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Actin cytoskeleton in the control of vesicle transport, cytoplasmic organization, and pollen tube tip growth
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inferredcites →https://doi.org/10.1002/(sici)1097-0169(1997)36:4<323::aid-cm3>3.0.co;2-6openalex-snapshot
Characterization and localization of profilin in pollen grains and tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1002/1873-3468.14343openalex-snapshot
Vesicle trafficking in Arabidopsis pollen tubes
inferredcites →https://doi.org/10.1002/cm.20181openalex-snapshot
Differential organelle movement on the actin cytoskeleton in lily pollen tubes
inferredcites →https://doi.org/10.1006/dbio.1996.0060openalex-snapshot
Tip-Localized Calcium Entry Fluctuates during Pollen Tube Growth
inferredcites →https://doi.org/10.1006/dbio.2000.9709openalex-snapshot
Periodic increases in elongation rate precede increases in cytosolic Ca2+ during pollen tube growth
inferredcites →https://doi.org/10.1007/bf01403385openalex-snapshot
Ultrastructure of freeze-substituted pollen tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1007/s00425-004-1423-2openalex-snapshot
Enhanced fixation reveals the apical cortical fringe of actin filaments as a consistent feature of the pollen tube
inferredcites →https://doi.org/10.1007/s00425-008-0802-5openalex-snapshot
Actin filament organization and polarity in pollen tubes revealed by myosin II subfragment 1 decoration
inferredcites →https://doi.org/10.1007/s00709-006-0231-xopenalex-snapshot
The function of actin-binding proteins in pollen tube growth
inferredcites →https://doi.org/10.1007/s00709-006-0233-8openalex-snapshot
Arabidopsis thaliana myosin XIK is involved in root hair as well as trichome morphogenesis on stems and leaves
inferredcites →https://doi.org/10.1007/s00709-021-01694-2openalex-snapshot
Apical pollen tube wall curvature correlates with growth and indicates localized changes in the yielding of the cell wall
inferredcites →https://doi.org/10.1007/s11427-019-9532-0openalex-snapshot
Arabidopsis AIP1-1 regulates the organization of apical actin filaments by promoting their turnover in pollen tubes
inferredcites →https://doi.org/10.1016/0012-1606(91)90278-bopenalex-snapshot
A cytoplasmic gradient of Ca2+ is correlated with the growth of lily pollen tubes
inferredcites →https://doi.org/10.1016/0092-8674(95)90363-1openalex-snapshot
GTPase cascades choreographing cellular behavior: Movement, morphogenesis, and more
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.10.009openalex-snapshot
Calcium - a central regulator of pollen germination and tube growth
inferredcites →https://doi.org/10.1016/j.bpj.2009.07.038openalex-snapshot
Microfilament Orientation Constrains Vesicle Flow and Spatial Distribution in Growing Pollen Tubes
inferredcites →https://doi.org/10.1016/j.bpj.2011.08.016openalex-snapshot
Chemically Mediated Mechanical Expansion of the Pollen Tube Cell Wall
inferredcites →https://doi.org/10.1016/j.ceb.2003.11.009openalex-snapshot
Cytoplasmic streaming in plants
inferredcites →https://doi.org/10.1016/j.chembiol.2009.10.006openalex-snapshot
Identification and Characterization of a Small Molecule Inhibitor of Formin-Mediated Actin Assembly
inferredcites →https://doi.org/10.1016/j.febslet.2011.05.019openalex-snapshot
Arabidopsis actin-depolymerizing factors (ADFs) 1 and 9 display antagonist activities
inferredcites →https://doi.org/10.1016/j.gde.2018.03.008openalex-snapshot
Cell mechanics of pollen tube growth
inferredcites →https://doi.org/10.1016/j.isci.2019.05.026openalex-snapshot
The Balance between Actin-Bundling Factors Controls Actin Architecture in Pollen Tubes
inferredcites →https://doi.org/10.1016/j.molp.2015.09.013openalex-snapshot
Profilin Regulates Apical Actin Polymerization to Control Polarized Pollen Tube Growth
