scholarly article | Q13442814 |
P50 | author | Thomas Bornschlögl | Q61014819 |
P2093 | author name string | Thomas Bornschlögl | |
P2860 | cites work | Signaling mechanisms in cortical axon growth, guidance, and branching | Q21131061 |
Cdc42Hs facilitates cytoskeletal reorganization and neurite outgrowth by localizing the 58-kD insulin receptor substrate to filamentous actin | Q24290738 | ||
Cdc42 induces filopodia by promoting the formation of an IRSp53:Mena complex | Q24291871 | ||
Myosin-X is a molecular motor that functions in filopodia formation | Q24299253 | ||
The RAC binding domain/IRSp53-MIM homology domain of IRSp53 induces RAC-dependent membrane deformation | Q24304626 | ||
A novel actin bundling/filopodium-forming domain conserved in insulin receptor tyrosine kinase substrate p53 and missing in metastasis protein | Q24306756 | ||
Structural basis of filopodia formation induced by the IRSp53/MIM homology domain of human IRSp53 | Q24557455 | ||
Actin in dendritic spines: connecting dynamics to function | Q24611930 | ||
An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal | Q24676711 | ||
Filopodia act as phagocytic tentacles and pull with discrete steps and a load-dependent velocity. | Q24677668 | ||
Reaching out for signals: filopodia sense EGF and respond by directed retrograde transport of activated receptors | Q24678987 | ||
Actin- and myosin-driven movement of viruses along filopodia precedes their entry into cells | Q24679320 | ||
A STUDY OF TISSUE CULTURE CELLS BY ELECTRON MICROSCOPY : METHODS AND PRELIMINARY OBSERVATIONS | Q24681186 | ||
Three-dimensional reconstruction of the membrane skeleton at the plasma membrane interface by electron tomography | Q24682964 | ||
Use the force: membrane tension as an organizer of cell shape and motility | Q27014729 | ||
Deconstructing the third dimension: how 3D culture microenvironments alter cellular cues | Q27023837 | ||
Properties of the force exerted by filopodia and lamellipodia and the involvement of cytoskeletal components | Q27302614 | ||
Visualization of endothelial actin cytoskeleton in the mouse retina | Q27313983 | ||
Human papillomavirus type 16 entry: retrograde cell surface transport along actin-rich protrusions | Q27318457 | ||
Eps8 regulates axonal filopodia in hippocampal neurons in response to brain-derived neurotrophic factor (BDNF) | Q27330089 | ||
Cellular motility driven by assembly and disassembly of actin filaments | Q27860676 | ||
Disruption of the Diaphanous-related formin Drf1 gene encoding mDia1 reveals a role for Drf3 as an effector for Cdc42 | Q28188673 | ||
Non-muscle myosin II takes centre stage in cell adhesion and migration | Q28262326 | ||
Filopodia: molecular architecture and cellular functions | Q28279460 | ||
Disoriented pathfinding by pioneer neurone growth cones deprived of filopodia by cytochalasin treatment | Q28304527 | ||
Regulation of cell shape by Cdc42 is mediated by the synergic actin-bundling activity of the Eps8-IRSp53 complex | Q28505970 | ||
Force fluctuations within focal adhesions mediate ECM-rigidity sensing to guide directed cell migration | Q28508256 | ||
The comings and goings of actin: coupling protrusion and retraction in cell motility | Q36228793 | ||
Delayed retraction of filopodia in gelsolin null mice | Q36254777 | ||
Regulated actin cytoskeleton assembly at filopodium tips controls their extension and retraction | Q36316633 | ||
The Diaphanous-related formin dDia2 is required for the formation and maintenance of filopodia. | Q46503087 | ||
Nonviral gene delivery vectors use syndecan-dependent transport mechanisms in filopodia to reach the cell surface | Q47310356 | ||
Membrane extensions are associated with proper anterior migration of muscle cells during Caenorhabditis elegans embryogenesis. | Q50514847 | ||
The asymmetric self-assembly mechanism of adherens junctions: a cellular push-pull unit. | Q50640288 | ||
Delta-promoted filopodia mediate long-range lateral inhibition in Drosophila. | Q52642002 | ||
Ross Harrison's "The outgrowth of the nerve fiber as a mode of protoplasmic movement". | Q53354418 | ||
Formation and Interaction of Membrane Tubes | Q57252588 | ||
Assembling an actin cytoskeleton for cell attachment and movement | Q58009796 | ||
Polarity of actin at the leading edge of cultured cells | Q59067967 | ||
A sensory role for neuronal growth cone filopodia | Q59067973 | ||
Essential role of filopodia in chemotropic turning of nerve growth cone induced by a glutamate gradient | Q70891412 | ||
