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Keep in contact: multiple roles of endoplasmic reticulum–membrane contact sites and the organelle interaction network in plants

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00385355openalex-snapshot

Low and high voltage electron microscopy of mitosis and cytokinesis in maize roots

inferredcites →https://doi.org/10.1007/bf01281685openalex-snapshot

Stereology and stereometry of endoplasmic reticulum during differentiation in the maize root cap

inferredcites →https://doi.org/10.1007/bf01282070openalex-snapshot

Endoplasmic reticulum in the formation of the cell plate and plasmodesmata

inferredcites →https://doi.org/10.1007/s12192-017-0854-1openalex-snapshot

Gene encoding vesicle-associated membrane protein-associated protein from Triticum aestivum (TaVAP) confers tolerance to drought stress

inferredcites →https://doi.org/10.1016/j.ceb.2006.06.011openalex-snapshot

Inter-organelle membrane contact sites: through a glass, darkly

inferredcites →https://doi.org/10.1016/j.cell.2005.11.047openalex-snapshot

A Class of Membrane Proteins Shaping the Tubular Endoplasmic Reticulum

inferredcites →https://doi.org/10.1016/j.cell.2006.07.019openalex-snapshot

Rough Sheets and Smooth Tubules

inferredcites →https://doi.org/10.1016/j.cell.2009.05.025openalex-snapshot

A Class of Dynamin-like GTPases Involved in the Generation of the Tubular ER Network

inferredcites →https://doi.org/10.1016/j.cell.2010.12.034openalex-snapshot

Osh Proteins Regulate Phosphoinositide Metabolism at ER-Plasma Membrane Contact Sites

inferredcites →https://doi.org/10.1016/j.cell.2013.06.031openalex-snapshot

Stacked Endoplasmic Reticulum Sheets Are Connected by Helicoidal Membrane Motifs

inferredcites →https://doi.org/10.1016/j.cell.2016.06.037openalex-snapshot

Endosome-ER Contacts Control Actin Nucleation and Retromer Function through VAP-Dependent Regulation of PI4P

inferredcites →https://doi.org/10.1016/j.celrep.2018.02.055openalex-snapshot

The PERK Arm of the Unfolded Protein Response Regulates Mitochondrial Morphology during Acute Endoplasmic Reticulum Stress

inferredcites →https://doi.org/10.1016/j.celrep.2018.04.091openalex-snapshot

Plant Endocytosis Requires the ER Membrane-Anchored Proteins VAP27-1 and VAP27-3

inferredcites →https://doi.org/10.1016/j.cub.2004.06.065openalex-snapshot

Arabidopsis NAP1 Is Essential for Arp2/3-Dependent Trichome Morphogenesis

inferredcites →https://doi.org/10.1016/j.cub.2010.11.059openalex-snapshot

THRUMIN1 Is a Light-Regulated Actin-Bundling Protein Involved in Chloroplast Motility

inferredcites →https://doi.org/10.1016/j.cub.2012.06.041openalex-snapshot

A Superfamily of Actin-Binding Proteins at the Actin-Membrane Nexus of Higher Plants

inferredcites →https://doi.org/10.1016/j.cub.2014.05.003openalex-snapshot

The Plant Cytoskeleton, NET3C, and VAP27 Mediate the Link between the Plasma Membrane and Endoplasmic Reticulum

inferredcites →https://doi.org/10.1016/j.cub.2015.06.015openalex-snapshot

Synaptotagmin SYTA Forms ER-Plasma Membrane Junctions that Are Recruited to Plasmodesmata for Plant Virus Movement

inferredcites →https://doi.org/10.1016/j.cub.2016.06.008openalex-snapshot

Arabidopsis NAP1 Regulates the Formation of Autophagosomes

inferredcites →https://doi.org/10.1016/j.cub.2016.10.024openalex-snapshot

SYP73 Anchors the ER to the Actin Cytoskeleton for Maintenance of ER Integrity and Streaming in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cub.2017.06.059openalex-snapshot