inferredcites →https://doi.org/10.1016/j.molp.2017.05.002openalex-snapshot
Organizational Innovation of Apical Actin Filaments Drives Rapid Pollen Tube Growth and Turning
inferredcites →https://doi.org/10.1016/j.molp.2017.06.001openalex-snapshot
Higher-Ordered Actin Structures Remodeled by Arabidopsis ACTIN-DEPOLYMERIZING FACTOR5 Are Important for Pollen Germination and Pollen Tube Growth
inferredcites →https://doi.org/10.1016/j.molp.2018.09.004openalex-snapshot
Actin Polymerization Mediated by AtFH5 Directs the Polarity Establishment and Vesicle Trafficking for Pollen Germination in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2006.09.013openalex-snapshot
Actin dynamics: old friends with new stories
inferredcites →https://doi.org/10.1016/j.pbi.2008.10.002openalex-snapshot
Tip growth: signaling in the apical dome
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.004openalex-snapshot
The cytoskeleton in the pollen tube
inferredcites →https://doi.org/10.1016/j.peptides.2021.170572openalex-snapshot
The role of diverse LURE-type cysteine-rich peptides as signaling molecules in plant reproduction
inferredcites →https://doi.org/10.1016/j.semcdb.2011.06.004openalex-snapshot
Rapid tip growth: Insights from pollen tubes
inferredcites →https://doi.org/10.1016/j.tplants.2006.04.003openalex-snapshot
RAC/ROP GTPases: ‘hubs’ for signal integration and diversification in plants
inferredcites →https://doi.org/10.1016/j.tplants.2006.10.002openalex-snapshot
Vesicular trafficking, cytoskeleton and signalling in root hairs and pollen tubes
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.010openalex-snapshot
Pollen tubes and the physical world
inferredcites →https://doi.org/10.1016/s0014-5793(01)02528-5openalex-snapshot
Phosphorylation of plant actin‐depolymerising factor by calmodulin‐like domain protein kinase
inferredcites →https://doi.org/10.1016/s0962-8924(99)01619-0openalex-snapshot
Putting a new twist on actin: ADF/cofilins modulate actin dynamics
inferredcites →https://doi.org/10.1016/s1360-1385(01)02130-6openalex-snapshot
Rop GTPase: a master switch of cell polarity development in plants
inferredcites →https://doi.org/10.1021/bi00420a027openalex-snapshot
Effect of pH on the mechanism of actin polymerization
inferredcites →https://doi.org/10.1038/nature17413openalex-snapshot
Tip-localized receptors control pollen tube growth and LURE sensing in Arabidopsis
inferredcites →https://doi.org/10.1038/ncb1238openalex-snapshot
Plant formin AtFH5 is an evolutionarily conserved actin nucleator involved in cytokinesis
inferredcites →https://doi.org/10.1038/s41467-020-16253-1openalex-snapshot
Plasma membrane H+-ATPases sustain pollen tube growth and fertilization
inferredcites →https://doi.org/10.1038/s41467-021-26827-2openalex-snapshot
MPK3- and MPK6-mediated VLN3 phosphorylation regulates actin dynamics during stomatal immunity in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00304.xopenalex-snapshot
A GFP‐mouse talin fusion protein labels plant actin filamentsin vivoand visualizes the actin cytoskeleton in growing pollen tubes
inferredcites →https://doi.org/10.1073/pnas.0810730105openalex-snapshot
Overlapping functions of the four class XI myosins in Arabidopsis growth, root hair elongation, and organelle motility
inferredcites →https://doi.org/10.1073/pnas.1008527107openalex-snapshot
A transmembrane formin nucleates subapical actin assembly and controls tip-focused growth in pollen tubes
inferredcites →https://doi.org/10.1073/pnas.1821639116openalex-snapshot
Mechanism of CAP1-mediated apical actin polymerization in pollen tubes
inferredcites →https://doi.org/10.1074/jbc.m116.730069openalex-snapshot
The Structurally Plastic CH2 Domain Is Linked to Distinct Functions of Fimbrins/Plastins
inferredcites →https://doi.org/10.1074/jbc.m312973200openalex-snapshot
A Gelsolin-like Protein from Papaver rhoeas Pollen (PrABP80) Stimulates Calcium-regulated Severing and Depolymerization of Actin Filaments
