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Tissue‐specific isolation of Arabidopsis/plant mitochondria – IMTACT (isolation of mitochondria tagged in specific cell types)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4899-3517-5_21openalex-snapshot
The Effects of Different Ionic-Conditions on the Activity of Cytochrome C-Oxidase in Purified Plant Mitochondria
inferredcites →https://doi.org/10.1007/bf00203657openalex-snapshot
The promoter of the Arabidopsis thaliana SUC2 sucrose-H+ symporter gene directs expression of ?-glucuronidase to the phloem: Evidence for phloem loading and unloading by SUC2
inferredcites →https://doi.org/10.1016/0005-2728(72)90035-7openalex-snapshot
Preparation of intact plant mitochondria
inferredcites →https://doi.org/10.1016/0092-8674(93)90459-4openalex-snapshot
Signal transduction mutants of arabidopsis uncouple nuclear CAB and RBCS gene expression from chloroplast development
inferredcites →https://doi.org/10.1016/0168-9452(88)90177-xopenalex-snapshot
Properties of mitochondria isolated from greening soybean and lupin tissues
inferredcites →https://doi.org/10.1016/0304-4211(78)90101-3openalex-snapshot
Preparatiön of mitochondria from gree leaves of spinach by differential centrifugation and phase partition
inferredcites →https://doi.org/10.1016/j.bbaexp.2003.12.004openalex-snapshot
Expression of a glycine decarboxylase complex H-protein in non-photosynthetic tissues of Populus tremuloides
inferredcites →https://doi.org/10.1016/j.bbrc.2017.09.168openalex-snapshot
A simple elution strategy for biotinylated proteins bound to streptavidin conjugated beads using excess biotin and heat
inferredcites →https://doi.org/10.1016/j.cell.2016.07.040openalex-snapshot
Absolute Quantification of Matrix Metabolites Reveals the Dynamics of Mitochondrial Metabolism
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.013openalex-snapshot
A Simple Method for Gene Expression and Chromatin Profiling of Individual Cell Types within a Tissue
inferredcites →https://doi.org/10.1016/j.devcel.2019.02.022openalex-snapshot
Spatiotemporal Developmental Trajectories in the Arabidopsis Root Revealed Using High-Throughput Single Cell RNA Sequencing
inferredcites →https://doi.org/10.1016/j.phytochem.2010.12.004openalex-snapshot
Combining proteomics of root and shoot mitochondria and transcript analysis to define constitutive and variable components in plant mitochondria
inferredcites →https://doi.org/10.1016/s0031-9422(00)88038-3openalex-snapshot
Mitochondrial preparations from the fruit of the apple—I.
inferredcites →https://doi.org/10.1038/s41598-019-46171-2openalex-snapshot
A unified multi-kingdom Golden Gate cloning platform
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1071/pp9850219openalex-snapshot
Biochemical Characterization of Chlorophyll-Free Mitochondria From Pea Leaves
inferredcites →https://doi.org/10.1091/mbc.e02-08-0509openalex-snapshot
The AtC–VPS Protein Complex Is Localized to the Tonoplast and the Prevacuolar Compartment in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erm034openalex-snapshot
The glycine decarboxylase complex multienzyme family in Populus
inferredcites →https://doi.org/10.1104/pp.003970openalex-snapshot
NPSN11 Is a Cell Plate-Associated SNARE Protein That Interacts with the Syntaxin KNOLLE
inferredcites →https://doi.org/10.1104/pp.010387openalex-snapshot
Analysis of the Arabidopsis Mitochondrial Proteome
inferredcites →https://doi.org/10.1104/pp.125.2.943openalex-snapshot
Purification and Characterization of the Preprotein Translocase of the Outer Mitochondrial Membrane from Arabidopsis. Identification of Multiple Forms of TOM20
inferredcites →https://doi.org/10.1104/pp.43.12.2001openalex-snapshot
Studies on Ultrastructure and Purification of Isolated Plant Mitochondria
inferredcites →https://doi.org/10.1104/pp.66.3.442openalex-snapshot
Method to Obtain a Chlorophyll-free Preparation of Intact Mitochondria from Spinach Leaves
inferredcites →https://doi.org/10.1104/pp.88.1.69openalex-snapshot
Influence of Photorespiration on ATP/ADP Ratios in the Chloroplasts, Mitochondria, and Cytosol, Studied by Rapid Fractionation of Barley (Hordeum vulgare) Protoplasts
inferredcites →https://doi.org/10.1105/tpc.107.050534openalex-snapshot
Functional Definition of Outer Membrane Proteins Involved in Preprotein Import into Mitochondria
