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Unconventional protein secretion in plants: a critical assessment

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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/j.1460-2075.1996.tb01039.xopenalex-snapshot
The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1002/mnfr.201300729openalex-snapshot
Interspecies communication between plant and mouse gut host cells through edible plant derived exosome‐like nanoparticles
inferredcites →https://doi.org/10.1002/pmic.200900514openalex-snapshot
Plant secretome: Unlocking secrets of the secreted proteins
inferredcites →https://doi.org/10.1006/scel.1993.1003openalex-snapshot
STE6, the yeast a-factor transporter
inferredcites →https://doi.org/10.1007/978-1-4939-3804-9openalex-snapshot
Unconventional Protein Secretion
inferredcites →https://doi.org/10.1007/s00018-007-7044-8openalex-snapshot
Galectins: matricellular glycan-binding proteins linking cell adhesion, migration, and survival
inferredcites →https://doi.org/10.1007/s00441-012-1428-2openalex-snapshot
Exosomes: vesicular carriers for intercellular communication in neurodegenerative disorders
inferredcites →https://doi.org/10.1007/s00497-014-0245-zopenalex-snapshot
High humidity partially rescues the Arabidopsis thaliana exo70A1 stigmatic defect for accepting compatible pollen
inferredcites →https://doi.org/10.1016/0092-8674(80)90128-2openalex-snapshot
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway
inferredcites →https://doi.org/10.1016/j.bbapap.2013.03.024openalex-snapshot
Plant secretome — From cellular process to biological activity
inferredcites →https://doi.org/10.1016/j.bcp.2011.02.011openalex-snapshot
Exosomes as intercellular signalosomes and pharmacological effectors
inferredcites →https://doi.org/10.1016/j.ceb.2007.12.002openalex-snapshot
ESCRT complexes and the biogenesis of multivesicular bodies
inferredcites →https://doi.org/10.1016/j.ceb.2009.03.007openalex-snapshot
Exosomes – vesicular carriers for intercellular communication
inferredcites →https://doi.org/10.1016/j.ceb.2009.04.007openalex-snapshot
The exocyst complex in polarized exocytosis
inferredcites →https://doi.org/10.1016/j.cell.2007.06.029openalex-snapshot
The Golgi-Associated Protein GRASP Is Required for Unconventional Protein Secretion during Development
inferredcites →https://doi.org/10.1016/j.cub.2010.03.011openalex-snapshot
Protein Secretion: Unconventional Exit by Exophagy
inferredcites →https://doi.org/10.1016/j.cub.2010.09.015openalex-snapshot
Multisubunit Tethering Complexes and Their Role in Membrane Fusion
inferredcites →https://doi.org/10.1016/j.cub.2014.09.014openalex-snapshot
A Unique Plant ESCRT Component, FREE1, Regulates Multivesicular Body Protein Sorting and Plant Growth
inferredcites →https://doi.org/10.1016/j.devcel.2013.07.007openalex-snapshot
Exo70 Generates Membrane Curvature for Morphogenesis and Cell Migration
inferredcites →https://doi.org/10.1016/j.devcel.2014.04.029openalex-snapshot
Plant Cytokinesis Is Orchestrated by the Sequential Action of the TRAPPII and Exocyst Tethering Complexes
inferredcites →https://doi.org/10.1016/j.febslet.2009.09.041openalex-snapshot
Vesicular fractions of sunflower apoplastic fluids are associated with potential exosome marker proteins
inferredcites →https://doi.org/10.1016/j.pbi.2013.10.013openalex-snapshot
Exocyst complexes multiple functions in plant cells secretory pathways
inferredcites →https://doi.org/10.1016/j.tcb.2013.09.006openalex-snapshot
Tethering the assembly of SNARE complexes
inferredcites →https://doi.org/10.1016/j.tplants.2012.06.004openalex-snapshot
Unconventional protein secretion
inferredcites →https://doi.org/10.1016/j.tplants.2013.06.002openalex-snapshot
Transcytosis shuts the door for an unwanted guest
inferredcites →https://doi.org/10.1016/s0076-6879(01)29071-5openalex-snapshot
[12] Purification and characterization of yeast exocyst complex
inferredcites →https://doi.org/10.1016/s0167-4889(03)00088-0openalex-snapshot
Long coiled-coil proteins and membrane traffic
inferredcites →https://doi.org/10.1016/s0896-6273(03)00031-xopenalex-snapshot
Mutations in the Exocyst Component Sec5 Disrupt Neuronal Membrane Traffic, but Neurotransmitter Release Persists
inferredcites →https://doi.org/10.1016/s0962-8924(99)01516-0openalex-snapshot
Targeting vesicles to specific sites on the plasma membrane: the role of the sec6/8 complex
inferredcites →https://doi.org/10.1021/pr200944zopenalex-snapshot
Low Temperature Stress Modulated Secretome Analysis and Purification of Antifreeze Protein from Hippophae rhamnoides, a Himalayan Wonder Plant
inferredcites →https://doi.org/10.1021/pr400827aopenalex-snapshot
Protein Secretome of Moss Plants (Physcomitrella patens) with Emphasis on Changes Induced by a Fungal Elicitor
inferredcites →https://doi.org/10.1034/j.1600-0854.2003.00072.xopenalex-snapshot
Recycling Compartments and the Internal Vesicles of Multivesicular Bodies Harbor Most of the Cholesterol Found in the Endocytic Pathway
inferredcites →https://doi.org/10.1038/emboj.2013.104openalex-snapshot
Unconventional protein secretion: an evolving mechanism
inferredcites →https://doi.org/10.1038/emboj.2013.246openalex-snapshot
Amphisomes: out of the autophagosome shadow?