inferredcites →https://doi.org/10.1083/jcb.136.6.1307openalex-snapshot
Actin Depolymerizing Factor (ADF/Cofilin) Enhances the Rate of Filament Turnover: Implication in Actin-based Motility
inferredcites →https://doi.org/10.1083/jcb.145.2.317openalex-snapshot
Rac Homologues and Compartmentalized Phosphatidylinositol 4, 5-Bisphosphate Act in a Common Pathway to Regulate Polar Pollen Tube Growth
inferredcites →https://doi.org/10.1083/jcb.152.5.1019openalex-snapshot
ROP Gtpase–Dependent Dynamics of Tip-Localized F-Actin Controls Tip Growth in Pollen Tubes
inferredcites →https://doi.org/10.1083/jcb.200409140openalex-snapshot
A Rho family GTPase controls actin dynamics and tip growth via two counteracting downstream pathways in pollen tubes
inferredcites →https://doi.org/10.1083/jcb.200806185openalex-snapshot
Actin filament dynamics are dominated by rapid growth and severing activity in the Arabidopsis cortical array
inferredcites →https://doi.org/10.1091/mbc.12.8.2534openalex-snapshot
Actin Polymerization Is Essential for Pollen Tube Growth
inferredcites →https://doi.org/10.1091/mbc.e06-11-1041openalex-snapshot
Identification of Arabidopsis Cyclase-associated Protein 1 as the First Nucleotide Exchange Factor for Plant Actin
inferredcites →https://doi.org/10.1091/mbc.e14-10-1482openalex-snapshot
Navigating the plant cell: intracellular transport logistics in the green kingdom
inferredcites →https://doi.org/10.1093/emboj/cdg130openalex-snapshot
Higher plant myosin XI moves processively on actin with 35 nm steps at high velocity
inferredcites →https://doi.org/10.1093/jxb/erg035openalex-snapshot
ROP GTPase regulation of pollen tube growth through the dynamics of tip-localized F-actin
inferredcites →https://doi.org/10.1093/jxb/erl122openalex-snapshot
Structural and functional compartmentalization in pollen tubes
inferredcites →https://doi.org/10.1093/jxb/erq012openalex-snapshot
Regulation of actin dynamics by actin-binding proteins in pollen
inferredcites →https://doi.org/10.1093/jxb/erw160openalex-snapshot
Arabidopsis FIM5 decorates apical actin filaments and regulates their organization in the pollen tube
inferredcites →https://doi.org/10.1093/jxb/erx195openalex-snapshot
Actin fringes of polar cell growth
inferredcites →https://doi.org/10.1093/mp/sss073openalex-snapshot
Actin Fringe Is Correlated with Tip Growth Velocity of Pollen Tubes
inferredcites →https://doi.org/10.1093/mp/sss101openalex-snapshot
Arabidopsis ROP1 and ROP6 Influence Germination Time, Root Morphology, the Formation of F-Actin Bundles, and Symbiotic Fungal Interactions
inferredcites →https://doi.org/10.1093/mp/sss103openalex-snapshot
AtPRK2 Promotes ROP1 Activation via RopGEFs in the Control of Polarized Pollen Tube Growth
inferredcites →https://doi.org/10.1093/mp/sst070openalex-snapshot
Signaling in Pollen Tube Growth: Crosstalk, Feedback, and Missing Links
inferredcites →https://doi.org/10.1093/pcp/pci185openalex-snapshot
Plant Villin, Lily P-135-ABP, Possesses G-Actin Binding Activity and Accelerates the Polymerization and Depolymerization of Actin in a Ca2+-Sensitive Manner
inferredcites →https://doi.org/10.1093/pcp/pcr068openalex-snapshot
Spatial and Temporal Expression of Actin Depolymerizing Factors ADF7 and ADF10 during Male Gametophyte Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/plcell/koab027openalex-snapshot
Profilin promotes formin-mediated actin filament assembly and vesicle transport during polarity formation in pollen
inferredcites →https://doi.org/10.1104/pp.013052openalex-snapshot
Analysis of the Small GTPase Gene Superfamily of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.113035openalex-snapshot
Pollen Tube Growth Oscillations and Intracellular Calcium Levels Are Reversibly Modulated by Actin Polymerization
inferredcites →https://doi.org/10.1104/pp.107.113654openalex-snapshot
