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Involvement of the Membrane Nanodomain Protein, AtFlot1, in Vesicular Transport of Plasma Membrane H+-ATPase in Arabidopsis thaliana under Salt Stress
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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/yea.3365openalex-snapshot
The plasma membrane H+‐ATPase, a simple polypeptide with a long history
inferredcites →https://doi.org/10.1007/s10555-020-09873-yopenalex-snapshot
Flotillin membrane domains in cancer
inferredcites →https://doi.org/10.1016/0076-6879(87)48054-3openalex-snapshot
[52] Preparation of high-purity plasma membranes
inferredcites →https://doi.org/10.1016/j.cub.2007.07.020openalex-snapshot
Abscisic Acid Triggers the Endocytosis of the Arabidopsis KAT1 K+ Channel and Its Recycling to the Plasma Membrane
inferredcites →https://doi.org/10.1016/j.febslet.2007.04.014openalex-snapshot
Na+ transport in plants
inferredcites →https://doi.org/10.1016/j.molp.2015.11.002openalex-snapshot
Plasma Membrane H + -ATPase Regulation in the Center of Plant Physiology
inferredcites →https://doi.org/10.1016/j.molp.2020.02.012openalex-snapshot
TOLs Function as Ubiquitin Receptors in the Early Steps of the ESCRT Pathway in Higher Plants
inferredcites →https://doi.org/10.1016/j.tplants.2015.03.014openalex-snapshot
Endocytosis and its regulation in plants
inferredcites →https://doi.org/10.1038/35025089openalex-snapshot
CAP defines a second signalling pathway required for insulin-stimulated glucose transport
inferredcites →https://doi.org/10.1038/msb.2011.72openalex-snapshot
Recycling, clustering, and endocytosis jointly maintain PIN auxin carrier polarity at the plasma membrane
inferredcites →https://doi.org/10.1038/ncb2270openalex-snapshot
A membrane trafficking pathway regulated by the plant-specific RAB GTPase ARA6
inferredcites →https://doi.org/10.1038/nplants.2016.17openalex-snapshot
Receptor-mediated sorting of soluble vacuolar proteins ends at the trans-Golgi network/early endosome
inferredcites →https://doi.org/10.1073/pnas.0604421103openalex-snapshot
Suppression of Arabidopsis vesicle-SNARE expression inhibited fusion of H 2 O 2 -containing vesicles with tonoplast and increased salt tolerance
inferredcites →https://doi.org/10.1073/pnas.0910744107openalex-snapshot
Polar localization and degradation of Arabidopsis boron transporters through distinct trafficking pathways
inferredcites →https://doi.org/10.1073/pnas.1100659108openalex-snapshot
Monoubiquitin-dependent endocytosis of the IRON-REGULATED TRANSPORTER 1 (IRT1) transporter controls iron uptake in plants
inferredcites →https://doi.org/10.1073/pnas.1710866114openalex-snapshot
Arabidopsis SH3P2 is an ubiquitin-binding protein that functions together with ESCRT-I and the deubiquitylating enzyme AMSH3
inferredcites →https://doi.org/10.1074/jbc.m110.101733openalex-snapshot
Molecular Characterization of Mutant Arabidopsis Plants with Reduced Plasma Membrane Proton Pump Activity
inferredcites →https://doi.org/10.1080/07352689.2016.1249690openalex-snapshot
Flotillins, Erlins, and HIRs: From Animal Base Camp to Plant New Horizons
inferredcites →https://doi.org/10.1093/jxb/erv069openalex-snapshot
Identification of rice cornichon as a possible cargo receptor for the Golgi-localized sodium transporter OsHKT1;3
inferredcites →https://doi.org/10.1093/jxb/erw222openalex-snapshot
Receptor-mediated sorting of soluble vacuolar proteins: myths, facts, and a new model
inferredcites →https://doi.org/10.1093/jxb/erx262openalex-snapshot
Protein secretion in plants: conventional and unconventional pathways and new techniques
inferredcites →https://doi.org/10.1093/pcp/pcp143openalex-snapshot
Dynamic Aspects of Ion Accumulation by Vesicle Traffic Under Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.102.010421openalex-snapshot
Na+/H+ Exchange Activity in the Plasma Membrane of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.025379openalex-snapshot
Induction of Salt and Osmotic Stress Tolerance by Overexpression of an Intracellular Vesicle Trafficking Protein AtRab7 (AtRabG3e)
inferredcites →https://doi.org/10.1104/pp.123.4.1217openalex-snapshot
Vesicle-Mediated Solute Transport between the Vacuole and the Plasma Membrane
inferredcites →https://doi.org/10.1104/pp.17.01117openalex-snapshot
Inroads into Internalization: Five Years of Endocytic Exploration
inferredcites →https://doi.org/10.1104/pp.19.00163openalex-snapshot
Calcium-Promoted Interaction between the C2-Domain Protein EHB1 and Metal Transporter IRT1 Inhibits Arabidopsis Iron Acquisition
inferredcites →https://doi.org/10.1105/tpc.111.091454openalex-snapshot
Single-Molecule Analysis of PIP2;1 Dynamics and Partitioning Reveals Multiple Modes of Arabidopsis Plasma Membrane Aquaporin Regulation
inferredcites →https://doi.org/10.1105/tpc.112.095695openalex-snapshot
A Membrane Microdomain-Associated Protein, Arabidopsis Flot1, Is Involved in a Clathrin-Independent Endocytic Pathway and Is Required for Seedling Development
inferredcites →https://doi.org/10.1105/tpc.113.122358openalex-snapshot
