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1 nhibition of the minus-end microtubule motor cytoplasmic dynein .
2 for the minus-end-directed microtubule motor cytoplasmic dynein.
3 first specific small-molecule antagonists of cytoplasmic dynein.
4  of the cellular functions and regulation of cytoplasmic dynein.
5 f two ~300-kilodalton motor domains of yeast cytoplasmic dynein.
6 1 in the regulation of the microtubule motor cytoplasmic dynein.
7  interact directly with one another and with cytoplasmic dynein.
8 e force-dependent stepping behavior of yeast cytoplasmic dynein.
9 back to the cytoplasm (retrograde) driven by cytoplasmic dynein.
10 gene, which is involved in the regulation of cytoplasmic dynein.
11 d by myosin V, heterotrimeric kinesin-2, and cytoplasmic dynein.
12 directly modulates the enzymatic activity of cytoplasmic dynein.
13 orged between Lis1 and the microtubule motor cytoplasmic dynein.
14 amine the interaction of neurofilaments with cytoplasmic dynein.
15 s partially dependent on Aurora-A kinase and cytoplasmic dynein.
16 oposed to regulate the multiple functions of cytoplasmic dynein.
17 ormation through developmental regulation of cytoplasmic dynein.
18  forces on astral microtubules (MTs) through cytoplasmic dynein.
19  driven exclusively by the microtubule motor cytoplasmic dynein.
20                                              Cytoplasmic dynein 1 (dynein) is a minus end-directed mi
21                                          The cytoplasmic dynein 1 cargo binding domain is formed by f
22                Recent experiment showed that cytoplasmic dynein 1, a molecular motor responsible for
23                                          The cytoplasmic dynein-1 (dynein) motor plays a central role
24                                              Cytoplasmic dynein-1 (dynein-1) plays roles in mitosis a
25 t a previously unrecognized link between the cytoplasmic dynein-1 and IFT dynein-2 motors.
26 novel model by which stationary complexes of cytoplasmic dynein-1 are responsible for the shuttling o
27                                              Cytoplasmic dynein-1 binds dynactin and cargo adaptor pr
28                              In human cells, cytoplasmic dynein-1 is essential for long-distance tran
29           DYNC1H1 encodes the heavy chain of cytoplasmic dynein-1, a 1.4-MDa motor complex that traff
30 gical and genetic manipulation, we show that cytoplasmic dynein-1, which localizes to the junction be
31 essential cofactor for the microtubule motor cytoplasmic dynein-1.
32         The microtubule motors kinesin-2 and cytoplasmic dynein 1b drive IFT particles (protein compl
33 re, we report that the retrograde IFT motor, cytoplasmic dynein 1b, is required in the cytoplasm for
34 d smaller groups are returned to the base by cytoplasmic dynein 1b.
35 nt away from the flagellar tip is powered by cytoplasmic dynein 1b/2.
36 his identifies potential novel components of cytoplasmic dynein 2 and furthermore provides fresh insi
37 nts IFT88, the kinesin-II subunit KIF3A, and cytoplasmic dynein 2 appeared compromised.
38 , a mammalian homologue of the Chlamydomonas cytoplasmic dynein 2 intermediate chain that also locali
39 both requiring the ciliary retrograde motor, cytoplasmic dynein 2, for ciliary exit.
40  Wdr34 gene encodes an intermediate chain of cytoplasmic dynein 2, the motor for retrograde intraflag
41                                              Cytoplasmic dynein-2 (dynein-2) performs intraflagellar
42  the light intermediate chain (D2LIC) of the cytoplasmic dynein-2 complex are essential for retrograd
43                            Zebrafish lacking cytoplasmic dynein-2 function exhibited small eyes, kidn
44                                      Loss of cytoplasmic dynein-2 function resulted in a significant
45 the first time, that the dync2-i1 subunit of cytoplasmic dynein-2 is necessary for retrograde IFT.
46 y mutations in a new disease-producing gene, cytoplasmic dynein-2 light intermediate chain 1, DYNC2LI
47 e present the crystal structure of the human cytoplasmic dynein-2 motor bound to the ATP-hydrolysis t
48 nally, the ERG results indicate that loss of cytoplasmic dynein-2 reduces the photoreceptor light res
49 nd intermediate chain (dync2-i1) subunits of cytoplasmic dynein-2 were injected into zebrafish embryo
50 oreceptors lacking the retrograde IFT motor, cytoplasmic dynein-2.
51 ould be phenocopied by RNAi directed against cytoplasmic dynein, a known LIS1 interactor.