Two Class XI Myosins Function in Organelle Trafficking and Root Hair Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.118604openalex-snapshot
An Actin-Binding Protein, LlLIM1, Mediates Calcium and Hydrogen Regulation of Actin Dynamics in Pollen Tubes
inferredcites →https://doi.org/10.1104/pp.108.120212openalex-snapshot
Magnitude and Direction of Vesicle Dynamics in Growing Pollen Tubes Using Spatiotemporal Image Correlation Spectroscopy and Fluorescence Recovery after Photobleaching
inferredcites →https://doi.org/10.1104/pp.114.242974openalex-snapshot
The Apical Actin Fringe Contributes to Localized Cell Wall Deposition and Polarized Growth in the Lily Pollen Tube
inferredcites →https://doi.org/10.1104/pp.114.244335openalex-snapshot
Arabidopsis Myosin XI: A Motor Rules the Tracks
inferredcites →https://doi.org/10.1104/pp.114.252742openalex-snapshot
Self-Incompatibility-Induced Programmed Cell Death in Field Poppy Pollen Involves Dramatic Acidification of the Incompatible Pollen Tube Cytosol
inferredcites →https://doi.org/10.1104/pp.124.3.959openalex-snapshot
Cell Surface Expansion in Polarly Growing Root Hairs ofMedicago truncatula
inferredcites →https://doi.org/10.1104/pp.15.01161openalex-snapshot
Class XI Myosins Move Specific Organelles in Pollen Tubes and are Required for Normal Fertility and Pollen Tube Growth in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.17.00753openalex-snapshot
F-Actin Mediated Focusing of Vesicles at the Cell Tip Is Essential for Polarized Growth
inferredcites →https://doi.org/10.1104/pp.17.01466openalex-snapshot
Interplay between Ions, the Cytoskeleton, and Cell Wall Properties during Tip Growth
inferredcites →https://doi.org/10.1104/pp.17.01519openalex-snapshot
The Actin Cytoskeleton: Functional Arrays for Cytoplasmic Organization and Cell Shape Control
inferredcites →https://doi.org/10.1104/pp.17.01759openalex-snapshot
Rice Morphology Determinant-Mediated Actin Filament Organization Contributes to Pollen Tube Growth
inferredcites →https://doi.org/10.1104/pp.19.01505openalex-snapshot
Durotropic Growth of Pollen Tubes
inferredcites →https://doi.org/10.1104/pp.20.00380openalex-snapshot
Quantitative Structural Organization of Bulk Apical Membrane Traffic in Pollen Tubes
inferredcites →https://doi.org/10.1105/tpc.002998openalex-snapshot
Signal-Mediated Depolymerization of Actin in Pollen during the Self-Incompatibility Response
inferredcites →https://doi.org/10.1105/tpc.003038openalex-snapshot
The Regulation of Actin Organization by Actin-Depolymerizing Factor in Elongating Pollen Tubes[W]
inferredcites →https://doi.org/10.1105/tpc.005363openalex-snapshot
Regulation of the Pollen-Specific Actin-Depolymerizing Factor LlADF1
inferredcites →https://doi.org/10.1105/tpc.007153openalex-snapshot
Actin-Depolymerizing Factor Mediates Rac/Rop GTPase–Regulated Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.010359openalex-snapshot
The Arabidopsis Rop2 GTPase Is a Positive Regulator of Both Root Hair Initiation and Tip Growth
inferredcites →https://doi.org/10.1105/tpc.104.028555openalex-snapshot
Arabidopsis VILLIN1 Generates Actin Filament Cables That Are Resistant to Depolymerization
inferredcites →https://doi.org/10.1105/tpc.106.044867openalex-snapshot
Oscillatory Increases in Alkalinity Anticipate Growth and May Regulate Actin Dynamics in Pollen Tubes of Lily
inferredcites →https://doi.org/10.1105/tpc.106.047423openalex-snapshot
Exclusion of a Proton ATPase from the Apical Membrane Is Associated with Cell Polarity and Tip Growth in Nicotiana tabacum Pollen Tubes
inferredcites →https://doi.org/10.1105/tpc.107.053413openalex-snapshot
Profilin Is Essential for Tip Growth in the MossPhyscomitrella patens
inferredcites →https://doi.org/10.1105/tpc.109.068700openalex-snapshot
ArabidopsisFormin3 Directs the Formation of Actin Cables and Polarized Growth in Pollen Tubes
