review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Russell E McConnell | Q80335995 |
Matthew John Tyska | Q90406485 | ||
P2093 | author name string | Rajalakshmi Nambiar | |
P2860 | cites work | Small espin: a third actin-bundling protein and potential forked protein ortholog in brush border microvilli | Q22003897 |
Myosin-X is a molecular motor that functions in filopodia formation | Q24299253 | ||
Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss | Q24301501 | ||
A new compartment at stereocilia tips defined by spatial and temporal patterns of myosin IIIa expression | Q24305683 | ||
Defective myosin VIIA gene responsible for Usher syndrome type 1B | Q24314638 | ||
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle | Q24337137 | ||
Cellular motions and thermal fluctuations: the Brownian ratchet | Q24531501 | ||
Membrane tether formation from blebbing cells | Q24537319 | ||
MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells | Q24537500 | ||
The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions | Q24538474 | ||
A motility in the eukaryotic flagellum unrelated to flagellar beating | Q24562713 | ||
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex | Q24597349 | ||
The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins. | Q24603825 | ||
A millennial myosin census | Q24633678 | ||
Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia | Q24633897 | ||
Flexibility of actin filaments derived from thermal fluctuations. Effect of bound nucleotide, phalloidin, and muscle regulatory proteins | Q72223294 | ||
Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse | Q72951118 | ||
A role for myosin VII in dynamic cell adhesion | Q73670214 | ||
A hydrodynamic mechanosensory hypothesis for brush border microvilli | Q74346369 | ||
Localization of myosin-Ibeta near both ends of tip links in frog saccular hair cells | Q77458696 | ||
Actin-binding proteins sensitively mediate F-actin bundle stiffness | Q80143400 | ||
Defective CFTR apical endocytosis and enterocyte brush border in myosin VI-deficient mice | Q80445304 | ||
Invadopodia | Q81225323 | ||
Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering | Q82457987 | ||
Dynamic length regulation of sensory stereocilia | Q24646242 | ||
Intestinal alkaline phosphatase detoxifies lipopolysaccharide and prevents inflammation in zebrafish in response to the gut microbiota | Q24648039 | ||
Cadherins and mechanotransduction by hair cells | Q24649559 | ||
Intestinal alkaline phosphatase is a gut mucosal defense factor maintained by enteral nutrition | Q24656115 | ||
An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal | Q24676711 | ||
Arp2/3 complex and actin depolymerizing factor/cofilin in dendritic organization and treadmilling of actin filament array in lamellipodia | Q24682164 | ||
Myosin VI undergoes cargo-mediated dimerization | Q27656929 | ||
Cellular motility driven by assembly and disassembly of actin filaments | Q27860676 | ||
Intraflagellar transport (IFT) role in ciliary assembly, resorption and signalling. | Q27967638 | ||
Myosin VI: two distinct roles in endocytosis | Q28191412 | ||
The lamellipodium: where motility begins | Q28202993 | ||
The myosin power stroke | Q28216645 | ||
How the ear's works work | Q28272150 | ||
Filopodia: molecular architecture and cellular functions | Q28279460 | ||
PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa | Q28507299 | ||
Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons | Q28507574 | ||
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells | Q28509764 | ||
Ezrin is essential for epithelial organization and villus morphogenesis in the developing intestine | Q28510081 | ||
Whirlin complexes with p55 at the stereocilia tip during hair cell development. | Q28510548 | ||
Myosin-1a is critical for normal brush border structure and composition | Q28512472 | ||
A type VII myosin encoded by the mouse deafness gene shaker-1 | Q28512902 | ||
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells | Q28513409 | ||
Characterization of the motor activity of mammalian myosin VIIA | Q28566322 | ||
Redistribution of myosin VI from top to base of proximal tubule microvilli during acute hypertension | Q28575058 | ||
Expression of myosin VI within the early endocytic pathway in adult and developing proximal tubules | Q28579268 | ||