52 complex required for the in vivo function of cytoplasmic dynein, a microtubule (MT)-based motor.
53 1 and an interacting protein, NDEL1, bind to cytoplasmic dynein, a microtubule motor protein.
54 nhibitor nocodazole and by the inhibition of cytoplasmic dynein, a microtubule-associated motor prote
55                                              Cytoplasmic dynein, a microtubule-based motor protein, t
56 , Nudel/NudE, and dynactin are regulators of cytoplasmic dynein, a minus end-directed, microtubule (M
57                                              Cytoplasmic dynein, a minus-end-directed microtubule mot
58                                              Cytoplasmic dynein, a minus-end-directed microtubule mot
59 nding immunophilins that link the complex to cytoplasmic dynein, a molecular motor that processes alo
60  is central to the functional versatility of cytoplasmic dynein, a motor involved in intracellular tr
61 uggesting that dop is involved in regulating cytoplasmic dynein activity through direct or indirect m
62                         Here we identify the cytoplasmic dynein adaptor Spindly as an additional comp
63 bunit forms two separate complexes, one with cytoplasmic dynein ("aggregation complex") and one with
64                                 In addition, cytoplasmic dynein also depended on EBA to track on most
65 antibody-Fab tag to mark the position of the cytoplasmic dynein amino-terminal tail domain, as it eme
66                             Contacts between cytoplasmic dynein and astral microtubules (MTs) at the
67 r migration (INM) that is driven apically by cytoplasmic dynein and basally by the kinesin KIF1A, whi
68                                              Cytoplasmic dynein and dynactin interact to drive microt
69                                              Cytoplasmic dynein and dynactin participate in retrograd
70                        The microtubule motor cytoplasmic dynein and its activator dynactin drive vesi
71 the trafficking of TYR and Pmel17 depends on cytoplasmic dynein and its interaction with the spectrin
72                        The microtubule motor cytoplasmic dynein and its partner complex dynactin driv
73  implicated others [encoding neurofilaments, cytoplasmic dynein and its processivity factor dynactin,
74                                              Cytoplasmic dynein and kinesin are both microtubule-base
75 t, bidirectional capsid motility mediated by cytoplasmic dynein and kinesin during entry, whereas egr
76                                              Cytoplasmic dynein and kinesin I are both unidirectional
77                                              Cytoplasmic dynein and kinesin-1 are microtubule-based m
78 endosomes are transported bidirectionally by cytoplasmic dynein and kinesin-3, but how the movements
79 udEL are related proteins that interact with cytoplasmic dynein and LIS1.
80 1 in developing hair cells causes defects in cytoplasmic dynein and microtubule organization, resulti
81 precursor migration and the effects of LIS1, cytoplasmic dynein and myosin II inhibition.
82                     In Aspergillus nidulans, cytoplasmic dynein and NUDF/LIS1 are found at the spindl
83                               Dynactin links cytoplasmic dynein and other motors to cargo and is invo
84 in is a multiprotein complex that works with cytoplasmic dynein and other motors to support a wide ra
85 that kinesin-5 works in part by antagonizing cytoplasmic dynein and that these motor-driven forces fu
86 telomere attachment sites must be coupled to cytoplasmic dynein and the microtubule system to ensure
87 chain is a bona fide component of Drosophila cytoplasmic dynein and use P element excision to generat
88 ation activities associated with NuMA (i.e., cytoplasmic dynein) and HSET are not necessary for pole
89 d moved by microtubule motors (kinesin-1 and cytoplasmic dynein), and that binding of motors and move
90 sported by microtubule motors, kinesin-2 and cytoplasmic dynein, and an actin motor, myosin-V.
91 ransport machinery: specifically, kinesin-1, cytoplasmic dynein, and the dynein regulators Lis1 and d
92                                  Kinesin and cytoplasmic dynein are microtubule-based motor proteins
93               Using Saccharomyces cerevisiae cytoplasmic dynein as a model system, we mutagenized res
94                        Our studies implicate cytoplasmic dynein as a more thermally tunable motor and
95                    We identify Kinesin-1 and cytoplasmic dynein as major PrP(C) vesicle motor complex
96  are integral parts of the microtubule motor cytoplasmic dynein, as they directly associate with dyne
97 ts, but not control transcripts, recruit the cytoplasmic Dynein-associated co-factors Bicaudal D (Bic
98                       A single major form of cytoplasmic dynein associates with membranous organelles
99              We find that PKA phosphorylates cytoplasmic dynein at a novel site in light intermediate
100 itotic checkpoint protein and the anchor for cytoplasmic dynein at mitotic kinetochores, though it is
101 ons to model the molecular motor function of cytoplasmic dynein at the single-molecule level.