inferredcites →https://doi.org/10.1038/nature06307openalex-snapshot
Identification of Tim4 as a phosphatidylserine receptor
inferredcites →https://doi.org/10.1038/nature07961openalex-snapshot
The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins
inferredcites →https://doi.org/10.1038/ncb1596openalex-snapshot
Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells
inferredcites →https://doi.org/10.1038/ncb1929openalex-snapshot
Multivesicular bodies associate with components of miRNA effector complexes and modulate miRNA activity
inferredcites →https://doi.org/10.1038/ncb2502openalex-snapshot
Syndecan–syntenin–ALIX regulates the biogenesis of exosomes
inferredcites →https://doi.org/10.1038/nrm2002openalex-snapshot
SNAREs — engines for membrane fusion
inferredcites →https://doi.org/10.1038/nrm2245openalex-snapshot
Autophagy: from phenomenology to molecular understanding in less than a decade
inferredcites →https://doi.org/10.1038/nsmb1097openalex-snapshot
The exocyst defrocked, a framework of rods revealed
inferredcites →https://doi.org/10.1038/sj.emboj.7601834openalex-snapshot
Exo70 interacts with phospholipids and mediates the targeting of the exocyst to the plasma membrane
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01673.xopenalex-snapshot
GFP‐tagging of cell components reveals the dynamics of subcellular re‐organization in response to infection of Arabidopsis by oomycete pathogens
inferredcites →https://doi.org/10.1073/pnas.1117596109openalex-snapshot
Arabidopsis ARF-GTP exchange factor, GNOM, mediates transport required for innate immunity and focal accumulation of syntaxin PEN1
inferredcites →https://doi.org/10.1073/pnas.1424856112openalex-snapshot
An early secretory pathway mediated by GNOM-LIKE 1 and GNOM is essential for basal polarity establishment in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.92.21.9613openalex-snapshot
rSec6 and rSec8, mammalian homologs of yeast proteins essential for secretion.
inferredcites →https://doi.org/10.1074/jbc.m112.381939openalex-snapshot
Phosphatidylinositol 4,5-Bisphosphate (PI(4,5)P2)-dependent Oligomerization of Fibroblast Growth Factor 2 (FGF2) Triggers the Formation of a Lipidic Membrane Pore Implicated in Unconventional Secretion
inferredcites →https://doi.org/10.1074/jbc.m114.622456openalex-snapshot
Formation of Disulfide Bridges Drives Oligomerization, Membrane Pore Formation, and Translocation of Fibroblast Growth Factor 2 to Cell Surfaces
inferredcites →https://doi.org/10.1083/jcb.200704128openalex-snapshot
Membrane association and functional regulation of Sec3 by phospholipids and Cdc42
inferredcites →https://doi.org/10.1083/jcb.200911149openalex-snapshot
Unconventional secretion of Pichia pastoris Acb1 is dependent on GRASP protein, peroxisomal functions, and autophagosome formation
inferredcites →https://doi.org/10.1083/jcb.200911154openalex-snapshot
Unconventional secretion of Acb1 is mediated by autophagosomes
inferredcites →https://doi.org/10.1083/jcb.201106098openalex-snapshot
Biogenesis of a novel compartment for autophagosome-mediated unconventional protein secretion
inferredcites →https://doi.org/10.1084/jem.183.3.1161openalex-snapshot
B lymphocytes secrete antigen-presenting vesicles.
inferredcites →https://doi.org/10.1091/mbc.e04-02-0140openalex-snapshot
The PEN1 Syntaxin Defines a Novel Cellular Compartment upon Fungal Attack and Is Required for the Timely Assembly of Papillae
inferredcites →https://doi.org/10.1091/mbc.e07-05-0461openalex-snapshot
Phosphatidylinositol 4,5-Bisphosphate Mediates the Targeting of the Exocyst to the Plasma Membrane for Exocytosis in Mammalian Cells
inferredcites →https://doi.org/10.1091/mbc.e13-10-0586openalex-snapshot
Exo70E2 is essential for exocyst subunit recruitment and EXPO formation in both plants and animals
inferredcites →https://doi.org/10.1093/jxb/erq402openalex-snapshot
The role for the exocyst complex subunits Exo70B2 and Exo70H1 in the plant–pathogen interaction
inferredcites →https://doi.org/10.1093/jxb/err007openalex-snapshot
Differential effects of the brefeldin A analogue (6R)-hydroxy-BFA in tobacco and Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ert345openalex-snapshot
Proteomics profiling reveals novel proteins and functions of the plant stigma exudate
inferredcites →https://doi.org/10.1093/mp/ssq082openalex-snapshot
Sub-Compartmental Organization of Golgi-Resident N-Glycan Processing Enzymes in Plants
inferredcites →https://doi.org/10.1093/mp/sst153openalex-snapshot
Nanovesicles Are Secreted during Pollen Germination and Pollen Tube Growth: A Possible Role in Fertilization
inferredcites →https://doi.org/10.1101/cshperspect.a016998openalex-snapshot
The Cell Biology of the Endocytic System from an Evolutionary Perspective
inferredcites →https://doi.org/10.1104/pp.111.2.645openalex-snapshot
PIP1 Aquaporins Are Concentrated in Plasmalemmasomes of Arabidopsis thaliana Mesophyll
inferredcites →https://doi.org/10.1104/pp.112.210757openalex-snapshot
Time-Resolved Fluorescence Imaging Reveals Differential Interactions ofN-Glycan Processing Enzymes across the Golgi Stack in Planta
inferredcites →https://doi.org/10.1104/pp.113.214536openalex-snapshot
Traffic of Human α-Mannosidase in Plant Cells Suggests the Presence of a New Endoplasmic Reticulum-to-Vacuole Pathway without Involving the Golgi Complex
inferredcites →https://doi.org/10.1104/pp.114.235804openalex-snapshot
