgeschichte des Blattes, mit besonderer Berücksichtigung von Stipular und Ligularbildungen
inferredcites →https://doi.org/10.1007/bf01946860openalex-snapshot
Über die Bildung der Stele aus dem Urmeristem von Pteridophyten und Spermatophyten
inferredcites →https://doi.org/10.1007/bf02870152openalex-snapshot
Leaf differentiation in angiosperms
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Growth and Differentiation in Plants
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Patterns in plant development (2nd edn)
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MORPHOLOGICAL ASPECTS OF LEAF DEVELOPMENT IN FERNS AND ANGIOSPERMS
inferredcites →https://doi.org/10.1017/cbo9780511574535openalex-snapshot
Pattern Formation in Plant Tissues
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Patterns in Plant Development
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Observations et expérimentation sur les feuilles juvéniles duPaulownia tomentosaH. Bn.
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The Relationship of Cells to Organisms in Plants: Problem and Implications of an Organismal Perspective
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The Relationship of Anatomy to Morphology in Plants: A New Theoretical Perspective
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Morphogenesis in Plants
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‘The Plant FormsCells, NotCells the Plant’: TheOrigin of de Bary's Aphorism
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Anatomy of Seed Plants
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Vergleichende Morphologie und Anatomie — Organismus und Zelle, ist eine Synthese möglich?
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THE DORSIVENTRALITY OF LEAF PRIMORDIA
inferredcites →https://doi.org/10.1139/b71-223openalex-snapshot
The initial protrusion of a leaf primordium can form without concurrent periclinal cell divisions
inferredcites →https://doi.org/10.1139/b76-291openalex-snapshot
The growth and development of the leaf in tomato (Lycopersicon esculentum). II. Leaf ontogeny
inferredcites →https://doi.org/10.1139/b84-381openalex-snapshot
Position et orientation des mitoses dans la zone organogène de jeunes feuilles de Fraxinus excelsior, Glechoma hederacea et Lycopus europaeus
inferredcites →https://doi.org/10.1139/b86-350openalex-snapshot
Heteroblastic seedlings of green ash. III. Cell division activity and marginal meristems
inferredcites →https://doi.org/10.15281/jplantres1887.70.108openalex-snapshot
On the Types of the Marginal Growth in Dicotyledonous Foliage Leaves
inferredcites →https://doi.org/10.15281/jplantres1887.74.303openalex-snapshot
Experimental Studies on Leaf Dorsiventrality in Sesamum indicum L.
inferredcites →https://doi.org/10.18756/edn.12.41openalex-snapshot
Troll, Wilhelm: Die Infloreszenzen, Typologie und Stellung im Aufbau des Vegetationskörpers. Jena, VEB Gustav Fischer Verlag. Band I: XV, 615 S. 553 Abb. Geb. M 112,50. 1964.
inferredcites →https://doi.org/10.2307/1311764openalex-snapshot
The Relationship of Cell and Organism in Vascular Plants
inferredcites →https://doi.org/10.2307/2419986openalex-snapshot
Vergleichende Morphologie Der Hoheren Pflanzen.
inferredcites →https://doi.org/10.2307/3244517openalex-snapshot
Phyllotaxis. A Systemic Study in Plant Morphogenesis
inferredcites →https://doi.org/10.2307/4114369openalex-snapshot
Plant Anatomy: Experiment and Interpretation. Part 2. Organs
inferredcites →https://doi.org/10.5962/bhl.title.1310openalex-snapshot
Die Lehre von der Pflanzenzelle
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Morphological trait evolution inSolanum(Solanaceae): Evolutionary lability of key taxonomic characters
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Genetic Control of Leaf Shape
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Evolutionary Morphology of Ferns (Monilophytes)
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Leaf Architecture: Regulation of Leaf Position, Shape and Internal Structure
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Evolutionary Morphology of Ferns (Monilophytes)
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Adaxial–abaxial polarity: The developmental basis of leaf shape diversity
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Developmental Genetics and Morphological Evolution of Flowering Plants, Especially Bladderworts (Utricularia): Fuzzy Arberian Morphology Complements Classical Morphology, , , , , , , , ,
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Patterns and symmetries in leaf development
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The Tomato Leaf as a Model System for Organogenesis
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Organisationsformen und Evolution des Sporophyten
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Grundorgane und Lebensweise