Role of myosin VI in the differentiation of cochlear hair cells | Q28585164 | ||
Elongation of hair cell stereocilia is defective in the mouse mutant whirler | Q28585988 | ||
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells | Q28592402 | ||
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia | Q28593953 | ||
Lamellipodial versus filopodial mode of the actin nanomachinery: pivotal role of the filament barbed end | Q28594452 | ||
Mechanism of filopodia initiation by reorganization of a dendritic network | Q29616648 | ||
Antagonism between Ena/VASP proteins and actin filament capping regulates fibroblast motility | Q29618423 | ||
ERM proteins and merlin: integrators at the cell cortex | Q29619893 | ||
Myosin-VIIb, a novel unconventional myosin, is a constituent of microvilli in transporting epithelia. | Q30168113 | ||
Myosin-1c, the hair cell's adaptation motor | Q34300171 | ||
Myosin-X provides a motor-based link between integrins and the cytoskeleton. | Q34322246 | ||
The physics of filopodial protrusion | Q34350863 | ||
Mechanics and dynamics of actin-driven thin membrane protrusions | Q34352886 | ||
Flow-activated transport events along the nephron | Q34558161 | ||
Kinetic mechanism of human myosin IIIA. | Q34577832 | ||
The enterocyte microvillus is a vesicle-generating organelle | Q34989756 | ||
Myosins and pathology: genetics and biology | Q35052489 | ||
The co-workers of actin filaments: from cell structures to signals | Q35887294 | ||
Role of fascin in filopodial protrusion | Q36118593 | ||
Myosins: tails (and heads) of functional diversity | Q36197820 | ||
The organization of actin filaments in the stereocilia of cochlear hair cells | Q36201573 | ||
Binding of brush border myosin I to phospholipid vesicles | Q36223375 | ||
Unconventional myosins in inner-ear sensory epithelia | Q36254696 | ||
Intraflagellar transport (IFT) cargo: IFT transports flagellar precursors to the tip and turnover products to the cell body | Q36322385 | ||
Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo. | Q36324725 | ||
Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors | Q36639095 | ||
Direct measurement of the torsional rigidity of single actin filaments | Q36831827 | ||
Myosin V from head to tail | Q37073565 | ||
Protrusive growth from giant liposomes driven by actin polymerization | Q37169750 | ||
Ena/VASP: proteins at the tip of the nervous system | Q37174967 | ||
Villin: The major microfilament-associated protein of the intestinal microvillus | Q37330654 | ||
Membrane-induced bundling of actin filaments | Q37336549 | ||
Cargo binding induces dimerization of myosin VI. | Q37366472 | ||
PTH-induced internalization of apical membrane NaPi2a: role of actin and myosin VI. | Q37474487 | ||
Intraflagellar transport and the generation of dynamic, structurally and functionally diverse cilia | Q37533442 | ||
The neck region of the myosin motor domain acts as a lever arm to generate movement | Q37640558 | ||
Identification of a myosin VII-talin complex. | Q38328088 | ||
Myosin VIIB from Drosophila is a high duty ratio motor | Q40391038 | ||
The cell biology of infection by intracellular bacterial pathogens. | Q41020962 | ||
Fimbrin, a new microfilament-associated protein present in microvilli and other cell surface structures | Q41270803 | ||
Myosin I can act as a molecular force sensor. | Q41334383 | ||
A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level | Q41978648 | ||
The kinase domain alters the kinetic properties of the myosin IIIA motor | Q42030609 | ||
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. | Q42455765 | ||
Hair cells require phosphatidylinositol 4,5-bisphosphate for mechanical transduction and adaptation. | Q42468923 | ||
Microvilli defects in retinas of ezrin knockout mice | Q42486471 | ||
Kinetic mechanism and regulation of myosin VI. | Q43651972 | ||
Elastic properties of lipid bilayers: theory and possible experiments | Q44282845 | ||
The mechanism of myosin VI translocation and its load-induced anchoring | Q44790017 | ||
Progressing actin: Formin as a processive elongation machine | Q45169141 | ||
A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells. | Q45712448 | ||
Immunohistochemical localization of several cytoskeletal proteins in inner ear sensory and supporting cells | Q46446795 | ||
Myosin X is a high duty ratio motor | Q46551350 | ||