A Novel Plasma Membrane-Anchored Protein Regulates Xylem Cell-Wall Deposition through Microtubule-Dependent Lateral Inhibition of Rho GTPase Domains

inferredcites →https://doi.org/10.1016/j.cub.2017.11.055openalex-snapshot

ER-PM Contacts Restrict Exocytic Sites for Polarized Morphogenesis

inferredcites →https://doi.org/10.1016/j.cub.2018.05.014openalex-snapshot

An Immune-Responsive Cytoskeletal-Plasma Membrane Feedback Loop in Plants

inferredcites →https://doi.org/10.1016/j.cub.2020.12.009openalex-snapshot

A novel plant actin-microtubule bridging complex regulates cytoskeletal and ER structure at ER-PM contact sites

inferredcites →https://doi.org/10.1016/j.devcel.2010.08.007openalex-snapshot

Extended-Synaptotagmin-2 Mediates FGF Receptor Endocytosis and ERK Activation In Vivo

inferredcites →https://doi.org/10.1016/j.devcel.2012.04.008openalex-snapshot

Role of Actin Cytoskeleton in Brassinosteroid Signaling and in Its Integration with the Auxin Response in Plants

inferredcites →https://doi.org/10.1016/j.devcel.2012.11.004openalex-snapshot

ER-to-Plasma Membrane Tethering Proteins Regulate Cell Signaling and ER Morphology

inferredcites →https://doi.org/10.1016/j.devcel.2016.06.032openalex-snapshot

Cellulose-Microtubule Uncoupling Proteins Prevent Lateral Displacement of Microtubules during Cellulose Synthesis in Arabidopsis

inferredcites →https://doi.org/10.1016/j.devcel.2016.10.022openalex-snapshot

A Tether Is a Tether Is a Tether: Tethering at Membrane Contact Sites

inferredcites →https://doi.org/10.1016/j.devcel.2021.02.008openalex-snapshot

Maintaining the structural and functional homeostasis of the plant endoplasmic reticulum

inferredcites →https://doi.org/10.1016/j.jplph.2021.153473openalex-snapshot

Plant cytoskeletons and the endoplasmic reticulum network organization

inferredcites →https://doi.org/10.1016/j.molcel.2017.01.020openalex-snapshot

The ER Stress Sensor PERK Coordinates ER-Plasma Membrane Contact Site Formation through Interaction with Filamin-A and F-Actin Remodeling

inferredcites →https://doi.org/10.1016/j.molcel.2020.07.019openalex-snapshot

A UPR-Induced Soluble ER-Phagy Receptor Acts with VAPs to Confer ER Stress Resistance

inferredcites →https://doi.org/10.1016/j.molp.2021.06.012openalex-snapshot

Distinct phosphoinositides define the biotrophic interface of plant–microbe interactions

inferredcites →https://doi.org/10.1016/j.steroids.2015.01.027openalex-snapshot

Sterol liganding of OSBP-related proteins (ORPs) regulates the subcellular distribution of ORP–VAPA complexes and their impacts on organelle structure

inferredcites →https://doi.org/10.1016/j.tcb.2016.05.007openalex-snapshot

Stitching Organelles: Organization and Function of Specialized Membrane Contact Sites in Plants

