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Vesicular trafficking, cytoskeleton and signalling in root hairs and pollen tubes

https://doi.org/10.1016/j.tplants.2006.10.002

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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/cm.20024openalex-snapshot

Green fluorescent protein fusions to Arabidopsis fimbrin 1 for spatio‐temporal imaging of F‐actin dynamics in roots

inferredcites →https://doi.org/10.1007/978-4-431-68370-4_1openalex-snapshot

Root Hair Ultrastructure and Tip Growth

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/s00497-005-0008-yopenalex-snapshot

Growth and development of conifer pollen tubes

inferredcites →https://doi.org/10.1007/s00497-006-0021-9openalex-snapshot

Imaging the actin cytoskeleton in growing pollen tubes

inferredcites →https://doi.org/10.1007/s00497-006-0024-6openalex-snapshot

Rop1Ps promote actin cytoskeleton dynamics and control the tip growth of lily pollen tube

inferredcites →https://doi.org/10.1007/s00709-005-0103-9openalex-snapshot

Endocytosis and vesicle trafficking during tip growth of root hairs

inferredcites →https://doi.org/10.1007/s00709-005-0132-4openalex-snapshot

Disturbance of endomembrane trafficking by brefeldin A and calyculin A reorganizes the actin cytoskeleton of Lilium longiflorum pollen tubes

inferredcites →https://doi.org/10.1016/j.devcel.2005.11.015openalex-snapshot

Endocytosis of Cell Surface Material Mediates Cell Plate Formation during Plant Cytokinesis

inferredcites →https://doi.org/10.1016/j.ejcb.2004.11.011openalex-snapshot

GFP-FABD2 fusion construct allows in vivo visualization of the dynamic actin cytoskeleton in all cells of Arabidopsis seedlings

inferredcites →https://doi.org/10.1016/j.ejcb.2004.12.029openalex-snapshot

Actin-based motility of endosomes is linked to the polar tip growth of root hairs

inferredcites →https://doi.org/10.1016/j.tcb.2005.06.006openalex-snapshot

The endocytic network in plants

inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot

Reactive oxygen species produced by NADPH oxidase regulate plant cell growth

inferredcites →https://doi.org/10.1038/nature02353openalex-snapshot

OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis

inferredcites →https://doi.org/10.1038/nature04198openalex-snapshot

A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells

inferredcites →https://doi.org/10.1038/nature04491openalex-snapshot

Compartmentalization of S-RNase and HT-B degradation in self-incompatible Nicotiana

inferredcites →https://doi.org/10.1038/sj.emboj.7600068openalex-snapshot

A protein kinase target of a PDK1 signalling pathway is involved in root hair growth in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01290.xopenalex-snapshot

The IRE gene encodes a protein kinase homologue and modulates root hair growth in Arabidopsis

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.200412074openalex-snapshot

A Sec14p-nodulin domain phosphatidylinositol transfer protein polarizes membrane growth of Arabidopsis thaliana root hairs

inferredcites →https://doi.org/10.1083/jcb.200508116openalex-snapshot

A role for the RabA4b effector protein PI-4Kβ1 in polarized expansion of root hair cells in Arabidopsis thaliana

inferredcites →https://doi.org/10.1091/mbc.e04-07-0562openalex-snapshot

Ectopic Expression of an Activated RAC inArabidopsisDisrupts Membrane Cycling

inferredcites →https://doi.org/10.1093/emboj/20.11.2779openalex-snapshot

Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth

inferredcites →https://doi.org/10.1093/emboj/cdf349openalex-snapshot

Involvement of the mitogen‐activated protein kinase SIMK in regulation of root hair tip growth

inferredcites →https://doi.org/10.1093/jxb/eri256openalex-snapshot

Calcium gradients in conifer pollen tubes; dynamic properties differ from those seen in angiosperms