Clathrin and Membrane Microdomains Cooperatively Regulate RbohD Dynamics and Activity in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00154openalex-snapshot
Salt-Induced Remodeling of Spatially Restricted Clathrin-Independent Endocytic Pathways in Arabidopsis Root
inferredcites →https://doi.org/10.1111/boc.202000118openalex-snapshot
Endocytosis in plants: Peculiarities and roles in the regulated trafficking of plant metal transporters
inferredcites →https://doi.org/10.1111/jipb.13005openalex-snapshot
SINAT E3 ligases regulate the stability of the ESCRT component FREE1 in response to iron deficiency in plants
inferredcites →https://doi.org/10.1111/nph.16018openalex-snapshot
At the intersection of exocytosis and endocytosis in plants
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1134/s102144370706012xopenalex-snapshot
Pinocytosis in the root cells of a salt-accumulating halophyte Suaeda altissima and its possible involvement in chloride transport
inferredcites →https://doi.org/10.1134/s1021443720020077openalex-snapshot
Arabidopsis thaliana Mutant with T-DNA Insertion in the Flot1 (At5g25250) Gene Promotor Possesses Increased Resistance to NaCl
inferredcites →https://doi.org/10.1134/s1021443722010198openalex-snapshot
Mutation of the ARA7/AtRabF2b Gene, That Increases the Content of the Ara7 Protein Regulating Endocytic Trafficking Pathways, Improves Salt Tolerance of the Arabidopsis thaliana (L.) Heynh Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-043015-112242openalex-snapshot
Endocytosis and Endosomal Trafficking in Plants
inferredcites →https://doi.org/10.1146/annurev-physiol-021113-170305openalex-snapshot
Exocytosis and Endocytosis: Modes, Functions, and Coupling Mechanisms
inferredcites →https://doi.org/10.1186/1743-422x-8-479openalex-snapshot
Research advances on flotillins
inferredcites →https://doi.org/10.1242/jcs.092015openalex-snapshot
The roles of flotillin microdomains – endocytosis and beyond
inferredcites →https://doi.org/10.1242/jcs.093559openalex-snapshot
Structure and function of endosomes in plant cells
inferredcites →https://doi.org/10.1242/jcs.203695openalex-snapshot
The retromer, sorting nexins and the plant endomembrane protein trafficking
inferredcites →https://doi.org/10.1534/genetics.111.136911openalex-snapshot
Gene Overexpression: Uses, Mechanisms, and Interpretation
inferredcites →https://doi.org/10.32615/bp.2019.017openalex-snapshot
Characterisation of Arabidopsis flotillins in response to stresses
inferredcites →https://doi.org/10.3389/fcell.2022.895853openalex-snapshot
Unconventional Pathways of Protein Secretion: Mammals vs. Plants
inferredcites →https://doi.org/10.3389/fpls.2018.00991openalex-snapshot
Mapping of Plasma Membrane Proteins Interacting With Arabidopsis thaliana Flotillin 2
inferredcites →https://doi.org/10.3389/fpls.2020.00425openalex-snapshot
A Diverse Membrane Interaction Network for Plant Multivesicular Bodies: Roles in Proteins Vacuolar Delivery and Unconventional Secretion
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4480360openalex-extracted
Synergism of Vesicle Trafficking and Cytoskeleton During Regulation of Plant Growth and Development: A Mechanistic Outlook
inferred← citeshttps://doi.org/10.1002/ptr.70040openalex-snapshot
From Plants to Patients: Advancing Cancer Therapy With Bioengineered Exosomes and AI ‐Driven Innovations
inferred← citeshttps://doi.org/10.1002/smtd.70973openalex-snapshot
A Nano‐Anchor for Anti‐Drift Vesicle Imaging
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21976openalex-snapshot
RETRACTED: Synergism of vesicle trafficking and cytoskeleton during regulation of plant growth and development: A mechanistic outlook
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101535openalex-snapshot
Spatiotemporal dynamics of AHA2 reveal that RALF1 induces its endocytosis and vacuolar degradation
inferred← citeshttps://doi.org/10.1111/nph.70614openalex-snapshot
Clathrin‐mediated endocytosis regulates root endodermal suberization via ROS
inferred← citeshttps://doi.org/10.1134/s1021443723600307openalex-snapshot
The Membrane Nanodomain Flot1 Protein Participates in Formation of the Early Endosomes in the Root Cells of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1134/s1021443724604269openalex-snapshot
Bacterial Elisitor Flg22-Induced Endocytosis in the Immune Reaction of Arabidopsis thaliana Root Cells
inferred← citeshttps://doi.org/10.31857/s0015330323600067openalex-snapshot
The Membrane Nanodomain Flot1 Protein Participates in Formation of the Early Endosomes in the Root Cells of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.31857/s0015330324010011openalex-snapshot
Индуцированный бактериальным элиситором flg22 эндоцитоз в иммунной реакции клеток корней Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms27041917openalex-snapshot
Temporal Transcriptomic and Metabolomic Reprogramming Unveils a Two-Phase Salt Tolerance Mechanism in Apocynum venetum
inferred← citeshttps://doi.org/10.64898/2026.04.27.721028openalex-snapshot
The lipid raft marker flotillin FloA drives relocalization of the plasma membrane H + -ATPase PmaA as a protective response to calcium stress
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