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1  of BIM1 eliminated Kar9p localization along cytoplasmic microtubules.
2  the cell, often coincident with the ends of cytoplasmic microtubules.
3 im1p localizes to dots at the distal ends of cytoplasmic microtubules.
4  envelope proteins, such as SUN-1, to access 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 d other chemical treatments that disassemble cytoplasmic microtubules.
13 onemes to stabilize flagellar beat or within cytoplasmic microtubules.
14 ses of the cell cycle, connecting the DSB to cytoplasmic microtubules.
15  and flagellar enrichment are facilitated by cytoplasmic microtubules.
16 f Drosophila melanogaster that depolymerizes cytoplasmic microtubules.
17  interact with the nuclear envelope (NE) and cytoplasmic microtubules.
18  microtubules without significantly altering cytoplasmic microtubules.
19 rtant for the organization/nucleation of all cytoplasmic microtubules.
20  oogenesis for the structure and function of cytoplasmic microtubules.
21 onfunctional spindle poles or the absence of cytoplasmic microtubules.
22 tion of KAR3 leads to a dramatic increase in cytoplasmic microtubules, a phenotype which is most pron
23 ether, we propose that kinesin-1 slides free cytoplasmic microtubules against cortically immobilized
24                           In yeast, oriented cytoplasmic microtubules align the mitotic spindle betwe
25 of dynein-green fluorescent protein (GFP) to cytoplasmic microtubules allowed us to obtain one of the
26 ther and bud via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud.
27 her-bud neck via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud.
28 somal region, induces profound disruption of cytoplasmic microtubules and a nuclear distortion phenot
29  In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed
30 ates, repair-protein condensates, nuclear or cytoplasmic microtubules and actin filaments, kinesin or
31 tribution but retain the ability to organize cytoplasmic microtubules and actin in anucleate hyphae.
32 ing of the mitotic spindle requires both the cytoplasmic microtubules and actin.
33 lights a framework for communication between cytoplasmic microtubules and chromatin.
34 ivity resulted in assembly of unusually long cytoplasmic microtubules and defects in spindle position
35        These bidirectional movements require cytoplasmic microtubules and microfilaments and depend o
36 uring mitosis, leading to the coexistence of cytoplasmic microtubules and nuclear spindles with massi
37 sembly of subdistal appendages, which anchor cytoplasmic microtubules and prime the mother centriole
38 iae that is mediated by interactions between cytoplasmic microtubules and the cell cortex.
39  in fungi have been shown to be dependent on cytoplasmic microtubules and the microtubule-associated
40 t depends on persistent interactions between cytoplasmic microtubules and the mother-bud neck, the fu
41 3], but the rapid apical enrichment requires cytoplasmic microtubules and the retrograde IFT motor, d
42 tes with an apico-basally polarized array of cytoplasmic microtubules, and returns to the cell surfac
43 show that Myo2 localizes to the plus ends of cytoplasmic microtubules, and that the rate of movement
44                    Secondly, abnormally long cytoplasmic microtubules appear that do not stop at the
45                                              Cytoplasmic microtubules are critical for establishing a
46                           Here, we show that cytoplasmic microtubules are mechanically coupled to the
47                                     In vivo, cytoplasmic microtubules are nucleated and anchored by t
48                        Consistent with this, cytoplasmic microtubules are often highly curved and app
49  yeast Schizosaccharomyces pombe, interphase cytoplasmic microtubules are organized into antiparallel
50                    Our findings suggest that cytoplasmic microtubules are used to monitor the locatio
51 portant for establishing a normal interphase cytoplasmic microtubule array.
52                              At 30 degrees C cytoplasmic microtubule arrays are abnormal and bundle i
53 rmal mitotic spindles and some have abnormal cytoplasmic microtubule arrays.
54 layed unusually long and numerous bundles of cytoplasmic microtubules as revealed by immunofluorescen
55  targeted to the distal plus ends of dynamic cytoplasmic microtubules, as is HC, and their targeting
56 t anaphase onset, the FEAR pathway activates cytoplasmic microtubule-associated forces that facilitat
57 d lack of TINA causes enhanced production of cytoplasmic microtubules at metaphase arrest, we suggest
58 osaccharomyces pombe, longitudinal arrays of cytoplasmic microtubule bundles regulate cell polarity a
59     A simple self-assembly pathway generates cytoplasmic microtubule bundles that can locate the cell
60 lpha 85E does not disrupt meiotic spindle or cytoplasmic microtubules but causes defects in morphogen
61 g a stochastic simulation that confirms that cytoplasmic microtubules can compete with flagella for a
62 stent with Bud6's role as a cortical cue for cytoplasmic microtubule capture.
63 other- bud axis through interactions between cytoplasmic microtubules (CMs) and the cell cortex.
64         The 'cMT-bud neck model' posits that cytoplasmic microtubule (cMT)-bud neck interactions prev
65  to the conclusion that biased nucleation of cytoplasmic microtubules (cMTs) is essential for directi
66 ughter cell by linking the associated set of cytoplasmic microtubules (cMTs) to the polarized actin n
67 sponsible for establishing cell polarity and cytoplasmic microtubules collaborate to establish MEN as
68 pression of the entire SPC72 results in more cytoplasmic microtubules compared with wild-type.