inferredcites →https://doi.org/10.1104/pp.005777openalex-snapshot

ACTIN2 Is Essential for Bulge Site Selection and Tip Growth during Root Hair Development of Arabidopsis

inferredcites →https://doi.org/10.1104/pp.104.040683openalex-snapshot

Endocytosis, Actin Cytoskeleton, and Signaling

inferredcites →https://doi.org/10.1104/pp.104.045427openalex-snapshot

A Role of Arabidopsis Inositol Polyphosphate Kinase, AtIPK2α, in Pollen Germination and Root Growth

inferredcites →https://doi.org/10.1104/pp.105.069765openalex-snapshot

Effects of Brefeldin A on Pollen Germination and Tube Growth. Antagonistic Effects on Endocytosis and Secretion

inferredcites →https://doi.org/10.1104/pp.106.077818openalex-snapshot

RPA, a Class II ARFGAP Protein, Activates ARF1 and U5 and Plays a Role in Root Hair Development in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.106.080168openalex-snapshot

Imaging of Dynamic Secretory Vesicles in Living Pollen Tubes of Picea meyeri Using Evanescent Wave Microscopy

inferredcites →https://doi.org/10.1104/pp.106.081703openalex-snapshot

Roles of the Ubiquitin/Proteasome Pathway in Pollen Tube Growth with Emphasis on MG132-Induced Alterations in Ultrastructure, Cytoskeleton, and Cell Wall Components

inferredcites →https://doi.org/10.1105/tpc.001248openalex-snapshot

hydra Mutants of Arabidopsis Are Defective in Sterol Profiles and Auxin and Ethylene Signaling

inferredcites →https://doi.org/10.1105/tpc.001537openalex-snapshot

The ROP2 GTPase Controls the Formation of Cortical Fine F-Actin and the Early Phase of Directional Cell Expansion during Arabidopsis Organogenesis

inferredcites →https://doi.org/10.1105/tpc.008433openalex-snapshot

Cell Polarity and PIN Protein Positioning in Arabidopsis Require STEROL METHYLTRANSFERASE1 Function

inferredcites →https://doi.org/10.1105/tpc.010218openalex-snapshot

A Genome-Wide Analysis of Arabidopsis Rop-Interactive CRIB Motif–Containing Proteins That Act as Rop GTPase Targets

inferredcites →https://doi.org/10.1105/tpc.010339openalex-snapshot

Uptake of a Fluorescent Marker in Plant Cells Is Sensitive to Brefeldin A and Wortmannin

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.019703openalex-snapshot

Identification of Multivesicular Bodies as Prevacuolar Compartments in Nicotiana tabacum BY-2 Cells[W]

inferredcites →https://doi.org/10.1105/tpc.021634openalex-snapshot

The Arabidopsis Rab GTPase RabA4b Localizes to the Tips of Growing Root Hair Cells[W]

inferredcites →https://doi.org/10.1105/tpc.104.028449openalex-snapshot

Dissection of Arabidopsis ADP-RIBOSYLATION FACTOR 1 Function in Epidermal Cell Polarity

inferredcites →https://doi.org/10.1105/tpc.105.032508openalex-snapshot

Calcium: A Central Regulator of Plant Growth and Development

inferredcites →https://doi.org/10.1105/tpc.105.033183openalex-snapshot

Rab11 GTPase-Regulated Membrane Trafficking Is Crucial for Tip-Focused Pollen Tube Growth in Tobacco

inferredcites →https://doi.org/10.1105/tpc.105.035394openalex-snapshot

RNA Interference Identifies a Calcium-Dependent Protein Kinase Involved inMedicago truncatulaRoot Development

inferredcites →https://doi.org/10.1105/tpc.105.036434openalex-snapshot

Members of a Novel Class of Arabidopsis Rho Guanine Nucleotide Exchange Factors Control Rho GTPase-Dependent Polar Growth

inferredcites →https://doi.org/10.1105/tpc.105.037135openalex-snapshot

Calcium-Dependent Protein Kinase Isoforms inPetuniaHave Distinct Functions in Pollen Tube Growth, Including Regulating Polarity

inferredcites →https://doi.org/10.1105/tpc.105.037978openalex-snapshot

Vacuolar H+-ATPase Activity Is Required for Endocytic and Secretory Trafficking in Arabidopsis