102    Dynamitin is a commonly used inhibitor of cytoplasmic dynein-based motility in living cells.
103 rotubules are polarity sorted in the axon by cytoplasmic dynein but that additional factors are also
104                    The velocity of mammalian cytoplasmic dynein, but not of mammalian kinesin-1, exhi
105  cellular functions of the microtubule motor cytoplasmic dynein, but the mechanism by which dynactin
106  in vivo evidence that distinct mutations in cytoplasmic dynein can either result in a pure sensory n
107 l trap, we were now able to demonstrate that cytoplasmic dynein can generate a discrete power stroke
108 tubule movements so that polarity sorting by cytoplasmic dynein can occur in a manner unimpeded by ot
109 ncoding the heavy chain subunit (DYNC1H1) of cytoplasmic dynein cause spinal muscular atrophy with lo
110       Converging studies suggest it requires cytoplasmic dynein, cell polarity genes, and microtubule
111                The microtubule motor protein cytoplasmic dynein clusters into a ring at the synapse,
112 at mutations in the minus-end-directed motor cytoplasmic dynein, completely block the increased DCVs
113 microtubule transport, the recombinant human cytoplasmic dynein complex is an active, microtubule min
114 n performed either with the native mammalian cytoplasmic dynein complex purified from tissue or, more
115             Here, we reconstitute a complete cytoplasmic dynein complex using recombinant human subun
116 ssed by disrupting the retrograde motor, the cytoplasmic dynein complex.
117 ays demonstrate that Bub3 interacts with the cytoplasmic dynein complex.
118 his nomenclature recognizes the two distinct cytoplasmic dynein complexes and has the flexibility to
119 n used in the literature for the subunits of cytoplasmic dynein complexes.
120                      We find that Drosophila cytoplasmic dynein components are direct PKA phosphoryla
121 essing of tagged and truncated Dictyostelium cytoplasmic dynein constructs, we show that the heart of
122 TrkB) signaling endosomes are transported by cytoplasmic dynein containing the neuron-specific IC-1B
123                           The heavy chain of cytoplasmic dynein contains four nucleotide-binding doma
124 minus-end directed microtubule motor protein cytoplasmic dynein contributes to many aspects of cell d
125 sitive to the addition of ATP, a hallmark of cytoplasmic dynein-dependent microtubule interactions.
126                 Specifically, MPP+ increased cytoplasmic dynein-dependent retrograde FAT and reduced
127 crotubule-associated proteins (MAPs) but not cytoplasmic dynein-depleted MAPs.
128 n of kinesin-1 (KLC1) and the heavy chain of cytoplasmic dynein (DHC1) on vesicles.
129 o measure stall forces of both kinesin-1 and cytoplasmic dynein-driven lipid droplets in Drosophila e
130 r et al. and Hashimoto-Tane et al. show that cytoplasmic dynein drives microcluster centralization al
131                                              Cytoplasmic dynein drives the majority of minus end-dire
132 ei migrate basally during G1, apically using cytoplasmic dynein during G2, and undergo mitosis at the
133                                              Cytoplasmic dynein, dynactin, and pericentrin are all re
134                           Single kinesin and cytoplasmic dynein-dynactin molecules fused with green-f
135  mutation in p150(Glued), a component of the cytoplasmic dynein/dynactin microtubule motor complex, r
136 of either kinesin-1 (kinesin heavy chain) or cytoplasmic dynein (dynein heavy chain) by RNA interfere
137                                 In contrast, cytoplasmic dynein efficiently navigates both axons and
138 , hexon, directly recruits the motor protein cytoplasmic dynein following virion entry.
139 plicated in targeting and binding cargoes to cytoplasmic dynein for retrograde or apical transport.
140 ond switch, depending on magnesium, converts cytoplasmic dynein from a nonprocessive to a processive
141      Bipolar spindle fusion was blocked when cytoplasmic dynein function was perturbed, suggesting a
142                                              Cytoplasmic dynein functions at several sites during mit
143                                              Cytoplasmic dynein functions in the checkpoint, apparent
144 ducts of the 6 kinesin gene family and the 1 cytoplasmic dynein gene.
