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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
22                           In yeast, oriented cytoplasmic microtubules align the mitotic spindle betwe
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.
29 ing of the mitotic spindle requires both the cytoplasmic microtubules and actin.
30 lights a framework for communication between cytoplasmic microtubules and chromatin.
31 ivity resulted in assembly of unusually long cytoplasmic microtubules and defects in spindle position
32        These bidirectional movements require cytoplasmic microtubules and microfilaments and depend o
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
35 iae that is mediated by interactions between cytoplasmic microtubules and the cell cortex.
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
39                    Secondly, abnormally long cytoplasmic microtubules appear that do not stop at the
40                                              Cytoplasmic microtubules are critical for establishing a
41                           Here, we show that cytoplasmic microtubules are mechanically coupled to the
42                                     In vivo, cytoplasmic microtubules are nucleated and anchored by t
43                        Consistent with this, cytoplasmic microtubules are often highly curved and app
44  yeast Schizosaccharomyces pombe, interphase cytoplasmic microtubules are organized into antiparallel
45                    Our findings suggest that cytoplasmic microtubules are used to monitor the locatio
46 portant for establishing a normal interphase cytoplasmic microtubule array.
47                              At 30 degrees C cytoplasmic microtubule arrays are abnormal and bundle i
48 rmal mitotic spindles and some have abnormal cytoplasmic microtubule arrays.
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
57 stent with Bud6's role as a cortical cue for cytoplasmic microtubule capture.
58 other- bud axis through interactions between cytoplasmic microtubules (CMs) and the cell cortex.
59         The 'cMT-bud neck model' posits that cytoplasmic microtubule (cMT)-bud neck interactions prev
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
63 pression of the entire SPC72 results in more cytoplasmic microtubules compared with wild-type.
64 ed to returned to interphase retain a normal cytoplasmic microtubule complex.
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
67                        The average number of cytoplasmic microtubules decreased from 3 in wild-type t
68                         This correlated with cytoplasmic microtubule defects.
69  induced rapid, anterograde IFT-independent, cytoplasmic microtubule-dependent redistribution of the
70                           Stathmin (STMN), a cytoplasmic microtubule-destabilizing phosphoprotein, re
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
73                                In germlings, cytoplasmic microtubules disassembled completely in mito
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
76     Our findings highlight the regulation of cytoplasmic microtubule dynamics as a role of the IFT54
77                             The reduction in cytoplasmic microtubule dynamics is due primarily to dec
78                    The pattern and extent of cytoplasmic microtubule dynamics modulation through the
79 highly conserved EB1 family, Bim1p, promotes cytoplasmic microtubule dynamics specifically during G1.
80                    These movements depend on cytoplasmic microtubules emanating from the nuclei that
81 oncentrate at cell ends by attaching it to a cytoplasmic microtubule end-binding protein.
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
86         To ensure proper mitotic spindle and cytoplasmic microtubule formation, the cell must maintai
87 leted variant of SPC72 (DeltaN-SPC72) impair cytoplasmic microtubule formation.
88  cells, mitotic exit was preceded by loss of cytoplasmic microtubules from the neck.
89 f TINA enhanced the nucleation of bundles of cytoplasmic microtubules from the spindle pole bodies.
90         Removal of the forces exerted by the cytoplasmic microtubules had no effect on fragmentation.
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
94  nuclear distribution phenotype but affected cytoplasmic microtubules in an unexpected manner.
95 ion of Stu2p leads to fewer and less dynamic cytoplasmic microtubules in both G1 and preanaphase cell
96                  We also identify defects in cytoplasmic microtubules in both the germ and follicle c
97 tion of microtubules in vitro and stabilizes cytoplasmic microtubules in heterologous cells.
98 assembly and cause breakdown of preassembled cytoplasmic microtubules in human polymorphonuclear leuk
99                      EB1 colocalized both to cytoplasmic microtubules in interphase cells and to spin
100          By indirect immunofluorescence, the cytoplasmic microtubules in kip2Delta were consistently
101  a similar process plays a role in orienting cytoplasmic microtubules in mating yeast cells.
102 , the bni1Delta mutant exhibited misoriented cytoplasmic microtubules in shmoos.
103  localized to the plus ends (distal tips) of cytoplasmic microtubules in the bud.