inferredcites →https://doi.org/10.1016/j.tibs.2019.10.008openalex-snapshot

Functional Diversification of ER Stress Responses in Arabidopsis

inferredcites →https://doi.org/10.1016/j.tplants.2016.11.008openalex-snapshot

Plant Endoplasmic Reticulum–Plasma Membrane Contact Sites

inferredcites →https://doi.org/10.1016/j.tplants.2018.05.002openalex-snapshot

Autophagosome Biogenesis and the Endoplasmic Reticulum: A Plant Perspective

inferredcites →https://doi.org/10.1016/j.tplants.2020.03.011openalex-snapshot

Autophagosome Biogenesis in Plants: An Actin Cytoskeleton Perspective

inferredcites →https://doi.org/10.1038/celldisc.2015.33openalex-snapshot

ER network homeostasis is critical for plant endosome streaming and endocytosis

inferredcites →https://doi.org/10.1038/nature08280openalex-snapshot

Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin

inferredcites →https://doi.org/10.1038/nature11320openalex-snapshot

Molecular machines governing exocytosis of synaptic vesicles

inferredcites →https://doi.org/10.1038/nature13474openalex-snapshot

Lipid landscapes and pipelines in membrane homeostasis

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/ncb2523openalex-snapshot

ER network formation requires a balance of the dynamin-like GTPase Sey1p and the Lunapark family member Lnp1p

inferredcites →https://doi.org/10.1038/ncb2647openalex-snapshot

Rab10 GTPase regulates ER dynamics and morphology

inferredcites →https://doi.org/10.1038/ncb3234openalex-snapshot

Proteomic mapping of ER–PM junctions identifies STIMATE as a regulator of Ca2+ influx

inferredcites →https://doi.org/10.1038/ncb3339openalex-snapshot

Control of plasma membrane lipid homeostasis by the extended synaptotagmins

inferredcites →https://doi.org/10.1038/ncomms4996openalex-snapshot

ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

inferredcites →https://doi.org/10.1038/nplants.2015.35openalex-snapshot

Physical interaction between peroxisomes and chloroplasts elucidated by in situ laser analysis

inferredcites →https://doi.org/10.1038/s41467-019-08893-9openalex-snapshot

Quantitative analysis of plant ER architecture and dynamics

inferredcites →https://doi.org/10.1038/s41467-019-12782-6openalex-snapshot

Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery

inferredcites →https://doi.org/10.1038/s41467-020-19343-2openalex-snapshot

Armadillo-repeat kinesin1 interacts with Arabidopsis atlastin RHD3 to move ER with plus-end of microtubules

inferredcites →https://doi.org/10.1038/s41467-022-32109-2openalex-snapshot

Phosphatidylinositol-4-phosphate controls autophagosome formation in Arabidopsis thaliana

inferredcites →https://doi.org/10.1038/s41467-022-33402-wopenalex-snapshot

TraB family proteins are components of ER-mitochondrial contact sites and regulate ER-mitochondrial interactions and mitophagy

inferredcites →https://doi.org/10.1038/s41477-020-0700-9openalex-snapshot

Global profiling of plant nuclear membrane proteome in Arabidopsis

inferredcites →https://doi.org/10.1038/s41598-017-16662-1openalex-snapshot

AKT-mTOR signaling modulates the dynamics of IRE1 RNAse activity by regulating ER-mitochondria contacts

inferredcites →https://doi.org/10.1038/s41598-018-20840-0openalex-snapshot

The odd one out: Arabidopsis reticulon 20 does not bend ER membranes but has a role in lipid regulation

inferredcites →https://doi.org/10.1038/s42003-020-0872-xopenalex-snapshot

Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells

inferredcites →https://doi.org/10.1038/s42003-021-02700-2openalex-snapshot

Arabidopsis thaliana myosin XIK is recruited to the Golgi through interaction with a MyoB receptor

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00208.xopenalex-snapshot

Stacks on tracks: the plant Golgi apparatus traffics on an actin/ER network†

inferredcites →https://doi.org/10.1073/pnas.0611725104openalex-snapshot

E-Syts, a family of membranous Ca 2+ -sensor proteins with multiple C 2 domains

inferredcites →https://doi.org/10.1073/pnas.0906250106openalex-snapshot

Short actin-based mechanism for light-directed chloroplast movement in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.0909080107openalex-snapshot