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The Regulation of Dorsiventral Symmetry in Plants
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Origin, Development and Differentiation of Leaves
inferred← citeshttps://doi.org/10.1007/bf00985044openalex-snapshot
Relations between submarginal and marginal sori in ferns
inferred← citeshttps://doi.org/10.1007/bf00985102openalex-snapshot
Towards an organismic concept of land plants: The marginal blastozone and the development of the vegetation body of selected frondose gametophytes of liverworts and ferns
inferred← citeshttps://doi.org/10.1007/bf02507157openalex-snapshot
Genetic evidence for polarities that regulate leaf morphogenesis
inferred← citeshttps://doi.org/10.1007/bf02704759openalex-snapshot
Role ofLLD, a new locus for leaflet/pinna morphogenesis inPisum sativum
inferred← citeshttps://doi.org/10.1007/s00299-013-1426-1openalex-snapshot
Usual and unusual development of the dicot leaf: involvement of transcription factors and hormones
inferred← citeshttps://doi.org/10.1007/s00344-025-11655-1openalex-snapshot
Characterization of the KNOX Gene Family in Regulating Alfalfa Compound Leaf Development
inferred← citeshttps://doi.org/10.1007/s00425-003-1100-xopenalex-snapshot
Roles for auxin during morphogenesis of the compound leaves of pea ( Pisum sativum )
inferred← citeshttps://doi.org/10.1007/s00425-007-0540-0openalex-snapshot
Meristem maintenance and compound-leaf patterning utilize common genetic mechanisms in tomato
inferred← citeshttps://doi.org/10.1007/s00425-007-0572-5openalex-snapshot
Negative regulation of KNOX expression in tomato leaves
inferred← citeshttps://doi.org/10.1007/s00425-009-0997-0openalex-snapshot
KNOX overexpression in transgenic Kohleria (Gesneriaceae) prolongs the activity of proximal leaf blastozones and drastically alters segment fate
inferred← citeshttps://doi.org/10.1007/s00427-005-0479-8openalex-snapshot
Developmental events leading to peltate leaf structure in Tropaeolum majus (Tropaeolaceae) are associated with expression domain changes of a YABBY gene
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The foliar change in two species of Melaleuca (Myrtaceae): a morpho-anatomic and ontogenetic approach
inferred← citeshttps://doi.org/10.1007/s00468-020-01955-2openalex-snapshot
Morphological and physiological changes during leaf ontogeny in genotypes of Eucalyptus young plants
inferred← citeshttps://doi.org/10.1007/s00606-007-0561-yopenalex-snapshot
Pinnately ramified ensiform leaves in the genus Marathrum, (Podostemaceae-Podostemoideae)
inferred← citeshttps://doi.org/10.1007/s10265-009-0256-2openalex-snapshot
Gene expression patterns in seed plant shoot meristems and leaves: homoplasy or homology?
inferred← citeshttps://doi.org/10.1007/s10265-009-0263-3openalex-snapshot
Weeds of change: Cardamine hirsuta as a new model system for studying dissected leaf development
inferred← citeshttps://doi.org/10.1007/s11103-005-4548-1openalex-snapshot
Expression patterns of STM-like KNOX and Histone H4 genes in shoot development of the dissected-leaved basal eudicot plants Chelidonium majus and Eschscholzia californica (Papaveraceae)
inferred← citeshttps://doi.org/10.1007/s11103-016-0436-0openalex-snapshot
A CURLY LEAF homologue controls both vegetative and reproductive development of tomato plants
inferred← citeshttps://doi.org/10.1007/s11434-015-0849-1openalex-snapshot
Stem cell lineage in body layer specialization and vascular patterning of rice root and leaf
inferred← citeshttps://doi.org/10.1007/s12041-010-0026-xopenalex-snapshot
Genetic control of leaf-blade morphogenesis by the INSECATUS gene in Pisum sativum
inferred← citeshttps://doi.org/10.1007/s40415-018-0480-xopenalex-snapshot
A new anatomical interpretation for abaxialization in unifacial leaf blade of stone plants (Aizoaceae, Caryophyllales)
inferred← citeshttps://doi.org/10.1007/s40502-017-0340-xopenalex-snapshot
The key role of small RNAs in the making of a leaf
inferred← citeshttps://doi.org/10.1016/b978-012088457-5/50025-3openalex-snapshot
The Evolutionary History of Roots and Leaves
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.11.006openalex-snapshot
Leaf development and evolution
inferred← citeshttps://doi.org/10.1016/j.cub.2006.07.067openalex-snapshot
Distinct Developmental Mechanisms Reflect the Independent Origins of Leaves in Vascular Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2017.08.042openalex-snapshot
Spatial Auxin Signaling Controls Leaf Flattening in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2022.09.055openalex-snapshot
Differential growth dynamics control aerial organ geometry
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.01.019openalex-snapshot
Regulation of Leaf Maturation by Chromatin-Mediated Modulation of Cytokinin Responses
inferred← citeshttps://doi.org/10.1016/j.flora.2007.04.003openalex-snapshot
The shoot apex of Podostemaceae: De novo structure or reduction of the conventional type?
