scholarly article | Q13442814 |
P2093 | author name string | Imogen Sparkes | |
Lawrence R Griffing | |||
Hongbo T Gao | |||
P2860 | cites work | Plant mitochondria move on F-actin, but their positioning in the cortical cytoplasm depends on both F-actin and microtubules. | Q43911322 |
Simultaneous visualization of peroxisomes and cytoskeletal elements reveals actin and not microtubule-based peroxisome motility in plants | Q43916222 | ||
Expression, splicing, and evolution of the myosin gene family in plants | Q44689547 | ||
A comparative study of the involvement of 17 Arabidopsis myosin family members on the motility of Golgi and other organelles | Q44793716 | ||
Peroxisomal localization of a myosin XI isoform in Arabidopsis thaliana | Q46406298 | ||
Myosin XI-i links the nuclear membrane to the cytoskeleton to control nuclear movement and shape in Arabidopsis. | Q47712889 | ||
Stop-and-go movements of plant Golgi stacks are mediated by the acto-myosin system. | Q47901945 | ||
Myosin XI-K Is required for rapid trafficking of Golgi stacks, peroxisomes, and mitochondria in leaf cells of Nicotiana benthamiana | Q48075591 | ||
Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants | Q48911126 | ||
Myosin XI-Dependent Formation of Tubular Structures from Endoplasmic Reticulum Isolated from Tobacco Cultured BY-2 Cells | Q50524504 | ||
Differential organelle movement on the actin cytoskeleton in lily pollen tubes | Q50700442 | ||
The endoplasmic reticulum exerts control over organelle streaming during cell expansion | Q63342583 | ||
Actomyosin-based motility of endoplasmic reticulum and chloroplasts in Vallisneria mesophyll cells | Q71481228 | ||
GFP-tagging of cell components reveals the dynamics of subcellular re-organization in response to infection of Arabidopsis by oomycete pathogens | Q73055876 | ||
Stacks on tracks: the plant Golgi apparatus traffics on an actin/ER network† | Q77338801 | ||
Organelle targeting of myosin XI is mediated by two globular tail subdomains with separate cargo binding sites | Q80328535 | ||
Two class XI myosins function in organelle trafficking and root hair development in Arabidopsis | Q80454657 | ||
Inter-dependence of dimerization and organelle binding in myosin XI | Q81134455 | ||
Movement and remodeling of the endoplasmic reticulum in nondividing cells of tobacco leaves | Q82361753 | ||
Opaque1 encodes a myosin XI motor protein that is required for endoplasmic reticulum motility and protein body formation in maize endosperm | Q84794192 | ||
Myosin XIK of Arabidopsis thaliana accumulates at the root hair tip and is required for fast root hair growth | Q27304586 | ||
Actin turnover is required for myosin-dependent mitochondrial movements in Arabidopsis root hairs | Q27347881 | ||
Truncated myosin XI tail fusions inhibit peroxisome, Golgi, and mitochondrial movement in tobacco leaf epidermal cells: a genetic tool for the next generation | Q30482261 | ||
Rapid and dynamic subcellular reorganization following mechanical stimulation of Arabidopsis epidermal cells mimics responses to fungal and oomycete attack | Q30482409 | ||
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 | ||
Arabidopsis Myosin XI-K Localizes to the Motile Endomembrane Vesicles Associated with F-actin | Q30524660 | ||
AtPEX2 and AtPEX10 are targeted to peroxisomes independently of known endoplasmic reticulum trafficking routes | Q30798381 | ||
Visualization of peroxisomes in living plant cells reveals acto-myosin-dependent cytoplasmic streaming and peroxisome budding | Q30834494 | ||
Developmental transitions and dynamics of the cortical ER of Arabidopsis cells seen with green fluorescent protein | Q30840428 | ||
Distribution and characterization of peroxisomes in Arabidopsis by visualization with GFP: dynamic morphology and actin-dependent movement | Q31045424 | ||