Arabidopsis synaptotagmin SYTA regulates endocytosis and virus movement protein cell-to-cell transport

inferredcites →https://doi.org/10.1073/pnas.0911482107openalex-snapshot

Myosin-dependent endoplasmic reticulum motility and F-actin organization in plant cells

inferredcites →https://doi.org/10.1073/pnas.1101643108openalex-snapshot

Structures of the atlastin GTPase provide insight into homotypic fusion of endoplasmic reticulum membranes

inferredcites →https://doi.org/10.1073/pnas.1105056108openalex-snapshot

Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain

inferredcites →https://doi.org/10.1073/pnas.1208385109openalex-snapshot

Lipid interaction of the C terminus and association of the transmembrane segments facilitate atlastin-mediated homotypic endoplasmic reticulum fusion

inferredcites →https://doi.org/10.1073/pnas.1423026112openalex-snapshot

Lunapark stabilizes nascent three-way junctions in the endoplasmic reticulum

inferredcites →https://doi.org/10.1073/pnas.1805757115openalex-snapshot

Kv2 potassium channels form endoplasmic reticulum/plasma membrane junctions via interaction with VAPA and VAPB

inferredcites →https://doi.org/10.1073/pnas.1818099116openalex-snapshot

Ionic stress enhances ER–PM connectivity via phosphoinositide-associated SYT1 contact site expansion in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1819077116openalex-snapshot

The cell wall regulates dynamics and size of plasma-membrane nanodomains in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1915386117openalex-snapshot

STIM2 targets Orai1/STIM1 to the AKAP79 signaling complex and confers coupling of Ca 2+ entry with NFAT1 activation

inferredcites →https://doi.org/10.1073/pnas.2117554119openalex-snapshot

ER-phagy requires the assembly of actin at sites of contact between the cortical ER and endocytic pits

inferredcites →https://doi.org/10.1073/pnas.2205314119openalex-snapshot

Arabidopsis ORP2A mediates ER–autophagosomal membrane contact sites and regulates PI3P in plant autophagy

inferredcites →https://doi.org/10.1073/pnas.93.20.11155openalex-snapshot

Invasion of minor veins of tobacco leaves inoculated with tobacco mosaic virus mutants defective in phloem-dependent movement.

inferredcites →https://doi.org/10.1074/jbc.m112.359174openalex-snapshot

Loss of Mitofusin 2 Promotes Endoplasmic Reticulum Stress

inferredcites →https://doi.org/10.1074/jbc.m116.737783openalex-snapshot

Lunapark Is a Component of a Ubiquitin Ligase Complex Localized to the Endoplasmic Reticulum Three-way Junctions

inferredcites →https://doi.org/10.1080/15548627.2021.1872886openalex-snapshot

ATI1 (ATG8-interacting protein 1) and ATI2 define a plant starvation-induced reticulophagy pathway and serve as MSBP1/MAPR5 cargo receptors

inferredcites →https://doi.org/10.1083/jcb.200708205openalex-snapshot

Inheritance of cortical ER in yeast is required for normal septin organization

inferredcites →https://doi.org/10.1083/jcb.201711151openalex-snapshot

EB1 binding restricts STIM1 translocation to ER–PM junctions and regulates store-operated Ca2+ entry

inferredcites →https://doi.org/10.1083/jcb.201809107openalex-snapshot

Dynamic nanoscale morphology of the ER surveyed by STED microscopy

inferredcites →https://doi.org/10.1083/jcb.201910161openalex-snapshot

Ist2 recruits the lipid transporters Osh6/7 to ER–PM contacts to maintain phospholipid metabolism

inferredcites →https://doi.org/10.1083/jcb.98.1.283openalex-snapshot

Three-dimensional structure of a membrane-microtubule complex.

inferredcites →https://doi.org/10.1093/emboj/cdg201openalex-snapshot

A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP

inferredcites →https://doi.org/10.1093/jxb/erad075openalex-snapshot

A tell tail sign: a conserved C-terminal tail-anchor domain targets a subset of pathogen effectors to the plant endoplasmic reticulum

inferredcites →https://doi.org/10.1093/jxb/ern114openalex-snapshot

Truncated myosin XI tail fusions inhibit peroxisome, Golgi, and mitochondrial movement in tobacco leaf epidermal cells: a genetic tool for the next generation

