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1 of BIM1 eliminated Kar9p localization along cytoplasmic microtubules.
2 envelope proteins, such as SUN-1, to access cytoplasmic microtubules.
3 the cell, often coincident with the ends of cytoplasmic microtubules.
4 im1p localizes to dots at the distal ends of cytoplasmic microtubules.
5 e mitotic spindle and the orientation of the cytoplasmic microtubules.
6 the pheromone-induced reorganization of the cytoplasmic microtubules.
7 t of a cortical adaptor complex that orients cytoplasmic microtubules.
8 d for the Kar9p-dependent orientation of the cytoplasmic microtubules.
9 reas GFP-Kip3p localized to both spindle and cytoplasmic microtubules.
10 gene product, neurofibromin, interacts with cytoplasmic microtubules.
11 les and chromosomes toward the minus ends of cytoplasmic microtubules.
12 ses of the cell cycle, connecting the DSB to cytoplasmic microtubules.
13 and flagellar enrichment are facilitated by cytoplasmic microtubules.
14 f Drosophila melanogaster that depolymerizes cytoplasmic microtubules.
15 interact with the nuclear envelope (NE) and cytoplasmic microtubules.
16 microtubules without significantly altering cytoplasmic microtubules.
17 rtant for the organization/nucleation of all cytoplasmic microtubules.
18 oogenesis for the structure and function of cytoplasmic microtubules.
19 onfunctional spindle poles or the absence of cytoplasmic microtubules.
20 tion of KAR3 leads to a dramatic increase in cytoplasmic microtubules, a phenotype which is most pron
21 ether, we propose that kinesin-1 slides free cytoplasmic microtubules against cortically immobilized
23 of dynein-green fluorescent protein (GFP) to cytoplasmic microtubules allowed us to obtain one of the
24 ther and bud via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud.
25 her-bud neck via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud.
26 somal region, induces profound disruption of cytoplasmic microtubules and a nuclear distortion phenot
27 In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed
28 tribution but retain the ability to organize cytoplasmic microtubules and actin in anucleate hyphae.
31 ivity resulted in assembly of unusually long cytoplasmic microtubules and defects in spindle position
33 uring mitosis, leading to the coexistence of cytoplasmic microtubules and nuclear spindles with massi
34 sembly of subdistal appendages, which anchor cytoplasmic microtubules and prime the mother centriole
36 in fungi have been shown to be dependent on cytoplasmic microtubules and the microtubule-associated
37 t depends on persistent interactions between cytoplasmic microtubules and the mother-bud neck, the fu
38 show that Myo2 localizes to the plus ends of cytoplasmic microtubules, and that the rate of movement
44 yeast Schizosaccharomyces pombe, interphase cytoplasmic microtubules are organized into antiparallel
49 layed unusually long and numerous bundles of cytoplasmic microtubules as revealed by immunofluorescen
50 targeted to the distal plus ends of dynamic cytoplasmic microtubules, as is HC, and their targeting
51 t anaphase onset, the FEAR pathway activates cytoplasmic microtubule-associated forces that facilitat
52 d lack of TINA causes enhanced production of cytoplasmic microtubules at metaphase arrest, we suggest
53 osaccharomyces pombe, longitudinal arrays of cytoplasmic microtubule bundles regulate cell polarity a
54 A simple self-assembly pathway generates cytoplasmic microtubule bundles that can locate the cell
55 lpha 85E does not disrupt meiotic spindle or cytoplasmic microtubules but causes defects in morphogen
56 g a stochastic simulation that confirms that cytoplasmic microtubules can compete with flagella for a
60 to the conclusion that biased nucleation of cytoplasmic microtubules (cMTs) is essential for directi
61 ughter cell by linking the associated set of cytoplasmic microtubules (cMTs) to the polarized actin n
62 sponsible for establishing cell polarity and cytoplasmic microtubules collaborate to establish MEN as
65 st cell elongates toward its mating partner, cytoplasmic microtubules connect the nucleus to the cell
66 rity relies on a precise temporal program of cytoplasmic microtubule-cortex interactions throughout s
69 induced rapid, anterograde IFT-independent, cytoplasmic microtubule-dependent redistribution of the
71 Saccharomyces cerevisiae cells lacking She1, cytoplasmic microtubules detach from the spindle pole bo
72 lagellar transport and cargo transport along cytoplasmic microtubules, differ from motors in the cano
74 ghout the vegetative cell cycle as they bind cytoplasmic microtubules during interphase, spindle micr
75 nation of metachronic cilia beating, whereas cytoplasmic microtubule dynamics are required for local
79 highly conserved EB1 family, Bim1p, promotes cytoplasmic microtubule dynamics specifically during G1.
