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The expa1-1 mutant reveals a new biophysical lateral root organogenesis checkpoint
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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/bies.950180704openalex-snapshot
Plant cell enlargement and the action of expansins
inferredcites →https://doi.org/10.1007/978-1-4939-6493-2_12openalex-snapshot
Carbohydrate Microarray Technology Applied to High-Throughput Mapping of Plant Cell Wall Glycans Using Comprehensive Microarray Polymer Profiling (CoMPP)
inferredcites →https://doi.org/10.1007/s00425-007-0656-2openalex-snapshot
Xyloglucan−pectin linkages are formed intra-protoplasmically, contribute to wall-assembly, and remain stable in the cell wall
inferredcites →https://doi.org/10.1007/s00709-011-0371-5openalex-snapshot
Growth control by cell wall pectins
inferredcites →https://doi.org/10.1007/s11103-005-4547-2openalex-snapshot
Lateral Root Initiation or the Birth of a New Meristem
inferredcites →https://doi.org/10.1007/s11103-008-9417-2openalex-snapshot
Hormone interactions during lateral root formation
inferredcites →https://doi.org/10.1016/j.carbpol.2008.05.004openalex-snapshot
Competitive binding of pectin and xyloglucan with primary cell wall cellulose
inferredcites →https://doi.org/10.1016/j.cub.2008.10.065openalex-snapshot
Arabidopsis Phyllotaxis Is Controlled by the Methyl-Esterification Status of Cell-Wall Pectins
inferredcites →https://doi.org/10.1016/j.cub.2010.09.007openalex-snapshot
A Novel Aux/IAA28 Signaling Cascade Activates GATA23-Dependent Specification of Lateral Root Founder Cell Identity
inferredcites →https://doi.org/10.1016/j.cub.2011.08.057openalex-snapshot
Pectin-Induced Changes in Cell Wall Mechanics Underlie Organ Initiation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2015.03.046openalex-snapshot
Root Cap-Derived Auxin Pre-patterns the Longitudinal Axis of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.tplants.2009.05.002openalex-snapshot
Arabidopsis lateral root development: an emerging story
inferredcites →https://doi.org/10.1016/j.tplants.2013.04.006openalex-snapshot
Lateral root development in Arabidopsis: fifty shades of auxin
inferredcites →https://doi.org/10.1021/ie50421a009openalex-snapshot
Kinetics of Wood Saccharification - Hydrolysis of Cellulose and Decomposition of Sugars in Dilute Acid at High Temperature
inferredcites →https://doi.org/10.1038/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1038/ncb2573openalex-snapshot
Auxin regulates aquaporin function to facilitate lateral root emergence
inferredcites →https://doi.org/10.1038/nrm3064openalex-snapshot
Asymmetric cell division in land plants and algae: the driving force for differentiation
inferredcites →https://doi.org/10.1042/bj2820821openalex-snapshot
Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00630.xopenalex-snapshot
Molecular domains of the cellulose/xyloglucan network in the cell walls of higher plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00703.xopenalex-snapshot
Degradation of Aux/IAA proteins is essential for normal auxin signalling
inferredcites →https://doi.org/10.1073/pnas.0308702101openalex-snapshot
Transcript profiling of early lateral root initiation
inferredcites →https://doi.org/10.1073/pnas.1210807110openalex-snapshot
Lateral root morphogenesis is dependent on the mechanical properties of the overlaying tissues
inferredcites →https://doi.org/10.1073/pnas.1316290110openalex-snapshot
Sensitivity-enhanced solid-state NMR detection of expansin’s target in plant cell walls
inferredcites →https://doi.org/10.1073/pnas.191380498openalex-snapshot
Local expression of expansin induces the entire process of leaf development and modifies leaf shape
inferredcites →https://doi.org/10.1093/jxb/eri268openalex-snapshot
The co-ordination of cell division, differentiation and morphogenesis in the shoot apical meristem: a perspective
inferredcites →https://doi.org/10.1093/pcp/pcu204openalex-snapshot
Xyloglucan and its Interactions with Other Components of the Growing Cell Wall
inferredcites →https://doi.org/10.1101/cshperspect.a001537openalex-snapshot
Auxin Control of Root Development
inferredcites →https://doi.org/10.1101/gad.276964.115openalex-snapshot
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation
inferredcites →https://doi.org/10.1104/pp.107.1.87openalex-snapshot
Expansin Mode of Action on Cell Walls (Analysis of Wall Hydrolysis, Stress Relaxation, and Binding)