inferredcites →https://doi.org/10.1093/jxb/erw381openalex-snapshot

Arabidopsis SYT1 maintains stability of cortical endoplasmic reticulum networks and VAP27-1-enriched endoplasmic reticulum–plasma membrane contact sites

inferredcites →https://doi.org/10.1093/jxb/erx047openalex-snapshot

NETWORKED 3B: a novel protein in the actin cytoskeleton-endoplasmic reticulum interaction

inferredcites →https://doi.org/10.1093/jxb/erx403openalex-snapshot

The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane

inferredcites →https://doi.org/10.1093/jxb/erz543openalex-snapshot

Defining the dance: quantification and classification of endoplasmic reticulum dynamics

inferredcites →https://doi.org/10.1093/pcp/pcw061openalex-snapshot

Synaptotagmin 1 Negatively Controls the Two Distinct Immune Secretory Pathways to Powdery Mildew Fungi in Arabidopsis

inferredcites →https://doi.org/10.1093/plcell/koab116openalex-snapshot

Arabidopsis myosin XIK interacts with the exocyst complex to facilitate vesicle tethering during exocytosis

inferredcites →https://doi.org/10.1093/plcell/koab122openalex-snapshot

Synaptotagmins at the endoplasmic reticulum–plasma membrane contact sites maintain diacylglycerol homeostasis during abiotic stress

inferredcites →https://doi.org/10.1093/plcell/koab247openalex-snapshot

A glossary of plant cell structures: Current insights and future questions

inferredcites →https://doi.org/10.1093/plcell/koac017openalex-snapshot

Reductive stress triggers ANAC017-mediated retrograde signaling to safeguard the endoplasmic reticulum by boosting mitochondrial respiratory capacity

inferredcites →https://doi.org/10.1093/plphys/kiab485openalex-snapshot

A correlative light electron microscopy approach reveals plasmodesmata ultrastructure at the graft interface

inferredcites →https://doi.org/10.1101/2021.09.29.461190openalex-snapshot

A NET4-RabG3 couple mediate the link between actin and the tonoplast and is essential for normal actin cytoskeletal remodelling in stomatal closure to flg22

inferredcites →https://doi.org/10.1101/gad.11.6.799openalex-snapshot

The ROOT HAIR DEFECTIVE3 gene encodes an evolutionarily conserved protein with GTP-binding motifs and is required for regulated cell enlargement in Arabidopsis.

inferredcites →https://doi.org/10.1104/pp.103.027250openalex-snapshot

Cytoskeleton-Plasma Membrane-Cell Wall Continuum in Plants. Emerging Links Revisited

inferredcites →https://doi.org/10.1104/pp.109.137083openalex-snapshot

Evidence for Unidirectional Flow through Plasmodesmata

inferredcites →https://doi.org/10.1104/pp.110.157941openalex-snapshot

Super-Resolution Imaging of Plasmodesmata Using Three-Dimensional Structured Illumination Microscopy

inferredcites →https://doi.org/10.1104/pp.114.235754openalex-snapshot

Quantitative Analysis of the Mitochondrial and Plastid Proteomes of the Moss Physcomitrella patens Reveals Protein Macrocompartmentation and Microcompartmentation

inferredcites →https://doi.org/10.1104/pp.114.252320openalex-snapshot

Microtubules Contribute to Tubule Elongation and Anchoring of Endoplasmic Reticulum, Resulting in High Network Complexity in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.15.00260openalex-snapshot

The Arabidopsis Synaptotagmin1 Is Enriched in Endoplasmic Reticulum-Plasma Membrane Contact Sites and Confers Cellular Resistance to Mechanical Stresses

inferredcites →https://doi.org/10.1104/pp.15.00668openalex-snapshot

Putting the Squeeze on Plasmodesmata: A Role for Reticulons in Primary Plasmodesmata Formation

inferredcites →https://doi.org/10.1104/pp.15.01172openalex-snapshot

Phosphorylation of the C Terminus of RHD3 Has a Critical Role in Homotypic ER Membrane Fusion in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.15.01529openalex-snapshot

