Reverse engineering of force integration during mitosis in the Drosophila embryo.
about
Towards a quantitative understanding of mitotic spindle assembly and mechanicsKinesin-5-dependent poleward flux and spindle length control in Drosophila embryo mitosisCoupling between microtubule sliding, plus-end growth and spindle length revealed by kinesin-8 depletionFinding the cell center by a balance of dynein and myosin pulling and microtubule pushing: a computational study.Physical determinants of bipolar mitotic spindle assembly and stability in fission yeast.Asymmetric friction of nonmotor MAPs can lead to their directional motion in active microtubule networks.Prometaphase spindle maintenance by an antagonistic motor-dependent force balance made robust by a disassembling lamin-B envelope.Robust transport by multiple motors with nonlinear force-velocity relations and stochastic load sharing.Actomyosin-dependent cortical dynamics contributes to the prophase force-balance in the early Drosophila embryoUsing micromanipulation to analyze control of vertebrate meiotic spindle sizeBiophysics of mitosisCell size modulates oscillation, positioning and length of mitotic spindles.Emergent Properties of the Metaphase Spindle.Building the Microtubule Cytoskeleton Piece by PieceInferring the Forces Controlling Metaphase Kinetochore Oscillations by Reverse Engineering System Dynamics.The elasticity of motor-microtubule bundles and shape of the mitotic spindle.Highly Transient Molecular Interactions Underlie the Stability of Kinetochore-Microtubule Attachment During Cell Division.Micromechanics of the vertebrate meiotic spindle examined by stretching along the pole-to-pole axis.Force and length in the mitotic spindle.A theoretical model of mitotic spindle elongation under experimental constraints.Dynamical scenarios for chromosome bi-orientation.Microtubule Sliding within the Bridging Fiber Pushes Kinetochore Fibers Apart to Segregate Chromosomes.APC/C is an essential regulator of centrosome clustering.Bidirectional motion of filaments: the role of motor proteins and passive cross linkers.Generation of stable overlaps between antiparallel filaments.Mechanical positioning of multiple nuclei in muscle cells.
P2860
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P2860
Reverse engineering of force integration during mitosis in the Drosophila embryo.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@ast
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@en
type
label
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@ast
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@en
prefLabel
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@ast
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@en
P2093
P2860
P356
P1476
Reverse engineering of force integration during mitosis in the Drosophila embryo.
@en
P2093
Gul Civelekoglu-Scholey
Jonathan M Scholey
Roy Wollman
P2860
P356
10.1038/MSB.2008.23
P577
2008-05-06T00:00:00Z