Compliance of the hair bundle associated with gating of mechanoelectrical transduction channels in the bullfrog's saccular hair cell | Q46565359 | ||
Dynamic compartmentalization of protein tyrosine phosphatase receptor Q at the proximal end of stereocilia: implication of myosin VI-based transport | Q46645141 | ||
Sisyphus, the Drosophila myosin XV homolog, traffics within filopodia transporting key sensory and adhesion cargos | Q47070932 | ||
Bending stiffness of a crystalline actin bundle | Q47995063 | ||
A microtubule-binding myosin required for nuclear anchoring and spindle assembly. | Q52560093 | ||
The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. | Q52857621 | ||
Limits of filopodium stability. | Q55514892 | ||
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression | Q57002730 | ||
Formation and Interaction of Membrane Tubes | Q57252588 | ||
A sensory role for neuronal growth cone filopodia | Q59067973 | ||
Cytoskeletal architecture of the chicken hair cells revealed with the quick-freeze, deep-etch technique | Q69570668 | ||
Purification of the intestinal microvillus cytoskeletal proteins villin, fimbrin, and ezrin | Q69761052 | ||
Identification of a 120 kd hair-bundle myosin located near stereociliary tips | Q70478366 | ||
Multiple unconventional myosin domains of the intestinal brush border cytoskeleton | Q72132429 | ||
Fast adaptation in vestibular hair cells requires myosin-1c activity | Q30437793 | ||
Organization of an actin filament-membrane complex. Filament polarity and membrane attachment in the microvilli of intestinal epithelial cells | Q30442456 | ||
Ena/VASP proteins have an anti-capping independent function in filopodia formation | Q30444426 | ||
Myo1c binds tightly and specifically to phosphatidylinositol 4,5-bisphosphate and inositol 1,4,5-trisphosphate | Q30477029 | ||
Hair bundles are specialized for ATP delivery via creatine kinase. | Q30479206 | ||
Direct measurement of force generation by actin filament polymerization using an optical trap | Q30479598 | ||
Myosin-1a powers the sliding of apical membrane along microvillar actin bundles. | Q30480441 | ||
The motor activity of myosin-X promotes actin fiber convergence at the cell periphery to initiate filopodia formation. | Q30480576 | ||
Cytoskeletal bundle mechanics | Q30481556 | ||
A myosin motor that selects bundled actin for motility | Q30482736 | ||
Control of cell membrane tension by myosin-I. | Q30489048 | ||
Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments | Q30490501 | ||
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle | Q30493544 | ||
Response latency of vertebrate hair cells | Q30503299 | ||
The light chain binding domain of expressed smooth muscle heavy meromyosin acts as a mechanical lever | Q30652709 | ||
Mechanosensory function of microvilli of the kidney proximal tubule | Q30832338 | ||
Phospholipase C activation by anesthetics decreases membrane-cytoskeleton adhesion | Q31030097 | ||
Myosin X transports Mena/VASP to the tip of filopodia. | Q31065358 | ||
Vertebrate myosin VIIb is a high duty ratio motor adapted for generating and maintaining tension | Q33223992 | ||
Load fluctuations drive actin network growth | Q33300313 | ||
A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells | Q33373673 | ||
MyosinVIIa interacts with Twinfilin-2 at the tips of mechanosensory stereocilia in the inner ear. | Q33506085 | ||
Microvillar Ca++ signaling: a new view of an old problem | Q33653975 | ||
Myosins and deafness. | Q33725399 | ||
Cloning and chromosomal localization of a human class III myosin | Q33913130 | ||
Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin. | Q33917620 | ||
Deformation and flow of membrane into tethers extracted from neuronal growth cones | Q34016984 | ||
Cell motility driven by actin polymerization | Q34041217 | ||
Tip links in hair cells: molecular composition and role in hearing loss | Q34066652 | ||
Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. | Q34115035 | ||
Shigella flexneri surface protein IcsA is sufficient to direct actin-based motility | Q34140727 | ||
The polymerization motor | Q34156477 | ||
Force generation by actin polymerization II: the elastic ratchet and tethered filaments | Q34180568 | ||
Cell control by membrane-cytoskeleton adhesion | Q34238066 | ||
P433 | issue | 8 | |
P304 | page(s) | 1239-1254 | |
P577 | publication date | 2010-01-27 | |