Identification of myosin XI receptors in Arabidopsis defines a distinct class of transport vesicles | Q31135362 | ||
Phosphatidic Acid (PA) Binds PP2AA1 to Regulate PP2A Activity and PIN1 Polar Localization | Q33355878 | ||
Grab a Golgi: laser trapping of Golgi bodies reveals in vivo interactions with the endoplasmic reticulum. | Q33409729 | ||
Peroxisome dynamics in Arabidopsis plants under oxidative stress induced by cadmium. | Q33504951 | ||
Mobile and immobile endoplasmic reticulum in onion bulb epidermis cells: short- and long-term observations with a confocal laser scanning microscope. | Q33683681 | ||
Chloroplast Movement | Q34264219 | ||
Myosins XI-K, XI-1, and XI-2 are required for development of pavement cells, trichomes, and stigmatic papillae in Arabidopsis | Q34294594 | ||
Polarized cell growth in higher plants. | Q34425154 | ||
Pre- and postinvasion defenses both contribute to nonhost resistance in Arabidopsis. | Q34468523 | ||
An isoform of myosin XI is responsible for the translocation of endoplasmic reticulum in tobacco cultured BY-2 cells | Q34767566 | ||
The tail that wags the dog: the globular tail domain defines the function of myosin V/XI. | Q37035339 | ||
Networking in the endoplasmic reticulum | Q37758946 | ||
FrontiERs: movers and shapers of the higher plant cortical endoplasmic reticulum. | Q37915033 | ||
Homotypic fusion of endoplasmic reticulum membranes in plant cells | Q38175396 | ||
Understanding myosin functions in plants: are we there yet? | Q38180450 | ||
A rab1 GTPase is required for transport between the endoplasmic reticulum and golgi apparatus and for normal golgi movement in plants | Q38306377 | ||
Myosin XIK is a major player in cytoplasm dynamics and is regulated by two amino acids in its tail | Q39980530 | ||
Class XI myosins are required for development, cell expansion, and F-Actin organization in Arabidopsis | Q43004259 | ||
P304 | page(s) | 218 | |
P577 | publication date | 2014-05-21 | |
P1433 | published in | Frontiers in Plant Science | Q27723840 |
P1476 | title | ER network dynamics are differentially controlled by myosins XI-K, XI-C, XI-E, XI-I, XI-1, and XI-2 | |
P478 | volume | 5 |
Q47635720 | Dancing with the Stars: Using Image Analysis to Study the Choreography of the Endoplasmic Reticulum and Its Partners and of Movement Within Its Tubules |
Q91771876 | Defining the dance: quantification and classification of endoplasmic reticulum dynamics |
Q34603476 | ER - the key to the highway |
Q49686769 | Emerging roles of cortical microtubule-membrane interactions |
Q34114263 | Endoplasmic reticulum-shape and function in stress translation |
Q38302658 | Formins: linking cytoskeleton and endomembranes in plant cells. |
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Q41815095 | NETWORKED 3B: a novel protein in the actin cytoskeleton-endoplasmic reticulum interaction |
Q30616957 | Nucleocapsid protein from fig mosaic virus forms cytoplasmic agglomerates that are hauled by endoplasmic reticulum streaming |
Q38255058 | Organelle trafficking, the cytoskeleton, and pollen tube growth |
Q42551738 | Passive virus movements with organelle dynamics |
Q27320208 | Phosphorylation of the C Terminus of RHD3 Has a Critical Role in Homotypic ER Membrane Fusion in Arabidopsis |
Q30833897 | Plant ER geometry and dynamics: biophysical and cytoskeletal control during growth and biotic response |
Q47784360 | Plasmolysis-deplasmolysis causes changes in endoplasmic reticulum form, movement, flow, and cytoskeletal association |
Q27306988 | Protein Bodies in Leaves Exchange Contents through the Endoplasmic Reticulum |
Q38246680 | Role of plant myosins in motile organelles: is a direct interaction required? |
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