The Plant Membrane-Associated REMORIN1.3 Accumulates in Discrete Perihaustorial Domains and Enhances Susceptibility to Phytophthora infestans
inferredcites →https://doi.org/10.1104/pp.15.00112openalex-snapshot
Cell Wall Maturation of Arabidopsis Trichomes Is Dependent on Exocyst Subunit EXO70H4 and Involves Callose Deposition
inferredcites →https://doi.org/10.1104/pp.15.00953openalex-snapshot
EXPO and Autophagosomes are Distinct Organelles in Plants
inferredcites →https://doi.org/10.1104/pp.98.1.264openalex-snapshot
Arabinogalactan-Rich Glycoproteins Are Localized on the Cell Surface and in Intravacuolar Multivesicular Bodies
inferredcites →https://doi.org/10.1105/tpc.108.059105openalex-snapshot
An Exocyst Complex Functions in Plant Cell Growth inArabidopsisand Tobacco
inferredcites →https://doi.org/10.1105/tpc.108.064865openalex-snapshot
The ESCRT-Related CHMP1A and B Proteins Mediate Multivesicular Body Sorting of Auxin Carriers in Arabidopsis and Are Required for Plant Development
inferredcites →https://doi.org/10.1105/tpc.110.080697openalex-snapshot
EXPO, an Exocyst-Positive Organelle Distinct from Multivesicular Endosomes and Autophagosomes, Mediates Cytosol to Cell Wall Exocytosis in Arabidopsis and Tobacco Cells
inferredcites →https://doi.org/10.1105/tpc.111.086918openalex-snapshot
Multivesicular Bodies Mature from the Trans -Golgi Network/Early Endosome in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.087254openalex-snapshot
The Arabidopsis Deubiquitinating Enzyme AMSH3 Interacts with ESCRT-III Subunits and Regulates Their Localization
inferredcites →https://doi.org/10.1105/tpc.114.125880openalex-snapshot
Insights into the Localization and Function of the Membrane Trafficking Regulator GNOM ARF-GEF at the Golgi Apparatus inArabidopsis
inferredcites →https://doi.org/10.1111/febs.12092openalex-snapshot
Vacuolar protein sorting mechanisms in plants
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00766.xopenalex-snapshot
Host‐induced gene silencing: a tool for understanding fungal host interaction and for developing novel disease control strategies
inferredcites →https://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
inferredcites →https://doi.org/10.1111/j.1439-0434.1991.tb01194.xopenalex-snapshot
Comparative Ultrastructural Observations of Plasmalemmasomes in PSTVd‐Infected Healthy and Artificially Stunted Tomato Leaves
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00683.xopenalex-snapshot
Multivesicular bodies participate in a cell wall-associated defence response in barley leaves attacked by the pathogenic powdery mildew fungus
inferredcites →https://doi.org/10.1111/j.1462-5822.2012.01751.xopenalex-snapshot
Patterns of plant subcellular responses to successful oomycete infections reveal differences in host cell reprogramming and endocytic trafficking
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01829.xopenalex-snapshot
Tête à tête inside a plant cell: establishing compatibility between plants and biotrophic fungi and oomycetes
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01844.xopenalex-snapshot
Multivesicular compartments proliferate in susceptible and resistant MLA12‐barley leaves in response to infection by the biotrophic powdery mildew fungus
inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00920.xopenalex-snapshot
Multivesicular Endosome Biogenesis in the Absence of ESCRTs
inferredcites →https://doi.org/10.1111/j.1600-0854.2012.01353.xopenalex-snapshot
Exorcising the Exocyst Complex
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00929.xopenalex-snapshot
The Plant Exocyst
inferredcites →https://doi.org/10.1111/nph.12236openalex-snapshot
The A rabidopsis exocyst subunit SEC 3 A is essential for embryo development and accumulates in transient puncta at the plasma membrane
inferredcites →https://doi.org/10.1111/tra.12101openalex-snapshot
Arabidopsis Exocyst Subcomplex Containing Subunit EXO70B1 Is Involved in Autophagy‐Related Transport to the Vacuole
inferredcites →https://doi.org/10.1111/tra.12203openalex-snapshot
Arabinogalactan Glycosyltransferases Target to a Unique Subcellular Compartment That May Function in Unconventional Secretion in Plants
inferredcites →https://doi.org/10.1111/tra.12245openalex-snapshot
Rerouting of Plant Late Endocytic Trafficking Toward a Pathogen Interface
inferredcites →https://doi.org/10.1126/science.1153124openalex-snapshot
Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes
inferredcites →https://doi.org/10.1126/science.1234740openalex-snapshot
Unconventional Secretion, Unconventional Solutions
inferredcites →https://doi.org/10.1146/annurev-cellbio-101512-122326openalex-snapshot
Biogenesis, Secretion, and Intercellular Interactions of Exosomes and Other Extracellular Vesicles
inferredcites →https://doi.org/10.1146/annurev-physiol-021014-071641openalex-snapshot
Exosomes: Vehicles of Intercellular Signaling, Biomarkers, and Vectors of Cell Therapy
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113327openalex-snapshot
Tethering Factors as Organizers of Intracellular Vesicular Traffic
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.105307openalex-snapshot
BI-DIRECTIONAL PROTEIN TRANSPORT BETWEEN THE ER AND GOLGI
inferredcites →https://doi.org/10.1146/annurev.cellbio.21.012704.133214openalex-snapshot
PROTEIN TRANSLOCATION BY THE SEC61/SECY CHANNEL