69 ed to returned to interphase retain a normal cytoplasmic microtubule complex.
70 st cell elongates toward its mating partner, cytoplasmic microtubules connect the nucleus to the cell
71 rity relies on a precise temporal program of cytoplasmic microtubule-cortex interactions throughout s
72                     Naegleria amoebae lack a cytoplasmic microtubule cytoskeleton and assemble microt
73                        The average number of cytoplasmic microtubules decreased from 3 in wild-type t
74                         This correlated with cytoplasmic microtubule defects.
75  induced rapid, anterograde IFT-independent, cytoplasmic microtubule-dependent redistribution of the
76                           Stathmin (STMN), a cytoplasmic microtubule-destabilizing phosphoprotein, re
77 Saccharomyces cerevisiae cells lacking She1, cytoplasmic microtubules detach from the spindle pole bo
78 lagellar transport and cargo transport along cytoplasmic microtubules, differ from motors in the cano
79                                In germlings, cytoplasmic microtubules disassembled completely in mito
80 ghout the vegetative cell cycle as they bind cytoplasmic microtubules during interphase, spindle micr
81 nation of metachronic cilia beating, whereas cytoplasmic microtubule dynamics are required for local
82     Our findings highlight the regulation of cytoplasmic microtubule dynamics as a role of the IFT54
83                             The reduction in cytoplasmic microtubule dynamics is due primarily to dec
84                    The pattern and extent of cytoplasmic microtubule dynamics modulation through the
85 highly conserved EB1 family, Bim1p, promotes cytoplasmic microtubule dynamics specifically during G1.
86                    These movements depend on cytoplasmic microtubules emanating from the nuclei that
87 oncentrate at cell ends by attaching it to a cytoplasmic microtubule end-binding protein.
88 chanism to delay cell cycle progression when cytoplasmic microtubules fail to orient the spindle.
89 gests a model in which flagella compete with cytoplasmic microtubules for a fixed pool of tubulin, wi
90 lium, with Gli2 but not Smo requiring intact cytoplasmic microtubules for ciliary entry and both requ
91  that a novel complex links the nucleus with cytoplasmic microtubules for the promotion of DNA repair
92         To ensure proper mitotic spindle and cytoplasmic microtubule formation, the cell must maintai
93 leted variant of SPC72 (DeltaN-SPC72) impair cytoplasmic microtubule formation.
94  cells, mitotic exit was preceded by loss of cytoplasmic microtubules from the neck.
95 f TINA enhanced the nucleation of bundles of cytoplasmic microtubules from the spindle pole bodies.
96         Removal of the forces exerted by the cytoplasmic microtubules had no effect on fragmentation.
97  Although effects of XMAP215/TOG proteins on cytoplasmic microtubules have not previously been shown
98  functions to limit the number and length of cytoplasmic microtubules in a cell cycle-specific manner
99 ons essential to mitosis and organization of cytoplasmic microtubules in addition to its well-documen
100  nuclear distribution phenotype but affected cytoplasmic microtubules in an unexpected manner.
101 ion of Stu2p leads to fewer and less dynamic cytoplasmic microtubules in both G1 and preanaphase cell
102                  We also identify defects in cytoplasmic microtubules in both the germ and follicle c
103 tion of microtubules in vitro and stabilizes cytoplasmic microtubules in heterologous cells.
104 assembly and cause breakdown of preassembled cytoplasmic microtubules in human polymorphonuclear leuk
105                      EB1 colocalized both to cytoplasmic microtubules in interphase cells and to spin
106          By indirect immunofluorescence, the cytoplasmic microtubules in kip2Delta were consistently
107  a similar process plays a role in orienting cytoplasmic microtubules in mating yeast cells.
108 , the bni1Delta mutant exhibited misoriented cytoplasmic microtubules in shmoos.
109  localized to the plus ends (distal tips) of cytoplasmic microtubules in the bud.
110 unctions without Lte1p and apparently senses cytoplasmic microtubules in the mother/bud neck [7-9].
111 avy chain Dyn1 also localized to the tips of cytoplasmic microtubules in wild-type cells.
112 nd yeast cells, this process is dependent on cytoplasmic microtubules interacting with the cortical a
113              By indirect immunofluorescence, cytoplasmic microtubules intersected the GFP-Kar9p dot.
114  and cell polarization, as well as Kar9p and cytoplasmic microtubule localization.
115 niversal function of kinesin-1 is to mediate cytoplasmic microtubule-microtubule sliding.