inferred← citeshttps://doi.org/10.1016/j.flora.2015.11.012openalex-snapshot
The shoot concept of the flower: Still up to date?
inferred← citeshttps://doi.org/10.1016/j.flora.2020.151658openalex-snapshot
Leaf development in some ferns with variable dissection patterns (Dryopteridaceae and Lomariopsidaceae)
inferred← citeshttps://doi.org/10.1016/j.molp.2018.06.006openalex-snapshot
Molecular Mechanisms of Leaf Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.09.017openalex-snapshot
Leaf development: what it needs to be complex
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.11.012openalex-snapshot
Comparative leaf development in angiosperms
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.10.007openalex-snapshot
Compound leaf development in model plant species
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102847openalex-snapshot
Multilayered regulatory control of compound leaf development
inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.12.011openalex-snapshot
CaHAM is autoregulated and regulates CaSTM expression and is required for shoot apical meristem organization in pepper
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.11.035openalex-snapshot
Leaf shape diversity with an emphasis on leaf contour variation, developmental background, and adaptation
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.019openalex-snapshot
Is auxin enough? Cytokinins and margin patterning in simple leaves
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Pedicel development in Arabidopsis thaliana: Contribution of vascular positioning and the role of the BREVIPEDICELLUS and ERECTA genes
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Hormones in tomato leaf development
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60384-1openalex-snapshot
8 Genetic, Molecular, and Morphological Analysis of Compound Leaf Development
inferred← citeshttps://doi.org/10.1016/s0074-7696(02)17011-2openalex-snapshot
Interpretation of mutants in leaf morphology: Genetic evidence for a compensatory system in leaf morphogenesis that provides a new link between cell and organismal theories
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Comparative analysis of leaf shape development in Papaveraceae-Papaveroideae
inferred← citeshttps://doi.org/10.1016/s0367-2530(17)30865-4openalex-snapshot
Comparative analysis of leaf shape development in Papaveraceae-Chelidonioideae
inferred← citeshttps://doi.org/10.1016/s0981-9428(98)80090-9openalex-snapshot
Leaf development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s1360-1385(97)90055-8openalex-snapshot
Simple and compound leaves: reduction or multiplication?
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00135-7openalex-snapshot
Vascular patterning and leaf shape
inferred← citeshttps://doi.org/10.1017/cbo9780511541827.004openalex-snapshot
Meristem organization and organ diversity
inferred← citeshttps://doi.org/10.1038/ng2036openalex-snapshot
Regulation of LANCEOLATE by miR319 is required for compound-leaf development in tomato
inferred← citeshttps://doi.org/10.1038/nrg1002openalex-snapshot
Comparative plant development: the time of the leaf?
inferred← citeshttps://doi.org/10.1038/s41438-020-00404-yopenalex-snapshot
WUSCHEL-related homeobox1 (WOX1) regulates vein patterning and leaf size in Cucumis sativus
inferred← citeshttps://doi.org/10.1038/s41438-021-00558-3openalex-snapshot
The diverse roles of cytokinins in regulating leaf development
inferred← citeshttps://doi.org/10.1046/j.1095-8339.2003.00199.xopenalex-snapshot
The marginal band, a new structural component of the developing angiosperm leaf
inferred← citeshttps://doi.org/10.1055/s-2003-42718openalex-snapshot
The Molecular Regulation of Leaf Form
inferred← citeshttps://doi.org/10.1073/pnas.1214300110openalex-snapshot
Trifoliate encodes an MYB transcription factor that modulates leaf and shoot architecture in tomato
inferred← citeshttps://doi.org/10.1073/pnas.1421878112openalex-snapshot
Auxin depletion from leaf primordia contributes to organ patterning
inferred← citeshttps://doi.org/10.1078/0367-2530-00056openalex-snapshot