inferredcites →https://doi.org/10.1104/pp.108.4.1579openalex-snapshot
Fractionation of Xyloglucan Fragments and Their Interaction with Cellulose
inferredcites →https://doi.org/10.1104/pp.110.156844openalex-snapshot
The XTH Gene Family: An Update on Enzyme Structure, Function, and Phylogeny in Xyloglucan Remodeling
inferredcites →https://doi.org/10.1104/pp.111.189779openalex-snapshot
Changes in Cell Wall Biomechanical Properties in the Xyloglucan-Deficient xxt1/xxt2 Mutant of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.192880openalex-snapshot
A Revised Architecture of Primary Cell Walls Based on Biomechanical Changes Induced by Substrate-Specific Endoglucanases
inferredcites →https://doi.org/10.1104/pp.15.00665openalex-snapshot
Cellulose-Pectin Spatial Contacts Are Inherent to Never-Dried Arabidopsis Primary Cell Walls: Evidence from Solid-State Nuclear Magnetic Resonance
inferredcites →https://doi.org/10.1104/pp.51.1.188openalex-snapshot
The Structure of Plant Cell Walls
inferredcites →https://doi.org/10.1104/pp.54.1.105openalex-snapshot
The Structure of Plant Cell Walls
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
inferredcites →https://doi.org/10.1105/tpc.018705openalex-snapshot
Downregulation of the Petunia hybrida α-Expansin Gene PhEXP1 Reduces the Amount of Crystalline Cellulose in Cell Walls and Leads to Phenotypic Changes in Petal Limbs
inferredcites →https://doi.org/10.1105/tpc.105.035493openalex-snapshot
Cell Cycle Progression in the Pericycle Is Not Sufficient for SOLITARY ROOT/IAA14-Mediated Lateral Root Initiation inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.16.00638openalex-snapshot
Periodic Lateral Root Priming: What Makes It Tick?
inferredcites →https://doi.org/10.1105/tpc.4.11.1425openalex-snapshot
Two Endogenous Proteins That Induce Cell Wall Extension in Plants
inferredcites →https://doi.org/10.1111/j.1365-313x.1993.tb00007.xopenalex-snapshot
Structural models of primary cell walls in flowering plants: consistency of molecular structure with the physical properties of the walls during growth
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03114.xopenalex-snapshot
High‐throughput mapping of cell‐wall polymers within and between plants using novel microarrays
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.1469-8137.2011.03996.xopenalex-snapshot
Lateral root initiation: one step at a time
inferredcites →https://doi.org/10.1126/science.1160158openalex-snapshot
Receptor-Like Kinase ACR4 Restricts Formative Cell Divisions in the Arabidopsis Root
inferredcites →https://doi.org/10.1126/science.1191937openalex-snapshot
Oscillating Gene Expression Determines Competence for Periodic Arabidopsis Root Branching
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/10.1126/science.276.5317.1415openalex-snapshot
Induction of Leaf Primordia by the Cell Wall Protein Expansin
inferredcites →https://doi.org/10.1155/2008/420747openalex-snapshot
Genevestigator V3: A Reference Expression Database for the Meta‐Analysis of Transcriptomes
inferredcites →https://doi.org/10.1242/dev.02753openalex-snapshot
Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis
inferredcites →https://doi.org/10.1242/dev.071928openalex-snapshot
The establishment of asymmetry in Arabidopsis lateral root founder cells is regulated by LBD16/ASL18 and related LBD/ASL proteins
inferredcites →https://doi.org/10.1242/dev.116459openalex-snapshot
Cell type-specific transcriptome analysis in the early Arabidopsis thaliana embryo
inferredcites →https://doi.org/10.1242/dev.124.1.33openalex-snapshot
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1263/jbb.104.34openalex-snapshot
Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation
inferredcites →https://doi.org/10.3791/4238openalex-snapshot
Glycan Profiling of Plant Cell Wall Polymers using Microarrays
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s10725-020-00588-2openalex-snapshot
Blue and red light upregulate α-expansin 1 (EXPA1) in transgenic Brassica rapa and its overexpression promotes leaf and root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2019.06.039openalex-snapshot
Cytoskeleton Dynamics Are Necessary for Early Events of Lateral Root Initiation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcab038openalex-snapshot
Integration of Cell Growth and Asymmetric Division during Lateral Root Initiation in Arabidopsis thaliana
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