inferredcites →https://doi.org/10.1182/blood-2008-08-174094openalex-snapshot
Activated T cells recruit exosomes secreted by dendritic cells via LFA-1
inferredcites →https://doi.org/10.1242/jcs.049791openalex-snapshot
An intrinsic quality-control mechanism ensures unconventional secretion of fibroblast growth factor 2 in a folded conformation
inferredcites →https://doi.org/10.1242/jcs.093559openalex-snapshot
Structure and function of endosomes in plant cells
inferredcites →https://doi.org/10.1242/jcs.103630openalex-snapshot
Diversity in unconventional protein secretion
inferredcites →https://doi.org/10.12703/p6-74openalex-snapshot
Membrane tethering
inferredcites →https://doi.org/10.1371/journal.pgen.1004945openalex-snapshot
A Truncated NLR Protein, TIR-NBS2, Is Required for Activated Defense Responses in the exo70B1 Mutant
inferredcites →https://doi.org/10.1371/journal.pone.0094077openalex-snapshot
Dissecting a Hidden Gene Duplication: The Arabidopsis thaliana SEC10 Locus
inferredcites →https://doi.org/10.1371/journal.ppat.1004243openalex-snapshot
Arabidopsis LIP5, a Positive Regulator of Multivesicular Body Biogenesis, Is a Critical Target of Pathogen-Responsive MAPK Cascade in Plant Basal Defense
inferredcites →https://doi.org/10.1371/journal.ppat.1004496openalex-snapshot
The Plasmodesmal Protein PDLP1 Localises to Haustoria-Associated Membranes during Downy Mildew Infection and Regulates Callose Deposition
inferredcites →https://doi.org/10.15252/embr.201439363openalex-snapshot
Exosomes and other extracellular vesicles in host–pathogen interactions
inferredcites →https://doi.org/10.2174/092986612799363163openalex-snapshot
Extracellular Sunflower Proteins: Evidence on Non-classical Secretion of a Jacalin-Related Lectin
inferredcites →https://doi.org/10.3389/fpls.2011.00111openalex-snapshot
Membrane Traffic and Fusion at Post-Golgi Compartments
inferredcites →https://doi.org/10.3389/fpls.2012.00159openalex-snapshot
Evolution of the Land Plant Exocyst Complexes
inferredcites →https://doi.org/10.3389/fpls.2013.00009openalex-snapshot
Plant secretome proteomics
inferredcites →https://doi.org/10.3389/fpls.2013.00111openalex-snapshot
Plant cell wall proteomics: the leadership of Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2015.00478openalex-snapshot
Proteomic analysis of apoplastic fluid of Coffea arabica leaves highlights novel biomarkers for resistance against Hemileia vastatrix
inferredcites →https://doi.org/10.3390/ijms15057611openalex-snapshot
Delivering of Proteins to the Plant Vacuole—An Update
inferredcites →https://doi.org/10.4161/15592324.2014.984524openalex-snapshot
Arabinogalactan biosynthesis: Implication of AtGALT29A enzyme activity regulated by phosphorylation and co-localized enzymes for nucleotide sugar metabolism in the compartments outside of the Golgi apparatus
inferredcites →https://doi.org/10.4161/auto.6.5.12066openalex-snapshot
Role of autophagy in unconventional protein secretion
inferredcites →https://doi.org/10.4161/cib.1.1.6639openalex-snapshot
A role for vesicular transport of macromolecules across cell walls in fungal pathogenesis
inferredcites →https://doi.org/10.4161/psb.19675openalex-snapshot
Apoplastic exosome-like vesicles: A new way of protein secretion in plants?
inferredcites →https://doi.org/10.4161/psb.26732openalex-snapshot
TheArabidopsisexocyst subcomplex subunits involved in a golgi-independent transport into the vacuole possess consensus autophagy-associated atg8 interacting motifs
inferredcites →https://doi.org/10.7490/f1000research.1091965.1openalex-snapshot
Evolution of the land plant exocyst complex

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/9780470015902.a0029216openalex-snapshot
Exocytosis, Endocytosis and Membrane Recycling in Plant Cells
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Small Extracellular Vesicles Secreted by Nigrostriatal Astrocytes Rescue Cell Death and Preserve Mitochondrial Function in Parkinson's Disease
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Structural and Functional Characterization of EXPO‐Derived Extracellular Vesicles in Plants
inferred← citeshttps://doi.org/10.1002/advs.202506590openalex-snapshot
Peptide Hormone‐Mediated Regulation of Plant Development and Environmental Adaptability
inferred← citeshttps://doi.org/10.1002/bies.202400150openalex-snapshot
Linking secretion and cytoskeleton in immunity– a case for Arabidopsis TGNap1
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Roles of Noncoding RNAs in Islet Biology
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Novel Pharmacological Targets for Pulmonary Arterial Hypertension
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inferred← citeshttps://doi.org/10.1002/j.2040-4603.2021.tb00182.xopenalex-snapshot
Novel Pharmacological Targets for Pulmonary Arterial Hypertension
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Metabolic labeling of cardiomyocyte‐derived small extracellular‐vesicle (sEV) miRNAs identifies miR‐208a in cardiac regulation of lung gene expression
inferred← citeshttps://doi.org/10.1002/mco2.543openalex-snapshot
miR‐1246 promotes osteosarcoma cell migration via NamiRNA‐enhancer network dependent on Argonaute 2
inferred← citeshttps://doi.org/10.1007/978-1-0716-4059-3_2openalex-snapshot
An Overview of Protein Secretion in Plant Cells
inferred← citeshttps://doi.org/10.1007/978-1-4939-7262-3_2openalex-snapshot
An Overview of Protein Secretion in Plant Cells
