scholarly article | Q13442814 |
P356 | DOI | 10.1111/JIPB.12297 |
P698 | PubMed publication ID | 25319240 |
P50 | author | Chris Hawes | Q60021837 |
Verena Kriechbaumer | Q41586008 | ||
P2093 | author name string | Petra Kiviniemi | |
P2860 | cites work | Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation | Q54330082 |
NAI2 is an endoplasmic reticulum body component that enables ER body formation in Arabidopsis thaliana | Q54516633 | ||
Five Arabidopsis reticulon isoforms share endoplasmic reticulum location, topology, and membrane-shaping properties. | Q55052860 | ||
Metabolons involving plant cytochrome P450s | Q57357493 | ||
High-curvature domains of the ER are important for the organization of ER exit sites in Saccharomyces cerevisiae | Q58480436 | ||
RNA Processing Bodies, Peroxisomes, Golgi Bodies, Mitochondria, and Endoplasmic Reticulum Tubule Junctions Frequently Pause at Cortical Microtubules | Q58480441 | ||
The reticulons: a family of proteins with diverse functions | Q21184131 | ||
Rab10 GTPase regulates ER dynamics and morphology | Q24306806 | ||
A class of dynamin-like GTPases involved in the generation of the tubular ER network | Q24322595 | ||
Plastid Stromule Branching Coincides with Contiguous Endoplasmic Reticulum Dynamics | Q24596646 | ||
Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology | Q24679382 | ||
Peroxisomes take shape | Q27027175 | ||
X-ray structure of a protein-conducting channel | Q27642744 | ||
A highly conserved binding site in vesicle-associated membrane protein-associated protein (VAP) for the FFAT motif of lipid-binding proteins | Q27930652 | ||
Rtn1p is involved in structuring the cortical endoplasmic reticulum | Q27931857 | ||
ER-to-plasma membrane tethering proteins regulate cell signaling and ER morphology | Q27936693 | ||
A class of membrane proteins shaping the tubular endoplasmic reticulum | Q27940194 | ||
Inheritance of cortical ER in yeast is required for normal septin organization. | Q27940243 | ||
The fluid mosaic model of the structure of cell membranes | Q28239890 | ||
Metabolic pathways as enzyme complexes: evidence for the synthesis of phenylpropanoids and flavonoids on membrane associated enzyme complexes | Q28307834 | ||
Sorting signals, N-terminal modifications and abundance of the chloroplast proteome | Q28472564 | ||
REEPs are membrane shaping adapter proteins that modulate specific g protein-coupled receptor trafficking by affecting ER cargo capacity | Q28507125 | ||
Truncated myosin XI tail fusions inhibit peroxisome, Golgi, and mitochondrial movement in tobacco leaf epidermal cells: a genetic tool for the next generation | Q30482261 | ||
Overlapping functions of the four class XI myosins in Arabidopsis growth, root hair elongation, and organelle motility | Q30484920 | ||
Myosin-dependent endoplasmic reticulum motility and F-actin organization in plant cells. | Q30494560 | ||
ER Import Sites and Their Relationship to ER Exit Sites: A New Model for Bidirectional ER-Golgi Transport in Higher Plants | Q30523967 | ||
Cytoskeleton‐dependent endomembrane organization in plant cells: an emerging role for microtubules | Q38104402 | ||
Cortical microtubule-associated ER sites: organization centers of cell polarity and communication | Q38165606 | ||
Redefining the metabolic continuity of chloroplasts and ER. | Q38200284 | ||
Formation and maintenance of the Golgi apparatus in plant cells. | Q38203975 | ||
Role of plant myosins in motile organelles: is a direct interaction required? | Q38246680 | ||
ER-to-Golgi carriers arise through direct en bloc protrusion and multistage maturation of specialized ER exit domains | Q40627644 | ||
Oleosins and oil bodies in seeds and other organs | Q41230989 | ||
Identification of a calmodulin-regulated Ca2+-ATPase in the endoplasmic reticulum | Q41645045 | ||
Fluxes through the prokaryotic and eukaryotic pathways of lipid synthesis in the '16:3' plant Arabidopsis thaliana | Q41877564 | ||
Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family | Q42174824 | ||
Arabidopsis myosin XI sub-domains homologous to the yeast myo2p organelle inheritance sub-domain target subcellular structures in plant cells | Q42251031 | ||
Nucleocapsid of Tomato spotted wilt tospovirus forms mobile particles that traffic on an actin/endoplasmic reticulum network driven by myosin XI-K. | Q42270006 | ||
Sequential depletion and acquisition of proteins during Golgi stack disassembly and reformation | Q42275199 | ||
Plant science. Dynamic metabolons | Q42787103 | ||