Morphology and morphogenesis of ensiform leaves in Apinagia multibranchiata and Mourera fluviatilis (Podostemaceae – Podostemoideae)
inferred← citeshttps://doi.org/10.1086/314165openalex-snapshot
Evolution of Leaf Morphogenesis: Evidence from Developmental and Phylogenetic Data in Papaveraceae
inferred← citeshttps://doi.org/10.1086/320137openalex-snapshot
Genetic Control of Leaf Development in Pea ( Pisum sativum )
inferred← citeshttps://doi.org/10.1086/320145openalex-snapshot
Leaf Morphogenesis in Dicotyledons: Current Issues
inferred← citeshttps://doi.org/10.1086/321924openalex-snapshot
Roles of theUniGene in Shoot and Leaf Development of Pea (Pisum sativum): Phenotypic Characterization and Leaf Development in theunianduni‐tacMutants
inferred← citeshttps://doi.org/10.1086/422048openalex-snapshot
Roles of Auxin andUniin Leaf Morphogenesis of theafilaGenotype of Pea (Pisum sativum)
inferred← citeshttps://doi.org/10.1086/513489openalex-snapshot
The Role of Abscission during Leaflet Separation inChamaedorea elegans(Arecaceae)
inferred← citeshttps://doi.org/10.1086/588067openalex-snapshot
Abscission‐Like Leaflet Separation in Chamaedorea seifrizii (Arecaceae)
inferred← citeshttps://doi.org/10.1086/684178openalex-snapshot
Different Ways to Build Succulent Leaves in Portulacineae (Caryophyllales)
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa066openalex-snapshot
Floral structure in Thismia (Thismiaceae: Dioscoreales): new insights from anatomy, vasculature and development
inferred← citeshttps://doi.org/10.1093/gigascience/giw008openalex-snapshot
Morphometric analysis of Passiflora leaves: the relationship between landmarks of the vasculature and elliptical Fourier descriptors of the blade
inferred← citeshttps://doi.org/10.1093/jxb/erae118openalex-snapshot
Shaping leaves through TALE homeodomain transcription factors
inferred← citeshttps://doi.org/10.1093/jxb/erp397openalex-snapshot
Co-ordination of developmental processes by small RNAs during leaf development
inferred← citeshttps://doi.org/10.1093/jxb/erw388openalex-snapshot
TomatoHAIRY MERISTEMgenes are involved in meristem maintenance and compound leaf morphogenesis
inferred← citeshttps://doi.org/10.1093/jxb/erz205openalex-snapshot
Growth and biomechanics of shoot organs
inferred← citeshttps://doi.org/10.1093/pcp/pcaa163openalex-snapshot
Interaction between the MtDELLA–MtGAF1 Complex and MtARF3 Mediates Transcriptional Control of MtGA3ox1 to Elaborate Leaf Margin Formation in Medicago truncatula
inferred← citeshttps://doi.org/10.1093/plcell/koaa012openalex-snapshot
Spatial transcriptional signatures define margin morphogenesis along the proximal–distal and medio-lateral axes in tomato ( Solanum lycopersicum ) leaves
inferred← citeshttps://doi.org/10.1093/plcell/koab190openalex-snapshot
The leaf meristem enigma: The relationship between the plate meristem and the marginal meristem
inferred← citeshttps://doi.org/10.1101/126466openalex-snapshot
Cell type boundaries organize plant development
inferred← citeshttps://doi.org/10.1101/2020.08.19.257550openalex-snapshot
Collaboration of multiple pathways in making a compound leaf
inferred← citeshttps://doi.org/10.1101/2022.03.15.484181openalex-snapshot
miR319-targeted TCP4/LANCEOLATE directly regulates OVATE and auxin responses to modulate tomato gynoecium patterning and fruit morphology
inferred← citeshttps://doi.org/10.1104/pp.117.3.771openalex-snapshot
Overexpression of a Homeobox Gene, LeT6, Reveals Indeterminate Features in the Tomato Compound Leaf1
inferred← citeshttps://doi.org/10.1105/tpc.001941openalex-snapshot
Ectopic Expression of BABY BOOM Triggers a Conversion from Vegetative to Embryonic Growth
inferred← citeshttps://doi.org/10.1105/tpc.004911openalex-snapshot
YABBY Polarity Genes Mediate the Repression of KNOX Homeobox Genes in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.019307openalex-snapshot
PHANTASTICA Regulates Development of the Adaxial Mesophyll in Nicotiana Leaves
inferred← citeshttps://doi.org/10.1105/tpc.021816openalex-snapshot
MicroRNA-Directed Cleavage of Nicotiana sylvestris PHAVOLUTA mRNA Regulates the Vascular Cambium and Structure of Apical Meristems
inferred← citeshttps://doi.org/10.1105/tpc.107.057521openalex-snapshot
