| P2093 | author name string | Tomohiro Uemura | |
| P2860 | cites work | Qa-SNAREs localized to the trans-Golgi network regulate multiple transport pathways and extracellular disease resistance in plants | Q24633544 |
| | The TRAPP complex is a nucleotide exchanger for Ypt1 and Ypt31/32. | Q27936185 |
| | Arabidopsis boron transporter for xylem loading. | Q27938492 |
| | Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth | Q28366139 |
| | Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex | Q28569612 |
| | SNAREs--engines for membrane fusion | Q29547230 |
| | Autophagy: process and function | Q29547296 |
| | Arabidopsis ALIX is required for the endosomal localization of the deubiquitinating enzyme AMSH3. | Q30009106 |
| | The ESCRT-III-interacting deubiquitinating enzyme AMSH3 is essential for degradation of ubiquitinated membrane proteins in Arabidopsis thaliana | Q30009488 |
| | The deubiquitinating enzyme AMSH1 and the ESCRT-III subunit VPS2.1 are required for autophagic degradation in Arabidopsis | Q30009879 |
| | Monoubiquitin-dependent endocytosis of the iron-regulated transporter 1 (IRT1) transporter controls iron uptake in plants. | Q30503486 |
| | ECHIDNA-mediated post-Golgi trafficking of auxin carriers for differential cell elongation | Q30548804 |
| | A unique HEAT repeat-containing protein SHOOT GRAVITROPISM6 is involved in vacuolar membrane dynamics in gravity-sensing cells of Arabidopsis inflorescence stem. | Q30575809 |
| | Macromolecular differentiation of Golgi stacks in root tips of Arabidopsis and Nicotiana seedlings as visualized in high pressure frozen and freeze-substituted samples. | Q33335962 |
| | Endocytosis and degradation of BOR1, a boron transporter of Arabidopsis thaliana, regulated by boron availability | Q33341481 |
| | Polar localization and degradation of Arabidopsis boron transporters through distinct trafficking pathways | Q33348692 |
| | Electron tomography of RabA4b- and PI-4Kβ1-labeled trans Golgi network compartments in Arabidopsis. | Q33350214 |
| | Endocytic and secretory traffic in Arabidopsis merge in the trans-Golgi network/early endosome, an independent and highly dynamic organelle | Q33570063 |
| | Organization of the ER-Golgi interface for membrane traffic control | Q33779916 |
| | Plant vacuoles | Q33859533 |
| | Syntaxin of plant proteins SYP123 and SYP132 mediate root hair tip growth in Arabidopsis thaliana. | Q50459255 |
| | Dynamic behavior of the trans-golgi network in root tissues of Arabidopsis revealed by super-resolution live imaging. | Q50463301 |
| | Dynamics and environmental responses of PATROL1 in Arabidopsis subsidiary cells. | Q50470134 |
| | A specific role for Arabidopsis TRAPPII in post-Golgi trafficking that is crucial for cytokinesis and cell polarity. | Q50518334 |
| | The Arabidopsis major intrinsic protein NIP5;1 is essential for efficient boron uptake and plant development under boron limitation. | Q50649614 |
| | Protein delivery to vacuole requires SAND protein-dependent Rab GTPase conversion for MVB-vacuole fusion. | Q50658765 |
| | Evidence for sequential action of Rab5 and Rab7 GTPases in prevacuolar organelle partitioning. | Q52844821 |
| | The Membrane-Associated Sec1/Munc18 KEULE is Required for Phragmoplast Microtubule Reorganization During Cytokinesis in Arabidopsis. | Q52893145 |
| | Plant vacuolar trafficking occurs through distinctly regulated pathways. | Q53798749 |
| | Plant Cytokinesis Is Orchestrated by the Sequential Action of the TRAPPII and Exocyst Tethering Complexes | Q58001228 |
| | Involvement of the vacuoles of the endodermis in the early process of shoot gravitropism in Arabidopsis | Q58480525 |
| | RME-8, a conserved J-domain protein, is required for endocytosis in Caenorhabditis elegans. | Q33937385 |
| | The trans Golgi network: sorting at the exit site of the Golgi complex. | Q34562583 |
| | Cell polarity and patterning by PIN trafficking through early endosomal compartments in Arabidopsis thaliana | Q34758259 |
| | Conserved Arabidopsis ECHIDNA protein mediates trans-Golgi-network trafficking and cell elongation | Q34977816 |
| | A SNARE complex containing SGR3/AtVAM3 and ZIG/VTI11 in gravity-sensing cells is important for Arabidopsis shoot gravitropism. | Q35168727 |
| | Wide-range high-resolution transmission electron microscopy reveals morphological and distributional changes of endomembrane compartments during log to stationary transition of growth phase in tobacco BY-2 cells. | Q35188252 |
| | Diversity and formation of endoplasmic reticulum-derived compartments in plants. Are these compartments specific to plant cells? | Q35948440 |