inferred← citeshttps://doi.org/10.1007/978-1-4939-7262-3_21openalex-snapshot
Analysis of Exocyst-Positive Organelle (EXPO)-Mediated Unconventional Protein Secretion (UPS) in Plant Cells
inferred← citeshttps://doi.org/10.1007/978-1-4939-7262-3_3openalex-snapshot
Bioinformatics Analysis of Protein Secretion in Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-73079-5_13openalex-snapshot
The Dialogue into the Sow Genital Tract: An Essential Process for Fertility
inferred← citeshttps://doi.org/10.1007/978-3-319-56645-0_6openalex-snapshot
Polar Protein Exocytosis: Lessons from Plant Pollen Tube
inferred← citeshttps://doi.org/10.1007/978-3-319-78655-1_11openalex-snapshot
Prologue: About DAMPs, PAMPs, and MAMPs
inferred← citeshttps://doi.org/10.1007/978-3-319-78655-1_22openalex-snapshot
Cellular Inflammatory Responses
inferred← citeshttps://doi.org/10.1007/s00122-019-03463-5openalex-snapshot
Association mapping of wheat Fusarium head blight resistance-related regions using a candidate-gene approach and their verification in a biparental population
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The cell-surface protein composition of a coral symbiont, Breviolum psygmophilum, reveals a mechanism for host specificity and displays dynamic regulation during temperature stress
inferred← citeshttps://doi.org/10.1007/s00299-026-03983-7openalex-snapshot
Extracellular vesicles released by in vitro plant cell cultures: emerging systems for vesicle-mediated communication and biomedical translation
inferred← citeshttps://doi.org/10.1007/s00497-015-0269-zopenalex-snapshot
Classification of EA1-box proteins and new insights into their role during reproduction in grasses
inferred← citeshttps://doi.org/10.1007/s00709-016-0952-4openalex-snapshot
The plant secretory pathway seen through the lens of the cell wall
inferred← citeshttps://doi.org/10.1007/s00709-019-01435-6openalex-snapshot
Plant extracellular vesicles
inferred← citeshttps://doi.org/10.1007/s00709-019-01478-9openalex-snapshot
At the border of the unknown—a plea for curiosity
inferred← citeshttps://doi.org/10.1007/s00709-025-02059-9openalex-snapshot
In memoriam: David G. Robinson
inferred← citeshttps://doi.org/10.1007/s11033-026-12327-3openalex-snapshot
GABARAPL2 and Alix mediate reciprocal regulation of autophagy and exosome pathways to facilitate cellular homeostasis
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Secretome profiling of Pinus nigra embryogenic cultures reveals a freely secreted protein fraction dominated by cell wall- and redox-related proteins
inferred← citeshttps://doi.org/10.1007/s11357-020-00204-1openalex-snapshot
Composition of Caenorhabditis elegans extracellular vesicles suggests roles in metabolism, immunity, and aging
inferred← citeshttps://doi.org/10.1007/s12015-022-10455-4openalex-snapshot
Stem Cell-derived Extracellular Vesicles: A Promising Nano Delivery Platform to the Brain?
inferred← citeshttps://doi.org/10.1016/b978-0-12-814371-1.16001-1openalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1016/b978-0-12-819453-9.00005-2openalex-snapshot
Chemical communication between Trichoderma and plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-21469-1.16001-4openalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1016/b978-0-443-23891-8.00003-2openalex-snapshot
Extracellular vesicles: unlocking therapeutic potential in regenerative medicine
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102712openalex-snapshot
Extracellular vesicles and bioactive peptides for regenerative medicine in cosmetology
inferred← citeshttps://doi.org/10.1016/j.canlet.2022.215979openalex-snapshot
Crosstalk between extracellular vesicles and tumor-associated macrophage in the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.cej.2026.177298openalex-snapshot
The application of Chinese herbal medicine-derived extracellular vesicles as drug carriers in drug delivery systems
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2023.08.005openalex-snapshot
Extracellular vesicles as a novel mediator of interkingdom communication
inferred← citeshttps://doi.org/10.1016/j.ejps.2016.09.022openalex-snapshot
Extracellular vesicles in food: Experimental evidence of their secretion in grape fruits
inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e41960openalex-snapshot
Small extracellular vesicles derived from miRNA-486 overexpressed dental pulp stem cells mitigate high altitude pulmonary edema through PTEN/PI3K/AKT/eNOS pathway
inferred← citeshttps://doi.org/10.1016/j.jconrel.2020.08.018openalex-snapshot
Cancer therapy based on extracellular vesicles as drug delivery vehicles
inferred← citeshttps://doi.org/10.1016/j.jconrel.2026.115265openalex-snapshot
Exosomes as next-generation drug carriers: Transforming cancer therapy
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2023.578064openalex-snapshot
Emerging role of extracellular vesicles in multiple sclerosis: From cellular surrogates to pathogenic mediators and beyond
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153467openalex-snapshot
Plants have neither synapses nor a nervous system
inferred← citeshttps://doi.org/10.1016/j.jprot.2025.105557openalex-snapshot
The protein cargo of extracellular vesicles. Recent advances in lung cancer research
inferred← citeshttps://doi.org/10.1016/j.mcpro.2025.101464openalex-snapshot