In Vivo Quantification of Peroxisome Tethering to Chloroplasts in Tobacco Epidermal Cells Using Optical Tweezers

inferredcites →https://doi.org/10.1104/pp.15.01865openalex-snapshot

A GTPase-Dependent Fine ER Is Required for Localized Secretion in Polarized Growth of Root Hairs

inferredcites →https://doi.org/10.1104/pp.16.01743openalex-snapshot

The IQD Family of Calmodulin-Binding Proteins Links Calcium Signaling to Microtubules, Membrane Subdomains, and the Nucleus

inferredcites →https://doi.org/10.1104/pp.18.00498openalex-snapshot

Synaptotagmin-Associated Endoplasmic Reticulum-Plasma Membrane Contact Sites Are Localized to Immobile ER Tubules

inferredcites →https://doi.org/10.1105/tpc.105.035212openalex-snapshot

Selective Membrane Protein Internalization Accompanies Movement from the Endoplasmic Reticulum to the Protein Storage Vacuole Pathway in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.108.058503openalex-snapshot

Analysis of Cortical Arrays from Tradescantia virginiana at High Resolution Reveals Discrete Microtubule Subpopulations and Demonstrates That Confocal Images of Arrays Can Be Misleading

inferredcites →https://doi.org/10.1105/tpc.108.063859openalex-snapshot

Arabidopsis Synaptotagmin 1 Is Required for the Maintenance of Plasma Membrane Integrity and Cell Viability

inferredcites →https://doi.org/10.1105/tpc.108.064212openalex-snapshot

Cucumber Mosaic VirusMovement Protein Severs Actin Filaments to Increase the Plasmodesmal Size Exclusion Limit in Tobacco

inferredcites →https://doi.org/10.1105/tpc.109.072249openalex-snapshot

Movement and Remodeling of the Endoplasmic Reticulum in Nondividing Cells of Tobacco Leaves

inferredcites →https://doi.org/10.1105/tpc.110.074385openalex-snapshot

Five Arabidopsis Reticulon Isoforms Share Endoplasmic Reticulum Location, Topology, and Membrane-Shaping Properties

inferredcites →https://doi.org/10.1105/tpc.111.093575openalex-snapshot

POM-POM2/CELLULOSE SYNTHASE INTERACTING1 Is Essential for the Functional Association of Cellulose Synthase and Microtubules in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.111.095398openalex-snapshot

Differential Coloring Reveals That Plastids Do Not Form Networks for Exchanging Macromolecules

inferredcites →https://doi.org/10.1105/tpc.112.096263openalex-snapshot

The ARP2/3 Complex Mediates Guard Cell Actin Reorganization and Stomatal Movement in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.114.123281openalex-snapshot

Tomato Pistil Factor STIG1 Promotes in Vivo Pollen Tube Growth by Binding to Phosphatidylinositol 3-Phosphate and the Extracellular Domain of the Pollen Receptor Kinase LePRK2

inferredcites →https://doi.org/10.1105/tpc.19.00771openalex-snapshot

SEIPIN Isoforms Interact with the Membrane-Tethering Protein VAP27-1 for Lipid Droplet Formation

inferredcites →https://doi.org/10.1105/tpc.19.00970openalex-snapshot

Specific Recruitment of Phosphoinositide Species to the Plant-Pathogen Interfacial Membrane Underlies Arabidopsis Susceptibility to Fungal Infection

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02435.xopenalex-snapshot

Arabidopsis IQD1, a novel calmodulin‐binding nuclear protein, stimulates glucosinolate accumulation and plant defense

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03863.xopenalex-snapshot

Peroxule extension over ER‐defined paths constitutes a rapid subcellular response to hydroxyl stress