A Protracted and Dynamic Maturation Schedule Underlies Arabidopsis Leaf Development
inferred← citeshttps://doi.org/10.1105/tpc.109.068148openalex-snapshot
Stage-Specific Regulation of Solanum lycopersicum Leaf Maturation by Class 1 KNOTTED1-LIKE HOMEOBOX Proteins
inferred← citeshttps://doi.org/10.1105/tpc.109.069948openalex-snapshot
LYRATE Is a Key Regulator of Leaflet Initiation and Lamina Outgrowth in Tomato
inferred← citeshttps://doi.org/10.1105/tpc.109.073601openalex-snapshot
Morphogenesis of Simple and Compound Leaves: A Critical Review
inferred← citeshttps://doi.org/10.1105/tpc.110.078253openalex-snapshot
Cytokinin Regulates Compound Leaf Development in Tomato
inferred← citeshttps://doi.org/10.1105/tpc.111.085340openalex-snapshot
STENOFOLIARegulates Blade Outgrowth and Leaf Vascular Patterning inMedicago truncatulaandNicotiana sylvestris
inferred← citeshttps://doi.org/10.1105/tpc.111.085464openalex-snapshot
Developmental Analysis of aMedicago truncatula smooth leaf margin1Mutant Reveals Context-Dependent Effects on Compound Leaf Development
inferred← citeshttps://doi.org/10.1105/tpc.111.089128openalex-snapshot
Regulation of Compound Leaf Development in Medicago truncatula by Fused Compound Leaf1, a Class M KNOX Gene
inferred← citeshttps://doi.org/10.1105/tpc.111.092858openalex-snapshot
Roles of the Middle Domain–Specific WUSCHEL-RELATED HOMEOBOX Genes in Early Development of Leaves in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.113.113035openalex-snapshot
A Role for APETALA1/FRUITFULL Transcription Factors in Tomato Leaf Development
inferred← citeshttps://doi.org/10.1105/tpc.113.121947openalex-snapshot
STENOFOLIA Recruits TOPLESS to RepressASYMMETRIC LEAVES2at the Leaf Margin and Promote Leaf Blade Outgrowth inMedicago truncatula
inferred← citeshttps://doi.org/10.1105/tpc.12.8.1279openalex-snapshot
Pea Compound Leaf Architecture Is Regulated by Interactions among the Genes UNIFOLIATA, COCHLEATA, AFILA, and TENDRIL-LESS
inferred← citeshttps://doi.org/10.1105/tpc.16.00211openalex-snapshot
CLAUSA is a MYB Transcription Factor that Promotes Leaf Differentiation by Attenuating Cytokinin Signaling
inferred← citeshttps://doi.org/10.1105/tpc.8.8.1277openalex-snapshot
KNAT1 Induces Lobed Leaves with Ectopic Meristems When Overexpressed in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.9.7.1077openalex-snapshot
Leaf morphogenesis in flowering plants.
inferred← citeshttps://doi.org/10.1105/tpc.9.7.1121openalex-snapshot
Leaf Vascular Pattern Formation.
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2006.00487.xopenalex-snapshot
Alternative modes of leaf dissection in monocotyledons
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2006.00497.xopenalex-snapshot
A feeling for the superorganism: expression of plant form in the lichen thallus
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2009.01004.xopenalex-snapshot
The Jambi gigantopterids and their place in gigantopterid classification
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04716.xopenalex-snapshot
Gibberellin partly mediates LANCEOLATE activity in tomato
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.04939.xopenalex-snapshot
ENTIRE and GOBLET promote leaflet development in tomato by modulating auxin response
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01466.xopenalex-snapshot
Evolution of leaf developmental mechanisms
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03951.xopenalex-snapshot
Keeping it simple: flowering plants tend to retain, and revert to, simple leaves
inferred← citeshttps://doi.org/10.1111/nph.12582openalex-snapshot
Acquisition and diversification of tendrilled leaves in B ignonieae ( B ignoniaceae) involved changes in expression patterns of SHOOTMERISTEMLESS ( STM ), LEAFY/FLORICAULA ( LFY / FLO ), and PHANTASTICA ( PHAN )
inferred← citeshttps://doi.org/10.1111/nph.13641openalex-snapshot
Divide et impera: boundaries shape the plant body and initiate new meristems
inferred← citeshttps://doi.org/10.1111/nph.14449openalex-snapshot
A common developmental program can produce diverse leaf shapes
inferred← citeshttps://doi.org/10.1111/nph.15073openalex-snapshot
The molecular control of tendril development in angiosperms