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.13.12.2841openalex-snapshot

A Genome-Wide Analysis of Arabidopsis Rop-Interactive CRIB Motif-Containing Proteins That Act as Rop GTPase Targets

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02091.xopenalex-snapshot

Calmodulin activity and cAMP signalling modulate growth and apical secretion in pollen tubes

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02245.xopenalex-snapshot

The Arabidopsis COW1 gene encodes a phosphatidylinositol transfer protein essential for root hair tip growth

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02609.xopenalex-snapshot

Analysis of the root‐hair morphogenesis transcriptome reveals the molecular identity of six genes with roles in root‐hair development in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02757.xopenalex-snapshot

Nt‐RhoGDI2 regulates Rac/Rop signaling and polar cell growth in tobacco pollen tubes

inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02783.xopenalex-snapshot

Differential display proteomic analysis of Picea meyeri pollen germination and pollen‐tube growth after inhibition of actin polymerization by latrunculin B

inferredcites →https://doi.org/10.1111/j.1600-0854.2005.00372.xopenalex-snapshot

Compound Exocytosis: Mechanisms and Functional Significance

inferredcites →https://doi.org/10.1146/annurev.cellbio.17.1.159openalex-snapshot

Polarized Cell Growth in Higher Plants

inferredcites →https://doi.org/10.1186/1471-2229-6-5openalex-snapshot

Polarization of the endomembrane system is an early event in fucoid zygote development

inferredcites →https://doi.org/10.1242/jcs.00468openalex-snapshot

Pollen tubes exhibit regular periodic membrane trafficking events in the absence of apical extension

inferredcites →https://doi.org/10.1242/jcs.114.14.2685openalex-snapshot

Dynamics of the apical vesicle accumulation and the rate of growth are related in individual pollen tubes

inferredcites →https://doi.org/10.4161/psb.1.3.2996openalex-snapshot

Fine Structural Analysis of Brefeldin A-Induced Compartment Formation After High-Pressure Freeze Fixation of Maize Root Epidermis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Spatial and temporal integration of signalling networks regulating pollen tube growth

inferred← citeshttps://doi.org/10.1093/jxb/ers023openalex-snapshot

The pollen-specific R-SNARE/longin PiVAMP726 mediates fusion of endo- and exocytic compartments in pollen tube tip growth

inferred← citeshttps://doi.org/10.1093/jxb/ers166openalex-snapshot

Nitric oxide is essential for vesicle formation and trafficking in Arabidopsis root hair growth

inferred← citeshttps://doi.org/10.1093/jxb/eru412openalex-snapshot

Rab geranylgeranyl transferase β subunit is essential for male fertility and tip growth in Arabidopsis

inferred← citeshttps://doi.org/10.1093/mp/ssn051openalex-snapshot

RIP1 (ROP Interactive Partner 1)/ICR1 Marks Pollen Germination Sites and May Act in the ROP1 Pathway in the Control of Polarized Pollen Growth

inferred← citeshttps://doi.org/10.1093/mp/ssp086openalex-snapshot

Ubiquitin-Specific Protease 14 (UBP14) Is Involved in Root Responses to Phosphate Deficiency in Arabidopsis

inferred← citeshttps://doi.org/10.1093/mp/ssr011openalex-snapshot

Vacuolar Sorting Receptor (VSR) Proteins Reach the Plasma Membrane in Germinating Pollen Tubes

inferred← citeshttps://doi.org/10.1093/mp/sss071openalex-snapshot

NAD+ Accumulation during Pollen Maturation in Arabidopsis Regulating Onset of Germination

inferred← citeshttps://doi.org/10.1093/mp/sst103openalex-snapshot

Control of Cell Wall Extensibility during Pollen Tube Growth

inferred← citeshttps://doi.org/10.1093/pcp/pcn197openalex-snapshot

Differential Expression Control and Polarized Distribution of Plasma Membrane-Resident SYP1 SNAREs in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/pcp/pct014openalex-snapshot