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04846.xopenalex-snapshot

In Arabidopsis, the spatial and dynamic organization of the endoplasmic reticulum and Golgi apparatus is influenced by the integrity of the C‐terminal domain of RHD3, a non‐essential GTPase

inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01218.xopenalex-snapshot

Cell biology of the plant Golgi apparatus

inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00670.xopenalex-snapshot

Overexpression of a Plant Reticulon Remodels the Lumen of the Cortical Endoplasmic Reticulum but Does not Perturb Protein Transport

inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00891.xopenalex-snapshot

Grab a Golgi: Laser Trapping of Golgi Bodies Reveals in vivo Interactions with the Endoplasmic Reticulum

inferredcites →https://doi.org/10.1111/jipb.12872openalex-snapshot

AtSec62 is critical for plant development and is involved in ER‐phagy in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/jmi.13139openalex-snapshot

intER‐ACTINg: The structure and dynamics of ER and actin are interlinked

inferredcites →https://doi.org/10.1111/mpp.13261openalex-snapshot

Reticulons 3 and 6 interact with viral movement proteins

inferredcites →https://doi.org/10.1111/nph.12038openalex-snapshot

An A rabidopsis reticulon and the atlastin homologue RHD3‐like2 act together in shaping the tubular endoplasmic reticulum

inferredcites →https://doi.org/10.1111/nph.13857openalex-snapshot

Plant VAP 27 proteins: domain characterization, intracellular localization and role in plant development

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.15228openalex-snapshot

Arabidopsis Lunapark proteins are involved in ER cisternae formation

inferredcites →https://doi.org/10.1111/nph.15365openalex-snapshot

Plant organelle dynamics: cytoskeletal control and membrane contact sites

inferredcites →https://doi.org/10.1111/nph.16369openalex-snapshot

Insights into endoplasmic reticulum‐associated degradation in plants

inferredcites →https://doi.org/10.1111/nph.16391openalex-snapshot

Structural and functional relationships between plasmodesmata and plant endoplasmic reticulum–plasma membrane contact sites consisting of three synaptotagmins

inferredcites →https://doi.org/10.1111/nph.16743openalex-snapshot

Plasma membrane aquaporins interact with the endoplasmic reticulum resident VAP27 proteins at ER–PM contact sites and endocytic structures

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/tra.12700openalex-snapshot

Actin‐spectrin scaffold supports open fenestrae in liver sinusoidal endothelial cells

inferredcites →https://doi.org/10.1111/tra.12844openalex-snapshot

Arabidopsis synaptotagmin 1 mediates lipid transport in a lipid composition‐dependent manner

inferredcites →https://doi.org/10.1126/science.1153634openalex-snapshot

Membrane Proteins of the Endoplasmic Reticulum Induce High-Curvature Tubules

inferredcites →https://doi.org/10.1126/science.aaf3928openalex-snapshot

Increased spatiotemporal resolution reveals highly dynamic dense tubular matrices in the peripheral ER

inferredcites →https://doi.org/10.1126/science.aah6152openalex-snapshot

Reticulon 3–dependent ER-PM contact sites control EGFR nonclathrin endocytosis

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Plants transfer lipids to sustain colonization by mutualistic mycorrhizal and parasitic fungi

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Fatty acids in arbuscular mycorrhizal fungi are synthesized by the host plant

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Developmental control of plant Rho GTPase nano-organization by the lipid phosphatidylserine

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Endoplasmic reticulum–associated degradation regulates mitochondrial dynamics in brown adipocytes

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A heat-sensitive Osh protein controls PI4P polarity

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Overexpression of vesicle-associated membrane protein PttVAP27-17 as a tool to improve biomass production and the overall saccharification yields in Populus trees

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The Secretory System of Arabidopsis

inferredcites →https://doi.org/10.1242/jcs.080762openalex-snapshot

Increased ER–mitochondrial coupling promotes mitochondrial respiration and bioenergetics during early phases of ER stress

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Arabidopsis RHD3 mediates the generation of the tubular ER network and is required for Golgi distribution and motility in plant cells

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ER stress signaling requires RHD3, a functionally conserved ER-shaping GTPase

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A novel fluorescent reporter detects plastic remodeling of mitochondria–ER contact sites