inferredcites →https://doi.org/10.1105/tpc.109.073288openalex-snapshot
Myosin XI Is Essential for Tip Growth inPhyscomitrella patens
inferredcites →https://doi.org/10.1105/tpc.11.12.2349openalex-snapshot
Latrunculin B Has Different Effects on Pollen Germination and Tube Growth
inferredcites →https://doi.org/10.1105/tpc.11.9.1731openalex-snapshot
Control of Pollen Tube Tip Growth by a Rop GTPase–Dependent Pathway That Leads to Tip-Localized Calcium Influx
inferredcites →https://doi.org/10.1105/tpc.110.075960openalex-snapshot
Arabidopsis LIM Proteins: A Family of Actin Bundlers with Distinct Expression Patterns and Modes of Regulation
inferredcites →https://doi.org/10.1105/tpc.110.076257openalex-snapshot
ArabidopsisVILLIN5, an Actin Filament Bundling and Severing Protein, Is Necessary for Normal Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.110.080283openalex-snapshot
Arabidopsis FIMBRIN5, an Actin Bundling Factor, Is Required for Pollen Germination and Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.110.081349openalex-snapshot
RICE MORPHOLOGY DETERMINANTEncodes the Type II Formin FH5 and Regulates Rice Morphogenesis
inferredcites →https://doi.org/10.1105/tpc.110.081802openalex-snapshot
BENT UPPERMOST INTERNODE1Encodes the Class II Formin FH5 Crucial for Actin Organization and Rice Development
inferredcites →https://doi.org/10.1105/tpc.111.090753openalex-snapshot
Actin Interacting Protein1 and Actin Depolymerizing Factor Drive Rapid Actin Dynamics inPhyscomitrella patens
inferredcites →https://doi.org/10.1105/tpc.112.099358openalex-snapshot
FIMBRIN1 Is Involved in Lily Pollen Tube Growth by Stabilizing the Actin Fringe
inferredcites →https://doi.org/10.1105/tpc.113.110528openalex-snapshot
MAP18 Regulates the Direction of Pollen Tube Growth in Arabidopsis by Modulating F-Actin Organization
inferredcites →https://doi.org/10.1105/tpc.113.110940openalex-snapshot
Arabidopsis Villins Promote Actin Turnover at Pollen Tube Tips and Facilitate the Construction of Actin Collars
inferredcites →https://doi.org/10.1105/tpc.113.117820openalex-snapshot
Arabidopsis ACTIN-DEPOLYMERIZING FACTOR7 Severs Actin Filaments and Regulates Actin Cable Turnover to Promote Normal Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.113.119768openalex-snapshot
Arabidopsis Microtubule-Destabilizing Protein 25 Functions in Pollen Tube Growth by Severing Actin Filaments
inferredcites →https://doi.org/10.1105/tpc.114.127381openalex-snapshot
Overexpression of the Tomato Pollen Receptor Kinase LePRK1 Rewires Pollen Tube Growth to a Blebbing Mode
inferredcites →https://doi.org/10.1105/tpc.114.135400openalex-snapshot
Arabidopsis RIC1 Severs Actin Filaments at the Apex to Regulate Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.12.4.583openalex-snapshot
Maize Profilin Isoforms Are Functionally Distinct
inferredcites →https://doi.org/10.1105/tpc.16.00690openalex-snapshot
Plant Actin-Depolymerizing Factors Possess Opposing Biochemical Properties Arising from Key Amino Acid Changes throughout Evolution
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02388.xopenalex-snapshot
Kinase partner protein interacts with the LePRK1 and LePRK2 receptor kinases and plays a role in polarized pollen tube growth
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03451.xopenalex-snapshot
Actin depolymerizing factor is essential for viability in plants, and its phosphoregulation is important for tip growth
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05044.xopenalex-snapshot
Arabidopsis VILLIN2 and VILLIN3 act redundantly in sclerenchyma development via bundling of actin filaments
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.01979.xopenalex-snapshot
Actin organization and root hair development are disrupted by ethanol‐induced overexpression of Arabidopsis actin interacting protein 1 (AIP1)