82 chanism to delay cell cycle progression when cytoplasmic microtubules fail to orient the spindle.
83 gests a model in which flagella compete with cytoplasmic microtubules for a fixed pool of tubulin, wi
84 lium, with Gli2 but not Smo requiring intact cytoplasmic microtubules for ciliary entry and both requ
85 that a novel complex links the nucleus with cytoplasmic microtubules for the promotion of DNA repair
89 f TINA enhanced the nucleation of bundles of cytoplasmic microtubules from the spindle pole bodies.
91 Although effects of XMAP215/TOG proteins on cytoplasmic microtubules have not previously been shown
92 functions to limit the number and length of cytoplasmic microtubules in a cell cycle-specific manner
93 ons essential to mitosis and organization of cytoplasmic microtubules in addition to its well-documen
95 ion of Stu2p leads to fewer and less dynamic cytoplasmic microtubules in both G1 and preanaphase cell
98 assembly and cause breakdown of preassembled cytoplasmic microtubules in human polymorphonuclear leuk
104 unctions without Lte1p and apparently senses cytoplasmic microtubules in the mother/bud neck [7-9].
106 nd yeast cells, this process is dependent on cytoplasmic microtubules interacting with the cortical a
114 evisiae kinesin-14 that functions to shorten cytoplasmic microtubules (MTs) during yeast mating yet m
118 osome positioning requires a radial array of cytoplasmic microtubules (MTs) that can exert pushing or
120 n fission yeast (Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the sp
122 d molecular motors and they travel along the cytoplasmic microtubule network towards the minus end of
123 iod marked by dramatic reorganization of the cytoplasmic microtubule network, endogenous MLK3 transie
128 in fission yeast Schizosaccharomyces pombe, cytoplasmic microtubule nucleation ceases simultaneously
130 rmation of these microtubule bundles include cytoplasmic microtubule nucleation, microtubule release
131 ein is targeted to the dynamic plus end of a cytoplasmic microtubule, offloads to the cortex, becomes
132 nclude that Kar9p's function is specific for cytoplasmic microtubule orientation and that Kar9p's rol
134 important to prevent excessive detachment of cytoplasmic microtubules, particularly in G1 cells.
136 tip-ward movement is similar to the rate of cytoplasmic microtubule polymerization toward the hyphal
141 ted tubulin pool, showing that alteration of cytoplasmic microtubule severing could be sufficient to
144 cells lack cytoplasmic microtubules; the few cytoplasmic microtubules that are observed are excessive
145 ch a highly elastic nucleus is surrounded by cytoplasmic microtubules that behave as a jelly-like vis
146 oison thiabendazole and have abnormally long cytoplasmic microtubules that can curl around the ends o
147 ubules anchored to the actin cortex and free cytoplasmic microtubules that moved in the ooplasm.
148 In addition, most spc72 mutant cells lack cytoplasmic microtubules; the few cytoplasmic microtubul
149 Klp5p-GFP and Klp6p-GFP both localize to cytoplasmic microtubules throughout the cell cycle and t
150 alization studies found Kip2p exclusively on cytoplasmic microtubules throughout the cell cycle, wher
151 marker protein, Tea1, that is transported by cytoplasmic microtubules to cell tips and recruits other
156 ules, and that the rate of movement of these cytoplasmic microtubules to the bud neck depends on the
157 elative contributions of the kinetochore and cytoplasmic microtubules to the forces involved in forma
158 mutants retain the ability to generate long cytoplasmic microtubule tracks, suggesting that the nucl
159 rc activity regulates the transition between cytoplasmic microtubule transport and actin-based motili
162 cells with nuclear positioning defects, the cytoplasmic microtubules were misoriented and failed to
165 e pole body (SPB), organizes the nuclear and cytoplasmic microtubules which are functionally and spat
166 ver, alp16 deletion displays abnormally long cytoplasmic microtubules, which curve around the cell ti
169 eriments demonstrate that the interaction of cytoplasmic microtubules with the Kar9p cortical attachm
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