Evidence that Proliferation of Golgi Apparatus Depends on Both De Novo Generation from the Endoplasmic Reticulum and Formation from Pre-Existing Stacks During the Growth of Tobacco BY-2 Cells

inferred← citeshttps://doi.org/10.1093/pcp/pcu018openalex-snapshot

Multiple BiP Genes of Arabidopsis thaliana are Required for Male Gametogenesis and Pollen Competitiveness

inferred← citeshttps://doi.org/10.1093/pcp/pcu048openalex-snapshot

Syntaxin of Plant Proteins SYP123 and SYP132 Mediate Root Hair Tip Growth in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/pcp/pcx138openalex-snapshot

Fimbrins 4 and 5 Act Synergistically During Polarized Pollen Tube Growth to Ensure Fertility in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koab131openalex-snapshot

LARP6C orchestrates posttranscriptional reprogramming of gene expression during hydration to promote pollen tube guidance

inferred← citeshttps://doi.org/10.1093/plcell/koad240openalex-snapshot

The SYP123–VAMP727 SNARE complex delivers secondary cell wall components for root hair shank hardening in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koad280openalex-snapshot

Evolution of the thermostability of actin-depolymerizing factors enhances the adaptation of pollen germination to high temperature

inferred← citeshttps://doi.org/10.1093/plphys/kiab595openalex-snapshot

ROOT HAIR DEFECTIVE 2 vesicular delivery to the apical plasma membrane domain during Arabidopsis root hair development

inferred← citeshttps://doi.org/10.1093/plphys/kiad203openalex-snapshot

Actin cytoskeleton in the control of vesicle transport, cytoplasmic organization, and pollen tube tip growth

inferred← citeshttps://doi.org/10.1093/plphys/kiad484openalex-snapshot

Spatiotemporal distribution of reactive oxygen species production, delivery, and use in Arabidopsis root hairs

inferred← citeshttps://doi.org/10.1093/plphys/kiaf659openalex-snapshot

RACK1A interacts and colocalizes with FSD1 in stress granules to regulate salt stress response in Arabidopsis

inferred← citeshttps://doi.org/10.1094/mpmi-08-10-0181openalex-snapshot

Invasion by Invitation: Rhizobial Infection in Legumes

inferred← citeshttps://doi.org/10.1094/mpmi-12-17-0289-ropenalex-snapshot

SNARE-Encoding Genes VdSec22 and VdSso1 Mediate Protein Secretion Required for Full Virulence in Verticillium dahliae

inferred← citeshttps://doi.org/10.1094/mpmi-22-6-0703openalex-snapshot

Multiple Activities of the Plant Pathogen Type III Effector Proteins WtsE and AvrE Require WxxxE Motifs

inferred← citeshttps://doi.org/10.1098/rsob.160028openalex-snapshot

NADPH oxidases as electrochemical generators to produce ion fluxes and turgor in fungi, plants and humans

inferred← citeshttps://doi.org/10.1101/2022.01.10.475584openalex-snapshot

Cell surface receptor kinase FERONIA linked to nutrient sensor TORC signaling controls root hair growth at low temperature linked to low nitrate in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1101/2023.01.05.522872openalex-snapshot

Spatiotemporal distribution of ROS production, delivery and utilization in Arabidopsis root hairs

inferred← citeshttps://doi.org/10.1101/2025.02.25.640159openalex-snapshot

Protein and genetic interactions between RACK1A and FSD1 modulate plant development and stress granule-dependent response to salt in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.107.102863openalex-snapshot