SnapShot: membrane curvature sensors and generators. | Q42919917 | ||
Class XI myosins are required for development, cell expansion, and F-Actin organization in Arabidopsis | Q43004259 | ||
Golgi membrane dynamics after induction of a dominant-negative mutant Sar1 GTPase in tobacco. | Q43253811 | ||
Pausing of Golgi bodies on microtubules regulates secretion of cellulose synthase complexes in Arabidopsis | Q43451848 | ||
An Arabidopsis reticulon and the atlastin homologue RHD3-like2 act together in shaping the tubular endoplasmic reticulum | Q43760692 | ||
A novel ER-derived compartment, the ER body, selectively accumulates a beta-glucosidase with an ER-retention signal in Arabidopsis | Q44311763 | ||
ATG5 defines a phagophore domain connected to the endoplasmic reticulum during autophagosome formation in plants | Q44631737 | ||
Sporopollenin Biosynthetic Enzymes Interact and Constitute a Metabolon Localized to the Endoplasmic Reticulum of Tapetum Cells | Q44720774 | ||
A comparative study of the involvement of 17 Arabidopsis myosin family members on the motility of Golgi and other organelles | Q44793716 | ||
The plant cytoskeleton, NET3C, and VAP27 mediate the link between the plasma membrane and endoplasmic reticulum | Q45741138 | ||
Changing Patterns of Localization of the Tobacco Mosaic Virus Movement Protein and Replicase to the Endoplasmic Reticulum and Microtubules during Infection | Q45754788 | ||
Patterning and lifetime of plasma membrane-localized cellulose synthase is dependent on actin organization in Arabidopsis interphase cells. | Q45964175 | ||
The life of the peroxisome: from birth to death | Q46833278 | ||
A novel method for monitoring the localization of cytochromes P450 and other endoplasmic reticulum membrane associated proteins: a tool for investigating the formation of metabolons. | Q46834906 | ||
ROOT HAIR DEFECTIVE3 Family of Dynamin-Like GTPases Mediates Homotypic Endoplasmic Reticulum Fusion and Is Essential for Arabidopsis Development | Q47841518 | ||
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system. | Q47901945 | ||
ER quality control can lead to retrograde transport from the ER lumen to the cytosol and the nucleoplasm in plants | Q47953927 | ||
The ROOT HAIR DEFECTIVE3 gene encodes an evolutionarily conserved protein with GTP-binding motifs and is required for regulated cell enlargement in Arabidopsis | Q48052577 | ||
Myosin XI-K Is required for rapid trafficking of Golgi stacks, peroxisomes, and mitochondria in leaf cells of Nicotiana benthamiana | Q48075591 | ||
Photoactivation of GFP reveals protein dynamics within the endoplasmic reticulum membrane. | Q48944416 | ||
Endoplasmic Reticulum: The Rising Compartment in Auxin Biology | Q49087716 | ||
Protein-protein and protein-membrane associations in the lignin pathway | Q50487635 | ||
A superfamily of actin-binding proteins at the actin-membrane nexus of higher plants | Q50492949 | ||
Purification and characterization of the preprotein translocase of the outer mitochondrial membrane from Arabidopsis. Identification of multiple forms of TOM20. | Q50507149 | ||
Localization and domain characterization of Arabidopsis golgin candidates | Q50650932 | ||
Peroxule extension over ER-defined paths constitutes a rapid subcellular response to hydroxyl stress | Q51765051 | ||
Arabidopsis RHD3 mediates the generation of the tubular ER network and is required for Golgi distribution and motility in plant cells | Q51864821 | ||
ER network dynamics are differentially controlled by myosins XI-K, XI-C, XI-E, XI-I, XI-1, and XI-2 | Q30578799 | ||
AtPEX2 and AtPEX10 are targeted to peroxisomes independently of known endoplasmic reticulum trafficking routes | Q30798381 | ||
Endoplasmic reticulum export sites and Golgi bodies behave as single mobile secretory units in plant cells | Q33203998 | ||
Optical manipulation reveals strong attracting forces at membrane contact sites between endoplasmic reticulum and chloroplasts | Q33262293 | ||
Formation of an endoplasmic reticulum ring associated with acetylated microtubules in the angiosperm preprophase band. | Q33353081 | ||
The endoplasmic reticulum is the main membrane source for biogenesis of the lytic vacuole in Arabidopsis. | Q33356485 | ||
Grab a Golgi: laser trapping of Golgi bodies reveals in vivo interactions with the endoplasmic reticulum. | Q33409729 | ||
Principles of macromolecular organization and cell function in bacteria and archaea | Q33875136 | ||
ER stress signaling requires RHD3, a functionally conserved ER-shaping GTPase | Q33980515 | ||