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03632.xopenalex-snapshot
Arabidopsis VILLIN4 is involved in root hair growth through regulating actin organization in a Ca2+‐dependent manner
inferredcites →https://doi.org/10.1111/j.1744-7909.2009.00850.xopenalex-snapshot
Regulation of Actin Dynamics in Pollen Tubes: Control of Actin Polymer Level
inferredcites →https://doi.org/10.1111/jipb.12289openalex-snapshot
Organelle trafficking, the cytoskeleton, and pollen tube growth
inferredcites →https://doi.org/10.1111/jipb.12293openalex-snapshot
Plant villins: Versatile actin regulatory proteins
inferredcites →https://doi.org/10.1111/jipb.12315openalex-snapshot
The pollen tube clear zone: Clues to the mechanism of polarized growth
inferredcites →https://doi.org/10.1111/jipb.12642openalex-snapshot
Calcium imaging in Arabidopsis pollen cells using G‐CaMP5
inferredcites →https://doi.org/10.1111/jipb.12981openalex-snapshot
Plasma membrane H+‐ATPases‐mediated cytosolic proton gradient regulates pollen tube growth
inferredcites →https://doi.org/10.1111/nph.14395openalex-snapshot
Ll FH 1‐mediated interaction between actin fringe and exocytic vesicles is involved in pollen tube tip growth
inferredcites →https://doi.org/10.1111/nph.14745openalex-snapshot
Actin–membrane interactions mediated by NETWORKED 2 in Arabidopsis pollen tubes through associations with Pollen Receptor‐Like Kinase 4 and 5
inferredcites →https://doi.org/10.1111/nph.17391openalex-snapshot
NETWORKED2‐subfamily proteins regulate the cortical actin cytoskeleton of growing pollen tubes and polarised pollen tube growth
inferredcites →https://doi.org/10.1111/tpj.12039openalex-snapshot
Apical myosin XI anticipates F ‐actin during polarized growth of P hyscomitrella patens cells
inferredcites →https://doi.org/10.1111/tpj.12065openalex-snapshot
Oryza sativa actin‐interacting protein 1 is required for rice growth by promoting actin turnover
inferredcites →https://doi.org/10.1111/tpj.12910openalex-snapshot
Arabidopsis ACT 11 modifies actin turnover to promote pollen germination and maintain the normal rate of tube growth
inferredcites →https://doi.org/10.1111/tpj.13668openalex-snapshot
Monomeric G‐actin is uniformly distributed in pollen tubes and is rapidly redistributed via cytoplasmic streaming during pollen tube growth
inferredcites →https://doi.org/10.1111/tpj.15030openalex-snapshot
Organelle movement and apical accumulation of secretory vesicles in pollen tubes ofArabidopsis thalianadepend on class XI myosins
inferredcites →https://doi.org/10.1111/tpj.15505openalex-snapshot
Myosin XI‐B is involved in the transport of vesicles and organelles in pollen tubes of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.15723openalex-snapshot
Functional non‐equivalence of pollen ADF isovariants in Arabidopsis
inferredcites →https://doi.org/10.1126/science.279.5350.509openalex-snapshot
Rho GTPases and the Actin Cytoskeleton
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120150openalex-snapshot
Growth Mechanisms in Tip-Growing Plant Cells
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-100133openalex-snapshot
A Fruitful Journey: Pollen Tube Navigation from Germination to Fertilization
inferredcites →https://doi.org/10.1146/annurev.arplant.48.1.461openalex-snapshot
POLLEN GERMINATION AND TUBE GROWTH
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092921openalex-snapshot
Structural and Signaling Networks for the Polar Cell Growth Machinery in Pollen Tubes
inferredcites →https://doi.org/10.1146/annurev.cellbio.23.090506.123233openalex-snapshot
Cell Polarity Signaling in Arabidopsis
inferredcites →https://doi.org/10.1186/gb-2001-2-7-research0024openalex-snapshot
Analysis of the myosins encoded in the recently completed Arabidopsis thaliana genome sequence
inferredcites →https://doi.org/10.1186/gb-2002-3-5-reviews3007openalex-snapshot
The ADF/cofilin family: actin-remodeling proteins.