inferred← citeshttps://doi.org/10.1111/nph.15371openalex-snapshot
On the mechanisms of development in monocot and eudicot leaves
inferred← citeshttps://doi.org/10.1111/nph.17124openalex-snapshot
Coordination of differentiation rate and local patterning in compound‐leaf development
inferred← citeshttps://doi.org/10.1111/ppl.14641openalex-snapshot
SlTCP29 and SlTCP24 participate in the morphological development of tomato compound leaves by integrating multiple pathways
inferred← citeshttps://doi.org/10.1111/ppl.70092openalex-snapshot
Synergistic effects of GmLFYa and GmLFYb on Compound Leaf Development in Soybean
inferred← citeshttps://doi.org/10.1111/ppl.70416openalex-snapshot
Transcription Factor ClTCP4 Regulates Leaf Size and Wavy Margin in Leaf Morphogenesis of Citrullus lanatus
inferred← citeshttps://doi.org/10.1111/tpj.12782openalex-snapshot
Lateral suppressor and Goblet act in hierarchical order to regulate ectopic meristem formation at the base of tomato leaflets
inferred← citeshttps://doi.org/10.1111/tpj.12936openalex-snapshot
CLAUSA restricts tomato leaf morphogenesis and GOBLET expression
inferred← citeshttps://doi.org/10.1111/tpj.13188openalex-snapshot
Auxin‐mediated lamina growth in tomato leaves is restricted by two parallel mechanisms
inferred← citeshttps://doi.org/10.1111/tpj.14073openalex-snapshot
Tuning of Sl ARF 10A dosage by sly‐miR160a is critical for auxin‐mediated compound leaf and flower development
inferred← citeshttps://doi.org/10.1111/tpj.14982openalex-snapshot
Leaflet initiation and blade expansion are separable in compound leaf development
inferred← citeshttps://doi.org/10.1111/tpj.70278openalex-snapshot
A suppressor screen of an Arabidopsis thalianaREDUCED COMPLEXITY (RCO)‐expressing strain provides insight into the genetics of leaf margin complexity
inferred← citeshttps://doi.org/10.1126/science.1070343openalex-snapshot
Homologies in Leaf Form Inferred from KNOXI Gene Expression During Development
inferred← citeshttps://doi.org/10.1134/s2079086421040083openalex-snapshot
Evolutionary History of the Leguminous Flower
inferred← citeshttps://doi.org/10.1139/b08-136openalex-snapshot
Leaf development in Aralia elata in relation to the partial-shoot concept
inferred← citeshttps://doi.org/10.1139/b09-043openalex-snapshot
A quantitative analysis of leaf growth parameters inMyriophyllum aquaticum(Haloragaceae)
inferred← citeshttps://doi.org/10.1139/b10-051openalex-snapshot
Leaflet initiation is temporally and spatially separated in simple and complex tomato (Solanum lycopersicum) leaf mutants: a developmental analysis
inferred← citeshttps://doi.org/10.1139/cjb-2013-0210openalex-snapshot
Development of leaf shape in two North American native species ofAmpelopsis(Vitaceae)
inferred← citeshttps://doi.org/10.1139/cjb-2015-0077openalex-snapshot
Extended expression of MaKN1 contributes to the leaf morphology in aquatic forms of Myriophyllum aquaticum
inferred← citeshttps://doi.org/10.1146/annurev-arplant-080720-101613openalex-snapshot
Leaf Shape Diversity: From Genetic Modules to Computational Models
inferred← citeshttps://doi.org/10.1146/annurev.arplant.50.1.419openalex-snapshot
LEAF DEVELOPMENT IN ANGIOSPERMS
inferred← citeshttps://doi.org/10.11606/d.41.2013.tde-19032014-093900openalex-snapshot
Desenvolvimento foliar em Ruschioideae (Aizoaceae), com ênfase na formação e estrutura dos feixes vasculares periféricos
inferred← citeshttps://doi.org/10.11606/d.41.2014.tde-11072014-100107openalex-snapshot
Ontogênese da região da axila foliar e filogenia molecular de Didiereaceae: a história de um caráter e suas implicações filogenéticas em Portulacineae
inferred← citeshttps://doi.org/10.11606/t.11.2016.tde-28032016-135123openalex-snapshot
Caracterização de uma variação genética natural de Solanum galapagense controlando o comprimento do entrenó e arquitetura foliar em tomateiro
inferred← citeshttps://doi.org/10.11606/t.41.2018.tde-21032018-134304openalex-snapshot
Desenvolvimento foliar e expressão do ortólogo de ASYMMETRIC LEAVES1/ROUGH SHEATH2/PHANTASTICA em Aizoaceae
inferred← citeshttps://doi.org/10.1186/2041-9139-5-47openalex-snapshot
What determines a leaf's shape?