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Enforced tethering elongates the cortical endoplasmic reticulum and limits store-operated Ca2+ entry

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Cortical endoplasmic reticulum in plants

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The cell wall regulates dynamics and size of plasma-membrane nanodomains in Arabidopsis.

inferredcites →https://doi.org/10.1371/journal.pbio.3000355openalex-snapshot

Reticulon and CLIMP-63 regulate nanodomain organization of peripheral ER tubules

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The Plant Actin Cytoskeleton Responds to Signals from Microbe-Associated Molecular Patterns

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Identification of VAPA and VAPB as Kv2 Channel-Interacting Proteins Defining Endoplasmic Reticulum–Plasma Membrane Junctions in Mammalian Brain Neurons

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GRIM REAPER peptide binds to receptor kinase PRK5 to trigger cell death in Arabidopsis

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ER–plasma membrane contact sites contribute to autophagosome biogenesis by regulation of local PI3P synthesis

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CALCOCO1 acts with VAMP‐associated proteins to mediate ER‐phagy

inferredcites →https://doi.org/10.15252/embr.201847182openalex-snapshot

Multiple C2 domains and transmembrane region proteins (MCTPs) tether membranes at plasmodesmata

inferredcites →https://doi.org/10.26508/lsa.201700014openalex-snapshot

The ER morphology-regulating lunapark protein induces the formation of stacked bilayer discs

inferredcites →https://doi.org/10.3389/fcell.2015.00078openalex-snapshot

Mitochondrial Dynamics and the ER: The Plant Perspective

inferredcites →https://doi.org/10.3389/fpls.2014.00350openalex-snapshot

The mitochondrial Ras-related GTPase Miro: views from inside and outside the metazoan kingdom

inferredcites →https://doi.org/10.3389/fpls.2014.00584openalex-snapshot

The Arabidopsis synaptotagmin SYTA regulates the cell-to-cell movement of diverse plant viruses

inferredcites →https://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

inferredcites →https://doi.org/10.3389/fpls.2019.00023openalex-snapshot

Plant ER-PM Contact Sites in Endocytosis and Autophagy: Does the Local Composition of Membrane Phospholipid Play a Role?

inferredcites →https://doi.org/10.3389/fpls.2019.00635openalex-snapshot

Manipulating Endoplasmic Reticulum-Plasma Membrane Tethering in Plants Through Fluorescent Protein Complementation

inferredcites →https://doi.org/10.3389/fpls.2019.01192openalex-snapshot

ER-Phagy and ER Stress Response (ERSR) in Plants

inferredcites →https://doi.org/10.3389/fpls.2022.1010569openalex-snapshot

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inferredcites →https://doi.org/10.3389/fpls.2022.817251openalex-snapshot

ROOT HAIR DEFECTIVE3 Is a Receptor for Selective Autophagy of the Endoplasmic Reticulum in Arabidopsis

inferredcites →https://doi.org/10.3389/fpls.2022.925863openalex-snapshot

Sensing Mechanisms: Calcium Signaling Mediated Abiotic Stress in Plants

inferredcites →https://doi.org/10.3390/cells11010145openalex-snapshot

Collisions of Cortical Microtubules with Membrane Associated Myosin VIII Tail

inferredcites →https://doi.org/10.4161/psb.2.3.3973openalex-snapshot

Membrane Contact Sites

inferredcites →https://doi.org/10.7554/elife.36316openalex-snapshot

Arabidopsis formin 2 regulates cell-to-cell trafficking by capping and stabilizing actin filaments at plasmodesmata

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Reticulon proteins modulate autophagy of the endoplasmic reticulum in maize endosperm

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A cross-kingdom conserved ER-phagy receptor maintains endoplasmic reticulum homeostasis during stress

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Unbiased proteomic and forward genetic screens reveal that mechanosensitive ion channel MSL10 functions at ER–plasma membrane contact sites in Arabidopsis thaliana

What points at this work

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

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COST1 stimulates RHD3 GTPase activity to maintain ER morphology and plant growth in Arabidopsis

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