| | Unique COPII component AtSar1a/AtSec23a pair is required for the distinct function of protein ER export in Arabidopsis thaliana | Q36306135 |
| | A Munc13-like protein in Arabidopsis mediates H+-ATPase translocation that is essential for stomatal responses | Q37064915 |
| | Chapter 4: functions of RAB and SNARE proteins in plant life | Q37435106 |
| | Membrane traffic within the Golgi apparatus | Q37540106 |
| | BEX1/ARF1A1C is required for BFA-sensitive recycling of PIN auxin transporters and auxin-mediated development in Arabidopsis. | Q37695393 |
| | New insights into the regulation of stomatal opening by blue light and plasma membrane H(+)-ATPase | Q37900408 |
| | Plant TGNs: dynamics and physiological functions | Q38119864 |
| | The plant secretory pathway: an essential factory for building the plant cell wall | Q38176744 |
| | Membrane trafficking pathways and their roles in plant-microbe interactions. | Q38195007 |
| | Formation and maintenance of the Golgi apparatus in plant cells. | Q38203975 |
| | Plant vacuolar trafficking driven by RAB and SNARE proteins | Q38280486 |
| | Endocytosis and its regulation in plants | Q38443287 |
| | Interactomics of Qa-SNARE in Arabidopsis thaliana | Q38479538 |
| | Autophagy in Plants--What's New on the Menu? | Q38644887 |
| | New Insight into the Mechanism and Function of Autophagy in Plant Cells | Q38651383 |
| | Drought stress-induced Rma1H1, a RING membrane-anchor E3 ubiquitin ligase homolog, regulates aquaporin levels via ubiquitination in transgenic Arabidopsis plants | Q39166445 |
| | The gravitropism defective 2 mutants of Arabidopsis are deficient in a protein implicated in endocytosis in Caenorhabditis elegans | Q39462156 |
| | SNARE Molecules in Marchantia polymorpha: Unique and Conserved Features of the Membrane Fusion Machinery. | Q40895232 |
| | UDP-D-galactose synthesis by UDP-glucose 4-epimerase 4 is required for organization of the trans-Golgi network/early endosome in Arabidopsis thaliana root epidermal cells | Q40899863 |
| | Binding of SEC11 indicates its role in SNARE recycling after vesicle fusion and identifies two pathways for vesicular traffic to the plasma membrane | Q41276510 |
| | Evolutionary Divergence of Plant Borate Exporters and Critical Amino Acid Residues for the Polar Localization and Boron-Dependent Vacuolar Sorting of AtBOR1. | Q41529342 |
| | High boron-induced ubiquitination regulates vacuolar sorting of the BOR1 borate transporter in Arabidopsis thaliana. | Q42692038 |
| | Identification and characterization of an Arabidopsis mutant with altered localization of NIP5;1, a plasma membrane boric acid channel, reveals the requirement for D-galactose in endomembrane organization | Q43601086 |
| | Cell wall polysaccharides are mislocalized to the Vacuole in echidna mutants | Q43874451 |
| | Assessment and optimization of autophagy monitoring methods in Arabidopsis roots indicate direct fusion of autophagosomes with vacuoles | Q44111994 |
| | CONTINUOUS VASCULAR RING (COV1) is a trans-Golgi network-localized membrane protein required for Golgi morphology and vacuolar protein sorting | Q44328784 |
| | Fluorescence imaging-based screen identifies ARF GEF component of early endosomal trafficking | Q46115710 |
| | Trans-Golgi network localized ECHIDNA/Ypt interacting protein complex is required for the secretion of cell wall polysaccharides in Arabidopsis | Q46285202 |
| | Different sets of ER-resident J-proteins regulate distinct polar nuclear-membrane fusion events in Arabidopsis thaliana | Q46837271 |
| | Vacuolar H+-ATPase activity is required for endocytic and secretory trafficking in Arabidopsis | Q46930624 |
| | The Arabidopsis Rab GTPase RabA4b localizes to the tips of growing root hair cells | Q47447236 |
| | ESCRT-III-Associated Protein ALIX Mediates High-Affinity Phosphate Transporter Trafficking to Maintain Phosphate Homeostasis in Arabidopsis. | Q48137297 |
| | Activation of the Rab7 GTPase by the MON1-CCZ1 Complex Is Essential for PVC-to-Vacuole Trafficking and Plant Growth in Arabidopsis. | Q48308717 |
| | SGR2, a phospholipase-like protein, and ZIG/SGR4, a SNARE, are involved in the shoot gravitropism of Arabidopsis. | Q48320261 |
| P433 | issue | 10 | |
| P1104 | number of pages | 7 | |
| P304 | page(s) | 2013-2019 | |
| P577 | publication date | 2016-09-20 | |
| P1433 | published in | Plant and Cell Physiology | Q2402845 |
| P1476 | title | Physiological Roles of Plant Post-Golgi Transport Pathways in Membrane Trafficking | |
| P478 | volume | 57 | |