inferred← citeshttps://doi.org/10.1186/s13007-020-00694-2openalex-snapshot
Characterization of the cytokinin sensor TCSv2 in arabidopsis and tomato
inferred← citeshttps://doi.org/10.1186/s40793-022-00397-2openalex-snapshot
Cytokinin-microbiome interactions regulate developmental functions
inferred← citeshttps://doi.org/10.1242/dev.031625openalex-snapshot
The NAC-domain transcription factor GOBLET specifies leaflet boundaries in compound tomato leaves
inferred← citeshttps://doi.org/10.1242/dev.033811openalex-snapshot
Auxin patternsSolanum lycopersicumleaf morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.056770openalex-snapshot
Dynamic growth program regulated by LANCEOLATE enables flexible leaf patterning
inferred← citeshttps://doi.org/10.1242/dev.106195openalex-snapshot
Leaf development and morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.125.21.4235openalex-snapshot
LAM1 is required for dorsoventrality and lateral growth of the leaf blade in Nicotiana
inferred← citeshttps://doi.org/10.1242/dev.126.2.305openalex-snapshot
Mosaic analysis of the dominant mutant,Gnarley1-R, reveals distinct lateral and transverse signaling pathways during maize leaf development
inferred← citeshttps://doi.org/10.1242/dev.161646openalex-snapshot
Getting leaves into shape: a molecular, cellular, environmental and evolutionary view
inferred← citeshttps://doi.org/10.1242/dev.205772openalex-snapshot
A two-step auxin–GA cross-talk regulates organ formation in tomato
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006649openalex-snapshot
Overexpression of the WOX gene STENOFOLIA improves biomass yield and sugar release in transgenic grasses and display altered cytokinin homeostasis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009633openalex-snapshot
The VIL gene CRAWLING ELEPHANT controls maturation and differentiation in tomato via polycomb silencing
inferred← citeshttps://doi.org/10.1371/journal.pone.0007968openalex-snapshot
A Global Regulation Inducing the Shape of Growing Folded Leaves
inferred← citeshttps://doi.org/10.1666/0094-8373(2002)028<0070:eodpat>2.0.co;2openalex-snapshot
Evolution of developmental potential and the multiple independent origins of leaves in Paleozoic vascular plants
inferred← citeshttps://doi.org/10.1666/0094-8373(2005)031<0117:posaci>2.0.co;2openalex-snapshot
Patterns of segregation and convergence in the evolution of fern and seed plant leaf morphologies
inferred← citeshttps://doi.org/10.18756/edn.108.101openalex-snapshot
Die Knospe als Organ und Verlauf der Formenreihen-Bildung. Herbsttagung «Evolving Morphology»
inferred← citeshttps://doi.org/10.18756/edn.88.39openalex-snapshot
Die Trennung der Geschlechter und die Bildung der Blütenorgane - Gestaltungsfreiheit
inferred← citeshttps://doi.org/10.2216/i0031-8884-37-6-478.1openalex-snapshot
Phylogenetic implications of patterns of cap development in selected species of Acetabularia/Polyphysa (Dasycladales, Chlorophyta)
inferred← citeshttps://doi.org/10.2298/bg20121227barisicklisaricopenalex-snapshot
Fluctuating asymmetry as an indicator of developmental stability of selected plant taxa in unpolluted environment and under anthropogenically induced stress
inferred← citeshttps://doi.org/10.3389/fgene.2018.00478openalex-snapshot
Mechanisms Underlying the Environmentally Induced Plasticity of Leaf Morphology
inferred← citeshttps://doi.org/10.3389/fgene.2021.648831openalex-snapshot
AGNEP: An Agglomerative Nesting Clustering Algorithm for Phenotypic Dimension Reduction in Joint Analysis of Multiple Phenotypes
inferred← citeshttps://doi.org/10.3389/fpls.2015.01135openalex-snapshot
Interspecies Gene Transfer as a Method for Understanding the Genetic Basis for Evolutionary Change: Progress, Pitfalls, and Prospects
inferred← citeshttps://doi.org/10.3390/genes9120577openalex-snapshot
The Analysis of Genes and Phytohormone Metabolic Pathways Associated with Leaf Shape Development in Liriodendron chinense via De Novo Transcriptome Sequencing