Ingestion of latex beads by filopodia of adherent mouse peritoneal macrophages. A scanning electron microscopical and reflection contrast microscopical study | Q71297801 | ||
The trkA receptor mediates growth cone turning toward a localized source of nerve growth factor | Q73470143 | ||
Myosin IIB is required for growth cone motility | Q74316064 | ||
Molecular dynamics and forces of a motile cell simultaneously visualized by TIRF and force microscopies | Q81267872 | ||
Spicules and the effect of rigid rods on enclosing membrane tubes | Q82125661 | ||
I-BAR domain proteins: linking actin and plasma membrane dynamics | Q82533830 | ||
Myosin II functions in actin-bundle turnover in neuronal growth cones | Q82661954 | ||
The making of filopodia | Q36335794 | ||
Dendritic filopodia, Ripped Pocket, NOMPC, and NMDARs contribute to the sense of touch in Drosophila larvae | Q36438843 | ||
Quantitative fluorescent speckle microscopy of cytoskeleton dynamics | Q36475406 | ||
WASP family members and formin proteins coordinate regulation of cell protrusions in carcinoma cells | Q36534637 | ||
The stochastic dynamics of filopodial growth | Q36632087 | ||
Filopodia: the fingers that do the walking | Q36915801 | ||
Ena/VASP: proteins at the tip of the nervous system | Q37174967 | ||
Unravelling the structure of the lamellipodium | Q37255349 | ||
The role of formins in filopodia formation | Q37378128 | ||
Epithelial resealing | Q37402619 | ||
Filopodia: Complex models for simple rods. | Q37477758 | ||
The heel and toe of the cell's foot: a multifaceted approach for understanding the structure and dynamics of focal adhesions | Q37550239 | ||
Cytoskeletal dynamics in growth-cone steering. | Q37610679 | ||
ADF/cofilin: a functional node in cell biology | Q37687604 | ||
Control of actin filament treadmilling in cell motility | Q37700675 | ||
Neurite outgrowth: this process, first discovered by Santiago Ramon y Cajal, is sustained by the exocytosis of two distinct types of vesicles | Q37769854 | ||
Force generation, transmission, and integration during cell and tissue morphogenesis | Q37899183 | ||
Nanoscopy of cell architecture: The actin-membrane interface | Q37922104 | ||
Filopodia initiation: focus on the Arp2/3 complex and formins | Q37942763 | ||
From filopodia to synapses: the role of actin-capping and anti-capping proteins. | Q37958909 | ||
Wiring through tunneling nanotubes--from electrical signals to organelle transfer | Q37991687 | ||
Quantifying traction stresses in adherent cells | Q38000684 | ||
United we stand: integrating the actin cytoskeleton and cell-matrix adhesions in cellular mechanotransduction. | Q38026497 | ||
Mechanical feedback between membrane tension and dynamics | Q38037852 | ||
Cytoneme-mediated cell-to-cell signaling during development | Q38084176 | ||
Formins regulate the actin-related protein 2/3 complex-independent polarization of the centrosome to the immunological synapse | Q39546199 | ||
Vangl2 promotes Wnt/planar cell polarity-like signaling by antagonizing Dvl1-mediated feedback inhibition in growth cone guidance | Q39726927 | ||
Missing-in-metastasis and IRSp53 deform PI(4,5)P2-rich membranes by an inverse BAR domain-like mechanism | Q39734937 | ||
Role of focal adhesions and mechanical stresses in the formation and progression of the lamellipodium-lamellum interface [corrected] | Q39806001 | ||
Micromechanics of filopodia mediated capture of pathogens by macrophages | Q40198042 | ||
Characterization of the turning response of dorsal root neurites toward nerve growth factor | Q41281495 | ||
On the mechanical stabilization of filopodia | Q41429724 | ||
The organization of myosin and actin in rapid frozen nerve growth cones | Q41564848 | ||
Organization of actin networks in intact filopodia | Q41625141 | ||
Specialized filopodia direct long-range transport of SHH during vertebrate tissue patterning | Q41944663 | ||
A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level | Q41978648 | ||
Dynamical control of the shape and size of stereocilia and microvilli | Q42468948 | ||
Pioneer growth cone steering decisions mediated by single filopodial contacts in situ. | Q42482885 | ||
Three functionally distinct adhesions in filopodia: shaft adhesions control lamellar extension. | Q42525821 | ||
The Rho family GTPase Rif induces filopodia through mDia2. | Q42818923 | ||
Nerve growth cone lamellipodia contain two populations of actin filaments that differ in organization and polarity | Q43108576 | ||
Forces for morphogenesis investigated with laser microsurgery and quantitative modeling | Q44307030 | ||