inferredcites →https://doi.org/10.1242/jcs.207738openalex-snapshot
ADF10 shapes the overall organization of apical actin filaments by promoting their turnover and ordering in pollen tubes
inferredcites →https://doi.org/10.1242/jcs.237404openalex-snapshot
Villin controls the formation and enlargement of punctate actin foci in pollen tubes
inferredcites →https://doi.org/10.1371/journal.pgen.1007789openalex-snapshot
Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
inferredcites →https://doi.org/10.1371/journal.pone.0001074openalex-snapshot
A Mutation in MRH2 Kinesin Enhances the Root Hair Tip Growth Defect Caused by Constitutively Activated ROP2 Small GTPase in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0005744openalex-snapshot
Lifeact-mEGFP Reveals a Dynamic Apical F-Actin Network in Tip Growing Plant Cells
inferredcites →https://doi.org/10.1371/journal.pone.0076745openalex-snapshot
Myosin XIK of Arabidopsis thaliana Accumulates at the Root Hair Tip and Is Required for Fast Root Hair Growth
inferredcites →https://doi.org/10.3389/fcell.2020.614821openalex-snapshot
Control of the Actin Cytoskeleton Within Apical and Subapical Regions of Pollen Tubes
inferredcites →https://doi.org/10.3389/fcell.2020.615447openalex-snapshot
Secretory Vesicles Targeted to Plasma Membrane During Pollen Germination and Tube Growth
inferredcites →https://doi.org/10.3389/fpls.2014.00786openalex-snapshot
Organization and regulation of the actin cytoskeleton in the pollen tube
inferredcites →https://doi.org/10.3389/fpls.2017.01349openalex-snapshot
Direct Comparison of the Performance of Commonly Employed In Vivo F-actin Markers (Lifeact-YFP, YFP-mTn and YFP-FABD2) in Tobacco Pollen Tubes
inferredcites →https://doi.org/10.3389/fpls.2020.589712openalex-snapshot
Mechanics of Pollen Tube Elongation: A Perspective
inferredcites →https://doi.org/10.3389/fpls.2021.599961openalex-snapshot
The Arabidopsis thaliana Class II Formin FH13 Modulates Pollen Tube Growth
inferredcites →https://doi.org/10.3390/ijms19113529openalex-snapshot
The Long Journey of Pollen Tube in the Pistil
inferredcites →https://doi.org/10.3390/plants9091098openalex-snapshot
Signalling Pinpointed to the Tip: The Complex Regulatory Network That Allows Pollen Tube Growth
inferredcites →https://doi.org/10.4161/cam.5.2.14403openalex-snapshot
Dynamics of the Rho-family small GTPases in actin regulation and motility
inferredcites →https://doi.org/10.4161/psb.20436openalex-snapshot
Actin depolymerizing factors ADF7 and ADF10 play distinct roles during pollen development and pollen tube growth
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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AtHMGB15 regulates tapetal apoptosis in pollen development and actin dynamics during pollen germination in arabidopsis
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inferred← citeshttps://doi.org/10.1038/s41467-025-58869-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1073/pnas.2410607121openalex-snapshot
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inferred← citeshttps://doi.org/10.1083/jcb.202206074openalex-snapshot
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inferred← citeshttps://doi.org/10.1083/jcb.202310012openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jxb/erae078openalex-snapshot
Transmembrane formins as active cargoes of membrane trafficking
inferred← citeshttps://doi.org/10.1093/jxb/erae387openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jxb/erag040openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jxb/erag298openalex-snapshot
SNAP30 forms a SNARE complex with VAMP726 and SYP131, and mediates vesicle secretion at the plasma membrane of the Arabidopsis pollen tube tip
inferred← citeshttps://doi.org/10.1093/plphys/kiad436openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/plphys/kiae087openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.70760openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/jcs.261920openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/jcs.262068openalex-snapshot
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inferred← citeshttps://doi.org/10.24180/ijaws.1388346openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms26052348openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants14010072openalex-snapshot
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inferred← citeshttps://doi.org/10.48130/seedbio-0024-0014openalex-snapshot
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