Complexes of sequential metabolic enzymes | Q34039557 | ||
Tales of tethers and tentacles: golgins in plants | Q34275325 | ||
The trafficking of the cellulose synthase complex in higher plants | Q34331422 | ||
Lipid rafts and little caves. Compartmentalized signalling in membrane microdomains | Q34532553 | ||
ER - the key to the highway | Q34603476 | ||
Viral protein targeting to the cortical endoplasmic reticulum is required for cell–cell spreading in plants | Q34918259 | ||
Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin | Q34994215 | ||
Study of the plant COPII vesicle coat subunits by functional complementation of yeast Saccharomyces cerevisiae mutants. | Q35108633 | ||
Intracellular Transport of Plant Viruses: Finding the Door out of the Cell | Q35243914 | ||
Metabolic channeling in plants. | Q36051376 | ||
Metabolon formation and metabolic channeling in the biosynthesis of plant natural products | Q36110243 | ||
The plant Golgi apparatus--going with the flow. | Q36142775 | ||
Lipid interaction of the C terminus and association of the transmembrane segments facilitate atlastin-mediated homotypic endoplasmic reticulum fusion | Q36167580 | ||
Golgi structure in three dimensions: functional insights from the normal rat kidney cell | Q36293363 | ||
Auxin biosynthesis in maize. | Q36523008 | ||
Untangling the web: mechanisms underlying ER network formation | Q37060463 | ||
Endoplasmic reticulum bodies: solving the insoluble. | Q37282057 | ||
Endoplasmic reticulum–mitochondria contacts: function of the junction | Q37417736 | ||
Membrane traffic within the Golgi apparatus | Q37540106 | ||
Mechanisms shaping the membranes of cellular organelles | Q37540213 | ||
The plant endoplasmic reticulum: a cell-wide web. | Q37601499 | ||
Lipid biochemists salute the genome | Q37735383 | ||
Networking in the endoplasmic reticulum | Q37758946 | ||
Biogenesis of the plant Golgi apparatus. | Q37758954 | ||
Motoring around the plant cell: insights from plant myosins | Q37758984 | ||
P433 | issue | 1 | |
P921 | main subject | endoplasmic reticulum | Q79927 |
P304 | page(s) | 50-62 | |
P577 | publication date | 2015-01-01 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Journal of Integrative Plant Biology | Q15760521 |
P1476 | title | The endoplasmic reticulum: a dynamic and well-connected organelle | |
P478 | volume | 57 |
Q36130932 | A C-terminal amphipathic helix is necessary for the in vivo tubule-shaping function of a plant reticulon |
Q99711594 | A Combinatorial Reporter Set to Visualize the Membrane Contact Sites Between Endoplasmic Reticulum and Other Organelles in Plant Cell |
Q88805163 | Arabidopsis Lunapark proteins are involved in ER cisternae formation |
Q101165995 | Armadillo-repeat kinesin1 interacts with Arabidopsis atlastin RHD3 to move ER with plus-end of microtubules |
Q37643392 | Assembly of Dynamic P450-Mediated Metabolons-Order Versus Chaos |
Q91771876 | Defining the dance: quantification and classification of endoplasmic reticulum dynamics |
Q52645971 | Endoplasmic Reticulum Stress in Spinal Cord Contributes to the Development of Morphine Tolerance |
Q36025182 | Localization and interactions between Arabidopsis auxin biosynthetic enzymes in the TAA/YUC-dependent pathway |
Q47635680 | Metabolons on the Plant ER. |
Q28067655 | Origin of the Autophagosomal Membrane in Plants |
Q39783066 | Plant VAP27 proteins: domain characterization, intracellular localization and role in plant development. |
Q27306988 | Protein Bodies in Leaves Exchange Contents through the Endoplasmic Reticulum |
Q35768442 | Reticulomics: Protein-Protein Interaction Studies with Two Plasmodesmata-Localized Reticulon Family Proteins Identify Binding Partners Enriched at Plasmodesmata, Endoplasmic Reticulum, and the Plasma Membrane. |
Q38246680 | Role of plant myosins in motile organelles: is a direct interaction required? |
Q55474343 | Sirt3-Mediated Autophagy Contributes to Resveratrol-Induced Protection against ER Stress in HT22 Cells. |
Q49358142 | The odd one out: Arabidopsis reticulon 20 does not bend ER membranes but has a role in lipid regulation |
Q38780940 | The plant secretory pathway seen through the lens of the cell wall |
Q38272246 | The pollen tube clear zone: clues to the mechanism of polarized growth |
Q93098936 | Wogonoside promotes apoptosis in gastric cancer AGS and SGC-7901 cells through induction of mitochondrial dysfunction and endoplasmic reticulum stress |
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