Oral Microbiome–Derived Proteins in Brain Extracellular Vesicles Circulate and Tie to Specific Dysbiotic and Neuropathological Profiles in Age-Related Dementias
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.09.001openalex-snapshot
A safe ride in extracellular vesicles – small RNA trafficking between plant hosts and pathogens
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2021.08.006openalex-snapshot
Intercellular communication through extracellular vesicles in cancer and evolutionary biology
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.108025openalex-snapshot
Extracellular vesicles in cardiovascular disease: Biological functions and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.03.020openalex-snapshot
Expression of CLAVATA3 fusions indicates rapid intracellular processing and a role of ERAD
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110979openalex-snapshot
Comparison of mass spectrometry data and bioinformatics predictions to assess the bona fide localization of proteins identified in cell wall proteomics studies
inferred← citeshttps://doi.org/10.1016/j.repbre.2022.11.001openalex-snapshot
Apical vesicles: Social networking at the pollen tube tip
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.11.007openalex-snapshot
Pathways of Unconventional Protein Secretion
inferred← citeshttps://doi.org/10.1016/j.vesic.2025.100075openalex-snapshot
Role of extracellular vesicles in immune modulation, angiogenesis, progression and therapeutic resistance of glioblastoma
inferred← citeshttps://doi.org/10.1016/j.yexcr.2020.112213openalex-snapshot
Increased release of microvesicles containing mitochondria is associated with the myeloid differentiation of AML-M5 leukaemia cells
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b05173openalex-snapshot
Charge Detection Mass Spectrometry Measurements of Exosomes and other Extracellular Particles Enriched from Bovine Milk
inferred← citeshttps://doi.org/10.1021/acsami.3c16839openalex-snapshot
Smart Nanoscale Extracellular Vesicles in the Brain: Unveiling their Biology, Diagnostic Potential, and Therapeutic Applications
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.5c00377openalex-snapshot
Optimizing Isolation Methods and Exploring the Therapeutic Potential of Lotus-Derived Extracellular Vesicles in Modulating Inflammation and Promoting Wound Healing
inferred← citeshttps://doi.org/10.1038/nrm.2017.125openalex-snapshot
Shedding light on the cell biology of extracellular vesicles
inferred← citeshttps://doi.org/10.1039/d3fo03503dopenalex-snapshot
Engineered plant extracellular vesicles for natural delivery across physiological barriers
inferred← citeshttps://doi.org/10.1039/d3tb02752jopenalex-snapshot
Plant-derived exosomes: a green approach for cancer drug delivery
inferred← citeshttps://doi.org/10.1080/10408363.2020.1751584openalex-snapshot
Clinical applications of extracellular vesicle long RNAs
inferred← citeshttps://doi.org/10.1080/11263504.2025.2531894openalex-snapshot
Highways and detours: routes for protein and polysaccharide secretion into the plant cell wall
inferred← citeshttps://doi.org/10.1080/15592324.2023.2291618openalex-snapshot
Exogenous abscisic acid treatment regulates protein secretion in sorghum cell suspension cultures
inferred← citeshttps://doi.org/10.1080/20013078.2019.1703480openalex-snapshot
Anti‐melanogenic effects of extracellular vesicles derived from plant leaves and stems in mouse melanoma cells and human healthy skin
inferred← citeshttps://doi.org/10.1083/jcb.202307066openalex-snapshot
Logistics of defense: The contribution of endomembranes to plant innate immunity
inferred← citeshttps://doi.org/10.1093/glycob/cww044openalex-snapshot
The plant secretory pathway for the trafficking of cell wall polysaccharides and glycoproteins
inferred← citeshttps://doi.org/10.1093/jxb/erac363openalex-snapshot
Do photosynthetic cells communicate with each other during cell death? From cyanobacteria to vascular plants
inferred← citeshttps://doi.org/10.1093/jxb/erx261openalex-snapshot
Merging roads: chemical tools and cell biology to study unconventional protein secretion
inferred← citeshttps://doi.org/10.1093/jxb/erx262openalex-snapshot
Protein secretion in plants: conventional and unconventional pathways and new techniques
inferred← citeshttps://doi.org/10.1093/jxb/erx286openalex-snapshot
The endoplasmic reticulum is a hub to sort proteins toward unconventional traffic pathways and endosymbiotic organelles
inferred← citeshttps://doi.org/10.1093/jxb/erx334openalex-snapshot
The roles of membranes and associated cytoskeleton in plant virus replication and cell-to-cell movement
inferred← citeshttps://doi.org/10.1093/jxb/erx355openalex-snapshot
Plant extracellular vesicles are incorporated by a fungal pathogen and inhibit its growth
inferred← citeshttps://doi.org/10.1093/jxb/erx363openalex-snapshot
Exocyst and autophagy-related membrane trafficking in plants
inferred← citeshttps://doi.org/10.1093/jxb/ery162openalex-snapshot
A broadly conserved NERD genetically interacts with the exocyst to affect root growth and cell expansion
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgag238openalex-snapshot
Nanotubes enable intercellular communication in early-branching eukaryotes
inferred← citeshttps://doi.org/10.1101/2021.04.23.441135openalex-snapshot
Small Extracellular Vesicles Secreted by Region-specific Astrocytes Ameliorate the Mitochondrial Function in a Cellular Model of Parkinson’s Disease