145                                              Cytoplasmic dynein has been implicated in diverse mitoti
146  The microtubule-associated molecular motor, cytoplasmic dynein, has been implicated in the retrograd
147           A few small-molecule inhibitors of cytoplasmic dynein have been identified.
148 ioning in different systems, associates with cytoplasmic dynein heavy chain (DYNC1H1) in a Galphai-re
149  comprises different subunits assembled on a cytoplasmic dynein heavy chain 1 (DYNC1H1) dimer.
150 ant, c.917A>G, in DYNC1H1, which encodes the cytoplasmic dynein heavy chain 1 (here, novel refers to
151 to identify a nine base-pair deletion in the cytoplasmic dynein heavy chain 1 gene (Dync1h1) in this
152   The library was examined for inhibition of cytoplasmic dynein heavy chain and cell growth.
153                         Partial depletion of cytoplasmic dynein heavy chain by RNA interference block
154 le-stimulated ATPase activity of recombinant cytoplasmic dynein heavy chain motor domain.
155  of CLIPA, green fluorescent protein-labeled cytoplasmic dynein heavy chain, p150(Glued) dynactin, an
156 ganelle movement by conventional kinesin and cytoplasmic dynein in a cell.
157 n hexon recruits the molecular motor protein cytoplasmic dynein in a pH-dependent manner, a function
158                     FAK also associated with cytoplasmic dynein in a Ser-732 phosphorylation-dependen
159                       Functional analysis of cytoplasmic dynein in Caenorhabditis elegans has reveale
160  RNA interference to investigate the role of cytoplasmic dynein in powering these transport events.
161                  These immunophilins link to cytoplasmic dynein indirectly through the association of
162 at both Hook1 and Hook3 effectively activate cytoplasmic dynein, inducing longer run lengths and high
163 d a genomic region that contained DYNC2H1, a cytoplasmic dynein involved in retrograde transport in t
164                                              Cytoplasmic dynein is a 1.2-MDa multisubunit motor prote
165                                              Cytoplasmic dynein is a complex containing heavy chains
166                                              Cytoplasmic dynein is a dimeric AAA(+) motor protein tha
167                                              Cytoplasmic dynein is a dimeric motor that transports in
168                                              Cytoplasmic dynein is a homodimeric AAA+ motor that tran
169                                              Cytoplasmic dynein is a homodimeric microtubule (MT) mot
170                                              Cytoplasmic dynein is a large minus end-directed motor c
171                                              Cytoplasmic dynein is a large multisubunit complex invol
172                                              Cytoplasmic dynein is a large multisubunit motor protein
173                                              Cytoplasmic dynein is a large, microtubule-dependent mol
174                                              Cytoplasmic dynein is a microtubule motor involved in ca
175                                              Cytoplasmic dynein is a microtubule-based molecular moto
176                                              Cytoplasmic dynein is a microtubule-based motor protein
177                                              Cytoplasmic dynein is a microtubule-based motor protein
178                                              Cytoplasmic dynein is a microtubule-based motor required
179                                              Cytoplasmic dynein is a minus-end-directed microtubule m
180                                              Cytoplasmic dynein is a molecular motor responsible for
181                                              Cytoplasmic dynein is a molecular motor that transports
182                                              Cytoplasmic dynein is a motor protein that walks along m
183                                              Cytoplasmic dynein is a multisubunit microtubule motor c
184 in vivo and in vitro, we found evidence that cytoplasmic dynein is active during minus- and plus-end
185                                              Cytoplasmic dynein is an abundant kinetochore protein wh
186  Here, we report that the stalk shaft of rat cytoplasmic dynein is an antiparallel alpha-helical coil
187                                              Cytoplasmic dynein is an approximately 1.4 MDa multi-pro
188                                              Cytoplasmic dynein is an enormous minus end-directed mic
189                  The functional diversity of cytoplasmic dynein is in part attributed to multiple int
190                                              Cytoplasmic dynein is involved in a multitude of essenti
191                                              Cytoplasmic dynein is involved in a wide range of cellul
192                        In higher eukaryotes, cytoplasmic dynein is involved in silencing the SAC by r
193  endosomes from the axon to the cell body by cytoplasmic dynein is necessary for axonal and neuronal
194                                              Cytoplasmic dynein is particularly important for neurons
195                                      Whereas cytoplasmic dynein is primarily known as a minus-end-dir
196         Previous studies have suggested that cytoplasmic dynein is required for efficient neurofilame
197                   Furthermore, we found that cytoplasmic dynein is required for the spindle pole accu
198                                              Cytoplasmic dynein is responsible for a wide range of ce
