about
Cell movement is guided by the rigidity of the substrate.Mechanical tension can specify axonal fate in hippocampal neuronsQuantifying mechanical force in axonal growth and guidanceMechanochemical regulation of growth cone motilityCartography and connectomesDrosophila growth cones advance by forward translocation of the neuronal cytoskeletal meshwork in vivoTubulin tyrosination is required for the proper organization and pathfinding of the growth coneRecycling of the cell adhesion molecule L1 in axonal growth cones.A physical model of axonal elongation: force, viscosity, and adhesions govern the mode of outgrowthShootin1 interacts with actin retrograde flow and L1-CAM to promote axon outgrowthDirect evidence for coherent low velocity axonal transport of mitochondria.Coordination of actin filament and microtubule dynamics during neurite outgrowth.Quantitative analysis of microtubule dynamics during adhesion-mediated growth cone guidanceA framework for modeling the growth and development of neurons and networks.A diffusion-based neurite length-sensing mechanism involved in neuronal symmetry breaking.Mechanical tension modulates local and global vesicle dynamics in neuronsNetrin-1 attracts axons through FAK-dependent mechanotransductionActive transport of vesicles in neurons is modulated by mechanical tensionDynamic peripheral traction forces balance stable neurite tension in regenerating Aplysia bag cell neurons.Low piconewton towing of CNS axons against diffusing and surface-bound repellents requires the inhibition of motor protein-associated pathways.Radixin is involved in lamellipodial stability during nerve growth cone motilityChanges in membrane trafficking and actin dynamics during axon formation in cultured hippocampal neurons.Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering.Towards a unified theory for morphomechanics.Discovery of long-range inhibitory signaling to ensure single axon formation.Self-organizing circuit assembly through spatiotemporally coordinated neuronal migration within geometric constraintsFilopodia and actin arcs guide the assembly and transport of two populations of microtubules with unique dynamic parameters in neuronal growth cones.Tensile force-dependent neurite elicitation via anti-beta1 integrin antibody-coated magnetic beads.Strength in the periphery: growth cone biomechanics and substrate rigidity response in peripheral and central nervous system neuronsCell guidance on nanogratings: a computational model of the interplay between PC12 growth cones and nanostructures.Role of myosin II in axon outgrowth.Axons pull on the brain, but tension does not drive cortical foldingMeasurement of subcellular force generation in neurons.Substrate Deformation Predicts Neuronal Growth Cone Advance.Residual stress in the adult mouse brain.The cytomechanics of axonal elongation and retraction.Extracellular matrix allows PC12 neurite elongation in the absence of microtubules.Growth cone behavior and production of traction force.Cytoskeletal remodeling during growth cone-target interactions.Measurements of growth cone adhesion to culture surfaces by micromanipulation
P2860
Q24537364-AAD5E909-910C-45A5-8C77-6DD6F83AC3F2Q24674320-EB33E92D-51AA-49F5-AF54-00443C80233AQ26781636-A58D2CB9-4751-4010-8560-1EDEE21607A6Q26799030-9CAB8EFC-6C59-4A54-9396-C2EEF486B5E6Q27003959-8DEDFCD9-87B6-4750-A47F-C122A1646920Q27302110-72633F2C-5E40-4641-B518-D05EF1B6F1FEQ27349475-9BF85C4D-285A-43CD-B309-7E3F02CEB77AQ27863668-2C853630-B16C-456C-80AF-B258CA34DB2BQ28263795-610F4CFA-B597-4B69-8EDB-1FC7A655D209Q28574182-17D3E077-0825-44C8-B9B5-8948B9AD03C5Q30480396-B5F606AD-40C1-4CFA-8A94-E5B1AA82B537Q30484871-3541CF39-27B0-4B22-B78E-668ED418E9E3Q30490287-0A7ECB25-596E-4FF7-BC2B-EED237FBAA2AQ30491952-46D8BCA0-77E6-4D8F-89F0-6A5CBD988956Q30496207-D0EBAE72-9179-411E-BA69-A66EF5CC719BQ30525094-28F7EAF4-EDCB-4290-ACEA-0526D125D37CQ30525348-4769DF34-BE2A-423B-89F5-99B96422A7AAQ30574743-3C4BED38-80F7-40E0-AB14-D122CE627BCDQ30577972-ABBB536D-84C8-4F8F-A906-26EB465EDEECQ30601245-A5055E93-C834-42A3-B448-6C9CC47AED95Q30629181-D3A76010-9B09-41A9-837C-D02A3D1CED6EQ33808584-4EEE036F-6ABE-4E9D-879F-04084392D9F4Q33817937-89B803DA-B0F3-4F0F-AD26-7E03D8E60702Q33834790-60D288F0-B889-4C2F-8945-C27ED2C2ED84Q33835262-FD38E6F7-6261-4F18-A5EA-D6CD79474F2DQ34088191-2A848CBD-51CE-4C4B-9E8A-001A8F064F8FQ34137487-5ED981F0-8D2D-4CC4-97C5-B523DC0B7DB0Q34182009-FDAEF980-FFC9-4BA1-80D7-8755642A124FQ34253602-4B4C85B5-C294-4D36-A0E2-B4A5A8EF4900Q34925352-AD577759-7518-44BC-AD0D-DDC44D8CEB80Q35087189-467B517A-8B86-41A3-A881-5945EEB6D54EQ35207844-F99FFC6F-78A5-4554-95F0-DD84DC01FCB1Q35221891-F2E14603-4565-44E2-9924-935F1DDD28A8Q36146813-058F0D24-27F3-4A4D-A76F-D8F20E1920A0Q36161361-74282ECB-1EF2-4331-B6F0-6C33D1C1F75DQ36222066-2D5B8547-1500-4543-AB39-8231050D6A54Q36222453-49C66CB0-6CAA-44AC-B950-ABAA8F8EAA7BQ36223976-E30D4134-613E-4AFD-8ED5-4B9FEDEAF932Q36232984-CE49B9FA-DD5E-4245-BC5D-8E252231B985Q36234993-0491DCB1-E8C0-412D-A85E-13439AA48415
P2860
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Direct evidence that growth cones pull.
@ast
Direct evidence that growth cones pull.
@en
Direct evidence that growth cones pull.
@nl
type
label
Direct evidence that growth cones pull.
@ast
Direct evidence that growth cones pull.
@en
Direct evidence that growth cones pull.
@nl
prefLabel
Direct evidence that growth cones pull.
@ast
Direct evidence that growth cones pull.
@en
Direct evidence that growth cones pull.
@nl
P2093
P356
P1433
P1476
Direct evidence that growth cones pull.
@en
P2093
Buxbaum RE
Heidemann SR
Lamoureux P
P2888
P304
P356
10.1038/340159A0
P407
P577
1989-07-01T00:00:00Z
P6179
1021455619