inferred← citeshttps://doi.org/10.1101/2024.11.02.621656openalex-snapshot
Reciprocal regulation of autophagy and exosome pathway is mediated by GABARAPL2 and Alix to facilitate cellular homeostasis
inferred← citeshttps://doi.org/10.1104/pp.16.00097openalex-snapshot
Pea Border Cell Maturation and Release Involve Complex Cell Wall Structural Dynamics
inferred← citeshttps://doi.org/10.1104/pp.16.00754openalex-snapshot
A Distinct Pathway for Polar Exocytosis in Plant Cell Wall Formation
inferred← citeshttps://doi.org/10.1104/pp.17.01239openalex-snapshot
The Plant Trans-Golgi Network: Not Just a Matter of Distinction
inferred← citeshttps://doi.org/10.1111/febs.16981openalex-snapshot
A guide to the expanding field of extracellular vesicles and their release in regulated cell death programs
inferred← citeshttps://doi.org/10.1111/jipb.12895openalex-snapshot
The roles of endomembrane trafficking in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1111/jipb.13181openalex-snapshot
Effective methods for isolation and purification of extracellular vesicles from plants
inferred← citeshttps://doi.org/10.1111/jph.13022openalex-snapshot
In situ and ex situ imaging of plant extracellular vesicles as nanovectors for cross‐domain communication
inferred← citeshttps://doi.org/10.1111/nph.14959openalex-snapshot
Plant–microbe interactions: organelles and the cytoskeleton in action
inferred← citeshttps://doi.org/10.1111/nph.18316openalex-snapshot
Unprocessed wheat γ‐gliadin reduces gluten accumulation associated with the endoplasmic reticulum stress and elevated cell death
inferred← citeshttps://doi.org/10.1111/nph.19134openalex-snapshot
Recent advances in plant endomembrane research and new microscopical techniques
inferred← citeshttps://doi.org/10.1111/tpj.15301openalex-snapshot
Ride to cell wall: Arabidopsis XTH11, XTH29 and XTH33 exhibit different secretion pathways and responses to heat and drought stress
inferred← citeshttps://doi.org/10.1111/tpj.17246openalex-snapshot
A cell fractionation and quantitative proteomics pipeline to enable functional analyses of cotton fiber development
inferred← citeshttps://doi.org/10.1134/s1021443726602351openalex-snapshot
Intracellular Localization of the Nicotiana benthamiana Glycoprotein KPILP is Determined by Its N-Glycosylation Sites
inferred← citeshttps://doi.org/10.1146/annurev-arplant-081519-035846openalex-snapshot
Dynamic Construction, Perception, and Remodeling of Plant Cell Walls
inferred← citeshttps://doi.org/10.1146/annurev-arplant-081720-010616openalex-snapshot
Message in a Bubble: Shuttling Small RNAs and Proteins Between Cells and Interacting Organisms Using Extracellular Vesicles
inferred← citeshttps://doi.org/10.1159/000508613openalex-snapshot
Liquid Biopsy in Uveal Melanoma: Are We There Yet?
inferred← citeshttps://doi.org/10.11606/t.42.2021.tde-18022022-122839openalex-snapshot
Perfil de microRNAs de vesículas extracelulares do soro de animais obesos e seu possível envolvimento na regulação do metabolismo energético.
inferred← citeshttps://doi.org/10.1167/iovs.18-26277openalex-snapshot
MMP14-Containing Exosomes Cleave VEGFR1 and Promote VEGFA-Induced Migration and Proliferation of Vascular Endothelial Cells
inferred← citeshttps://doi.org/10.1186/s12917-022-03137-3openalex-snapshot
Extracellular vesicles in low volume uterine lavage and serum: novel and promising biomarker for endometritis in Arabian mares
inferred← citeshttps://doi.org/10.1186/s12951-025-03602-9openalex-snapshot
Exploring the bioactivity of MicroRNAs Originated from Plant-derived Exosome-like Nanoparticles (PELNs): current perspectives
inferred← citeshttps://doi.org/10.1186/s12951-026-04484-1openalex-snapshot
Plant-derived nanovesicles: the intelligent nanoplatforms for therapeutics and drug delivery
inferred← citeshttps://doi.org/10.1186/s12964-019-0319-5openalex-snapshot
Extracellular vesicles in bone: “dogrobbers” in the “eternal battle field”
inferred← citeshttps://doi.org/10.1186/s12964-022-00889-1openalex-snapshot
Plant-derived extracellular vesicles: a novel nanomedicine approach with advantages and challenges
inferred← citeshttps://doi.org/10.1186/s13578-021-00537-0openalex-snapshot
The versatile role of exosomes in human retroviral infections: from immunopathogenesis to clinical application
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012748openalex-snapshot
H5 subtype avian influenza virus induces Golgi apparatus stress response via TFE3 pathway to promote virus replication
inferred← citeshttps://doi.org/10.18174/509627openalex-snapshot
Glyco-engineering in plants : Fucosyltransferase characterisation and application for the production of immunomodulatory helminth glycoproteins
inferred← citeshttps://doi.org/10.20868/upm.thesis.52072openalex-snapshot
Papel relevante de la proteína P3 del virus del mosaico del nabo (TUMV) en la alteración del patrón de desarrollo de plantas infectadas de Arabidopsis thaliana
inferred← citeshttps://doi.org/10.2147/ijn.s597419openalex-snapshot
Bacterial Extracellular Vesicles in Aging: Mechanisms and Therapeutic Prospects
inferred← citeshttps://doi.org/10.2174/0929866527666200408142827openalex-snapshot
Proteomics-Based Characterization of the Effects of MMP14 on the Protein Content of Exosomes from Corneal Fibroblasts
inferred← citeshttps://doi.org/10.3233/jad-215666openalex-snapshot