104 unctions without Lte1p and apparently senses cytoplasmic microtubules in the mother/bud neck [7-9].
105 avy chain Dyn1 also localized to the tips of cytoplasmic microtubules in wild-type cells.
106 nd yeast cells, this process is dependent on cytoplasmic microtubules interacting with the cortical a
107              By indirect immunofluorescence, cytoplasmic microtubules intersected the GFP-Kar9p dot.
108  and cell polarization, as well as Kar9p and cytoplasmic microtubule localization.
109 niversal function of kinesin-1 is to mediate cytoplasmic microtubule-microtubule sliding.
110                   These results suggest that cytoplasmic microtubules might be arranged with plus end
111                                          The cytoplasmic microtubule modulator RanBP10 is a Ran and b
112                                              Cytoplasmic microtubules (MTs) continuously grow and sho
113                                              Cytoplasmic microtubules (MTs) continuously grow and sho
114 evisiae kinesin-14 that functions to shorten cytoplasmic microtubules (MTs) during yeast mating yet m
115        CB also disrupted the organization of cytoplasmic microtubules (MTs) in stage VI oocytes.
116                      The ability to nucleate cytoplasmic microtubules (MTs) is a property of the surr
117                                              Cytoplasmic microtubules (MTs) serve as a rate-limiting
118 osome positioning requires a radial array of cytoplasmic microtubules (MTs) that can exert pushing or
119                   Polarized radial arrays of cytoplasmic microtubules (MTs) with minus ends clustered
120 n fission yeast (Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the sp
121                          They have a reduced cytoplasmic microtubule network and display severe morph
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
124 nters establish transient connections to the cytoplasmic microtubule network.
125  knockdown causes the disorganization of the cytoplasmic microtubule network.
126  KIF3A but not by chemical disruption of the cytoplasmic microtubule network.
127        Furthermore, in the bim1 mutants, the cytoplasmic microtubules no longer intersected the corti
128  in fission yeast Schizosaccharomyces pombe, cytoplasmic microtubule nucleation ceases simultaneously
129                                              Cytoplasmic microtubule nucleation in fission yeast depe
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
133                 In fission yeast, interphase cytoplasmic microtubules originate from poorly character
134 important to prevent excessive detachment of cytoplasmic microtubules, particularly in G1 cells.
135         Unexpectedly, BBIP10 is required for cytoplasmic microtubule polymerization and acetylation,
136  tip-ward movement is similar to the rate of cytoplasmic microtubule polymerization toward the hyphal
137                 Thus, SPBs are able to sense cytoplasmic microtubule properties and regulate the Bfa1
138                        Further, Kms1 and the cytoplasmic microtubule regulator Mto1 promote the repai
139                              The behavior of cytoplasmic microtubules revealed distinct interactions
140 2, bld1 mutants have normal basal bodies and cytoplasmic microtubule rootlets.
141 ted tubulin pool, showing that alteration of cytoplasmic microtubule severing could be sufficient to
142                           We further observe cytoplasmic microtubule sliding in Xenopus and Ptk2 cell
143                                           On cytoplasmic microtubules, Stu2 and Bim1 act cooperativel
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
152                        Others operate on the cytoplasmic microtubules to effect spindle and nuclear p
153       These findings support that nuclei use cytoplasmic microtubules to establish "cells within cell
154                    In response to defects of cytoplasmic microtubules to interact with the cell corte
155  the cell because they impede the ability of cytoplasmic microtubules to orient the spindle.
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
160                                Indeed, while cytoplasmic microtubules vanish, the spindle pole body (
161                                              Cytoplasmic microtubules were largely bundled, spindle a
162  cells with nuclear positioning defects, the cytoplasmic microtubules were misoriented and failed to
163 tic nuclei remained widely separated and the cytoplasmic microtubules were misoriented.
164       In contrast, in kip3Delta strains, the cytoplasmic microtubules were significantly longer than
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
167 itotic spindle depends on the interaction of cytoplasmic microtubules with the cell cortex.
168     Both movements depend on interactions of cytoplasmic microtubules with the cortex.
169 eriments demonstrate that the interaction of cytoplasmic microtubules with the Kar9p cortical attachm
170        It is the differential interaction of cytoplasmic microtubules with the mother and bud cortex

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