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1 Cytoplasmic dynein is the major microtubule minus end-directed motor.
2 lasmic Dynein 1, or Dynein, is a microtubule minus end-directed motor.
3 but not KIF13B undergoes a tug-of-war with a minus-end directed motor.
4 a gal suggests that the head of Nod may be a minus-end-directed motor.
5 on antagonistic activities of plus end- and minus end-directed motors.
6 ongression depends on the cooperation of two minus end-directed motors.
7 T, the human homologue of the KAR3 family of minus end-directed motors.
8 ng, suggesting that they were transported by minus end-directed motors.
9 by the opposing activities of plus end- and minus end-directed motors.
10 bidirectionally, employing both plus-end and minus-end directed motors.
11 ytoskeleton has pointed instead to roles for minus-end-directed motors.
12 be created by complexes combining plus- and minus-end-directed motors.
13 rucial role in the coordination of plus- and minus-end-directed motors.
14 formation of aggresomes, suggesting that the minus-end-directed motor activities of cytoplasmic dynei
15 ndrites indicate that models suggesting that minus end-directed motor activity is sufficient for dend
17 tor, the clustering of their minus ends by a minus-end-directed motor, and the loss of MTs by dynamic
18 plored how the balance between plus end- and minus end-directed motors, as well as the influence of m
21 eraction of microtubules with both plus- and minus-end directed motors bound to a fluid membrane.
22 ve studied the shape of myosin VI, the actin minus-end directed motor, by negative stain and metal sh
25 dynein/dynactin, a multi-subunit microtubule minus-end-directed motor complex, and NuMA, a microtubul
26 Our data reveal the novel finding that a minus-end-directed motor contributes to the organization
27 es (MTs) are substrates upon which plus- and minus-end directed motors control the directional moveme
28 d simulations, we propose a model on how two minus end-directed motors cooperate to ensure spindle po
29 -end binding proteins, suggesting that these minus-end-directed motors could interact with growing mi
30 r to translocation of the MTOC, in which the minus end-directed motor cytoplasmic dynein, localized a
33 plus end-directed motor, kinesin-II, and the minus end-directed motor, cytoplasmic dynein in highly p
38 Inhibitory antibodies indicated that the minus-end-directed motor dynein is required to prevent p
39 the transport of a subset of cargoes by the minus-end-directed motor dynein, although the full exten
41 Here, we have characterized the roles of two minus end-directed motors, dynein and Ncd, in such proce
43 ac-man model, in which 1) kinetochore-based, minus end-directed motors generate poleward forces for a
44 cortex required Bud6p, Bim1p, and dynein, a minus-end-directed motor helping tether the receding plu
45 involved in organelle transport) and ncd (a minus-end-directed motor involved in chromosome segregat
47 Cell biologists have long speculated that a minus end-directed motor localized at kinetochores contr
49 motors containing the stalk and neck of the minus-end-directed motor, Ncd, fused to the motor domain
50 se mitotic spindles with inactive kinesin-14 minus-end-directed motors often have shorter spindle len
51 ng of nuclear congression and identified two minus end-directed motors operating in parallel in this
52 Cytoplasmic dynein 1 (dynein) is the primary minus end-directed motor protein in most eukaryotic cell
56 mobilized on microtubules by the activity of minus end-directed motor proteins that interact either d
60 nein-1 (dynein) is a microtubule-associated, minus end-directed motor that traffics hundreds of diffe
61 Drosophila Ncd, the other well characterized minus-end directed motor that is a homodimer, Kar3 is a
64 -directed motors are balanced by forces from minus-end-directed motors that pull spindle poles togeth
65 act at microtubule tips synergistically with minus-end directed motors to produce a system that can g
66 ative actions of the bipolar kinesin-5 and a minus-end-directed motor, which then pulls the sliding M