inferredcites →https://doi.org/10.1105/tpc.16.00249openalex-snapshot
Lost in Transit: Long-Distance Trafficking and Phloem Unloading of Protein Signals in Arabidopsis Homografts
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02298.xopenalex-snapshot
Expression of GFP‐fusions in Arabidopsis companion cells reveals non‐specific protein trafficking into sieve elements and identifies a novel post‐phloem domain in roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03253.xopenalex-snapshot
TECHNICAL ADVANCE: Free‐flow electrophoresis for purification of plant mitochondria by surface charge
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00521.xopenalex-snapshot
Preparation of leaf mitochondria from Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0088218openalex-snapshot
A Modular Plasmid Assembly Kit for Multigene Expression, Gene Silencing and Silencing Rescue in Plants
inferredcites →https://doi.org/10.1371/journal.pone.0118122openalex-snapshot
Live Imaging of Companion Cells and Sieve Elements in Arabidopsis Leaves
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Dynamic Shift in Mitochondria from Mature Pollen Grains
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Tissue‐Specific Isolation of Tagged Arabidopsis Plastids
inferred← citeshttps://doi.org/10.1007/978-1-0716-1653-6_2openalex-snapshot
Cell Type–Specific Isolation of Mitochondria in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1653-6_3openalex-snapshot
Isolation of Plant Mitochondria Using Affinity Purification
inferred← citeshttps://doi.org/10.1007/978-981-99-4890-1_11openalex-snapshot
Exploring Plant-Pathogen Interactions through Subcellular Proteomics: Insights and Challenges
inferred← citeshttps://doi.org/10.1007/s12268-021-1674-5openalex-snapshot
Die Proteinausstattung eines einzelnen pflanzlichen Mitochondriums
inferred← citeshttps://doi.org/10.1016/j.bbabio.2021.148443openalex-snapshot
Protein interaction patterns in Arabidopsis thaliana leaf mitochondria change in dependence to light
inferred← citeshttps://doi.org/10.1016/j.cell.2026.08.027openalex-snapshot
A high-confidence plant mitochondrial proteome via protein correlation profiling
inferred← citeshttps://doi.org/10.1016/j.cub.2024.12.037openalex-snapshot
The atypical proteome of mitochondria from mature pollen grains
inferred← citeshttps://doi.org/10.1016/j.mitoco.2024.09.002openalex-snapshot
Innovative methods for isolating highly purified mitochondria essential for biomedical studies
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100015openalex-snapshot
In the symbiosome: Cross-kingdom dating under the moonlight
inferred← citeshttps://doi.org/10.1016/j.ncrops.2025.100081openalex-snapshot
Current advances in plant mitochondria: Application revolution of cytoplasmic male sterility
inferred← citeshttps://doi.org/10.1016/j.tibs.2025.06.010openalex-snapshot
Cell-specific mitoproteomics reveals mitochondrial plasticity and applications
inferred← citeshttps://doi.org/10.1038/s41438-021-00470-wopenalex-snapshot
Isolation and comparative proteomic analysis of mitochondria from the pulp of ripening citrus fruit
inferred← citeshttps://doi.org/10.1038/s41467-025-62652-7openalex-snapshot
Ribosome biogenesis in plants requires the nuclear envelope and mitochondria localized OPENER complex
inferred← citeshttps://doi.org/10.1039/d5cc06838jopenalex-snapshot
A small-molecule AIE fluorescent probe targeting plant mitochondria and its application in super-resolution imaging
inferred← citeshttps://doi.org/10.1080/01140671.2022.2139730openalex-snapshot
An approach for vacuole isolation and vacuolar protein identification by proteomics in apple
inferred← citeshttps://doi.org/10.1093/jxb/erad133openalex-snapshot
Comparison of plastid proteomes points towards a higher plastidial redox turnover in vascular tissues than in mesophyll cells
inferred← citeshttps://doi.org/10.1093/jxb/erae214openalex-snapshot
The mitochondrial orf117Sha gene desynchronizes pollen development and causes pollen abortion in Arabidopsis Sha cytoplasmic male sterility
inferred← citeshttps://doi.org/10.1093/jxb/eraf490openalex-snapshot
Illuminating the subcellular maze: fluorescence-activated organelle sorting in plant sciences
inferred← citeshttps://doi.org/10.1093/plphys/kiad540openalex-snapshot
PLANT UNCOUPLING MITOCHONDRIAL PROTEIN 2 localizes to the Golgi