Molecular Dissection of Endosomal Compartments in Plants

inferred← citeshttps://doi.org/10.1104/pp.108.118604openalex-snapshot

An Actin-Binding Protein, LlLIM1, Mediates Calcium and Hydrogen Regulation of Actin Dynamics in Pollen Tubes

inferred← citeshttps://doi.org/10.1104/pp.108.119529openalex-snapshot

A Class I ADP-Ribosylation Factor GTPase-Activating Protein Is Critical for Maintaining Directional Root Hair Growth in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.108.120105openalex-snapshot

The Endosomal System of Plants: Charting New and Familiar Territories

inferred← citeshttps://doi.org/10.1104/pp.108.122226openalex-snapshot

ThePRA1Gene Family in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.108.127514openalex-snapshot

Combined Proteomic and Cytological Analysis of Ca2+-Calmodulin Regulation in Picea meyeri Pollen Tube Growth

inferred← citeshttps://doi.org/10.1104/pp.108.131649openalex-snapshot

Establishment of a Protein Reference Map for Soybean Root Hair Cells

inferred← citeshttps://doi.org/10.1104/pp.109.142349openalex-snapshot

Interdependence of Endomembrane Trafficking and Actin Dynamics during Polarized Growth of Arabidopsis Pollen Tubes

inferred← citeshttps://doi.org/10.1104/pp.109.146159openalex-snapshot

Arabidopsis FAB1/PIKfyve Proteins Are Essential for Development of Viable Pollen

inferred← citeshttps://doi.org/10.1104/pp.109.148700openalex-snapshot

A Systems Model of Vesicle Trafficking in Arabidopsis Pollen Tubes

inferred← citeshttps://doi.org/10.1104/pp.19.00180openalex-snapshot

Two Pathways for Trafficking the Borate Receptor BOR1

inferred← citeshttps://doi.org/10.1104/pp.20.00380openalex-snapshot

Quantitative Structural Organization of Bulk Apical Membrane Traffic in Pollen Tubes

inferred← citeshttps://doi.org/10.1105/tpc.107.052621openalex-snapshot

Class-Specific Interaction of Profilin and ADF Isovariants with Actin in the Regulation of Plant Development

inferred← citeshttps://doi.org/10.1105/tpc.108.059428openalex-snapshot

Dynamics of Arabidopsis Dynamin-Related Protein 1C and a Clathrin Light Chain at the Plasma Membrane

inferred← citeshttps://doi.org/10.1105/tpc.108.063420openalex-snapshot

A Small GTPase of the Rab Family Is Required for Root Hair Formation and Preinfection Stages of the Common Bean–RhizobiumSymbiotic Association

inferred← citeshttps://doi.org/10.1105/tpc.108.063693openalex-snapshot

Rearrangement of Actin Cytoskeleton Mediates Invasion of Lotus japonicus Roots by Mesorhizobium loti

inferred← citeshttps://doi.org/10.1105/tpc.109.069880openalex-snapshot

Structural Sterols Are Involved in Both the Initiation and Tip Growth of Root Hairs inArabidopsis thaliana

inferred← citeshttps://doi.org/10.1105/tpc.110.079426openalex-snapshot

The Arabidopsis Intracellular Na+/H+ Antiporters NHX5 and NHX6 Are Endosome Associated and Necessary for Plant Growth and Development

inferred← citeshttps://doi.org/10.1105/tpc.113.118273openalex-snapshot

Actin-Dependent and -Independent Functions of Cortical Microtubules in the Differentiation ofArabidopsisLeaf Trichomes

inferred← citeshttps://doi.org/10.1105/tpc.20.00109openalex-snapshot

SPIKE1 Activates the GTPase ROP6 to Guide the Polarized Growth of Infection Threads in Lotus japonicus

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2008.03743.xopenalex-snapshot