P1433 | published in | Cellular and Molecular Life Sciences | Q5058352 |
P1476 | title | Myosin motor function: the ins and outs of actin-based membrane protrusions | |
P478 | volume | 67 |
Q50352962 | A Salutary Role of Reactive Oxygen Species in Intercellular Tunnel-Mediated Communication. |
Q38072662 | A two-segment model for thin filament architecture in skeletal muscle |
Q47766718 | Application of Quasi-Steady-State Methods to Nonlinear Models of Intracellular Transport by Molecular Motors |
Q34570309 | CD44: target for antiangiogenesis therapy |
Q35795161 | CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI. |
Q34337954 | Caenorhabditis elegans chaperonin CCT/TRiC is required for actin and tubulin biogenesis and microvillus formation in intestinal epithelial cells |
Q38735421 | Disruption of Rab8a and Rab11a causes formation of basolateral microvilli in neonatal enteropathy. |
Q38242492 | Diversity and convergence in the mechanisms establishing L/R asymmetry in metazoa. |
Q35456797 | Ectoplasm, ghost in the R cell machine? |
Q92082941 | Emergence and Evolution of ERM Proteins and Merlin in Metazoans |
Q30846657 | Fatty acid synthase cooperates with protrudin to facilitate membrane outgrowth of cellular protrusions |
Q26823315 | Filopodia and adhesion in cancer cell motility |
Q30383741 | Ganglioside GM3 is essential for the structural integrity and function of cochlear hair cells |
Q51067426 | Generic Transport Mechanisms for Molecular Traffic in Cellular Protrusions. |
Q38130179 | How filopodia pull: what we know about the mechanics and dynamics of filopodia. |
Q47199341 | Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss |
Q37107569 | Insights into the origin of metazoan filopodia and microvilli |
Q28743071 | Lever-arm mechanics of processive myosins |
Q30544040 | Live-cell imaging of Marburg virus-infected cells uncovers actin-dependent transport of nucleocapsids over long distances |
Q41428935 | Mechanically enforced bond dissociation reports synergistic influence of Mn2+ and Mg2+ on the interaction between integrin α7β1 and invasin |
Q42510246 | Microtubules regulate brush border formation |
Q53296434 | Modulators of endothelial cell filopodia: PECAM-1 joins the club. |
Q34974055 | Myo1e impairment results in actin reorganization, podocyte dysfunction, and proteinuria in zebrafish and cultured podocytes |
Q27310298 | Myosin 1b functions as an effector of EphB signaling to control cell repulsion |
Q52626809 | Myosin 1b promotes axon formation by regulating actin wave propagation and growth cone dynamics. |
Q30528813 | Myosin Vs organize actin cables in fission yeast |
Q30513876 | Myosin-1A targets to microvilli using multiple membrane binding motifs in the tail homology 1 (TH1) domain |
Q35576442 | Myosin-X: a MyTH-FERM myosin at the tips of filopodia |
Q37219083 | Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function. |
Q35193732 | Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children. |
Q37047004 | Oxidized low-density lipoproteins induce rapid platelet activation and shape change through tyrosine kinase and Rho kinase-signaling pathways |
Q37884613 | Principles of unconventional myosin function and targeting |
Q24338447 | Prominin-2 expression increases protrusions, decreases caveolae and inhibits Cdc42 dependent fluid phase endocytosis |
Q34804549 | Proteomics approach to study the functions of Drosophila myosin VI through identification of multiple cargo-binding proteins |
Q50491249 | Radiogenomics: Identification of Genomic Predictors for Radiation Toxicity. |
Q39174495 | Redox regulation of the actin cytoskeleton and its role in the vascular system |
Q37549911 | Self-organization of actin networks by a monomeric myosin |
Q30663513 | Self-organization of waves and pulse trains by molecular motors in cellular protrusions |
Q34566715 | Shaping the intestinal brush border |
Q27329412 | Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like |
Q43058873 | Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins. |
Q47236946 | The Actin Cytoskeleton and Actin-Based Motility |
Q27011868 | The myosin superfamily at a glance. |
Q27333926 | Theoretical model for cellular shapes driven by protrusive and adhesive forces |
Q44592173 | Unusual anchor of a motor complex (MyoD-MLC2) to the plasma membrane of Toxoplasma gondii |
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