199                                              Cytoplasmic dynein is responsible for many aspects of ce
200                          The molecular motor cytoplasmic dynein is responsible for most minus-end-dir
201     The minus end-directed microtubule motor cytoplasmic dynein is responsible for the intracellular
202                                              Cytoplasmic dynein is responsible for transport of sever
203                                              Cytoplasmic dynein is the main retrograde motor in all e
204                                              Cytoplasmic dynein is the major microtubule minus end-di
205                                              Cytoplasmic dynein is the major microtubule minus-end-di
206                                              Cytoplasmic dynein is the major minus end-directed micro
207                                              Cytoplasmic dynein is the major motor protein responsibl
208                                              Cytoplasmic dynein is the molecular motor responsible fo
209         We have previously demonstrated that cytoplasmic dynein is the motor involved in the perinucl
210                                              Cytoplasmic dynein is the motor protein responsible for
211                                              Cytoplasmic dynein is the multisubunit motor protein for
212                                              Cytoplasmic dynein is the multisubunit protein complex r
213                                              Cytoplasmic dynein is the predominant minus-end-directed
214                                              Cytoplasmic dynein is the primary minus-end-directed mic
215                                              Cytoplasmic dynein is the primary molecular motor respon
216                                              Cytoplasmic dynein is well characterized as an organelle
217                        Previously, the 8-kDa cytoplasmic dynein light chain (LC8) was demonstrated to
218 ture of isoform 1 of the mouse Roadblock/LC7 cytoplasmic dynein light chain (robl1_mouse) by NMR spec
219 nal kinesin, reductions in the levels of the cytoplasmic dynein light chain Tctex type 3 subunit were
220              In this paper, we show that the cytoplasmic dynein light chain Tctex-1 plays a key role
221  studies, we show that in rodents Tctex-1, a cytoplasmic dynein light chain, is selectively enriched
222                        Dominant mutations in cytoplasmic dynein (Loa or Cra) have been reported to pr
223  MTOC, in which the minus end-directed motor cytoplasmic dynein, localized at the synapse through an
224   This is especially important for mammalian cytoplasmic dyneins, many subunits of which are encoded
225  is a highly conserved protein necessary for cytoplasmic dynein-mediated nuclear migration in Aspergi
226 say was used to evaluate the hypothesis that cytoplasmic dynein mediates AAV interaction with microtu
227                                              Cytoplasmic dynein mediates retrograde transport in axon
228                                              Cytoplasmic dynein mediates spindle orientation from the
229                                              Cytoplasmic dynein mediates spindle positioning in buddi
230   Recently, an x-ray structure of the murine cytoplasmic dynein microtubule binding domain (MTBD) in
231  a mutation in dhc-1, the heavy chain of the cytoplasmic dynein minus-end directed microtubule motor,
232 along microtubules is powered by kinesin and cytoplasmic dynein molecular motors.
233                                              Cytoplasmic dynein motility along microtubules is critic
234 ight chain LC8 is an integral subunit of the cytoplasmic dynein motor complex that binds directly to
235      Tctex-1, a light-chain component of the cytoplasmic dynein motor complex, can function independe
236                        We show that a single cytoplasmic dynein motor frequently transitions into an
237                                          The cytoplasmic dynein motor generates pulling forces to cen
238 ion of a specific role for these proteins in cytoplasmic dynein motor regulation has remained elusive
239 lization to elucidate relative kinesin-1 and cytoplasmic dynein motor subunit composition of individu
240         Dynactin is an essential part of the cytoplasmic dynein motor that enhances motor processivit
241 , dynactin, is an essential component of the cytoplasmic dynein motor.
242          Our data also suggest kinesin-1 and cytoplasmic dynein motors assemble in stable mixtures on
243 re under the influence of forces mediated by cytoplasmic dynein motors associated with the cell corte
244  MTs to test the hypothesis that immobilized cytoplasmic dynein motors transport short MTs with their
245                                     Metazoan cytoplasmic dynein moves processively along microtubules
246                                              Cytoplasmic dynein moves processively along microtubules
247                     Our results suggest that cytoplasmic dynein moves processively through the coordi
248  microtubules in the cell periphery, whereas cytoplasmic dynein moves to the minus ends in the cell c
249 We report the crystal structure of the mouse cytoplasmic dynein MTBD and a portion of the coiled coil
250 single molecule motility properties of yeast cytoplasmic dynein mutants bearing mutations that preven
251  (chromokinesin and Eg5) and minus-directed (cytoplasmic dynein oligomers) motors walking on microtub
252 litates the localization of Mcp5 and that of cytoplasmic dynein on the membrane.