Potential Roles of Extracellular Vesicles as Diagnosis Biomarkers and Therapeutic Approaches for Cognitive Impairment in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.33549/physiolres.934886openalex-snapshot
Plant extracellular vesicles and their potential in human health research, the practical approach
inferred← citeshttps://doi.org/10.3389/fcell.2020.577084openalex-snapshot
Extracellular Vesicles: Recent Developments in Aging and Reproductive Diseases
inferred← citeshttps://doi.org/10.3389/fcell.2022.883841openalex-snapshot
Unconventional Secretion of Plant Extracellular Vesicles and Their Benefits to Human Health: A Mini Review
inferred← citeshttps://doi.org/10.3389/fcell.2022.895853openalex-snapshot
Unconventional Pathways of Protein Secretion: Mammals vs. Plants
inferred← citeshttps://doi.org/10.3389/fendo.2024.1444940openalex-snapshot
Extracellular vesicular microRNAs and cardiac hypertrophy
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1713012openalex-snapshot
Bronchial epithelial cell-derived extracellular vesicles drive inflammasome activation and NTHi infection in COPD
inferred← citeshttps://doi.org/10.3389/fpls.2016.01451openalex-snapshot
Better Than Nothing? Limitations of the Prediction Tool SecretomeP in the Search for Leaderless Secretory Proteins (LSPs) in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.652337openalex-snapshot
The Exocyst Complex Subunit EXO70E1-V From Haynaldia villosa Interacts With Wheat Powdery Mildew Resistance Gene CMPG1-V
inferred← citeshttps://doi.org/10.3389/fpls.2023.1171957openalex-snapshot
The EXO70 inhibitor Endosidin2 alters plasma membrane protein composition in Arabidopsis roots
inferred← citeshttps://doi.org/10.3390/biom10091327openalex-snapshot
Extracellular Vesicles as Nanotherapeutics for Parkinson’s Disease
inferred← citeshttps://doi.org/10.3390/biom15081055openalex-snapshot
Plant-Derived Vesicle-like Nanoparticles: Pioneering Sustainable and Effective Approaches for Tissue Repair and Regeneration
inferred← citeshttps://doi.org/10.3390/biom8030094openalex-snapshot
Plasma Membrane Lipid Domains as Platforms for Vesicle Biogenesis and Shedding?
inferred← citeshttps://doi.org/10.3390/biomedicines11030728openalex-snapshot
Extracellular Vesicles, Cell-Penetrating Peptides and miRNAs as Future Novel Therapeutic Interventions for Parkinson’s and Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/cells8040337openalex-snapshot
Diverse Role of SNARE Protein Sec22 in Vesicle Trafficking, Membrane Fusion, and Autophagy
inferred← citeshttps://doi.org/10.3390/cells9112505openalex-snapshot
Mechanisms of Action of EGFR Tyrosine Kinase Receptor Incorporated in Extracellular Vesicles
inferred← citeshttps://doi.org/10.3390/f15122081openalex-snapshot
Identification of the P24 Gene Family Related to Vesicular Transport in Cyclocarya paliurus and Their Expression Analysis Under Salt Stress
inferred← citeshttps://doi.org/10.3390/iecps2020-08695openalex-snapshot
Abiotic Stress Upregulates the Expression of Genes Involved in PSV and Autophagy Routes
inferred← citeshttps://doi.org/10.3390/ijms18040703openalex-snapshot
Unconventional Transport Routes of Soluble and Membrane Proteins and Their Role in Developmental Biology
inferred← citeshttps://doi.org/10.3390/ijms20010060openalex-snapshot
Identification and Characterization of the EXO70 Gene Family in Polyploid Wheat and Related Species
inferred← citeshttps://doi.org/10.3390/ijms24010424openalex-snapshot
Relevance of the Exocyst in Arabidopsis exo70e2 Mutant for Cellular Homeostasis under Stress
inferred← citeshttps://doi.org/10.3390/ijms25021154openalex-snapshot
microRNAs: Key Regulators in Plant Responses to Abiotic and Biotic Stresses via Endogenous and Cross-Kingdom Mechanisms
inferred← citeshttps://doi.org/10.3390/life14091169openalex-snapshot
The RING-Type E3 Ligase BOI Interacts with EXO70E2 and Mediates Its Ubiquitination in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ph15060708openalex-snapshot
Focusing on Future Applications and Current Challenges of Plant Derived Extracellular Vesicles
inferred← citeshttps://doi.org/10.3390/pharmaceutics16081029openalex-snapshot
Extracellular Vesicles as Drug Delivery System for Cancer Therapy
inferred← citeshttps://doi.org/10.3390/plants12071428openalex-snapshot
LSPpred Suite: Tools for Leaderless Secretory Protein Prediction in Plants
inferred← citeshttps://doi.org/10.3390/polym15020318openalex-snapshot
Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery
inferred← citeshttps://doi.org/10.3390/proteomes8040029openalex-snapshot
Heat Stress Triggers Differential Protein Accumulation in the Extracellular Matrix of Sorghum Cell Suspension Cultures
inferred← citeshttps://doi.org/10.35537/10915/71433openalex-snapshot
Cambios en el apoplasto asociados a la senescencia foliar
inferred← citeshttps://doi.org/10.70675/12155076z603ez4c55zbedfz05c58338e7adopenalex-snapshot
Caractérisation du rôle des vésicules extracellulaires sur le microenvironnement du lymphome folliculaire
inferred← citeshttps://doi.org/10.70675/4c1c1220ze70dz4948z9cddz682d3502dce2openalex-snapshot
Exploring the potential of extracellular vesicles as therapeutic protein delivery vectors
inferred← citeshttps://doi.org/10.7150/ijbs.26518openalex-snapshot
Extracellular Vesicles: Potential Participants in Circadian Rhythm Synchronization
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