116                   These results suggest that cytoplasmic microtubules might be arranged with plus end
117              beta4B-tubulin was localized to cytoplasmic microtubules, mitotic spindles, manchette, a
118                                          The cytoplasmic microtubule modulator RanBP10 is a Ran and b
119                                              Cytoplasmic microtubules (MTs) continuously grow and sho
120                                              Cytoplasmic microtubules (MTs) continuously grow and sho
121 evisiae kinesin-14 that functions to shorten cytoplasmic microtubules (MTs) during yeast mating yet m
122        CB also disrupted the organization of cytoplasmic microtubules (MTs) in stage VI oocytes.
123                      The ability to nucleate cytoplasmic microtubules (MTs) is a property of the surr
124                                              Cytoplasmic microtubules (MTs) serve as a rate-limiting
125 osome positioning requires a radial array of cytoplasmic microtubules (MTs) that can exert pushing or
126                   Polarized radial arrays of cytoplasmic microtubules (MTs) with minus ends clustered
127 n fission yeast (Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the sp
128                          They have a reduced cytoplasmic microtubule network and display severe morph
129 d molecular motors and they travel along the cytoplasmic microtubule network towards the minus end of
130 iod marked by dramatic reorganization of the cytoplasmic microtubule network, endogenous MLK3 transie
131 nters establish transient connections to the cytoplasmic microtubule network.
132  knockdown causes the disorganization of the cytoplasmic microtubule network.
133  KIF3A but not by chemical disruption of the cytoplasmic microtubule network.
134        Furthermore, in the bim1 mutants, the cytoplasmic microtubules no longer intersected the corti
135  in fission yeast Schizosaccharomyces pombe, cytoplasmic microtubule nucleation ceases simultaneously
136                                              Cytoplasmic microtubule nucleation in fission yeast depe
137 rmation of these microtubule bundles include cytoplasmic microtubule nucleation, microtubule release
138 ein is targeted to the dynamic plus end of a cytoplasmic microtubule, offloads to the cortex, becomes
139 nclude that Kar9p's function is specific for cytoplasmic microtubule orientation and that Kar9p's rol
140                 In fission yeast, interphase cytoplasmic microtubules originate from poorly character
141 important to prevent excessive detachment of cytoplasmic microtubules, particularly in G1 cells.
142         Unexpectedly, BBIP10 is required for cytoplasmic microtubule polymerization and acetylation,
143  tip-ward movement is similar to the rate of cytoplasmic microtubule polymerization toward the hyphal
144                 Thus, SPBs are able to sense cytoplasmic microtubule properties and regulate the Bfa1
145                        Further, Kms1 and the cytoplasmic microtubule regulator Mto1 promote the repai
146                              The behavior of cytoplasmic microtubules revealed distinct interactions
147 2, bld1 mutants have normal basal bodies and cytoplasmic microtubule rootlets.
148 ted tubulin pool, showing that alteration of cytoplasmic microtubule severing could be sufficient to
149                           We further observe cytoplasmic microtubule sliding in Xenopus and Ptk2 cell
150                                           On cytoplasmic microtubules, Stu2 and Bim1 act cooperativel
151 cells lack cytoplasmic microtubules; the few cytoplasmic microtubules that are observed are excessive
152 ch a highly elastic nucleus is surrounded by cytoplasmic microtubules that behave as a jelly-like vis
153 oison thiabendazole and have abnormally long cytoplasmic microtubules that can curl around the ends o
154 ubules anchored to the actin cortex and free cytoplasmic microtubules that moved in the ooplasm.
155    In addition, most spc72 mutant cells lack cytoplasmic microtubules; the few cytoplasmic microtubul
156     Klp5p-GFP and Klp6p-GFP both localize to cytoplasmic microtubules throughout the cell cycle and t
157 alization studies found Kip2p exclusively on cytoplasmic microtubules throughout the cell cycle, wher
158 marker protein, Tea1, that is transported by cytoplasmic microtubules to cell tips and recruits other
159                        Others operate on the cytoplasmic microtubules to effect spindle and nuclear p
160       These findings support that nuclei use cytoplasmic microtubules to establish "cells within cell
161                    In response to defects of cytoplasmic microtubules to interact with the cell corte
162  the cell because they impede the ability of cytoplasmic microtubules to orient the spindle.
163 ules, and that the rate of movement of these cytoplasmic microtubules to the bud neck depends on the
164 elative contributions of the kinetochore and cytoplasmic microtubules to the forces involved in forma
165  mutants retain the ability to generate long cytoplasmic microtubule tracks, suggesting that the nucl
166 rc activity regulates the transition between cytoplasmic microtubule transport and actin-based motili
167                                Indeed, while cytoplasmic microtubules vanish, the spindle pole body (
168                                              Cytoplasmic microtubules were largely bundled, spindle a
169  cells with nuclear positioning defects, the cytoplasmic microtubules were misoriented and failed to
170 tic nuclei remained widely separated and the cytoplasmic microtubules were misoriented.
171       In contrast, in kip3Delta strains, the cytoplasmic microtubules were significantly longer than
172 e pole body (SPB), organizes the nuclear and cytoplasmic microtubules which are functionally and spat
173 ver, alp16 deletion displays abnormally long cytoplasmic microtubules, which curve around the cell ti
174 itotic spindle depends on the interaction of cytoplasmic microtubules with the cell cortex.
175     Both movements depend on interactions of cytoplasmic microtubules with the cortex.
176 eriments demonstrate that the interaction of cytoplasmic microtubules with the Kar9p cortical attachm
177        It is the differential interaction of cytoplasmic microtubules with the mother and bud cortex

 
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