Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
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In vivo analysis of interactions between GFP-labeled microfilaments and plastid stromules.Plant protein glycosylationProfilin as a regulator of the membrane-actin cytoskeleton interface in plant cellsREGULATOR OF BULB BIOGENESIS1 (RBB1) Is Involved in Vacuole Bulb Formation in ArabidopsisArabidopsis COG Complex Subunits COG3 and COG8 Modulate Golgi Morphology, Vesicle Trafficking Homeostasis and Are Essential for Pollen Tube GrowthHLB1 Is a Tetratricopeptide Repeat Domain-Containing Protein That Operates at the Intersection of the Exocytic and Endocytic Pathways at the TGN/EE in ArabidopsisTubule-guided cell-to-cell movement of a plant virus requires class XI myosin motorsIntracellular localization of the peanut clump virus replication complex in tobacco BY-2 protoplasts containing green fluorescent protein-labeled endoplasmic reticulum or Golgi apparatus.The arabidopsis cell plate-associated dynamin-like protein, ADL1Ap, is required for multiple stages of plant growth and developmentFunctional characterization and subcellular localization of poplar (Populus trichocarpa x Populus deltoides) cinnamate 4-hydroxylaseFRIENDLY regulates mitochondrial distribution, fusion, and quality control in ArabidopsisThe evolution of the actin binding NET superfamilyIdentification and characterization of COPIa- and COPIb-type vesicle classes associated with plant and algal Golgi.Association of six YFP-myosin XI-tail fusions with mobile plant cell organelles.Different subcellular localizations and functions of Arabidopsis myosin VIIITruncated myosin XI tail fusions inhibit peroxisome, Golgi, and mitochondrial movement in tobacco leaf epidermal cells: a genetic tool for the next generation.Multidimensional fluorescence microscopy of multiple organelles in Arabidopsis seedlings.Sequential recruitment of the endoplasmic reticulum and chloroplasts for plant potyvirus replication.pH-sensitivity of YFP provides an intracellular indicator of programmed cell deathER Import Sites and Their Relationship to ER Exit Sites: A New Model for Bidirectional ER-Golgi Transport in Higher PlantsImpact on the endoplasmic reticulum and Golgi apparatus of turnip mosaic virus infection.Cis-Golgi cisternal assembly and biosynthetic activation occur sequentially in plants and algae.ER network dynamics are differentially controlled by myosins XI-K, XI-C, XI-E, XI-I, XI-1, and XI-2Nucleocapsid protein from fig mosaic virus forms cytoplasmic agglomerates that are hauled by endoplasmic reticulum streaming.The WASP-Arp2/3 complex signal cascade is involved in actin-dependent sperm nuclei migration during double fertilization in tobacco and maizeHigh-throughput viral expression of cDNA-green fluorescent protein fusions reveals novel subcellular addresses and identifies unique proteins that interact with plasmodesmata.Novel type Arabidopsis thaliana H(+)-PPase is localized to the Golgi apparatus.Vacuolar membrane dynamics revealed by GFP-AtVam3 fusion protein.Identification of myosin XI receptors in Arabidopsis defines a distinct class of transport vesicles.Why green fluorescent fusion proteins have not been observed in the vacuoles of higher plants.The transport of prolamine RNAs to prolamine protein bodies in living rice endosperm cells.Endoplasmic reticulum export sites and Golgi bodies behave as single mobile secretory units in plant cells.Dynamics of COPII vesicles and the Golgi apparatus in cultured Nicotiana tabacum BY-2 cells provides evidence for transient association of Golgi stacks with endoplasmic reticulum exit sites.An Arabidopsis endo-1,4-beta-D-glucanase involved in cellulose synthesis undergoes regulated intracellular cycling.Endosidin1 defines a compartment involved in endocytosis of the brassinosteroid receptor BRI1 and the auxin transporters PIN2 and AUX1.AtKinesin-13A is located on Golgi-associated vesicle and involved in vesicle formation/budding in Arabidopsis root-cap peripheral cellsHead-neck domain of Arabidopsis myosin XI, MYA2, fused with GFP produces F-actin patterns that coincide with fast organelle streaming in different plant cellsElectron tomography of RabA4b- and PI-4Kβ1-labeled trans Golgi network compartments in Arabidopsis.Shrinkage and fragmentation of the trans-Golgi network in non-meristematic plant cells.Emerging aspects of ER organization in root hair tip growth: lessons from RHD3 and Atlastin.
P2860
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P2860
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@en
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@nl
type
label
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@en
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@nl
prefLabel
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@en
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system.
@nl
P2093
P2860
P356
P1433
P1476
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system
@en
P2093
A M Mazurkiewicz
J A Frohlick
L A Gallagher
T G Dunahay
P2860
P304
P356
10.1104/PP.121.4.1127
P407
P577
1999-12-01T00:00:00Z