Formin is a processive motor that requires profilin to accelerate actin assembly and associated ATP hydrolysis | Q45126402 | ||
Process entanglement as a neuronal anchorage mechanism to rough surfaces. | Q46024671 | ||
Arp2/3 complex is important for filopodia formation, growth cone motility, and neuritogenesis in neuronal cells | Q28576273 | ||
Lamellipodial versus filopodial mode of the actin nanomachinery: pivotal role of the filament barbed end | Q28594452 | ||
Building the actin cytoskeleton: filopodia contribute to the construction of contractile bundles in the lamella | Q28755150 | ||
Traction stress in focal adhesions correlates biphasically with actin retrograde flow speed | Q29030465 | ||
Actin cortex mechanics and cellular morphogenesis | Q29392541 | ||
Mechanism of filopodia initiation by reorganization of a dendritic network | Q29616648 | ||
Two distinct actin networks drive the protrusion of migrating cells | Q29617078 | ||
Directed actin polymerization is the driving force for epithelial cell-cell adhesion | Q29618861 | ||
I-BAR domains, IRSp53 and filopodium formation | Q30157055 | ||
Long-distance relationships: do membrane nanotubes regulate cell-cell communication and disease progression? | Q30418602 | ||
Molecular architecture of synaptic actin cytoskeleton in hippocampal neurons reveals a mechanism of dendritic spine morphogenesis | Q30436753 | ||
Ena/VASP proteins have an anti-capping independent function in filopodia formation | Q30444426 | ||
Twigs into branches: how a filopodium becomes a dendrite | Q30477226 | ||
Filopodia formation in the absence of functional WAVE- and Arp2/3-complexes | Q30477396 | ||
Nonmuscle myosin IIA-dependent force inhibits cell spreading and drives F-actin flow | Q30478216 | ||
Direct measurement of force generation by actin filament polymerization using an optical trap | Q30479598 | ||
Arp2/3 complex interactions and actin network turnover in lamellipodia. | Q30481401 | ||
Dynamic analysis of filopodial interactions during the zippering phase of Drosophila dorsal closure | Q30482461 | ||
Retrograde flow and myosin II activity within the leading cell edge deliver F-actin to the lamella to seed the formation of graded polarity actomyosin II filament bundles in migrating fibroblasts | Q30484304 | ||
Retroviruses can establish filopodial bridges for efficient cell-to-cell transmission. | Q30485520 | ||
Arp2 depletion inhibits sheet-like protrusions but not linear protrusions of fibroblasts and lymphocytes | Q30490773 | ||
Myosin-X induces filopodia by multiple elongation mechanism | Q30494868 | ||
Contribution of Filopodia to Cell Migration: A Mechanical Link between Protrusion and Contraction | Q30495706 | ||
Spatial and temporal relationships between actin-filament nucleation, capping, and disassembly | Q30499668 | ||
Polarization of actin cytoskeleton is reduced in dendritic protrusions during early spine development in hippocampal neuron | Q30524154 | ||
Filopodium retraction is controlled by adhesion to its tip. | Q30530913 | ||
The role of filopodia in the recognition of nanotopographies | Q30538842 | ||
Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination | Q30538857 | ||
Myosin II contributes to cell-scale actin network treadmilling through network disassembly | Q30540043 | ||
Cofilin cooperates with fascin to disassemble filopodial actin filaments | Q30581893 | ||
Rapid epithelial-sheet sealing in the Caenorhabditis elegans embryo requires cadherin-dependent filopodial priming | Q30798313 | ||
Insertional assembly of actin filament barbed ends in association with formins produces piconewton forces | Q31113561 | ||
Actin dynamics in growth cones | Q33264497 | ||
Coordination of membrane and actin cytoskeleton dynamics during filopodia protrusion | Q33455812 | ||
Visualizing cellular processes at the molecular level by cryo-electron tomography | Q33518979 | ||
Autonomous right-screw rotation of growth cone filopodia drives neurite turning. | Q33643751 | ||
Cytonemes: cellular processes that project to the principal signaling center in Drosophila imaginal discs | Q33864771 | ||
Dynamic actin-based epithelial adhesion and cell matching during Drosophila dorsal closure. | Q33927041 | ||
The key feature for early migratory processes: Dependence of adhesion, actin bundles, force generation and transmission on filopodia | Q33977473 | ||
Cell-matrix entanglement and mechanical anchorage of fibroblasts in three-dimensional collagen matrices | Q34099482 | ||
Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. | Q34115035 | ||
Dynamic filopodia transmit intermittent Delta-Notch signaling to drive pattern refinement during lateral inhibition | Q34126867 | ||
Mechanical properties of neuronal growth cone membranes studied by tether formation with laser optical tweezers | Q34128706 | ||
Filopodia and actin arcs guide the assembly and transport of two populations of microtubules with unique dynamic parameters in neuronal growth cones | Q34137487 | ||
Stresses at the cell-to-substrate interface during locomotion of fibroblasts | Q34170351 | ||
Mechanism of lateral movement of filopodia and radial actin bundles across neuronal growth cones | Q34172550 | ||
Specificity of Drosophila cytonemes for distinct signaling pathways | Q34178455 | ||
Direct determination of actin polarity in the cell | Q34213007 | ||
Cell control by membrane-cytoskeleton adhesion | Q34238066 | ||
Nanotubular highways for intercellular organelle transport | Q34298770 | ||
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 | ||
Dependence of Drosophila wing imaginal disc cytonemes on Decapentaplegic | Q34452981 | ||
Cytonemes and tunneling nanotubules in cell-cell communication and viral pathogenesis | Q34808767 | ||
Traction dynamics of filopodia on compliant substrates. | Q34901393 | ||
Myosin motor function: the ins and outs of actin-based membrane protrusions. | Q34985570 | ||
Forcing a connection: impacts of single-molecule force spectroscopy on in vivo tension sensing | Q34990311 | ||
Do filopodia enable the growth cone to find its way? | Q35132220 | ||
Extension of filopodia by motor-dependent actin assembly | Q35477000 | ||
The filopodium: a stable structure with highly regulated repetitive cycles of elongation and persistence depending on the actin cross-linker fascin. | Q35557009 | ||
Regulation of growth cone actin filaments by guidance cues | Q35575896 | ||
ATP-mediated Erk1/2 activation stimulates bacterial capture by filopodia, which precedes Shigella invasion of epithelial cells | Q35586337 | ||
Attachment conditions control actin filament buckling and the production of forces | Q35781252 | ||
Membrane tension, myosin force, and actin turnover maintain actin treadmill in the nerve growth cone | Q35866817 | ||
Role of fascin in filopodial protrusion | Q36118593 | ||
The cytomechanics of axonal elongation and retraction | Q36222066 | ||
Growth cone behavior and production of traction force | Q36223976 | ||
P433 | issue | 10 | |
P304 | page(s) | 590-603 | |
P577 | publication date | 2013-09-03 | |
P1433 | published in | Cytoskeleton | Q2196987 |
P1476 | title | How filopodia pull: what we know about the mechanics and dynamics of filopodia | |
P478 | volume | 70 |
Q50495381 | Actin Filament Structures in Migrating Cells. |
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Q38383035 | An updated look at actin dynamics in filopodia. |
Q36342251 | Analysis of host microRNA function uncovers a role for miR-29b-2-5p in Shigella capture by filopodia. |
Q37000324 | Competition between Coiled-Coil Structures and the Impact on Myosin-10 Bundle Selection |
Q48591142 | Computational simulation of formin-mediated actin polymerization predicts homologue-dependent mechanosensitivity |
Q38806123 | Correlative STED and Atomic Force Microscopy on Live Astrocytes Reveals Plasticity of Cytoskeletal Structure and Membrane Physical Properties during Polarized Migration |
Q36124196 | Dynamic buckling of actin within filopodia |
Q30826764 | Exosomes surf on filopodia to enter cells at endocytic hot spots, traffic within endosomes, and are targeted to the ER |
Q27323167 | Fast, label-free super-resolution live-cell imaging using rotating coherent scattering (ROCS) microscopy |
Q26751070 | Filopodia and Viruses: An Analysis of Membrane Processes in Entry Mechanisms |
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Q27316224 | Filopodial-Tension Model of Convergent-Extension of Tissues |
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Q37041149 | Matrix metalloproteinase-9-dependent mechanisms of reduced contractility and increased stiffness in the aging heart |
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Q47139973 | Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. |
Q52364597 | New insights into the formation and the function of lamellipodia and ruffles in mesenchymal cell migration. |
Q55322531 | Perspectives on Intra- and Intercellular Trafficking of Hedgehog for Tissue Patterning. |
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