253 y distribution of melanosomes transported by cytoplasmic dynein or kinesin-2 under conditions of aggr
254 terfering RNA (siRNA)-mediated inhibition of cytoplasmic dynein or the kinesin 1 heavy chain KIF5B de
255                              Proteins in the cytoplasmic dynein pathway accumulate at the microtubule
256                                              Cytoplasmic dynein performs multiple cellular tasks but
257  phenotype than the control, indicating that cytoplasmic dynein plays a role in chromosome segregatio
258                                              Cytoplasmic dynein plays important roles in membrane tra
259           During mitosis, the motor molecule cytoplasmic dynein plays key direct and indirect roles i
260                                              Cytoplasmic dynein powers intracellular movement of carg
261                     In axons of PNS neurons, cytoplasmic dynein provides force for retrograde movemen
262 e compelling evidence that the motor protein cytoplasmic dynein provides the necessary force for micr
263                        The AAA+ ATPase motor cytoplasmic dynein regulates ciliary trafficking, mitoti
264 erkinetic nuclear migration, consistent with cytoplasmic dynein regulation.
265                          We propose that the cytoplasmic dynein regulators are a critical component o
266   It is specifically blocked by RNAi for the cytoplasmic dynein regulators LIS1 and NudE/L (Nde1/Ndel
267                                          The cytoplasmic dynein regulatory factor Lis1, which induces
268                                Kinesin-1 and cytoplasmic dynein require each other for bidirectional
269             The spindle pole localization of cytoplasmic dynein requires the function of the anaphase
270  motor axons are kinesin-1 (anterograde) and cytoplasmic dynein (retrograde), and interestingly that
271                                Regulation of cytoplasmic dynein's motor activity is essential for div
272 cture we are able to draw new conclusions on cytoplasmic dynein's stepping mechanism.
273 motor, the function of NUDF is important for cytoplasmic dynein's targeting to the spindle poles.
274           In contrast, the velocity of yeast cytoplasmic dynein showed a break from Arrhenius behavio
275                        RNAi directed against cytoplasmic dynein specifically inhibited nuclear moveme
276           We propose names for the mammalian cytoplasmic dynein subunit genes and proteins that refle
277 ctions in levels of conventional kinesin and cytoplasmic dynein subunits were recapitulated in a rat
278 is a highly conserved light-chain subunit of cytoplasmic dynein that interacts with a wide variety of
279                                              Cytoplasmic dynein, the 1.2 MDa motor driving minus-end-
280 an interaction between the microtubule motor cytoplasmic dynein, the adenomatous polyposis coli tumor
281  contain a large number of kinesins but lack cytoplasmic dynein, the foremost processive retrograde t
282                                              Cytoplasmic dynein, the major motor driving retrograde a
283 orted to regulate the mechanical behavior of cytoplasmic dynein, the primary minus-end-directed micro
284                               The ability of cytoplasmic dynein to recognize such diverse forms of ca
285  binding to Trk initiates the recruitment of cytoplasmic dynein to signaling endosomes through ERK1/2
286 es attachment of the microtubule-based motor cytoplasmic dynein to the cortex, where it exerts a pull
287  nuclear INT complex promotes recruitment of cytoplasmic dynein to the NE, possibly via a mechanism i
288 pAR63, nearly eliminates the localization of cytoplasmic dynein to the spindle poles, but it has no a
289       To do this, we fused the MTBD of mouse cytoplasmic dynein, together with 12-36 residues of its
290                                              Cytoplasmic dynein transports cargoes for a variety of c
291                                              Cytoplasmic dynein transports membranous cargoes along m
292                                              Cytoplasmic dynein transports various cellular cargoes i
293     The minus end-directed microtubule motor cytoplasmic dynein transports various cellular cargoes,
294 s proplatelet elongation and is dependent on cytoplasmic dynein under static and physiological shear
295                        The microtubule motor cytoplasmic dynein was a critical part of this coalescin
296                    In view of new results on cytoplasmic dynein, we attempt to rationalize how these
297 s varying DNA sequences, and to myosin V and cytoplasmic dynein, which may advance by variable increm
298 sitioning, are mediated by the motor protein cytoplasmic dynein, which produces force on the microtub
299     We also predict that acute inhibition of cytoplasmic dynein will disrupt the polarity sorting of
300 oups of motor proteins, such as kinesins and cytoplasmic dynein, work together to ensure the supply a

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