Extracellular transport and integration of plant secretory proteins into pathogen‐induced cell wall compartments

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2009.03954.xopenalex-snapshot

IRREGULAR TRICHOME BRANCH 2 (ITB2) encodes a putative aminophospholipid translocase that regulates trichome branch elongation in Arabidopsis

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2009.04007.xopenalex-snapshot

BFA‐induced compartments from the Golgi apparatus and trans‐Golgi network/early endosome are distinct in plant cells

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2009.04111.xopenalex-snapshot

Vacuolar sorting receptors (VSRs) and secretory carrier membrane proteins (SCAMPs) are essential for pollen tube growth

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04856.xopenalex-snapshot

AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity

inferred← citeshttps://doi.org/10.1111/j.1438-8677.2010.00413.xopenalex-snapshot

Actin‐dependent deposition of putative endosomes and endoplasmic reticulum during early stages of wound healing in characean internodal cells

inferred← citeshttps://doi.org/10.1111/j.1467-7652.2008.00367.xopenalex-snapshot

Down‐regulation of GhADF1 gene expression affects cotton fibre properties

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02444.xopenalex-snapshot

NtGNL1 is involved in embryonic cell division patterning, root elongation, and pollen tube growth in tobacco

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02457.xopenalex-snapshot

Diverse cell signalling pathways regulate pollen‐stigma interactions: the search for consensus

inferred← citeshttps://doi.org/10.1111/j.1529-8817.2009.00713.xopenalex-snapshot

CELL‐WALL DEVELOPMENT AND BIPOLAR GROWTH IN THE DESMID PENIUM MARGARITACEUM (ZYGNEMATOPHYCEAE, STREPTOPHYTA). ASYMMETRY IN A SYMMETRIC WORLD1

inferred← citeshttps://doi.org/10.1111/j.1600-0854.2008.00773.xopenalex-snapshot

The Plant ER–Golgi Interface

inferred← citeshttps://doi.org/10.1111/j.1672-9072.2007.00520.xopenalex-snapshot

Diversification of the RAB Guanosine Triphosphatase Family in Dicots and Monocots

inferred← citeshttps://doi.org/10.1111/j.1672-9072.2007.00546.xopenalex-snapshot

The Villin/Gelsolin/Fragmin Superfamily Proteins in Plants

inferred← citeshttps://doi.org/10.1111/j.1744-7909.2011.01059.xopenalex-snapshot

Adenosine Diphosphate Ribosylation Factor-GTPase-Activating Protein Stimulates the Transport of AUX1 Endosome, Which Relies on Actin Cytoskeletal Organization in Rice Root Development

inferred← citeshttps://doi.org/10.1111/jipb.12315openalex-snapshot

The pollen tube clear zone: Clues to the mechanism of polarized growth

inferred← citeshttps://doi.org/10.1111/jipb.12459openalex-snapshot

AtTMEM18 plays important roles in pollen tube and vegetative growth in Arabidopsis

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1111/nph.18723openalex-snapshot

Cell surface receptor kinase FERONIA linked to nutrient sensor TORC signaling controls root hair growth at low temperature linked to low nitrate in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1111/tpj.12206openalex-snapshot

Developmental transcriptional profiling reveals key insights into T riticeae reproductive development

inferred← citeshttps://doi.org/10.1111/tpj.15086openalex-snapshot

The AGCVIII kinase Dw2 modulates cell proliferation, endomembrane trafficking, and MLG/xylan cell wall localization in elongating stem internodes of Sorghum bicolor

inferred← citeshttps://doi.org/10.1126/science.1152505openalex-snapshot

Local Positive Feedback Regulation Determines Cell Shape in Root Hair Cells

inferred← citeshttps://doi.org/10.1128/spectrum.01872-22openalex-snapshot

SNARE Protein DdVam7 of the Nematode-Trapping Fungus Drechslerella dactyloides Regulates Vegetative Growth, Conidiation, and the Predatory Process via Vacuole Assembly

inferred← citeshttps://doi.org/10.1134/s1021443712040085openalex-snapshot

Mechanisms and physiological role of polarity in plants

inferred← citeshttps://doi.org/10.1146/annurev-genet-110410-132549openalex-snapshot