inferred← citeshttps://doi.org/10.3390/ijms241814205openalex-snapshot
BrrA02.LMI1 Encodes a Homeobox Protein That Affects Leaf Margin Development in Brassica rapa
inferred← citeshttps://doi.org/10.3390/plants13182566openalex-snapshot
The Effects of Auxin Transport Inhibition on the Formation of Various Leaf and Vein Patterns
inferred← citeshttps://doi.org/10.3390/plants2020317openalex-snapshot
TALE and Shape: How to Make a Leaf Different
inferred← citeshttps://doi.org/10.3390/plants3010001openalex-snapshot
Regulation of Compound Leaf Development
inferred← citeshttps://doi.org/10.3390/plants8070243openalex-snapshot
The Diverse Roles of Auxin in Regulating Leaf Development
inferred← citeshttps://doi.org/10.3390/sym11030321openalex-snapshot
Interaction between Floral Merism and Symmetry: Evidence from Fasciated Mutant of Lupinus angustifolius L. (Leguminosae)
inferred← citeshttps://doi.org/10.3410/f.713998001.789452951openalex-snapshot
Faculty Opinions recommendation of Roles of the middle domain-specific WUSCHEL-RELATED HOMEOBOX genes in early development of leaves in Arabidopsis.
inferred← citeshttps://doi.org/10.3410/f.726818075.793545596openalex-snapshot
Faculty Opinions recommendation of Active suppression of a leaf meristem orchestrates determinate leaf growth.
inferred← citeshttps://doi.org/10.3417/2011018openalex-snapshot
Evolution and Development of Tendrils in Bignonieae (Lamiales, Bignoniaceae)1
inferred← citeshttps://doi.org/10.3732/ajb.1100101openalex-snapshot
Compound leaf development in the palm Chamaedorea elegans is KNOX‐independent
inferred← citeshttps://doi.org/10.3732/ajb.1200560openalex-snapshot
Precocious progression of tissue maturation instructs basipetal initiation of leaflets in Chelidonium majus subsp. asiaticum (Papaveraceae)
inferred← citeshttps://doi.org/10.3732/ajb.91.3.306openalex-snapshot
Comparative analysis of leaf shape development in Eschscholzia californica and other Papaveraceae‐Eschscholzioideae
inferred← citeshttps://doi.org/10.4161/psb.21550openalex-snapshot
Auxin and LANCEOLATE affect leaf shape in tomato via different developmental processes
inferred← citeshttps://doi.org/10.4161/psb.5.9.12640openalex-snapshot
Palmate-like pentafoliata1 encodes a novel Cys(2)His(2) zinc finger transcription factor essential for compound leaf morphogenesis in Medicago truncatula
inferred← citeshttps://doi.org/10.55360/cpn493.jb736openalex-snapshot
Evolution of the Cephalotus pitcher
inferred← citeshttps://doi.org/10.6084/m9.figshare.13245983openalex-snapshot
Additional file 1 of Characterization of the cytokinin sensor TCSv2 in arabidopsis and tomato
inferred← citeshttps://doi.org/10.70675/05fa1f88zde47z439fz86a5z3f2b0b390f67openalex-snapshot
A front propagation model of leaf growth
inferred← citeshttps://doi.org/10.70675/1cc63732zc8c7z46e6zb8e0zd9b73d2fa863openalex-snapshot
Inhibition de la bractée lors de la transition florale chez Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/2f5b8228zda99z4b3fza028zef4d9f2f1e95openalex-snapshot
The roles of the NOOT-BOP-COCH-LIKE genes in plant development and in the symbiotic organ identity
inferred← citeshttps://doi.org/10.70675/41962612za8d4z49a7z8ea6z603cb1b6d1d6openalex-snapshot
The roles of the NOOT-BOP-COCH-LIKE genes in the symbiotic organ identity and in plant development
inferred← citeshttps://doi.org/10.70675/e5636752z919dz4397z89aezf2b808d81d4copenalex-snapshot
Ontogenetic variations in leaf traits of the homoblastic species Dipterocarpus alatus under two light conditions at Cat Tien national park, Vietnam
inferred← citeshttps://doi.org/10.7554/elife.15023openalex-snapshot
Active suppression of a leaf meristem orchestrates determinate leaf growth
inferred← citeshttps://doi.org/10.7554/elife.27421openalex-snapshot
Cell type boundaries organize plant development
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