inferred← citeshttps://doi.org/10.1101/2021.10.31.466655openalex-snapshot
A versatile mitochondria isolation- and analysis-pipeline generates 3D nano-topographies and mechano-physical surface maps of single organelles
inferred← citeshttps://doi.org/10.1101/2023.03.03.531038openalex-snapshot
A proximity-dependent biotinylation map of cytosol-facing organelle outer membrane proteome in living Arabidopsis cells
inferred← citeshttps://doi.org/10.1101/2024.01.17.575984openalex-snapshot
The mitochondrial orf117Sha gene desynchronizes pollen development and causes pollen abortion in the Arabidopsis Sha CMS
inferred← citeshttps://doi.org/10.1101/2024.10.14.617781openalex-snapshot
GCS-H2 is essential for growth as it acts as the main relay for mitochondrial lipoylation in heterotrophic tissues of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2025.09.19.677279openalex-snapshot
The seed mitochondrial proteome of Lupinus albus provides insight into energy metabolism during germination
inferred← citeshttps://doi.org/10.1105/tpc.20.00241openalex-snapshot
In Vivo NADH/NAD + Biosensing Reveals the Dynamics of Cytosolic Redox Metabolism in Plants
inferred← citeshttps://doi.org/10.1111/nph.20317openalex-snapshot
Synergistic role of Rubisco inhibitor release and degradation in photosynthesis
inferred← citeshttps://doi.org/10.1111/ppl.70465openalex-snapshot
Comparative Study of the Mitochondrial Proteome From Mesophyll, Vascular, and Guard Cells in Response to Carbon Starvation
inferred← citeshttps://doi.org/10.1111/ppl.70529openalex-snapshot
Proteomic Analysis Infers Optimized ATP ‐Production in Guard Cell Mitochondria
inferred← citeshttps://doi.org/10.1111/ppl.70579openalex-snapshot
Mitochondrial Cell‐Type‐Specific Profiling: Differential Function of Mesophyll and Guard Cells is Reflected by Their Mitochondrial Proteome
inferred← citeshttps://doi.org/10.1111/tpj.15495openalex-snapshot
Plant mitochondria – past, present and future
inferred← citeshttps://doi.org/10.1111/tpj.16456openalex-snapshot
Fluorescence‐activated multi‐organelle mapping of subcellular plant hormone distribution
inferred← citeshttps://doi.org/10.1146/annurev-arplant-071425-085632openalex-snapshot
In Vivo Monitoring of Energy Metabolism with Genetically Encoded Fluorescent Biosensors
inferred← citeshttps://doi.org/10.1186/s13007-020-00663-9openalex-snapshot
Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.3389/fpls.2026.1763082openalex-snapshot
Newly assembled mitochondrial genomes of Hypericum (Hypericaceae) provide insights into phylogenetic relationships and inter-organellar conflict
inferred← citeshttps://doi.org/10.3390/ijms22179370openalex-snapshot
Auxin Metabolome Profiling in the Arabidopsis Endoplasmic Reticulum Using an Optimised Organelle Isolation Protocol
inferred← citeshttps://doi.org/10.3410/f.738489609.793579222openalex-snapshot
Faculty Opinions recommendation of In vivo NADH/NAD+ biosensing reveals the dynamics of cytosolic redox metabolism in plants.
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904679openalex-snapshot
Additional file 1 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904682openalex-snapshot
Additional file 2 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904685openalex-snapshot
Additional file 3 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904688openalex-snapshot
Additional file 4 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904691openalex-snapshot
Additional file 5 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904694openalex-snapshot
Additional file 6 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904697openalex-snapshot
Additional file 7 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904700openalex-snapshot
Additional file 8 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
inferred← citeshttps://doi.org/10.6084/m9.figshare.12904703openalex-snapshot
Additional file 9 of Tagging and catching: rapid isolation and efficient labeling of organelles using the covalent Spy-System in planta
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Assembly of respiratory complex I in plants
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Dissection des interactions moléculaires de la glutarédoxine S15 mitochondriale chez les plantes
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