The Rules of Engagement in the Legume-Rhizobial Symbiosis

inferred← citeshttps://doi.org/10.1146/annurev-phyto-072910-095426openalex-snapshot

The Pathogen-Actin Connection: A Platform for Defense Signaling in Plants

inferred← citeshttps://doi.org/10.1146/annurev.arplant.59.032607.092921openalex-snapshot

Structural and Signaling Networks for the Polar Cell Growth Machinery in Pollen Tubes

inferred← citeshttps://doi.org/10.1146/annurev.cellbio.23.090506.123233openalex-snapshot

Cell Polarity Signaling in Arabidopsis

inferred← citeshttps://doi.org/10.1186/s12870-014-0197-3openalex-snapshot

Transcriptional profiling of Arabidopsis root hairs and pollen defines an apical cell growth signature

inferred← citeshttps://doi.org/10.1186/s12870-014-0332-1openalex-snapshot

Patatin-related phospholipase pPLAIIIδ influences auxin-responsive cell morphology and organ size in Arabidopsis and Brassica napus

inferred← citeshttps://doi.org/10.1186/s12870-015-0441-5openalex-snapshot

Protein palmitoylation is critical for the polar growth of root hairs in Arabidopsis

inferred← citeshttps://doi.org/10.1186/s40529-017-0181-yopenalex-snapshot

Genome-wide characterization of the Rab gene family in Gossypium by comparative analysis

inferred← citeshttps://doi.org/10.1201/b18597-11openalex-snapshot

New Insights into the Role of Protein Prenylation and Processing in Plant Development, Phytohormone Signaling, and Secondary Metabolism

inferred← citeshttps://doi.org/10.1242/jcs.093559openalex-snapshot

Structure and function of endosomes in plant cells

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1371/journal.pone.0068681openalex-snapshot

Genome-Wide Identification, Phylogeny and Expression Profile of Vesicle Fusion Components in Verticillium dahliae

inferred← citeshttps://doi.org/10.1371/journal.pone.0076660openalex-snapshot

2, 6-dichlorobenzonitrile Causes Multiple Effects on Pollen Tube Growth beyond Altering Cellulose Synthesis in Pinus bungeana Zucc

inferred← citeshttps://doi.org/10.1515/nbec-2017-0003openalex-snapshot

Transient expression of green fluorescent protein in parasitic dodder as a tool for studying of cytoskeleton

inferred← citeshttps://doi.org/10.2147/chc.s57108openalex-snapshot

Cytoskeleton and Golgi-apparatus interactions: a two-way road of function and structure

inferred← citeshttps://doi.org/10.2478/v10052-010-0003-9openalex-snapshot

Pollen Transcriptome and Proteome: Molecular and Functional Analysis

inferred← citeshttps://doi.org/10.3109/10409238.2013.853024openalex-snapshot

Cinderella story: PI4P goes from precursor to key signaling molecule

inferred← citeshttps://doi.org/10.3389/fcell.2020.614821openalex-snapshot

Control of the Actin Cytoskeleton Within Apical and Subapical Regions of Pollen Tubes

inferred← citeshttps://doi.org/10.3389/fpls.2014.00120openalex-snapshot

Senescence and programmed cell death in plants: polyamine action mediated by transglutaminase

inferred← citeshttps://doi.org/10.3389/fpls.2014.00138openalex-snapshot

Callose homeostasis at plasmodesmata: molecular regulators and developmental relevance

inferred← citeshttps://doi.org/10.3389/fpls.2015.00131openalex-snapshot

Considerations for designing chemical screening strategies in plant biology

inferred← citeshttps://doi.org/10.3389/fpls.2015.00246openalex-snapshot

Knockin' on pollen's door: live cell imaging of early polarization events in germinating Arabidopsis pollen

inferred← citeshttps://doi.org/10.3389/fpls.2015.01262openalex-snapshot

Endosomal Interactions during Root Hair Growth

inferred← citeshttps://doi.org/10.3389/fpls.2017.00201openalex-snapshot

Interface Symbiotic Membrane Formation in Root Nodules of Medicago truncatula: the Role of Synaptotagmins MtSyt1, MtSyt2 and MtSyt3

inferred← citeshttps://doi.org/10.3389/fpls.2021.666229openalex-snapshot

TALEN-Based HvMPK3 Knock-Out Attenuates Proteome and Root Hair Phenotypic Responses to flg22 in Barley

inferred← citeshttps://doi.org/10.3389/fpls.2023.1120307openalex-snapshot

VPS45 is required for both diffuse and tip growth of Arabidopsis thaliana cells

inferred← citeshttps://doi.org/10.3390/cells9092016openalex-snapshot

Regulation and Functions of ROP GTPases in Plant–Microbe Interactions

inferred← citeshttps://doi.org/10.3390/genes13020193openalex-snapshot

MtWRP1, a Novel Fabacean Specific Gene, Regulates Root Nodulation and Plant Growth in Medicago truncatula

inferred← citeshttps://doi.org/10.3390/ijms22179642openalex-snapshot

Tissue-Specific Proteome and Subcellular Microscopic Analyses Reveal the Effect of High Salt Concentration on Actin Cytoskeleton and Vacuolization in Aleurone Cells during Early Germination of Barley

inferred← citeshttps://doi.org/10.3390/ijms222212212openalex-snapshot

A Decade of Pollen Phosphoproteomics

inferred← citeshttps://doi.org/10.3390/ijms24010126openalex-snapshot

Genome-Wide Analysis of the Rab Gene Family in Melilotus albus Reveals Their Role in Salt Tolerance

inferred← citeshttps://doi.org/10.3390/plants14121759openalex-snapshot

Protein Prenylation in Plants: Mechanisms and Functional Implications

inferred← citeshttps://doi.org/10.3390/plants2010148openalex-snapshot

Polar Expansion Dynamics in the Plant Kingdom: A Diverse and Multifunctional Journey on the Path to Pollen Tubes

inferred← citeshttps://doi.org/10.3390/plants2040650openalex-snapshot

Calcium: The Missing Link in Auxin Action

inferred← citeshttps://doi.org/10.3934/dcdss.2011.4.1429openalex-snapshot

Equilibrium submanifold for a biological system

inferred← citeshttps://doi.org/10.4161/psb.19669openalex-snapshot

Rapid endocytosis is triggered upon imbibition in Arabidopsis seeds

inferred← citeshttps://doi.org/10.4161/psb.6.11.17477openalex-snapshot

Emerging aspects of ER organization in root hair tip growth: Lessons from RHD3 and atlastin

inferred← citeshttps://doi.org/10.4238/vol9-2gmr768openalex-snapshot

Effects of low-energy argon ion implantation on the dynamic organization of the actin cytoskeleton during maize pollen germination

inferred← citeshttps://doi.org/10.4995/thesis/10251/202903openalex-snapshot

Los péptidos DEVIL: estudio de su papel en el control de la proliferación celular y la morfogénesis de las plantas

inferred← citeshttps://doi.org/10.70675/917f8984z2ee2z45e3z9c87zeab6272a42aaopenalex-snapshot

Biophysical and cellular mechanisms of tip-growth in the brown alga Ectocarpus sp.

inferred← citeshttps://doi.org/10.7273/000005793openalex-snapshot

Investigation into the functions of the pollen specific genes PiVAMP721 and PiSCP1 in pollen tube growth

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